Bone Marrow Aspirate Concentrate-Enhanced Marrow Stimulation of Chondral Defects

Madry, Henning; Gao, Liang; Eichler, Hermann; Orth, Patrick; Cucchiarini, Magali

doi:https://doi.org/10.1155/2017/1609685

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Volume 2017 | Article ID 1609685 | https://doi.org/10.1155/2017/1609685

Bone Marrow Aspirate Concentrate-Enhanced Marrow Stimulation of Chondral Defects

Henning Madry,^1,2Liang Gao,¹Hermann Eichler,³Patrick Orth,^1,2and Magali Cucchiarini¹

Academic Editor: Mitsuo Ochi

Received29 Jan 2017

Revised15 Mar 2017

Accepted12 Apr 2017

Published18 May 2017

Abstract

Mesenchymal stem cells (MSCs) from bone marrow play a critical role in osteochondral repair. A bone marrow clot forms within the cartilage defect either as a result of marrow stimulation or during the course of the spontaneous repair of osteochondral defects. Mobilized pluripotent MSCs from the subchondral bone migrate into the defect filled with the clot, differentiate into chondrocytes and osteoblasts, and form a repair tissue over time. The additional application of a bone marrow aspirate (BMA) to the procedure of marrow stimulation is thought to enhance cartilage repair as it may provide both an additional cell population capable of chondrogenesis and a source of growth factors stimulating cartilage repair. Moreover, the BMA clot provides a three-dimensional environment, possibly further supporting chondrogenesis and protecting the subchondral bone from structural alterations. The purpose of this review is to bridge the gap in our understanding between the basic science knowledge on MSCs and BMA and the clinical and technical aspects of marrow stimulation-based cartilage repair by examining available data on the role and mechanisms of MSCs and BMA in osteochondral repair. Implications of findings from both translational and clinical studies using BMA concentrate-enhanced marrow stimulation are discussed.

1. Introduction

Mesenchymal stem cells (MSCs) play a key role in articular cartilage repair. MSCs have multilineage differentiation potential, allowing them to differentiate, for example, into chondrocytes and osteoblasts, the key cells from the two tissues that constitute the osteochondral unit. They were first isolated from the bone marrow, and the potency of MSCs is currently being employed in the techniques of marrow stimulation for symptomatic small chondral defects. If bone marrow fills a cartilage defect either as a result of marrow stimulation for chondral defects or the course of the spontaneous repair of osteochondral defects, a bone marrow clot forms within the cartilage defect. Pluripotent MSCs from the subchondral bone marrow are subsequently mobilized, migrate into the defect filled with the clot, and differentiate into chondrocytes and osteoblasts. Over time, they form a fibrocartilaginous repair tissue in the defect and close the connection with the subchondral bone.

Bone marrow stem cells have been successfully transformed into several cell types among which chondrocytes, osteoblasts, adipocytes, angioblasts [1], and neural cells [2], to potentially be used to treat a variety of illnesses [3–6]. In the orthopaedic field, additional application of a bone marrow aspirate (BMA) to the procedure of marrow stimulation has been recently studied, since the bone marrow itself is both a source of MSCs, providing a cell population capable of chondrogenesis and of various growth factors stimulating cartilage repair [7–10]. Moreover, the bone marrow clot provides a three-dimensional (3D) environment which supports the chondrogenesis of MSCs. Finally, it is possible that it protects the subchondral bone plate and the subarticular spongiosa from structural alterations of its microarchitecture.

In contrast to the cost- and labor-intensive cultivation and propagation of cells such as MSCs or articular chondrocytes, the clinical use of “minimally processed” autologous BMA that can be prepared in the operation room as a single-step procedure appears straightforward. Native and concentrated BMA have been intensively studied in the context of articular cartilage repair. Such enhanced techniques of marrow stimulation have been shown to improve articular cartilage repair in both animal models and patients.

The purpose of this review is to bridge the gap in our understanding between the basic science knowledge about MSCs and BMA on one side and the clinical and technical aspects of marrow stimulation-based cartilage repair on the other side by examining available data on the role and mechanisms of MSCs and BMA in osteochondral repair. A focus is on the steps of mobilization of cells from the subchondral bone and repair tissue formation, including adherence of the bone marrow clot to the subchondral bone. The implications of findings from both translational and clinical studies using BMA concentrate-enhanced marrow stimulation are also discussed.

2. Marrow Stimulation-Based Cartilage Repair

Marrow stimulation techniques are the most important first-line treatment options for small symptomatic articular cartilage defects [11]. Their principle is to establish a communication of the cartilage defect with the subchondral bone marrow compartment (Figure 1). First, the cartilage defect is surgically prepared in a meticulous fashion, including removal of cartilage fragments and generation of stable and vertically oriented margins of the peripheral cartilage. The next step is the preparation of the bony defect base. Here, the entire calcified cartilage layer has to be removed, thereby exposing the superficial part of the subchondral bone plate without damaging it.

Figure 1

Principle of bone marrow aspirate concentrate- (BMAC-) enhanced marrow stimulation. (a) Schematic view of a full-thickness focal chondral defect. (b) Marrow stimulation can be performed with microfracture (b1), subchondral drilling (b2), or abrasion arthroplasty (b3). The subchondral bone plate can be perforated with a microfracture awl (microfracture), a Kirschner wire or a drill bit (subchondral drilling), or a motorized burr (abrasion arthroplasty) (c). After marrow stimulation, bone marrow containing mesenchymal stem cells ascends from the marrow cavity of the underlying subchondral bone via the channels generated by the marrow stimulation procedures. The defects are filled with a clot of autologous BMAC, containing mesenchymal stem cells and growth factors which possibly favor new tissue formation. (d) Defects thus contain bone marrow both from the subchondral bone and the additional BMAC application, and gradually a cartilaginous repair tissue forms within them. Red dashed lines (c1, d1, c2, and d2) show the outline of holes created by microfracture and subchondral drilling. Red arrows (c1, c2, and c3) within the subchondral bone denote the migration direction of the liquid bone marrow.

Marrow stimulation is performed by one of three different techniques. Microfracture induces multiple holes of the subchondral bone plate [12]. These focal perforations are the result of forcing the sharp tip of a microfracture awl into the subchondral bone plate. The impaction of the conical or polyhedral awl tip induces multiple small injuries of the adjacent bone. Subchondral drilling, proposed already in 1957 [13], is often termed Pridie drilling [14]. Here, the tip of a small diameter bone cutting device such as a drill bit or a Kirschner wire (K-wire) is placed on the base of the prepared cartilage defect and, at high speed, the rotating instrument cuts through the subchondral bone plate into the subarticular spongiosa. A defined number of standardized cylindrical holes are the result of subchondral drilling. Abrasion arthroplasty, in contrast, refers to a generalized abrasion of the subchondral bone plate of limited depth [15]. The small bony canals within the subchondral bone plate are opened following an abrasion with a round burr by removing about 1.0–1.5 mm of its thickness without completely eliminating the subchondral bone plate. This exposes the vascularity of the subchondral bone plate, providing the connecting link to the subchondral bone marrow. Although it has been suggested that larger holes may allow for an amplified access of reparative elements from the subchondral bone [5], recent data from translational models support the use of small diameter devices, most likely due to a lesser structural disturbance of the microarchitecture of the subchondral bone plate and subarticular spongiosa [16, 17].

After the communication of the cartilage defect with the subchondral bone marrow compartment has been established, bone marrow from the subchondral bone fills the defect, a clot forms, and more pluripotent progenitor cells from the subchondral compartment subsequently migrate into the defect, differentiate into chondrocytes, and, over time, form a fibrocartilaginous repair tissue. This repair tissue also serves to stabilize the adjacent cartilage and prevent early osteoarthritic degeneration.

3. Mesenchymal Stem Cells and Their Role in Osteochondral Repair

3.1. Definitions

MSCs represent a small fraction (0.001–0.01%) of nonhematopoietic, multipotent cells of the bone marrow. They are also present in other tissues including the synovium, periosteum, trabecular bone, adipose tissue, skeletal muscle, circulatory system, placenta, umbilical cord blood, and Wharton’s jelly [18].

MSCs exhibit a potent ability for self-renewal, stemness, and commitment toward cells of the mesodermal lineage (cartilage, bone, fat, muscle, meniscus, and tendons/ligaments) [19, 20]. MSCs have been defined by the Mesenchymal and Tissue Stem Cell Committee of the International Society for Cellular Therapy via a minimal set of standard criteria as being plastic-adherent in standard culture conditions, expressing CD105, CD73, and CD90 at their surface while lacking CD45, CD34, CD14 (or CD11b), CD79α (or CD19), and HLA-DR, and being able to differentiate in chondrocytes, osteoblasts, and adipocytes in vitro [21].

MSCs have homing, reparative, and trophic properties, migrating in damaged tissues upon recruitment from the circulation from the perivascular niche via activation of adhesion molecules (integrins, chemokine receptors) upon the release of factors from injured cells (chemokines) [22]. Once mobilized, MSCs produce a number of factors that can impact the healing responses locally by reduction of cell apoptosis, fibrosis, and inflammation and by activation of cell proliferation, mobilization, differentiation, and angiogenesis via paracrine and autocrine pathways [23]. Key agents involved in these processes include the vascular endothelial growth factor (VEGF), hepatocyte growth factor (HGF), insulin-like growth factor I (IGF-I), basic fibroblast growth factor (FGF-2), transforming growth factor beta (TGF-β), granulocyte-macrophage colony-stimulating factor (GMCSF), monocyte chemotactic protein-1 (MCP-1), macrophage inflammatory proteins-1 (MIP-1α, MIP-1β), regulated upon activation, normal T-cell expressed and secreted (RANTES), growth-related genes (GROα, GROβ), stromal-derived factor 1 (SDF-1), interleukin 6 (IL-6), angiopoietin-1, and stem cell factor (SCF). Such factors most likely coexist especially when MSCs are provided in a site of tissue injury like in a BMA. In such a setup, these agents may thus have the potential to cointeract in order to exert their specific activities via molecular interplays and subsequently to promote optimal MSC-associated therapeutic tissue healing in particular in a highly concentrated environment [24]. MSCs also have immunosuppressive activities, balancing or even inhibiting the activation of NK cells, dendritic cells, macrophages, and T and B lymphocytes [25]. In this regard, there is evidence that MSCs display advantageous anti-inflammatory and antifibrotic activities together with a potency for migration within a site of inflammation [26, 27], allowing to favorize their safe implantation and therapeutic effects in tissue lesions.

3.2. MSCs in Osteochondral Repair

Bone marrow MSCs undergo both chondrogenic and osteogenic differentiation processes [28, 29] that may promote the healing of the entire, damaged osteochondral unit:

(1) Chondrogenic MSC differentiation and subsequent cartilage formation are characterized by the expression of cartilage-specific markers (sex-determining region Y SRY-box transcription factors 5, 6, and 9; SOX5, SOX6, and SOX9; aggrecan; biglycan; type II, type IX, and type XI collagen; decorin; cartilage oligomeric matrix protein; COMP; scleraxis).

(2) Osteogenic MSC differentiation and subsequent bone formation are noted upon expression of bone-specific markers (Runt-related transcription factor 2 (RUNX2); alkaline phosphatase (ALP); type I collagen; bone sialoprotein (BSP); osteopontin (OPN); osteocalcin (OCN); calcium-rich mineralized matrix).

4. Mobilization of Cells from the Subchondral Bone into Sites of Articular Cartilage Damage

Mobilization of cells from the subchondral bone into sites of articular cartilage damage is possible once a communication of the defect with the subchondral bone marrow has been established. Liquid bone marrow fills the defect, and a clot forms. Theoretically, a bone marrow clot completely filling a full-thickness chondral defect of 2 cm in diameter in the medial femoral condyle would have a volume of about 300 μl (assuming a mean cartilage thickness at this topographical location of 2 mm) [30].

The cascade of bone marrow clotting is initiated by thrombocytes. They adhere to the exposed collagen of the subchondral bone with the aid of von Willebrand factor which creates a bridge between the platelets and the basis of the defect. Interestingly, platelets do not adhere to normal (uninjured) articular cartilage, and cartilage does not induce platelet aggregation in vivo, a discovery ascribed to the proteoglycans which block lysine sites on the collagen molecule [31]. If cartilage is treated with proteolytic enzymes such as trypsin, the tissue is rendered active as a platelet aggregant and adhesion and aggregation of platelets on the surface of the lesions results [31]. This highlights the importance of preparing the cartilage defect to be able to induce such platelet-subchondral bone/cartilage interactions. The aggregated platelets then degranulate, releasing several factors among which ILs and growth factors such as platelet-derived growth factor (PDGF), VEGF, and TGF-β which further potentiate their activation. PDGF, TGF-β, and other factors such as IGF-I also serve as chemoattractants. Next, the complement, kinin, plasminogen, and clotting cascades are activated. Fibrin is formed by polymerization through the clotting cascade, generating a mesh of long strands of insoluble protein that trap the cells, thus forming a clot in the cartilage defect that serves as a scaffold for adhesion. Little is known on the specific mechanisms on how cells are recruited to the site of the defect and how the cells move through the subchondral space. In accordance with wound healing, neutrophils and monocytes concentrate at the site of injury and direct the breakdown of the clot. The macrophages release chemoattractant substances and growth factors that recruit additional cells and stimulate collagen production. Over a period of several weeks, more pluripotent progenitor cells migrate through the openings of the subchondral bone into the articular cartilage defect. In the defect, they proliferate and undergo differentiation, together with matrix deposition and osteochondral remodeling.

From the classical paper of Shapiro et al. in a rabbit model [32], the time course of chondro- and osteogenesis in an osteochondral defect is well known. Fibrinous arcades are established in the first days across the defect, spanning both edges of the adjacent uninjured cartilage. Undifferentiated MSC ingrowth from the subchondral bone marrow can be seen after 7 days. The MSCs proliferate and differentiate into fibroblasts, articular chondroblasts, and osteoblasts. The first evidence of synthesis of a cartilaginous extracellular matrix, as defined by safranin-O staining, appears at about 10 days. The new repair tissue first contains flattened fibrocartilaginous cells and then round cells similar to chondrocytes. The defect is completely repopulated after about 6 weeks, with synthesis of repair cartilage and bone matrices in their appropriate locations. At 24 weeks, both the tidemark and the subchondral bone plate are re-established. The initially formed cancellous woven bone is replaced by the lamellar cancellous bone. Over time, the penetrations of the subchondral bone plate are closed with newly deposited bone. The cellular contribution to cartilage repair from the adjacent cartilage is very low [32].

During the repair of the osteochondral unit, osteogenesis is supported by the mobilization of perivascular cells and blood vessels within the subchondral bone compartment [33]. Under physiologic conditions, numerous arterial terminal branches and venous plexus are located in the subchondral bone plate [34, 35] and the blood flow rate is up to 10 times higher than in the cancellous bone, ensuring nutrient and water supply to the articular cartilage [35]. The physiological avascularity of the articular cartilage [36] is retained by the presence of antiangiogenic factors such as thrombospondin-1 [37, 38], thrombospondin-2 [39], troponin-I [40], tenascin [41], tissue inhibitors of metalloproteinases (TIMP) 1 and 2 [42], and chondromodulin-1 [37, 43–45]. While original hyaline articular cartilage is rich in these proteins, fibrocartilaginous repair tissue has been shown to lack such factors [37, 43], consequently permitting blood vessel invasion and stimulation of both endochondral and intramembranous bone formation [32]. Furthermore, in certain pathologies such as osteochondral defects [46], osteoarthritis [42, 47–49], and inflammatory joint diseases [50–53], chondrocytes have been demonstrated to express various proangiogenic factors, including VEGF [46, 54–56], connective tissue growth factor (CTGF) [57], FGF-2 [42], tumor necrosis factor-α (TNF-α) [58], and matrix metalloproteinases (MMP) 9 and 13 [59, 60]. Interestingly, blocking VEGF with its soluble antagonist (sFlt1) [61] or the antibody bevacizumab [62] improved the chondrogenic potential of stem cells [61] and articular cartilage repair in vivo [62]. Thus, although vascularization is beneficial for osteogenesis and subchondral bone reconstitution, it may critically disturb the repair of the overlying articular cartilage.

5. Bone Marrow Aspirate and Its Concentrate

5.1. Bone Marrow Aspirate

Bone marrow produces the red blood cells during hematopoiesis and is a major component of the immune system by producing lymphocytes. It mainly consists of hematopoietic tissue and fat cells. In the stroma of the bone marrow, supporting cells such as fibroblasts, macrophages, adipocytes, osteoblasts, osteoclasts, and endothelial cells are present. Myelopoietic and erythropoietic cells together with the lymphocytes are the major cell types. The bone marrow also contains hematopoietic cells and MSCs (also termed marrow stromal cells). Bone marrow aspiration can be performed with local anesthetic under guidance of ultrasound or fluoroscopic imaging to improve accuracy and efficiency.

5.2. Bone Marrow Aspirate Concentrate

Unprocessed BMA is been rarely used. As only about 0.001% of nucleated cells from BMA are MSCs [63], attempts are made to increase their number, usually by concentrating the autologous BMA by density-gradient centrifugation. This concept of concentrating BMA to produce BMA concentrate (BMAC) allows increasing not only the numbers of MSCs but also platelets containing growth factors and hematopoietic stem cells (HSCs) per sample volume. MSCs present strong self-renewal abilities with a differentiation capacity to form chondrocytes, osteocytes, and adipocytes. The platelet component of BMAC releases growth factors to initiate stem cell migration to the injury site and provides adhesion sites for the migrating stem cells [10]. Moreover, HSCs provide support to the vasculature system by differentiating into blood cells and maintain cell-to-cell contact with MSCs, stimulating osteogenesis.

6. Bone Marrow Aspirate-Enhanced Marrow Stimulation

BMA-enhanced marrow stimulation is based on a prior treatment of the subchondral bone plate in the defects with marrow stimulation, although BMA has been also applied in few cases to cartilage defects that were only debrided down to the subchondral bone. Microfracture is the main marrow stimulation technique performed, providing a more roughened base of the defect caused by the several microfracture holes and possible minute fractures. By definition, the continuous bleeding from the microfracture holes may always contribute to the final composition of the bone marrow clot. As the stability of the clot has been highlighted since a long time, alternative methods seek to enhance the security of the bone marrow clot. These include the application of bioresorbable membranes, thought to provide an additional 3D environment for the cells undergoing chondrogenesis in the cartilage defect.

7. Effects of Bone Marrow Aspirate-Enhanced Marrow Stimulation on Articular Cartilage Repair

7.1. Translational Evidence of BMAC-Enhanced Marrow Stimulation

The effect of unconcentrated BMA to enhance osteochondral repair has, to the best of our knowledge, currently not been reported to date in either translational or clinical settings. Only two preclinical studies applied marrow stimulation enhanced with BMAC (termed BMAC-enhanced marrow stimulation) to analyze the repair of chondral lesions (Table 1). Both studies were performed in the knee joint of large animal models (goat [64] and horse [65], respectively). Despite the availability of data regarding BMAC-enhanced repair of osteochondral lesions by the use of gene vectors [7, 66] or scaffolds [67–70], the particular effect of BMAC-enhanced marrow stimulation for chondral lesions has not yet been evaluated in other joints or experimental animals. Such scaffolds may aid to provide a stable environment for the clot and subsequent repair tissue development. However, little is known about the mechanisms of their interaction with the BMAC-enhanced marrow stimulation process.

Fortier et al. treated 12 young adult horses with full-thickness chondral defects (15 mm in diameter, 3 mm in depth) in the trochlear ridge with microfracture alone (6 microfracture holes per defect) or BMAC-enhanced microfracture [65]. BMA was harvested from two sternal marrow spaces (35 ml each) into syringes containing preservative-free heparin (final concentration: 15 U heparin/ml BMA). The marrow aspirate was processed with a centrifuge to yield 6 ml of BMAC. Arthroscopically, BMAC and thrombin (10 : 1 volume ratio) were injected into the microfracture-treated defects using a syringe. The animals were confined to rest for two weeks, followed by increasing weight bearing and a second-look arthroscopy at 12 weeks. At sacrifice after 8 months, an MRI-based radiological evaluation revealed a significantly increased defect filling and improved integration with the surrounding cartilage in the BMAC-enhanced microfracture group compared with microfracture alone. BMAC treatment also yielded a significantly increased type II collagen and glycosaminoglycan contents with improved collagen fiber orientation of the repair tissue.

Saw et al. reported on the treatment of 15 young goats with full-thickness chondral defects (4 mm in diameter) in the intercondylar area of the knee treated with either subchondral drilling (9 drill holes per defect, 5 mm in depth, 0.6 mm in diameter), subchondral drilling with additional intra-articular injection of sodium hyaluronate (HA) (HA group), or subchondral drilling with intra-articular injection of both HA and BMAC (HA-BMAC group) [64]. The injections were administered on a weekly basis for 3 weeks, starting one week after surgery with defect creation and subchondral drilling. The BMA was harvested from the iliac crest and centrifuged to remove red blood cells and plasma and yielded a mean final volume of 4.4 ml BMAC. In the HA-BMAC group, each defect was injected with 400 μl BMAC. Animals were mobilized without restrictions. At 6 months postoperatively, similar macroscopic findings were reported between drilling alone and the HA group. However, defects of the HA-BMAC group were almost completely filled and exhibited a smooth surface well in level with the adjacent normal cartilage. Histological evaluation revealed that BMAC/HA-enhanced marrow stimulation induced a significantly better histological grading of the articular cartilage repair with increased proteoglycan content and an improved lateral integration.

7.2. Clinical Evidence of BMAC-Enhanced Marrow Stimulation for Articular Cartilage Repair

Only four studies have been performed to investigate the specific clinical outcome of BMAC-enhanced marrow stimulation for chondral lesions. These were conducted in either the knee [71, 72] or the ankle joint [73, 74] (Table 2). Microfracture was the main marrow stimulation technique, applied in three studies [71–73], subchondral drilling only once [74]. In all the investigations, BMA was harvested from the iliac crest and processed with various commercially available centrifuge systems to generate BMAC.

De Girolamo et al. examined cellular characteristics and pain or adverse events in 11 patients with chondral lesions (Outerbridge types III or IV [75]) undergoing microfracture in combination with implantation of a type I/III porcine collagen matrix and application of BMAC [71]. Bone marrow from the iliac crest was harvested and centrifuged to obtain a concentrated phase containing mononuclear cells. Cellular characteristics were compared with samples obtained from the microfractured defect site. The authors reported that more cells with an MSC phenotype (CD34⁻/CD45^low/CD271^high) were found in the bone marrow from the iliac crest (0.04%) than from the subchondral location of the defect (0.02%). Clinically, no pain or adverse events were seen. The clinical outcome was not compared to a negative control group. Gobbi et al. treated 50 patients with chondral lesions of the knee (ICRS grade IV) with microfracture (microfracture group; median lesion size of 4.5 cm²) or a hyaluronan- (HA-) based scaffold plus BMAC (HA-BMAC group; median lesion size of 6.5 cm²) [72]. BMA was centrifuged to obtain a concentration of bone marrow cells approximately 6 times the baseline value. The hemotoxin batroxobin, also known as reptilase, was added to activate BMAC (from the iliac crest) to produce an adhesive clot. The clot was implanted into the cartilage defect that was prepared in a similar manner as for the microfracture group. It was covered with a HA-based scaffold and secured to the surrounding cartilage by sutures and/or fibrin glue. Weight bearing was restricted for the initial 4 weeks postoperatively. After 2 years, the HA-BMAC group obtained a normal or nearly normal International Knee Documentation Committee (IKDC) objective score in 100%, the microfracture group only in 64%. HA-BMAC-treated patients maintained a significantly improved knee function at 5 years according to Tegner and IKDC objective scores compared with microfracture-treated patients.

The concept of applying BMAC to improve cartilage repair has been also studied for defects of the talus [9]. Hannon et al. compared microfracture alone with BMAC-enhanced microfracture of talar defects in 34 patients [73]. Approximately 60 ml of BMA was extracted from the iliac crest and centrifuged to generate 3 ml of BMAC for each defect site. In the BMAC-enhanced microfracture group, BMAC was injected into the defect site under arthroscopic control after the subchondral plate had been penetrated with multiple microfractures. The Foot and Ankle Outcome Score (FAOS) pain score and the short form 12 (SF-12) general health questionnaire physical component summary (SF-12 PCS) score improved significantly from before to after surgery in both groups. Yet, the Magnetic Resonance Observation of Cartilage Repair Tissue (MOCART) score in the BMAC-enhanced microfracture group was significantly higher than that in microfracture alone group, indicating a significantly better morphological outcome compared with the microfracture alone group. MRI also revealed that BMAC-enhanced microfracture induced significantly less fissuring and fibrillation of the articular cartilage surface than microfracture treatment without adjunct. Lanham et al. evaluated 12 patients with full-thickness chondral defects of the talus (6-7 mm in depth) treated either with BMAC-enhanced subchondral drilling covered by a collagen scaffold or with particulated juvenile articular cartilage [74]. The collagen scaffold consisted of a hydrated matrix of bovine collagen and glycosaminoglycans. Approximately 60 ml of BMA was harvested from the iliac crest and centrifuged to obtain 6 ml of BMAC. After a mean follow-up of 2 years (range 12–42 months), the American Orthopaedic Foot and Ankle Surgeons (AOFAS) score as well as the Foot and Ankle Ability Measure (FAAM; activities of daily living subscale) showed a statistically significant improvement in favor of particulated juvenile articular cartilage compared with BMAC-enhanced marrow stimulation in these 12 patients. The SF-12 health status questionnaire [76] revealed no significant differences between both treatment groups.

8. Effects of Bone Marrow Aspirate-Enhanced Marrow Stimulation on Subchondral Bone Repair

Marrow stimulation affects not only articular cartilage but also subchondral bone repair. Relevant changes of the subchondral bone that have been observed include, for example, the upward migration of the subchondral bone plate, the formation of intralesional osteophytes and of subchondral bone cysts, and a generalized impairment of the osseous microarchitecture below the treated defects [77]. Of note, no study has been performed to date to the best of our knowledge to assess the effect of BMAC-enhanced marrow stimulation on the subchondral bone compartment compared with marrow stimulation alone. Given the abovementioned specifications and biological features of BMA and BMAC, such a biological adjunct may possibly have a beneficial impact not only on the articular cartilage but also on its supporting osseous bed.

9. Conclusions and Future Directions

In summary, there is good evidence from translational studies that BMAC-enhanced microfracture results in a significantly increased defect filling, better structural parameters of the repair tissue, and improved integration compared with microfracture alone. The study of Gobbi et al. shows after 2 years significant improvements in clinical scores of patients with relatively large chondral defects (median lesion size: 6.5 cm²) treated with BMAC that was additionally covered with a Hyaluronan scaffold compared to microfracture-treated patients [72].

Interestingly, no study investigated the effect of unconcentrated BMA for osteochondral repair in either translational or clinical settings so far. Such a treatment might constitute an interesting negative control and also shed more light on the possible effect of concentration on repair. Also, no standard technique or protocol for BMA harvesting exists. The commercially available systems including centrifuges do not provide equivalent cell numbers and concentrations. The ideal volume of required BMA or BMAC for the treatment of a specific defect volume remains to be determined. Standardizations of all of these factors are needed, as they may provide a more scientific way of evaluating possible effects, especially as there is a large interindividual variety in the number of produced and secreted growth factors by the many cells within the BMA. As marrow stimulation affects the entire osteochondral unit, further research is also mandatory to investigate possible effects of BMA on the important aspect of subchondral bone changes following cartilage repair procedures.

Although the structural [78] and functional [79] clinical results of marrow stimulation are usually good, the fibrocartilaginous repair tissue is inferior to the original hyaline cartilage. Possibly, application of novel insights to the problem of fibrosis with its excess deposition of an inferior fibrous tissue may show new avenues towards the goal of achieving true hyaline articular cartilage regeneration. For skeletal muscle, numerous approaches have been developed to inhibit the fibrotic cascade [80] that may also be studied in articular cartilage repair [81]. As discussed earlier, a combination of simultaneously blocking angiogenesis and fibrosis could also be investigated for its effects on cartilage repair [82].

Another future opportunity of enhancing the possible therapeutic potential of BMA is to increase the rate of MSC survival, leading to improved therapeutic functions. Little is known on the viability of migrated MSCs at the site of the cartilage defect, when exposed to biomechanical stresses and the synovial fluid. Possibly, strategies to regulate apoptotic signaling and enhance cell adhesion, such as hypoxic preconditioning [83] or application of growth or antiapoptotic factors by in situ genetic modifications [84, 85], may improve the in situ survival of the MSCs [86, 87].

Forthcoming translational and clinical studies will help to address the effect of BMAC-enhanced marrow stimulation of chondral defects more in detail.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

References

A. A. Kocher, M. D. Schuster, M. J. Szabolcs et al., “Neovascularization of ischemic myocardium by human bone-marrow-derived angioblasts prevents cardiomyocyte apoptosis, reduces remodeling and improves cardiac function,” Nature Medicine, vol. 7, no. 4, pp. 430–436, 2001.
View at: Publisher Site | Google Scholar
L. L. Johnson, “Arthroscopic abrasion arthroplasty historical and pathologic perspective: present status,” Arthroscopy, vol. 2, no. 1, pp. 54–69, 1986.
View at: Publisher Site | Google Scholar
J. F. Stoltz, N. de Isla, Y. P. Li et al., “Stem cells and regenerative medicine: myth or reality of the 21th century,” Stem Cells International, vol. 2015, Article ID 734731, p. 19, 2015.
View at: Publisher Site | Google Scholar
A. I. Caplan, “Adult Mesenchymal stem cells: When, where, and how,” Stem Cells International, vol. 2015, Article ID 628767, p. 6, 2015.
View at: Publisher Site | Google Scholar
B. H. Min, W. H. Choi, Y. S. Lee et al., “Effect of different bone marrow stimulation techniques (BSTs) on MSCs mobilization,” Journal of Orthopaedic Research, vol. 31, no. 11, pp. 1814–1819, 2013.
View at: Publisher Site | Google Scholar
E. Tateishi-Yuyama, H. Matsubara, T. Murohara et al., “Therapeutic angiogenesis for patients with limb ischaemia by autologous transplantation of bone-marrow cells: a pilot study and a randomised controlled trial,” Lancet, vol. 360, no. 9331, pp. 427–435, 2002.
View at: Publisher Site | Google Scholar
A. Ivkovic, A. Pascher, D. Hudetz et al., “Articular cartilage repair by genetically modified bone marrow aspirate in sheep,” Gene Therapy, vol. 17, no. 6, pp. 779–789, 2010.
View at: Publisher Site | Google Scholar
J. Holton, M. Imam, J. Ward, and M. Snow, “The basic science of bone marrow aspirate concentrate in chondral injuries,” Orthopedic Reviews, vol. 8, no. 3, p. 6659, 2016.
View at: Publisher Site | Google Scholar
J. Chahla, M. E. Cinque, J. M. Shon et al., “Bone marrow aspirate concentrate for the treatment of osteochondral lesions of the talus: a systematic review of outcomes,” Journal Experimental Orthopaedics, vol. 3, no. 1, p. 33, 2016.
View at: Publisher Site | Google Scholar
J. Holton, M. A. Imam, and M. Snow, “Bone marrow aspirate in the treatment of chondral injuries,” Frontiers in Surgery, vol. 3, p. 33, 2016.
View at: Publisher Site | Google Scholar
G. Smith, G. Knutsen, and J. Richardson, “A clinical review of cartilage repair techniques,” Journal of Bone and Joint Surgery (British Volume), vol. 87, no. 4, pp. 445–449, 2005.
View at: Publisher Site | Google Scholar
J. R. Steadman, W. G. Rodkey, and J. J. Rodrigo, “Microfracture: surgical technique and rehabilitation to treat chondral defects,” Clinical Orthopaedics and Related Research, Supplement 391, pp. S362–S369, 2001.
View at: Google Scholar
I. Smillie, “Treatment of osteochondritis dissecans,” Journal of Bone and Joint Surgery (British Volume), vol. 39, no. 2, pp. 248–260, 1957.
View at: Google Scholar
K. Pridie and G. Gordon, “A method of resurfacing osteoarthritic knee joints,” Journal of Bone and Joint Surgery (British Volume), vol. 41, no. 3, pp. 618-619, 1959.
View at: Google Scholar
L. L. Johnson, “Arthroscopic abrasion arthroplasty historical and pathologic perspective: present status,” Arthroscopy: The Journal of Arthroscopic & Related Surgery, vol. 2, no. 1, pp. 54–69, 1986.
View at: Google Scholar
M. Eldracher, P. Orth, M. Cucchiarini, D. Pape, and H. Madry, “Small subchondral drill holes improve marrow stimulation of articular cartilage defects,” American Journal of Sports Medicine, vol. 42, no. 11, pp. 2741–2750, 2014.
View at: Publisher Site | Google Scholar
P. Orth, J. Duffner, D. Zurakowski, M. Cucchiarini, and H. Madry, “Small-diameter awls improve articular cartilage repair after microfracture treatment in a translational animal model,” American Journal of Sports Medicine, vol. 44, no. 1, pp. 209–219, 2016.
View at: Publisher Site | Google Scholar
M. Cucchiarini, J. K. Venkatesan, M. Ekici, G. Schmitt, and H. Madry, “Human mesenchymal stem cells overexpressing therapeutic genes: from basic science to clinical applications for articular cartilage repair,” Bio-Medical Materials and Engineering, vol. 22, no. 4, pp. 197–208, 2012.
View at: Publisher Site | Google Scholar
D. J. Prockop, “Marrow stromal cells as stem cells for nonhematopoietic tissues,” Science, vol. 276, no. 5309, pp. 71–74, 1997.
View at: Publisher Site | Google Scholar
A. I. Caplan, “Mesenchymal stem cells,” Journal of Orthopaedic Research, vol. 9, no. 5, pp. 641–650, 1991.
View at: Publisher Site | Google Scholar
M. Dominici, K. Le Blanc, I. Mueller et al., “Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement,” Cytotherapy, vol. 8, no. 4, pp. 315–317, 2006.
View at: Publisher Site | Google Scholar
C. M. Kolf, E. Cho, and R. S. Tuan, “Mesenchymal stromal cells. Biology of adult mesenchymal stem cells: regulation of niche, self-renewal and differentiation,” Arthritis Research & Therapy, vol. 9, no. 1, p. 204, 2007.
View at: Publisher Site | Google Scholar
A. I. Caplan and J. E. Dennis, “Mesenchymal stem cells as trophic mediators,” Journal of Cellular Biochemistry, vol. 98, no. 5, pp. 1076–1084, 2006.
View at: Publisher Site | Google Scholar
J. M. Cassano, J. G. Kennedy, K. A. Ross, E. J. Fraser, M. B. Goodale, and L. A. Fortier, “Bone marrow concentrate and platelet-rich plasma differ in cell distribution and interleukin 1 receptor antagonist protein concentration,” Knee Surgery, Sports Traumatology, Arthroscopy, pp. 1–10, 2016.
View at: Publisher Site | Google Scholar
A. Uccelli, V. Pistoia, and L. Moretta, “Mesenchymal stem cells: a new strategy for immunosuppression?” Trends in Immunology, vol. 28, no. 5, pp. 219–226, 2007.
View at: Publisher Site | Google Scholar
S. Aggarwal and M. F. Pittenger, “Human mesenchymal stem cells modulate allogeneic immune cell responses,” Blood, vol. 105, no. 4, pp. 1815–1822, 2005.
View at: Publisher Site | Google Scholar
E. L. Fong, C. K. Chan, and S. B. Goodman, “Stem cell homing in musculoskeletal injury,” Biomaterials, vol. 32, no. 2, pp. 395–409, 2011.
View at: Publisher Site | Google Scholar
M. F. Pittenger, A. M. Mackay, S. C. Beck et al., “Multilineage potential of adult human mesenchymal stem cells,” Science, vol. 284, no. 5411, pp. 143–147, 1999.
View at: Publisher Site | Google Scholar
A. Augello and C. De Bari, “The regulation of differentiation in mesenchymal stem cells,” Human Gene Therapy, vol. 21, no. 10, pp. 1226–1238, 2010.
View at: Publisher Site | Google Scholar
D. E. Shepherd and B. B. Seedhom, “Thickness of human articular cartilage in joints of the lower limb,” Annals of the Rheumatic Diseases, vol. 58, no. 1, pp. 27–34, 1999.
View at: Publisher Site | Google Scholar
D. Zucker-Franklin and L. Drosenberg, “Platelet interaction with modified articular cartilage. Its possible relevance to joint repair,” Journal of Clinical Investigation, vol. 59, no. 4, pp. 641–651, 1977.
View at: Publisher Site | Google Scholar
F. Shapiro, S. Koide, and M. J. Glimcher, “Cell origin and differentiation in the repair of full-thickness defects of articular cartilage,” Journal of Bone and Joint Surgery (American Volume), vol. 75, no. 4, pp. 532–553, 1993.
View at: Google Scholar
P. Orth and H. Madry, “Advancement of the subchondral bone plate in translational models of osteochondral repair: implications for tissue engineering approaches,” Tissue Engineering Part B: Reviews, vol. 21, no. 6, pp. 504–520, 2015.
View at: Publisher Site | Google Scholar
C. Mathieu, A. Chevrier, V. Lascau-Coman, G. E. Rivard, and C. D. Hoemann, “Stereological analysis of subchondral angiogenesis induced by chitosan and coagulation factors in microdrilled articular cartilage defects,” Osteoarthritis and Cartilage, vol. 21, no. 6, pp. 849–859, 2013.
View at: Publisher Site | Google Scholar
H. Imhof, I. Sulzbacher, S. Grampp, C. Czerny, S. Youssefzadeh, and F. Kainberger, “Subchondral bone and cartilage disease: a rediscovered functional unit,” Investigative Radiology, vol. 35, no. 10, pp. 581–588, 2000.
View at: Publisher Site | Google Scholar
H. Brem and J. Folkman, “Inhibition of tumor angiogenesis mediated by cartilage,” Journal of Experimental Medicine, vol. 141, no. 2, pp. 427–439, 1975.
View at: Publisher Site | Google Scholar
M. Blanke, H. D. Carl, P. Klinger, B. Swoboda, F. Hennig, and K. Gelse, “Transplanted chondrocytes inhibit endochondral ossification within cartilage repair tissue,” Calcified Tissue International, vol. 85, no. 5, pp. 421–433, 2009.
View at: Publisher Site | Google Scholar
D. Pfander, T. Cramer, D. Deuerling, G. Weseloh, and B. Swoboda, “Expression of thrombospondin-1 and its receptor CD36 in human osteoarthritic cartilage,” Annals of the Rheumatic Diseases, vol. 59, no. 6, pp. 448–454, 2000.
View at: Publisher Site | Google Scholar
D. K. Taylor, J. A. Meganck, S. Terkhorn et al., “Thrombospondin-2 influences the proportion of cartilage and bone during fracture healing,” Journal of Bone and Mineral Research, vol. 24, no. 6, pp. 1043–1054, 2009.
View at: Publisher Site | Google Scholar
M. A. Moses, D. Wiederschain, I. Wu et al., “Troponin I is present in human cartilage and inhibits angiogenesis,” Proceedings of the National Academy of Sciences of the United States of America, vol. 96, no. 6, pp. 2645–2650, 1999.
View at: Publisher Site | Google Scholar
X. Chevalier, N. Groult, B. Larget-Piet, L. Zardi, and W. Hornebeck, “Tenascin distribution in articular cartilage from normal subjects and from patients with osteoarthritis and rheumatoid arthritis,” Arthritis and Rheumatism, vol. 37, no. 7, pp. 1013–1022, 1994.
View at: Publisher Site | Google Scholar
L. Pesesse, C. Sanchez, and Y. Henrotin, “Osteochondral plate angiogenesis: A new treatment target in osteoarthritis,” Joint, Bone, Spine: Revue du Rhumatisme, vol. 78, no. 2, pp. 144–149, 2011.
View at: Publisher Site | Google Scholar
P. Klinger, C. Surmann-Schmitt, M. Brem et al., “Chondromodulin 1 stabilizes the chondrocyte phenotype and inhibits endochondral ossification of porcine cartilage repair tissue,” Arthritis and Rheumatism, vol. 63, no. 9, pp. 2721–2731, 2011.
View at: Publisher Site | Google Scholar
K. Kusafuka, Y. Hiraki, C. Shukunami, T. Kayano, and T. Takemura, “Cartilage-specific matrix protein, chondromodulin-I (ChM-I), is a strong angio-inhibitor in endochondral ossification of human neonatal vertebral tissues in vivo: relationship with angiogenic factors in the cartilage,” Acta Histochemica, vol. 104, no. 2, pp. 167–175, 2002.
View at: Publisher Site | Google Scholar
C. Shukunami and Y. Hiraki, “Role of cartilage-derived anti-angiogenic factor, chondromodulin-I, during endochondral bone formation,” Osteoarthritis and Cartilage, vol. 9, Supplement A, pp. S91–S101, 2001.
View at: Google Scholar
R. Sakata, T. Kokubu, I. Nagura et al., “Localization of vascular endothelial growth factor during the early stages of osteochondral regeneration using a bioabsorbable synthetic polymer scaffold,” Journal of Orthopaedic Research, vol. 30, no. 2, pp. 252–259, 2012.
View at: Publisher Site | Google Scholar
D. A. Walsh, “Angiogenesis in osteoarthritis and spondylosis: successful repair with undesirable outcomes,” Current Opinion in Rheumatology, vol. 16, no. 5, pp. 609–615, 2004.
View at: Publisher Site | Google Scholar
Y. Henrotin, L. Pesesse, and C. Sanchez, “Subchondral bone in osteoarthritis physiopathology: state-of-the art and perspectives,” Bio-Medical Materials and Engineering, vol. 19, no. 4-5, pp. 311–316, 2009.
View at: Publisher Site | Google Scholar
T. Matsumoto, G. M. Cooper, B. Gharaibeh et al., “Cartilage repair in a rat model of osteoarthritis through intraarticular transplantation of muscle-derived stem cells expressing bone morphogenetic protein 4 and soluble Flt-1,” Arthritis and Rheumatism, vol. 60, no. 5, pp. 1390–1405, 2009.
View at: Publisher Site | Google Scholar
D. Walsh, “Angiogenesis and arthritis,” Rheumatology, vol. 38, no. 2, pp. 103–112, 1999.
View at: Publisher Site | Google Scholar
D. Walsh and L. Haywood, “Angiogenesis: a therapeutic target in arthritis,” Current Opinion in Investigational Drugs (London, England: 2000), vol. 2, no. 8, pp. 1054–1063, 2001.
View at: Google Scholar
S. C. Ballara, J. M. Miotla, and E. M. Paleolog, “New vessels, new approaches: angiogenesis as a therapeutic target in musculoskeletal disorders,” International Journal of Experimental Pathology, vol. 80, no. 5, pp. 235–250, 1999.
View at: Google Scholar
T. Saber, D. J. Veale, E. Balogh et al., “Toll-like receptor 2 induced angiogenesis and invasion is mediated through the Tie2 signalling pathway in rheumatoid arthritis,” PLoS One, vol. 6, no. 8, article e23540, 2011.
View at: Publisher Site | Google Scholar
H.-P. Gerber, T. H. Vu, A. M. Ryan, J. Kowalski, Z. Werb, and N. Ferrara, “VEGF couples hypertrophic cartilage remodeling, ossification and angiogenesis during endochondral bone formation,” Nature Medicine, vol. 5, no. 6, pp. 623–628, 1999.
View at: Publisher Site | Google Scholar
M. Murata, K. Yudoh, and K. Masuko, “The potential role of vascular endothelial growth factor (VEGF) in cartilage: how the angiogenic factor could be involved in the pathogenesis of osteoarthritis?” Osteoarthritis and Cartilage, vol. 16, no. 3, pp. 279–286, 2008.
View at: Publisher Site | Google Scholar
H. Enomoto, I. Inoki, K. Komiya et al., “Vascular endothelial growth factor isoforms and their receptors are expressed in human osteoarthritic cartilage,” The American Journal of Pathology, vol. 162, no. 1, pp. 171–181, 2003.
View at: Publisher Site | Google Scholar
T. Shimo, T. Nakanishi, Y. Kimura et al., “Inhibition of endogenous expression of connective tissue growth factor by its antisense oligonucleotide and antisense RNA suppresses proliferation and migration of vascular endothelial cells,” The Journal of Biochemistry, vol. 124, no. 1, pp. 130–140, 1998.
View at: Publisher Site | Google Scholar
D. A. Walsh and C. I. Pearson, “Angiogenesis in the pathogenesis of inflammatory joint and lung diseases,” Arthritis Research & Therapy, vol. 3, no. 3, pp. 147–153, 2001.
View at: Publisher Site | Google Scholar
G. Hashimoto, I. Inoki, Y. Fujii, T. Aoki, E. Ikeda, and Y. Okada, “Matrix metalloproteinases cleave connective tissue growth factor and reactivate angiogenic activity of vascular endothelial growth factor 165,” Journal of Biological Chemistry, vol. 277, no. 39, pp. 36288–36295, 2002.
View at: Publisher Site | Google Scholar
J. T. K. Melton, N. M. Clarke, and H. I. Roach, “Matrix metalloproteinase-9 induces the formation of cartilage canals in the chondroepiphysis of the neonatal rabbit,” The Journal of Bone & Joint Surgery, vol. 88, Supplement 3, pp. 155–161, 2006.
View at: Publisher Site | Google Scholar
S. Kubo, G. M. Cooper, T. Matsumoto et al., “Blocking vascular endothelial growth factor with soluble Flt-1 improves the chondrogenic potential of mouse skeletal muscle–derived stem cells,” Arthritis and Rheumatism, vol. 60, no. 1, pp. 155–165, 2009.
View at: Publisher Site | Google Scholar
T. Nagai, M. Sato, T. Kutsuna et al., “Intravenous administration of anti-vascular endothelial growth factor humanized monoclonal antibody bevacizumab improves articular cartilage repair,” Arthritis Research & Therapy, vol. 12, no. 5, p. R178, 2010.
View at: Publisher Site | Google Scholar
P. Kasten, I. Beyen, M. Egermann et al., “Instant stem cell therapy: characterization and concentration of human mesenchymal stem cells in vitro,” European Cells & Materials, vol. 16, pp. 47–55, 2008.
View at: Publisher Site | Google Scholar
K. Y. Saw, P. Hussin, S. C. Loke et al., “Articular cartilage regeneration with autologous marrow aspirate and hyaluronic acid: an experimental study in a goat model,” Arthroscopy, vol. 25, no. 12, pp. 1391–1400, 2009.
View at: Publisher Site | Google Scholar
L. A. Fortier, H. G. Potter, E. J. Rickey et al., “Concentrated bone marrow aspirate improves full-thickness cartilage repair compared with microfracture in the equine model,” Journal of Bone and Joint Surgery (American Volume), vol. 92, no. 10, pp. 1927–1937, 2010.
View at: Publisher Site | Google Scholar
A. Pascher, G. Palmer, A. Steinert et al., “Gene delivery to cartilage defects using coagulated bone marrow aspirate,” Gene Therapy, vol. 11, no. 2, pp. 133–141, 2004.
View at: Publisher Site | Google Scholar
J. Iwasa, L. Engebretsen, Y. Shima, and M. Ochi, “Clinical application of scaffolds for cartilage tissue engineering,” Knee Surgery, Sports Traumatology, Arthroscopy, vol. 17, no. 6, pp. 561–577, 2009.
View at: Publisher Site | Google Scholar
M. Betsch, J. Schneppendahl, S. Thuns et al., “Bone marrow aspiration concentrate and platelet rich plasma for osteochondral repair in a porcine osteochondral defect model,” PLoS One, vol. 8, no. 8, article e71602, 2013.
View at: Publisher Site | Google Scholar
M. Betsch, S. Thelen, L. Santak et al., “The role of erythropoietin and bone marrow concentrate in the treatment of osteochondral defects in mini-pigs,” PLoS One, vol. 9, no. 3, article e92766, 2014.
View at: Publisher Site | Google Scholar
A. Getgood, F. Henson, C. Skelton et al., “The augmentation of a collagen/glycosaminoglycan biphasic osteochondral scaffold with platelet-rich plasma and concentrated bone marrow aspirate for osteochondral defect repair in sheep: a pilot study,” Cartilage, vol. 3, no. 4, pp. 351–363, 2012.
View at: Publisher Site | Google Scholar
L. de Girolamo, G. Bertolini, M. Cervellin, G. Sozzi, and P. Volpi, “Treatment of chondral defects of the knee with one step matrix-assisted technique enhanced by autologous concentrated bone marrow: in vitro characterisation of mesenchymal stem cells from iliac crest and subchondral bone,” Injury, vol. 41, no. 11, pp. 1172–1177, 2010.
View at: Publisher Site | Google Scholar
A. Gobbi and G. P. Whyte, “One-stage cartilage repair using a hyaluronic acid-based scaffold with activated bone marrow-derived mesenchymal stem cells compared with microfracture: five-year follow-up,” American Journal of Sports Medicine, vol. 44, no. 11, pp. 2846–2854, 2016.
View at: Publisher Site | Google Scholar
C. P. Hannon, K. A. Ross, C. D. Murawski et al., “Arthroscopic bone marrow stimulation and concentrated bone marrow aspirate for osteochondral lesions of the talus: a case-control study of functional and magnetic resonance observation of cartilage repair tissue outcomes,” Arthroscopy, vol. 32, no. 2, pp. 339–347, 2016.
View at: Publisher Site | Google Scholar
N. S. Lanham, J. J. Carroll, M. T. Cooper, V. Perumal, and J. S. Park, “A comparison of outcomes of particulated juvenile articular cartilage and bone marrow aspirate concentrate for articular cartilage lesions of the talus,” Foot & Ankle Specialist, 2016.
View at: Publisher Site | Google Scholar
R. E. Outerbridge, “The etiology of chondromalacia patellae,” Journal of Bone and Joint Surgery (British Volume), vol. 43-B, no. 4, pp. 752–757, 1961.
View at: Google Scholar
K. E. Webster and J. A. Feller, “Comparison of the short form-12 (SF-12) health status questionnaire with the SF-36 in patients with knee osteoarthritis who have replacement surgery,” Knee Surgery, Sports Traumatology, Arthroscopy, vol. 24, no. 8, pp. 2620–2626, 2016.
View at: Publisher Site | Google Scholar
P. Orth, M. Cucchiarini, D. Kohn, and H. Madry, “Alterations of the subchondral bone in osteochondral repair—translational data and clinical evidence,” European Cells & Materials, vol. 25, pp. 299–316, 2013.
View at: Google Scholar
G. Kaul, M. Cucchiarini, K. Remberger, D. Kohn, and H. Madry, “Failed cartilage repair for early osteoarthritis defects: A biochemical, histological and immunohistochemical analysis of the repair tissue after treatment with marrow-stimulation techniques,” Knee Surgery, Sports Traumatology, Arthroscopy, vol. 20, no. 11, pp. 2315–2324, 2012.
View at: Publisher Site | Google Scholar
A. Gobbi, G. Karnatzikos, and A. Kumar, “Long-term results after microfracture treatment for full-thickness knee chondral lesions in athletes,” Knee Surgery, Sports Traumatology, Arthroscopy, vol. 22, no. 9, pp. 1986–1996, 2014.
View at: Publisher Site | Google Scholar
W. Foster, Y. Li, A. Usas, G. Somogyi, and J. Huard, “Gamma interferon as an antifibrosis agent in skeletal muscle,” Journal of Orthopaedic Research, vol. 21, no. 5, pp. 798–804, 2003.
View at: Publisher Site | Google Scholar
T. Laumonier and J. Menetrey, “Muscle injuries and strategies for improving their repair,” Journal Experimental Orthopaedics, vol. 3, no. 1, p. 15, 2016.
View at: Publisher Site | Google Scholar
J. Zhu, Y. Li, A. Lu et al., “Follistatin improves skeletal muscle healing after injury and disease through an interaction with muscle regeneration, angiogenesis, and fibrosis,” American Journal of Pathology, vol. 179, no. 2, pp. 915–930, 2011.
View at: Publisher Site | Google Scholar
Y. Zhang, W. Lei, W. Yan et al., “microRNA-206 is involved in survival of hypoxia preconditioned mesenchymal stem cells through targeting Pim-1 kinase,” Stem Cell Research & Therapy, vol. 7, no. 1, p. 61, 2016.
View at: Publisher Site | Google Scholar
J. Frisch, A. Rey-Rico, J. K. Venkatesan, G. Schmitt, H. Madry, and M. Cucchiarini, “rAAV-mediated overexpression of sox9, TGF-beta and IGF-I in minipig bone marrow aspirates to enhance the chondrogenic processes for cartilage repair,” Gene Therapy, vol. 23, no. 3, pp. 247–255, 2016.
View at: Publisher Site | Google Scholar
K. Tao, A. Rey-Rico, J. Frisch et al., “Effects of combined rAAV-mediated TGF-beta and sox9 gene transfer and overexpression on the metabolic and chondrogenic activities in human bone marrow aspirates,” Journal Experimental Orthopaedics, vol. 4, no. 1, p. 4, 2017.
View at: Publisher Site | Google Scholar
L. Li, X. Chen, W. E. Wang, and C. Zeng, “How to improve the survival of transplanted mesenchymal stem cell in ischemic heart?” Stem Cells International, vol. 2016, Article ID 9682757, p. 14, 2016.
View at: Publisher Site | Google Scholar
S. Lee, E. Choi, M. J. Cha, and K. C. Hwang, “Cell adhesion and long-term survival of transplanted mesenchymal stem cells: a prerequisite for cell therapy,” Oxidative Medicine and Cellular Longevity, vol. 2015, Article ID 632902, p. 9, 2015.
View at: Publisher Site | Google Scholar

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