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BioMed Research International
Volume 2013 (2013), Article ID 626258, 8 pages
Isolation and Characterization of Chicken Dermis-Derived Mesenchymal Stem/Progenitor Cells
1Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, China
2College of Wildlife Resources, Northeast Forestry University, Harbin 150040, China
Received 19 May 2013; Revised 30 June 2013; Accepted 2 July 2013
Academic Editor: Ken-ichi Isobe
Copyright © 2013 Yuhua Gao et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Dermis-derived mesenchymal stem/progenitor cells (DMS/PCs) were isolated from the skin tissue of 16-day-old chick embryos and then characterized by immunofluorescence and RT-PCR. We found that primary DMS/PCs could be expanded for 15 passages. Expression of β-integrin, CD44, CD71, and CD73 was observed by immunofluorescence and RT-PCR. Passage 3 DMS/PCs were successfully induced to differentiate into osteoblasts, adipocytes, and neurocytes. The results indicate the potential for multilineage differentiation of DMS/PCs that may represent an ideal candidate for cellular transplantation therapy.
Mesenchymal stem cells (MSCs) were first discovered in bone marrow (BMSCs), which have a strong proliferative capacity and can be differentiated into adipocytes [1, 2], osteoblasts [3–5], myoblasts [6–8], and neurons [9, 10].
However, the proliferation, differentiation, and number of BMSCs are significantly decreased with aging. In addition, because of possible virus infection , researchers began to search for MSCs in other tissues. In recent years, MSCs have been found in muscles, amniotic fluid, umbilical cord blood, fat, and other tissues [12–14].
The dermis contains mostly differentiated cells including fibroblasts that only participate in scar tissue formation during skin repair . Therefore, the dermis is often regarded as a negative control for studies of stem cells . Following isolation and characterization of BMSCs in the 1990s , significant progress has been made in studies of dermis-derived mesenchymal stem/progenitor cells (DMS/PCs), including their separation and culture. Moreover, DMS/PCs can be induced to differentiate into osteoblasts, adipocytes, and ectodermal cell types. Considering the easy accessibility of DMS/PCs, these cells have become an ideal cellular source in tissue engineering.
Current research of stem cells focuses on humans, mice, rabbits, and other mammals, but little research has been performed on poultry. As an animal model, the chicken possesses abundant dermal tissues. Furthermore, the chicken is an endemic species that is important in the global economy. In this study, we carried out a pilot study on the separation, culture, and differentiation potential of chicken DMS/PCs.
2. Materials and Methods
2.1. Isolation and Culture of DMS/PCs
Animal experiments were performed in accordance with the guidelines established by the Institutional Animal Care and Use Committee of the Chinese Academy of Agriculture of Sciences.
Dorsal skin tissues were isolated from 30 16-day-old chick embryos. The dermal layer was isolated from the epidermal layer by digestion with 0.25% dispase II (Gibco, Carlsbad, CA, USA) for 1.5–2 h at 37°C. The dermis was cut into approximately 1 cm2 pieces and then digested with 0.25% trypsin (Gibco) for about 15 min. Then, the enzymatic activity was neutralized with fetal bovine serum (FBS) (Gibco). The digested tissue was passed through a 200 μm mesh filter and then centrifuged at 1200 r/min for 6 min at room temperature. The supernatant was discarded, and the pellet was re-suspended with an optimized culture medium. The viability of DMS/PCs was determined by trypan blue exclusion. As a result, cells were yielded from 1 cm2 of chick embryo skin. The cell suspension was seeded in six-well plates and incubated at 37°C with 5% CO2. After 48 h of culture, the cells were washed twice with PBS to remove nonadherent cells. At 70–80% confluence, the cells were passaged with 0.25% trypsin. Generally, after 3-4 passages, the cells were homogenous.
2.2. Optimization of Cell Culture Systems for DMS/PCs
DMS/PC culture at passage 3 was assessed in three culture systems: culture system I (L-Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10% FBS), culture system II (L-DMEM supplemented with 2 mM L-glutamine, 1 mM sodium pyruvate, and 10% FBS), and culture system III (L-DMEM supplemented with 20 ng/mL epidermal growth factor (EGF), 20 ng/mL basic fibroblast growth factor (bFGF), 10% FBS, 2 mM L-glutamine, and 1 mM sodium pyruvate). Cells were harvested and reseeded in six-well plates at cells/well. The cells were cultured further and the generation time in each culture system was counted three times. Culture system III was subsequently used to culture DMS/PCs.
2.3. Markers of DMS/PCs
DMS/PCs were fixed in 4% paraformaldehyde for 15 min and then washed three times in PBS (5 min each). Cells were permeabilized with 0.2% Triton X-100 for 15–20 min and then washed three times (5 min each) in PBS. The cells were blocked with 10% normal goat serum (Santa Cruz Biotechnology, Santa Cruz, CA, USA) for 30 min and then incubated at room temperature for 1 h in 3% bovine serum albumin (BSA) containing the following antibodies: mouse anti-β-integrin (1 : 100; Abcam, Cambridge, MA, USA), mouse anti-CD44 (1 : 200; Abcam), mouse anti-nestin (1 : 200; Abcam), rabbit anti-synaptophysin (SYP) (1 : 100; Bioss, Beijing, China), rabbit anti-CD71 (1 : 200; Bioss), rabbit anti-CD73 (1 : 200; Bioss), rabbit anti-neurofilament (NF) (1 : 200; Bioss), or goat anti-β-III tubulin (1 : 200; Santa Cruz Biotechnology). Then, the cells were washed three times (10 min each) with PBS and then incubated in PBS containing secondary antibodies at 37°C for 1 h. Secondary antibodies were Cy5.5-conjugated goat anti-mouse and donkey anti-rabbit IgGs, and fluoroisothiocyanate-conjugated goat anti-rabbit and donkey anti-goat IgGs (Santa Cruz Biotechnology).
Cells were examined under a TE-2000-E inverted fluorescence microscope (Nikon, Yokohama, Kanagawa Japan). Cells were counterstained with DAPI (Sigma-Aldrich, St. Louis, MO, USA).
RNA was isolated from cells using Trizol reagent (Invitrogen). cDNA was synthesized using a reverse transcription system (Takara, Dalian, Liaoning, China) and amplified by PCR using specific primers (Table 1). PCR products were visualized by 2% agarose gel electrophoresis.
2.5. Adipogenic Differentiation of DMS/PCs
Cells were divided into two groups: induced and control groups. At 50–60% confluence, cells in the induced group were incubated in adipogenic medium containing 1 mM dexamethasone (Sigma), 0.5 mM isobutyl-methylxanthine (IBMX; Sigma), and 10 μg/mL insulin (Sigma). Cells in the control group were cultured in complete medium without any inducers. After 2 weeks of differentiation, the cells were stained with oil red O to assess intracellular lipid accumulation. RNA was also isolated for RT-PCR analysis.
2.6. Osteogenic Differentiation of DMS/PCs
Passage 3 cells were seeded in six-well plates at cells/well. The cells were also divided into inducted and control groups. At 50–60% confluence, cells in the induced group were cultured in osteogenic medium containing 0.5 mM dexamethasone (Sigma), 10 mM β-glycerophosphate (Sigma), and 50 μg/mL vitamin C. Cells in the control group were cultured in complete medium without any inducers. Media were changed every 2 days. After 2 weeks of differentiation, the capacity for calcium node formation was detected by alizarin red staining and osteoblast-specific gene expression was analyzed by RT-PCR.
2.7. Neurogenic Differentiation of DMS/PCs
Cells were seeded and divided into the two groups as described above. Neural-like cell differentiation was accomplished in L-DMEM supplemented with 10% FBS, 1 μM all-trans-retinoic acid, and 100 μM 2-mercaptoethanol (Sigma) . After 10 days, the cells were harvested and neural-specific marker expression was detected by immunofluorescence and RT-PCR.
3.1. Isolation, Culture, and Morphology of DMS/PCs
Primary cells isolated from the dermis adhered to the culture plates and began to elongate after 24 h (Figure 1(a)-A). After about 5 days, the cells exhibited a fibroblast-like morphology (Figure 1(a)-B) and grew to 80–90% confluence (Figure 1(a)-C).
3.2. Optimization of DMS/PC Culture
There was no significant difference between culture systems I and II (). The generation time was about 8 days for both systems. Culture system III and the other culture systems were significantly different and resulted in a generation time of about 3 days () (Figure 1(b)). These results indicated that EGF and bFGF promote DMS/PC proliferation, and culture system III is suitable for expansion of DMS/PCs.
No obvious morphological differences were observed among passages, and the characteristics of the cells were stable after passaging. The cells were cultured to passage 16 and showed the representative appearance of senescence, such as blebbing and karyopyknosis in most cells. Moreover, cells cultured for more than 16 passages became detached from the plates.
3.3. Characterization of DMS/PCs
3.3.1. Markers of DMS/PCs
We detected markers of DMS/PCs by immunofluorescence and RT-PCR. The immunofluorescence (Figure 2) and RT-PCR (Figure 3) results showed that DMS/PCs expressed β-integrin, CD44, CD71, and CD73 but did not express CD34 (a hematopoietic cell marker). There were no apparent differences in these markers at different passages.
3.4. Adipogenic Differentiation of DMS/PCs
Adipogenic differentiation of DMS/PCs was demonstrated by oil red O staining . After incubation in adipogenic medium for 7 days, DMS/PCs changed from a shuttle shape to an oblate shape and contained many intracellular lipid droplets. As differentiation progressed, the number of lipid droplets increased and aggregated to form larger droplets (Figure 4(b)). As a negative control, cells cultured in complete medium were negative for oil red O staining (Figure 4(a)).
After induction, RT-PCR results showed that the cells expressed adipocyte-specific genes peroxisome proliferator-activated receptor-γ (PPAR-γ) and lipoprotein lipase (LPL), whereas these genes were not expressed in the control group (Figure 4(c)).
3.5. Osteogenic Differentiation of DMS/PCs
After incubation in osteogenic medium for 7 days, DMS/PCs showed obvious morphological changes. After 14 days of differentiation, the cells became aggregated and formed mineralized nodules that were stained with alizarin red. In addition, the number and size of nodules were increased (Figure 5(b)), whereas control cells showed no such effects (Figure 5(a)).
Osteogenic differentiation of DMS/PCs was also analyzed by RT-PCR. Osteogenic-specific genes alkaline phosphatase (AKP) and osteopontin (OPN) were expressed in the induced group but not in the control group (Figure 5(c)).
3.6. Neurogenic Differentiation of DMS/PCs
After incubation in neural differentiation medium for 14 days, DMS/PCs exhibited elongated cell bodies with neurites (Figures 6(b) and 6(c)). There were no obvious morphological changes in the control group (Figure 6(a)). Moreover, immunofluorescence demonstrated that cells in the inducted group expressed neural cell markers nestin (Figure 6(d)), β-III tubulin (Figure 6(e)), NF (Figure 6(g)), and SYP (Figure 6(h)). RT-PCR analysis demonstrated expression of the nestin gene in both inducted and control groups, but the relative expression level in the inducted group was significantly higher than that in the control group (Figure 6(j), lanes 1 and 2). In addition, the NF gene was expressed in the induction group (Figure 6(j), lanes 3 and 4). These results indicate that DMS/PCs can differentiate into neurocytes .
In this study, DMS/PCs were successfully isolated from the dermis of 16-day-old chick embryos. Obvious differences in cell viability were observed between cells isolated from 16-day-old and 21-day-old embryos (data not show), indicating that younger animals are more suitable and the conditions to separate the dermis should be considered carefully.
The markers of DMS/PCs resemble those of BMSCs. Both cell types express some surface markers of MSCs. We examined the expression of β-integrin, CD44, CD71, and CD73 by immunofluorescence and RT-PCR. β-integrin is an integrin unit associated with very late antigen receptors. It is involved in cell adhesion and recognition in various biological processes including embryogenesis, hemostasis, tissue repair, immune responses, and metastatic diffusion of tumor cells. CD44 is a cell surface glycoprotein involved in cell-cell interactions, adhesion, and migration. This protein participates in a variety of cellular functions including lymphocyte activation, recirculation and homing, hematopoiesis, and tumor metastasis. CD71 is a member of the transferrin receptor family that is required for the import of iron into cells and is regulated in response to intracellular iron concentrations. Low iron concentrations increase the levels of transferrin receptors to increase iron intake into cells. Thus, the transferrin receptor maintains cellular iron homeostasis. CD73, also known as ecto-5′-nucleotidase, is an enzyme used as a marker of lymphocyte differentiation .
Multilineage differentiation of stem cells is the most notable characteristic for homotransplantation. Because of easy accessibility, DMS/PCs have become an ideal cell source in tissue engineering. In vivo, the development and function of tissue stem cells are related to transcription factors and extracellular signals . However, in vitro, the mechanisms of differentiation are unclear. In our study, we differentiated chicken DMS/PCs into osteoblasts, adipocytes, and neurocytes, and then examined relevant gene expression of these cell types. The results showed that different induction factors affect the differentiation of DMS/PCs. In addition, DMS/PCs originating from mesoblastema can be induced to differentiate into mesodermal and ectodermal cells. The homotransplantation feature of DMS/PCs, together with their putative multipotency and ease of procurement, suggests that these cells are an excellent choice for many tissue engineering strategies and cell-based therapies. The chick embryo is a classic model of vertebrate developmental biology, which has been used for many decades . Although the multi-lineage differentiation of DMS/PCs was successful in vitro, there are many drawbacks for the use of these cells in tissue regeneration in vivo, such as a higher decline rate and unstable phenotype. Therefore, more consideration may be needed for further research.
In this study, we isolated DMS/PCs from the dermis of 16-day-old chick embryos and then examined their ability to expand and differentiate in vitro. These results have implications for the potential utility of the dermis as a source of stem cells for regenerative medical therapies.
Yuhua Gao and Chunyu Bai contributed equally to this work.
Conflict of Interests
The authors have declared that there is no conflict of interests.
This research was supported by the Ministry of Agriculture of China for Transgenic Research Program (2011ZX08009-003-006, 2011ZX08012-002-06), the central level, scientific research institutes for R&D special fund business (2011cj-9, 2012zl072), and the project of National Infrastructure of Animal Germplasm Resources (2013 year).
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