Review Article

Management of Fibrosis: The Mesenchymal Stromal Cells Breakthrough

Table 3

MSC treatment on preclinical kidney fibrosis models.

ReferencesOrganismModelTreatmentMSC sourceTimingQuantityRouteOutcome

[60]MouseR-UUO10 days UUOBM10 days after UUO106 cellsRenal artery(i) Decreased expression of TNF-α, TGF-β1, and α-SMA
(ii) Increased expression of E-cadherin

[61]PigARASIrritant coil placed in the main renal arteryAT6 weeks after ARAS 106 cellsLocal(i) Reduced fibrotic area
(ii) Reduced number of CD163 + macrophages
(iii) Increased number of regulatory macrophages
(iv) Increased expression of IL-10
(v) Decreased expression of TNF-α
(vi) Reduced concentration of MMP-2
(vii) Increased expression of VEGF, FLK-1, and HIF1-α
(viii) Reduced MCP-1 positive area

[62]RatAlbumin-overload + uninephrectomyNephrectomy followed by 5 intraperitoneal injections of BSA (10 mg/g) per weeks during 4 weeksBM7 days after the first BSA injection106 cells weekly for 4 weeksIV(i) Reduced expression and concentration of MCP-1 and CCL-5
(ii) Reduced expression and concentration of α-SMA
(iii) Reduced expression and concentration of collagen IV

[63]RatAllograftBi-nephrectomization and single kidney allograftBM (melatonin treated)11 weeks after graft5.105 cellsTail vein(i) Decreased expression of IL-6, IL-7r, IL-23a, and IL-10
(ii) Decreased concentration of CTGF and α-SMA
(iii) Decreased expression of fibronectin
(iv) Decreased expression of bFGF

[64]RatNIRCExcision of the right kidney, 45-minutes ischemia in the left kidney followed by 28-day cyclosporine A treatmentBM7 or 14 days after ischemia-reperfusion3.106 cellsLocalMSC transplantation 7 days after ischemia reperfusion:
(i) Decreased fibrotic area
(ii) Decreased expression of collagen types I, III, and IV
(iii) Reduced number of α-SMA-positive cells
(iv) Decreased activity of MMP-2 (sham level)
MSC transplantation 14 days after ischemia reperfusion showed no significant improvement

[65]RatRKM5/6 nephrectomyBM2 weeks after surgical procedure−2.105 cells or −2.105 cells every other week (weeks 2, 4, and 6)IV(i) Reduced fibrotic area
(ii) Increased expression of IL-4 and IL-10
(iii) Decreased expression of IL-6 and TNF-α
(iv) Decreased expression of TGF-β1, Smad3, α-SMA, FSP-1, and vimentin
(v) Decreased expression of collagen type I, collagen type III, fibronectin, and TIMP-1/MMP-9 ratio
(vi) Increased expression of HO-1
(vii) Decreased expression of MCP-1
(viii) Increased expression of HGF

[66]RatUUO1 to 4 weeks obstructionBMPrior to UUO106 cellsRenal artery(i) Decreased collagen concentration
(ii) Decreased expression of TNF-α
(iii) Decreased concentration of TNF-α
(iv) Decreased expression of α-SMA
(v) Decreased number of FSP-1 positive cells
(vi) Increased expression of E-cadherin

Influence of fibrosis induction methods, MSC source, timing of injection, quantity of MSCs transplanted, and transplantation route. Outcomes are expressed compared to control groups (i.e., groups treated but not transplanted with MSCs) unless stated otherwise (α-SMA: α-smooth muscle actin; ARAS: atherosclerotic renal artery stenosis; AT: adipose tissue; BSA: bovine serum albumin; CCL: chemokine ligand; CTGF: connective tissue growth factor; FGF: fibroblast growth factor; FLK: fetal liver kinase; FSP: fibroblast specific protein; HGF: hepatocyte growth factor; HIF: hypoxia-inducible factor; HO-1: heme oxygenase 1; IL: interleukin; IV: intravenous; MCP: monocyte chemoattractant protein; MMP: matrix metalloproteinase; MSC: mesenchymal stromal cell; NIRC: nephrectomy + ischemia-reperfusion + cyclosporine; R-UUO: reversible unilateral ureteral obstruction; TGF-β: transforming growth factor-β; TIMP: tissue inhibitor of metalloproteinase; TNF-α: tumor necrosis factor-α; UUO: unilateral ureteral obstruction; VEGF: vascular endothelial growth factor).