Cavaglieri R C, Martini D, Sogayar M C, Noronha I L
Laboratory of Cellular and Molecular Nephrology, Faculty of Medicine, University of São Paulo, São Paulo, Brazil.
Transplant Proc. 2009 Apr;41(3):947-51. doi: 10.1016/j.transproceed.2009.01.072.
Stem cells (SC) are potential therapeutic tools in the treatment of chronic renal diseases. Number and engraftment of SC in the injured sites are important for possible differentiation into renal cells and paracrine effect. The aim of this study was to analyze the effect of subcapsular injection of mesenchymal stem cells (MSC) in the 5/6 nephrectomy model (5/6 Nx). MSC obtained from Wistar rats were isolated by their capacity to adhere to plastic surfaces, characterized by flow cytometry, and analyzed by their differentiation potential into osteoblasts. MSC (2 x 10(5)) were injected into the subcapsule of the remnant kidney of male Wistar rats, and were followed for 15 or 30 days. 5/6 Nx rats showed significant hypertension at 15 and 30 days, which was reduced by MSC at 30 days. Increased albuminuria and serum creatinine at 15 and 30 days in 5/6 Nx rats were also reduced by subcapsular injection of MSC. We also observed a significant reduction of glomerulosclerosis index 30 days after injection of MSC. 4-6 diamidino-2-phenylindole dihydrochloride (DAPI)-stained MSC showed a migration of these cells into renal parenchyma 5, 15, and 30 days after subcapsular injection. In conclusion, our data demonstrated that subcapsular injection of MSC in 5/6 Nx rats is associated with renoprotective effects. These results suggest that locally implanted MSC in the kidney allow a large number of cells to migrate into the injured sites and demonstrate that subcapsular injection represent an effective route for MSC delivery.
干细胞是治疗慢性肾脏疾病的潜在治疗工具。干细胞在损伤部位的数量和植入对于其分化为肾细胞及旁分泌作用至关重要。本研究旨在分析在5/6肾切除模型(5/6 Nx)中肾包膜下注射间充质干细胞(MSC)的效果。从Wistar大鼠分离获得的MSC通过其贴壁能力进行分离,采用流式细胞术进行鉴定,并分析其向成骨细胞的分化潜能。将2×10⁵个MSC注射到雄性Wistar大鼠残余肾脏的包膜下,随后观察15天或30天。5/6 Nx大鼠在15天和30天时出现明显高血压,而在30天时MSC使其血压降低。5/6 Nx大鼠在15天和30天时蛋白尿和血清肌酐增加,肾包膜下注射MSC也使其降低。我们还观察到注射MSC 30天后肾小球硬化指数显著降低。4',6-二脒基-2-苯基吲哚二盐酸盐(DAPI)染色的MSC显示在肾包膜下注射后5天、15天和30天这些细胞迁移至肾实质。总之,我们的数据表明在5/6 Nx大鼠中肾包膜下注射MSC具有肾脏保护作用。这些结果表明,在肾脏局部植入MSC可使大量细胞迁移至损伤部位,并证明肾包膜下注射是MSC递送的有效途径。