Caldas Heloisa Cristina, de Paula Couto Thaís Amarante Peres, Fernandes Ida Maria Maximina, Baptista Maria Alice Sperto Ferreira, Kawasaki-Oyama Rosa Sayoko, Goloni-Bertollo Eny Maria, Braile Domingo Marcolino, Abbud-Filho Mario
Laboratory of Immunology and Experimental Transplantation-LITEX, Department of Medicine/Nephrology, Medical School, FAMERP-HB/FUNFARME, Av Brigadeiro Faria Lima 5416, Sao Jose do Rio Preto, SP, 15090-000, Brazil.
Genetics and Molecular Biology Research Unit Laboratory-UPGEM, Department of Medicine/Nephrology, Medical School, FAMERP-HB/FUNFARME, Sao Jose do Rio Preto, SP, Brazil.
Clin Exp Nephrol. 2015 Oct;19(5):783-9. doi: 10.1007/s10157-015-1079-1. Epub 2015 Jan 29.
The therapeutic potential of adult stem cells in the treatment of chronic diseases is becoming increasingly evident. In the present study, we sought to assess whether treatment with mesenchymal stem cells (MSCs) efficiently retards progression of chronic renal failure (CRF) when administered to experimental models of less severe CRF.
We used two renal mass reduction models to simulate different stages of CRF (5/6 or 2/3 mass renal reduction). Renal functional parameters measured were serum creatinine (SCr), creatinine clearance (CCr), rate of decline in CCr (RCCr), and 24-h proteinuria (PT24h). We also evaluated renal morphology by histology and immunohistochemistry. MSCs were obtained from bone marrow aspirates and injected into the renal parenchyma of the remnant kidneys of both groups of rats with CRF (MSC5/6 or MSC2/3).
Animals from groups MSC5/6 and CRF2/3 seemed to benefit from MSC therapy because they showed significantly reduction in SCr and PT24h, increase in CCr and slowed the RCCr after 90 days. Treatment reduced glomerulosclerosis but significant improvement did occur in the tubulointerstitial compartment with much less fibrosis and atrophy. MSC therapy reduced inflammation by decreasing macrophage accumulation proliferative activity (PCNA-positive cells) and fibrosis (α-SM-actin). Comparisons of renal functional and morphological parameters responses between the two groups showed that rats MSC2/3 were more responsive to MSC therapy than MSC5/6.
This study showed that MSC therapy is efficient to retard CRF progression and might be more effective when administered during less severe stages of CRF.
成体干细胞在慢性疾病治疗中的潜力日益显著。在本研究中,我们试图评估当将间充质干细胞(MSC)应用于病情较轻的慢性肾衰竭(CRF)实验模型时,其是否能有效延缓CRF的进展。
我们使用两种肾质量减少模型来模拟CRF的不同阶段(5/6或2/3肾质量减少)。测量的肾功能参数包括血清肌酐(SCr)、肌酐清除率(CCr)、CCr下降率(RCCr)和24小时蛋白尿(PT24h)。我们还通过组织学和免疫组织化学评估肾脏形态。从骨髓抽吸物中获取MSC,并将其注射到两组CRF大鼠残余肾脏的肾实质中(MSC5/6或MSC2/3)。
MSC5/6组和CRF2/3组的动物似乎从MSC治疗中获益,因为在90天后,它们的SCr和PT24h显著降低,CCr增加,RCCr减缓。治疗减少了肾小球硬化,但肾小管间质区有显著改善,纤维化和萎缩程度明显减轻。MSC治疗通过减少巨噬细胞积聚、增殖活性(PCNA阳性细胞)和纤维化(α-平滑肌肌动蛋白)减轻了炎症。两组之间肾功能和形态学参数反应的比较表明,MSC2/3组大鼠对MSC治疗的反应比MSC5/6组更敏感。
本研究表明,MSC治疗可有效延缓CRF进展,在CRF病情较轻阶段进行治疗可能更有效。