肾脏疾病中的干细胞。

Q4 Biochemistry, Genetics and Molecular Biology
María José Soler, Ortiz-Pérez José Tomas
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引用次数: 0

摘要

循环骨髓来源的内皮祖细胞(EPCs)似乎在血管生成和血管稳态中起着至关重要的作用。慢性肾脏疾病是一种内皮功能障碍、动脉粥样硬化加速进展和心血管风险高的状态。因此,心血管疾病是终末期肾病(ESRD)患者死亡的主要原因。研究表明,晚期肾衰竭患者骨髓内皮祖细胞数量减少,内皮祖细胞功能受损。此外,在肾移植患者中,移植肾功能与EPC数显著相关。ESRD患者EPCs数量减少归因于尿毒症。因此,改善透析患者尿毒症状态的治疗方法,如夜间血液透析,与受损EPCs数量和迁移功能的恢复有关。事实上,慢性肾脏疾病患者的一些常见治疗方法,如促红细胞生成素、他汀类药物和血管紧张素II受体拮抗剂,会增加EPCs的数量。如今,越来越多的证据表明,在病理生理条件下,来自骨髓的干细胞(SCs)能够在损伤的肾脏中迁移,并且它们似乎在肾小球和肾小管再生中发挥作用。急性肾小管损伤后,存活的小管上皮细胞和假定的肾干细胞增殖分化为小管上皮细胞,促进结构和功能修复。此外,骨髓干细胞,包括造血干细胞和间充质干细胞也可以通过增殖和分化成肾系参与修复过程。例如,间充质干细胞已被证明可以减少炎症并促进肾脏再生。体外扩增的骨髓间充质SCs已被证明在各种急性肾功能衰竭的实验模型中是有益的。强调这种有益作用的机制仍然是一个有争议的问题。因此,基于体外扩增的SC或刺激局部祖细胞/SC群体的扩增和分化,旨在纠正干细胞再生潜力的治疗策略是未来研究的另一个令人兴奋的领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Stem cells in kidney diseases.

Circulating bone marrow-derived endothelial progenitor cells (EPCs) seem to play a crucial role in both vasculogenesis and vascular homeostasis. Chronic kidney disease is a state of endothelial dysfunction, accelerated progression of atherosclerosis and high cardiovascular risk. As a consequence, cardiovascular disorders are the main cause of death in end-stage renal disease (ESRD). It has been shown that patients with advanced renal failure have decreased number of bone marrow-derived endothelial progenitor cells and impaired EPCs function. Moreover, in kidney transplant patients, renal graft function significantly correlated with EPC number. The reduced number of EPCs in patients with ESRD has been ascribed to the uremia. Therefore, therapies that improve the uremic status in dialysis patients such as nocturnal hemodialysis are associated with restoration of impaired EPCs number and migratory function. In fact, some of the common treatments for patients with chronic kidney disease such as erythropoietin, statins and angiotensin II receptor antagonist increase the number of EPCs. Nowadays, there is growing evidence indicating that, under pathophysiological conditions, stem cells (SCs) derived from bone marrow are able to migrate in the injured kidney, and they seem to play a role in glomerular and tubular regeneration. After acute tubular renal injury, surviving tubular epithelial cells and putative renal stem cells proliferate and differentiate into tubular epithelial cells to promote structural and functional repair. Moreover, bone marrow stem cells, including hematopoietic stem cells and mesenchymal stem cells can also participate in the repair process by proliferation and differentiation into renal lineages. For instance, mesenchymal SCs have been shown to decrease inflammation and enhance renal regeneration. The administration of ex vivo expanded bone marrow-derived mesenchymal SCs have been proved to be beneficial in various experimental models of acute renal failure. The mechanisms underlining this beneficial effect are still a matter of debate. Thus, therapeutic strategies aimed at correcting the regenerative potential of stem cells based on the administration of ex vivo expanded SCs or stimulating expansion and differentiation of local progenitor/SC populations are another exciting area of future research.

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来源期刊
Journal of Stem Cells
Journal of Stem Cells Medicine-Transplantation
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