Regenerating the kidney using human pluripotent stem cells and renal progenitors

被引:26
作者
Becherucci, Francesca [1 ]
Mazzinghi, Benedetta [1 ]
Allinovi, Marco [2 ]
Angelotti, Maria Lucia [2 ]
Romagnani, Paola [1 ,2 ]
机构
[1] Meyer Childrens Univ Hosp, Nephrol & Dialysis Unit, Florence, Italy
[2] Univ Florence, Dept Biomed Expt & Clin Sci Mario Serio, Florence, Italy
基金
欧洲研究理事会;
关键词
iPSCs; kidney; regeneration; stem cells; renal progenitor cells; DIRECTED DIFFERENTIATION; EPITHELIAL-CELLS; LONG-TERM; INTERMEDIATE MESODERM; PODOCYTE REGENERATION; TUBULAR CELLS; GROWTH-FACTOR; DISEASE; GENERATION; INDUCTION;
D O I
10.1080/14712598.2018.1492546
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction: Chronic kidney disease is a major health-care problem worldwide and its cost is becoming no longer affordable. Indeed, restoring damaged renal structures or building a new kidney represents an ambitious and ideal alternative to renal replacement therapy. Streams of research have explored the possible application of pluripotent stem cells (SCs) (embryonic SCs and induced pluripotent SCs) in different strategies aimed at regenerate functioning nephrons and at understanding the mechanisms of kidney regeneration.Areas covered: In this review, we will focus on the main potential applications of human pluripotent SCs to kidney regeneration, including those leading to rebuilding new kidneys or part of them (organoids, scaffolds, biological microdevices) as well as those aimed at understanding the pathophysiological mechanisms of renal disease and regenerative processes (modeling of kidney disease, genome editing). Moreover, we will discuss the role of endogenous renal progenitors cells in order to understand and promote kidney regeneration, as an attractive alternative to pluripotent SCs.Expert opinion: Opportunities and pitfalls of all these strategies will be underlined, finally leading to the conclusion that a deeper knowledge of the biology of pluripotent SCs is mandatory, in order to allow us to hypothesize their clinical application.
引用
收藏
页码:795 / 806
页数:12
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