Recent Progress in Stem Cell Therapy for Diabetic Nephropathy

被引:32
作者
Liu, Yang [1 ]
Tang, Sydney C. W. [1 ]
机构
[1] Univ Hong Kong, Queen Mary Hosp, Div Nephrol, Dept Med, Hong Kong, Hong Kong, Peoples R China
关键词
Diabetic nephropathy; Stem cell therapy; Mesenchymal stem cells; Induced pluripotent stem cells; TUBULAR EPITHELIAL-CELLS; INSULIN-PRODUCING CELLS; INDUCED PLURIPOTENT; BONE-MARROW; KIDNEY-DISEASE; STROMAL CELLS; PROXIMAL TUBULE; PODOCYTE INJURY; ADIPOSE-TISSUE; GENERATION;
D O I
10.1159/000441913
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Diabetic nephropathy (DN) represents the leading cause of end-stage renal disease. Current therapeutic strategies for DN are very limited, and none of them can stop end-stage renal disease progression. Stem cell-based therapy showed encouraging outcomes in kidney disease, including experimental DN. Summary: Both podocytes and proximal tubular epithelial cells play key roles in the pathogenesis of DN and, accordingly, could be regarded as treatment targets. Multiple kinds of stem cells contribute to the regeneration of the injured kidney, including embryonic stem cells (ESCs), mesenchymal stem cells, and induced pluripotent stem cells (iPSCs). Stem cells exert reparatory effects mainly by homing to injured sites, directing differentiation, paracrine action, and immunoregulation. However, poor survival after transplantation under diabetic conditions and unsatisfactory animal models of advanced DN are major obstacles for achieving an efficacious therapeutic effect from stem cell transplantation. Recently, remarkable progress has been made both in the direct differentiation of human ESCs and iPSCs into renal cells and in the generation of tissue- and patient-specific iPSCs, offering a powerful tool to investigate DN mechanisms and to identify the ideal candidate cell for future clinical application. Key Message: This review provides updated information on recent progress and limitations of stem cell-based therapy for DN. (C) 2015 S. Karger AG, Basel
引用
收藏
页码:20 / 27
页数:8
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