Development of insulin-producing cells from primitive biologic precursors

被引:12
作者
Evans-Molina, Carmella [1 ,2 ]
Vestermark, George L. [1 ]
Mirmira, Raghavendra G. [1 ,2 ,3 ]
机构
[1] Indiana Univ, Sch Med, Dept Med, Indianapolis, IN 46202 USA
[2] Indiana Univ, Sch Med, Herman B Wells Ctr Pediat Res, Indianapolis, IN 46202 USA
[3] Indiana Univ, Sch Med, Dept Pediat, Indianapolis, IN 46202 USA
关键词
beta cells; differentiation protocols; human embryonic stem cells; insulin-producing cells; EMBRYONIC STEM-CELLS; PANCREATIC BETA-CELLS; IN-VITRO DIFFERENTIATION; DIRECTED DIFFERENTIATION; ENDOCRINE PANCREAS; PROGENITOR CELLS; DEFINITIVE ENDODERM; DIABETES-MELLITUS; MICE LACKING; ALPHA-CELLS;
D O I
10.1097/MOT.0b013e3283186fc1
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Purpose of review The differentiation of pluripotent and multipotent stem cells into insulin-producing cells has the potential to create a renewable supply of replacement beta cells with tremendous utility in the treatment of diabetes. The purpose of this review is to summarize recent advancements in the field, with emphasis on the limitations of this technology as it relates to the beta cell. Recent findings Multiple groups have developed successful in-vitro protocols to differentiate human embryonic stem cells and selected tissue specific stem cells into progenitors capable of insulin production and glucose-stimulated insulin secretion. The resulting cells are immature beta cell-like cells that coexpress multiple islet hormones and lack the full complement of genes necessary for normal function. Protocols that include in-vivo maturation in immune-compromised mice produce cells with a more mature phenotype. Summary Although tremendous progress has been made in differentiating stem cells into insulin-producing cells, there is still more research needed to produce a fully functional adult beta cell.
引用
收藏
页码:56 / 63
页数:8
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