Concise Review: Mesenchymal Stem Cells for Diabetes

被引:63
|
作者
Dominguez-Bendala, Juan [1 ,2 ]
Lanzoni, Giacomo [1 ]
Inverardi, Luca [1 ,3 ]
Ricordi, Camillo [1 ,2 ]
机构
[1] Univ Miami, Leonard M Miller Sch Med, Diabet Res Inst, Miami, FL USA
[2] Univ Miami, Leonard M Miller Sch Med, Dept Surg, Miami, FL USA
[3] Univ Miami, Leonard M Miller Sch Med, Dept Med, Div Endocrinol Diabet & Metab, Miami, FL USA
基金
美国国家卫生研究院;
关键词
Diabetes; Mesenchymal stem cells; Plasticity; Stem cell transplantation; Stem cells; Adult stem cells; INSULIN-PRODUCING CELLS; HUMAN BONE-MARROW; IN-VITRO CULTIVATION; HUMAN AMNIOTIC-FLUID; STROMAL CELLS; MULTIPOTENTIAL NESTIN; TRANSCRIPTION FACTORS; PANCREATIC ENDOCRINE; DIFFERENTIATION; TRANSPLANTATION;
D O I
10.5966/sctm.2011-0017
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Mesenchymal stem cells (MSCs) have already made their mark in the young field of regenerative medicine. Easily derived from many adult tissues, their therapeutic worth has already been validated for a number of conditions. Unlike embryonic stem cells, neither their procurement nor their use is deemed controversial. Here we review the potential use of MSCs for the treatment of type 1 diabetes mellitus, a devastating chronic disease in which the insulin-producing cells of the pancreas (the beta-cells) are the target of an autoimmune process. It has been hypothesized that stem cell-derived beta-cells may be used to replenish the islet mass in diabetic patients, making islet transplantation (a form of cell therapy that has already proven effective at clinically restoring normoglycemia) available to millions of prospective patients. Here we review the most current advances in the design and application of protocols for the differentiation of transplantable beta-cells, with a special emphasis in analyzing MSC potency according to their tissue of origin. Although no single method appears to be ripe enough for clinical trials yet, recent progress in reprogramming (a biotechnological breakthrough that relativizes the thus far insurmountable barriers between embryonal germ layers) bodes well for the rise of MSCs as a potential weapon of choice to develop personalized therapies for type 1 diabetes. STEM CELLS TRANSLATIONAL MEDICINE 2012;1:59-63
引用
收藏
页码:59 / 63
页数:5
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