Toward beta cell replacement for diabetes

被引:37
作者
Johannesson, Bjarki [1 ]
Sui, Lina [2 ,3 ]
Freytes, Donald O. [1 ]
Creusot, Remi J. [4 ,5 ]
Egli, Dieter [1 ,2 ,3 ]
机构
[1] New York Stem Cell Fdn Res Inst, New York, NY 10023 USA
[2] Columbia Univ, Coll Phys & Surg, Naomi Berrie Diabet Ctr, New York, NY USA
[3] Columbia Univ, Dept Pediat, Coll Phys & Surg, New York, NY 10027 USA
[4] Columbia Univ, Dept Med, Columbia Ctr Translat Immunol, New York, NY USA
[5] Columbia Univ, Naomi Berrie Diabet Ctr, New York, NY USA
关键词
beta cells; cell replacement therapy; stem cells; type; 1; diabetes; PLURIPOTENT STEM-CELLS; INSULIN-PRODUCING CELLS; REGULATORY T-CELLS; CLASS-I EXPRESSION; LONG-TERM CULTURE; EXTRACELLULAR-MATRIX; EFFICIENT DIFFERENTIATION; DIRECTED DIFFERENTIATION; PANCREAS PROGENITORS; IMMUNE SURVEILLANCE;
D O I
10.15252/embj.201490685
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The discovery of insulin more than 90 years ago introduced a life-saving treatment for patients with type 1 diabetes, and since then, significant progress has been made in clinical care for all forms of diabetes. However, no method of insulin delivery matches the ability of the human pancreas to reliably and automatically maintain glucose levels within a tight range. Transplantation of human islets or of an intact pancreas can in principle cure diabetes, but this approach is generally reserved for cases with simultaneous transplantation of a kidney, where immunosuppression is already a requirement. Recent advances in cell reprogramming and beta cell differentiation now allow the generation of personalized stem cells, providing an unlimited source of beta cells for research and for developing autologous cell therapies. In this review, we will discuss the utility of stem cell-derived beta cells to investigate the mechanisms of beta cell failure in diabetes, and the challenges to develop beta cell replacement therapies. These challenges include appropriate quality controls of the cells being used, the ability to generate beta cell grafts of stable cellular composition, and in the case of type 1 diabetes, protecting implanted cells from autoimmune destruction without compromising other aspects of the immune system or the functionality of the graft. Such novel treatments will need to match or exceed the relative safety and efficacy of available care for diabetes.
引用
收藏
页码:841 / 855
页数:15
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