Section on Islet Cell and Regenerative Biology, Research Division, Joslin Diabetes Center, One Joslin Place, Boston, MA 02215, USA, and the Department of Medicine, Harvard Medical School, 25 Shattuck Street, Boston, MA 02115, USA.
Genome Med. 2011 Sep 27;3(9):61. doi: 10.1186/gm277.
Stem cells hold great promise for pancreatic beta cell replacement therapy for diabetes. In type 1 diabetes, beta cells are mostly destroyed, and in type 2 diabetes beta cell numbers are reduced by 40% to 60%. The proof-of-principle that cellular transplants of pancreatic islets, which contain insulin-secreting beta cells, can reverse the hyperglycemia of type 1 diabetes has been established, and there is now a need to find an adequate source of islet cells. Human embryonic stem cells can be directed to become fully developed beta cells and there is expectation that induced pluripotent stem (iPS) cells can be similarly directed. iPS cells can also be generated from patients with diabetes to allow studies of the genomics and pathogenesis of the disease. Some alternative approaches for replacing beta cells include finding ways to enhance the replication of existing beta cells, stimulating neogenesis (the formation of new islets in postnatal life), and reprogramming of pancreatic exocrine cells to insulin-producing cells. Stem-cell-based approaches could also be used for modulation of the immune system in type 1 diabetes, or to address the problems of obesity and insulin resistance in type 2 diabetes. Herein, we review recent advances in our understanding of diabetes and beta cell biology at the genomic level, and we discuss how stem-cell-based approaches might be used for replacing beta cells and for treating diabetes.
干细胞为糖尿病的胰岛β细胞替代治疗带来了巨大的希望。在 1 型糖尿病中,β细胞几乎被完全破坏,而在 2 型糖尿病中,β细胞数量减少了 40%至 60%。胰岛细胞的细胞移植可以逆转 1 型糖尿病的高血糖,这一原理已经得到证实,现在需要寻找足够的胰岛细胞来源。人类胚胎干细胞可以被诱导分化为成熟的β细胞,人们期望诱导多能干细胞(iPS 细胞)也可以被类似地诱导分化。iPS 细胞也可以从糖尿病患者中产生,以允许对疾病的基因组学和发病机制进行研究。替代β细胞的一些其他方法包括寻找增强现有β细胞复制的方法、刺激新生成(出生后形成新胰岛)以及将胰腺外分泌细胞重编程为产生胰岛素的细胞。基于干细胞的方法也可用于调节 1 型糖尿病的免疫系统,或解决 2 型糖尿病的肥胖和胰岛素抵抗问题。在此,我们综述了近年来在基因组水平上对糖尿病和胰岛β细胞生物学的理解方面的最新进展,并讨论了基于干细胞的方法如何用于替代β细胞和治疗糖尿病。