Prasadan Krishna, Shiota Chiyo, Xiangwei Xiao, Ricks David, Fusco Joseph, Gittes George
Rangos Research Center, Children's Hospital of University of Pittsburgh, 4401 Penn Avenue, Pittsburgh, PA, 15224, USA.
Cell Mol Life Sci. 2016 Oct;73(19):3623-37. doi: 10.1007/s00018-016-2231-0. Epub 2016 Apr 22.
The insulin-secreting beta cells in the endocrine pancreas regulate blood glucose levels, and loss of functional beta cells leads to insulin deficiency, hyperglycemia (high blood glucose) and diabetes mellitus. Current treatment strategies for type-1 (autoimmune) diabetes are islet transplantation, which has significant risks and limitations, or normalization of blood glucose with insulin injections, which is clearly not ideal. The type-1 patients can lack insulin counter-regulatory mechanism; therefore, hypoglycemia is a potential risk. Hence, a cell-based therapy offers a better alternative for the treatment of diabetes. Past research was focused on attempting to generate replacement beta cells from stem cells; however, recently there has been an increasing interest in identifying mechanisms that will lead to the conversion of pre-existing differentiated endocrine cells into beta cells. The goal of this review is to provide an overview of several of the key factors that regulate new beta cell formation (neogenesis) and beta cell proliferation.
内分泌胰腺中分泌胰岛素的β细胞调节血糖水平,功能性β细胞的丧失会导致胰岛素缺乏、高血糖(血糖升高)和糖尿病。目前1型(自身免疫性)糖尿病的治疗策略是胰岛移植,该方法存在重大风险和局限性,或者通过注射胰岛素使血糖正常化,但这显然并不理想。1型糖尿病患者可能缺乏胰岛素反调节机制;因此,低血糖是一个潜在风险。因此,基于细胞的疗法为糖尿病治疗提供了更好的选择。过去的研究主要集中在试图从干细胞生成替代β细胞;然而,最近人们越来越关注确定能使已分化的内分泌细胞转化为β细胞的机制。这篇综述的目的是概述调节新β细胞形成(新生)和β细胞增殖的几个关键因素。