Glucose Mediated Regulation of Beta Cell Proliferation

A. García-Ocaña, Laura C. Alonso
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引用次数: 11

Abstract

The pancreatic beta cell, as the sole source of circulating insulin, is indispensible for normal glucose metabolism. All forms of diabetes are characterized by insufficient insulin to meet metabolic needs, and inadequate beta cell mass is present in most forms of diabetes. Beta cell regenerative therapies provide one potential avenue for the prevention or cure of diabetes. Study of the pathways and mechanisms involved in endogenous beta cell proliferation can provide important clues to how regeneration occurs. Glucose is one important regulator of beta cell replication. Here we review the published literature investigating the effect of glucose on beta cell proliferation, and then describe the data supporting various known mechanisms of action. First, in vitro studies on fetal and adult beta cells from rodents and humans are reviewed. Next, we review evidence that circulating blood glucose regulates beta cell proliferation in living animals. These studies encompass a variety of in vivo models, including dietary manipulation, partial pancreatectomy, intravenous infusion of glucose, islet transplantation, and studies on diabetic hyperglycemia. Finally, mechanistic studies, both in vitro and in vivo, point to several different mitogenic pathways activated by glucose. Especially prominent are insulin signaling pathway members, glucose metabolism, and glucose impact on signaling by other growth factors. Multiple unanswered questions remain, and are highlighted throughout. With today's technologies we can now address questions first raised in the early 1900s, and hopefully develop new approaches to assuage the devastation of clinical diabetes.
葡萄糖介导的β细胞增殖调节
胰腺细胞作为循环胰岛素的唯一来源,对正常的葡萄糖代谢是不可缺少的。所有形式的糖尿病的特点都是胰岛素不足以满足代谢需要,而β细胞质量不足存在于大多数形式的糖尿病中。细胞再生疗法为预防或治疗糖尿病提供了一条潜在的途径。研究内源性β细胞增殖的途径和机制可以为研究再生如何发生提供重要线索。葡萄糖是β细胞复制的重要调节因子。在这里,我们回顾了已发表的研究葡萄糖对β细胞增殖影响的文献,然后描述了支持各种已知作用机制的数据。首先,本文综述了啮齿动物和人类胎儿和成人β细胞的体外研究。接下来,我们回顾了循环血糖调节活体动物β细胞增殖的证据。这些研究包括多种体内模型,包括饮食控制、部分胰腺切除术、静脉输注葡萄糖、胰岛移植和糖尿病高血糖的研究。最后,体外和体内的机制研究指出了葡萄糖激活的几种不同的有丝分裂途径。尤其突出的是胰岛素信号通路成员、葡萄糖代谢和葡萄糖对其他生长因子信号传导的影响。许多未解决的问题仍然存在,并且贯穿始终。有了今天的技术,我们现在可以解决20世纪初首次提出的问题,并有希望开发新的方法来减轻临床糖尿病的破坏。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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