Paris Descartes University, Paris, France.
Stem Cells Transl Med. 2013 Jan;2(1):61-7. doi: 10.5966/sctm.2012-0120. Epub 2012 Dec 19.
It is well-established that insulin-producing pancreatic beta cells are central in diabetes. In type 1 diabetes, beta cells are destroyed by an autoimmune mechanism, whereas in type 2 diabetes, there is a decrease in functional beta-cell mass. In this context, studying beta cells is of major importance. Beta cells represent only 1% of total pancreatic cells and are found dispersed in the pancreatic gland. During the past decades, many tools and approaches have been developed to study rodent beta cells that efficiently pushed the field forward. However, rodent and human beta cells are not identical, and our knowledge of human beta cells has not progressed as quickly as our understanding of rodent beta cells. We believe that one of the reasons for this inefficient progress is the difficulty of accessing unlimited sources of functional human pancreatic beta cells. The main focus of this review concerns recent strategies to generate new sources of human pancreatic beta cells.
众所周知,产生胰岛素的胰腺β细胞是糖尿病的核心。在 1 型糖尿病中,β细胞被自身免疫机制破坏,而在 2 型糖尿病中,β细胞的功能数量减少。在这种情况下,研究β细胞是非常重要的。β细胞仅占胰腺细胞总数的 1%,并且分散在胰腺中。在过去的几十年中,已经开发出许多研究啮齿动物β细胞的工具和方法,这些方法有效地推动了该领域的发展。然而,啮齿动物和人类的β细胞并不完全相同,我们对人类β细胞的了解并没有像对啮齿动物β细胞那样迅速。我们认为,导致这种进展缓慢的原因之一是难以获得无限来源的功能性人类胰腺β细胞。本篇综述的主要重点是生成新的人类胰腺β细胞来源的最新策略。