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胰岛细胞发育。

Islet cell development.

机构信息

Andalusian Center of Molecular Biology and Regenerative Medicine (CABIMER), CIBERDEM, 41092 Seville, Spain.

出版信息

Adv Exp Med Biol. 2010;654:59-75. doi: 10.1007/978-90-481-3271-3_4.

Abstract

Over the last years, there has been great success in driving stem cells toward insulin-expressing cells. However, the protocols developed to date have some limitations, such as low reliability and low insulin production. The most successful protocols used for generation of insulin-producing cells from stem cells mimic in vitro pancreatic organogenesis by directing the stem cells through stages that resemble several pancreatic developmental stages. Islet cell fate is coordinated by a complex network of inductive signals and regulatory transcription factors that, in a combinatorial way, determine pancreatic organ specification, differentiation, growth, and lineage. Together, these signals and factors direct the progression from multipotent progenitor cells to mature pancreatic cells. Later in development and adult life, several of these factors also contribute to maintain the differentiated phenotype of islet cells. A detailed understanding of the processes that operate in the pancreas during embryogenesis will help us to develop a suitable source of cells for diabetes therapy. In this chapter, we will discuss the main transcription factors involved in pancreas specification and beta-cell formation.

摘要

在过去的几年中,在将干细胞诱导为胰岛素表达细胞方面取得了巨大的成功。然而,迄今为止开发的方案存在一些局限性,例如可靠性低和胰岛素产量低。最成功的从干细胞生成产生胰岛素的细胞的方案通过引导干细胞经历类似于几个胰腺发育阶段的阶段来模拟体外胰腺发生。胰岛细胞命运由诱导信号和调节转录因子的复杂网络协调,这些信号和转录因子以组合方式决定胰腺器官的特化、分化、生长和谱系。这些信号和因子共同指导从多能祖细胞向成熟胰腺细胞的进展。在发育后期和成年期,这些因子中的一些也有助于维持胰岛细胞的分化表型。详细了解胚胎发生过程中胰腺中发生的过程将有助于我们为糖尿病治疗开发合适的细胞来源。在本章中,我们将讨论参与胰腺特化和β细胞形成的主要转录因子。

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