Larsen Hjalte List, Grapin-Botton Anne
DanStem, University of Copenhagen, 3 B Blegdamsvej, DK-2200 Copenhagen N, Denmark.
DanStem, University of Copenhagen, 3 B Blegdamsvej, DK-2200 Copenhagen N, Denmark.
Semin Cell Dev Biol. 2017 Jun;66:51-68. doi: 10.1016/j.semcdb.2017.01.005. Epub 2017 Jan 12.
The pancreas is an essential endoderm-derived organ that ensures nutrient metabolism via its endocrine and exocrine functions. Here we review the essential processes governing the embryonic and early postnatal development of the pancreas discussing both the mechanisms and molecules controlling progenitor specification, expansion and differentiation. We elaborate on how these processes are orchestrated in space and coordinated with morphogenesis. We draw mainly from experiments conducted in the mouse model but also from investigations in other model organisms, complementing a recent comprehensive review of human pancreas development (Jennings et al., 2015) [1]. The understanding of pancreas development in model organisms provides a framework to interpret how human mutations lead to neonatal diabetes and may contribute to other forms of diabetes and to guide the production of desired pancreatic cell types from pluripotent stem cells for therapeutic purposes.
胰腺是一个重要的内胚层来源器官,通过其内分泌和外分泌功能确保营养物质的代谢。在此,我们回顾了胰腺胚胎期和出生后早期发育的关键过程,讨论了控制祖细胞特化、扩增和分化的机制及分子。我们阐述了这些过程如何在空间上进行协调,并与形态发生过程相配合。我们主要借鉴了在小鼠模型中进行的实验,同时也参考了其他模式生物的研究,补充了最近一篇关于人类胰腺发育的全面综述(Jennings等人,2015年)[1]。对模式生物胰腺发育的理解为解释人类突变如何导致新生儿糖尿病提供了一个框架,可能有助于理解其他形式的糖尿病,并指导从多能干细胞中产生所需的胰腺细胞类型用于治疗目的。