Kim Seung K, MacDonald Raymond J
Departments of Developmental Biology and Medicine (Oncology Division), Stanford UniversityStanford, California, 94305-5329, USA.
Curr Opin Genet Dev. 2002 Oct;12(5):540-7. doi: 10.1016/s0959-437x(02)00338-6.
The results of several new studies encourage a revision of fundamental hypotheses concerning the cellular and molecular mechanisms underlying pancreatic morphogenesis and cell differentiation in the embryo. The roles of FGF- and BMP-signaling indicate a fundamental difference in the induction of the dorsal and the ventral pancreatic anlage. Final commitment to the pancreatic fate requires the action of several transcriptional regulators including IPF1/PDX1, PBX1 and PTF1-P48 after the onset of pancreatic bud formation. Two, largely independent endocrine cell lineages develop during the formation of the embryonic pancreas. Lineage tracing has begun to refine our understanding of the origins of the acinar, ductal and islet cells.
几项新研究的结果促使人们对有关胚胎胰腺形态发生和细胞分化的细胞与分子机制的基本假设进行修订。FGF信号和BMP信号的作用表明,背侧和腹侧胰腺原基的诱导存在根本差异。胰腺命运的最终确定需要在胰腺芽形成后,包括IPF1/PDX1、PBX1和PTF1-P48在内的几种转录调节因子发挥作用。在胚胎胰腺形成过程中,主要发育出两个基本独立的内分泌细胞谱系。谱系追踪已开始深化我们对腺泡细胞、导管细胞和胰岛细胞起源的理解。