Hua Hong, Sarvetnick Nora
Department of Immunology, The Scripps Research Institute, 10550 N. Torrey Pines Rd, IMM-23, La Jolla, CA 92037, USA.
Endocrine. 2007 Dec;32(3):280-6. doi: 10.1007/s12020-008-9036-3. Epub 2008 Mar 6.
Several key transcription factors are necessary for alpha cell development in the pancreas. In this study, we describe the expression of Inhibition of DNA-binding protein 1 (Id1) in the developing as well as the normal adult pancreas. We found co-expression of Id1 with bone morphogenetic protein (BMP) receptor in alpha cells. Inhibition of BMP4 signaling with a specific neutralizing antibody slightly decreases the proportion of glucagon cells in the adult pancreas but had a significant effect in a model of pancreas regeneration. In late embryonic pancreas, Id1 co-localized with GATA4, a transcription factor known for its critical function in glucagon cell development. However, in early postnatal period, the expression of Id1 and GATA4 diverged with Id1 identified in glucagon cells and GATA4 restricted to the acinar pancreas.
几种关键转录因子对胰腺中α细胞的发育至关重要。在本研究中,我们描述了DNA结合抑制蛋白1(Id1)在发育中的以及正常成年胰腺中的表达。我们发现Id1与α细胞中的骨形态发生蛋白(BMP)受体共表达。用特异性中和抗体抑制BMP4信号通路可使成年胰腺中胰高血糖素细胞的比例略有降低,但在胰腺再生模型中具有显著作用。在胚胎后期胰腺中,Id1与GATA4共定位,GATA4是一种在胰高血糖素细胞发育中具有关键功能的转录因子。然而,在出生后早期,Id1和GATA4的表达出现分化,Id1在胰高血糖素细胞中表达,而GATA4局限于腺泡胰腺。