Endocrinology and Diabetes Group, Manchester Academic Health Science Centre, University of Manchester, A V Hill Building, Oxford Road, Manchester M13 9PT, UK.
J Endocrinol. 2010 Nov;207(2):151-61. doi: 10.1677/JOE-10-0120. Epub 2010 Aug 31.
Neurogenin 3 (NGN3) commits pancreatic progenitors to an islet cell fate. We have induced NGN3 expression and identified upregulation of the gene encoding the Ras-associated small molecular mass GTP-binding protein, RAB3B. RAB3B localised to the cytoplasm of human β-cells, both during the foetal period and post natally. Genes encoding alternative RAB3 proteins and RAB27A were unaltered by NGN3 expression and in human adult islets their transcripts were many fold less prevalent than those of RAB3B. The regulation of insulin exocytosis in rodent β-cells and responsiveness to incretins are reliant on Rab family members, notably Rab3a and Rab27a, but not Rab3b. Our results support an important inter-species difference in regulating insulin exocytosis where RAB3B is the most expressed isoform in human islets.
神经基因 3(NGN3)促使胰腺祖细胞向胰岛细胞命运分化。我们已经诱导了 NGN3 的表达,并发现编码 Ras 相关小分子 GTP 结合蛋白 RAB3B 的基因上调。RAB3B 在人类β细胞的细胞质中定位,无论是在胎儿期还是出生后。编码替代 RAB3 蛋白和 RAB27A 的基因不受 NGN3 表达的影响,在人类成年胰岛中,其转录本的丰度比 RAB3B 低得多。在啮齿动物β细胞中,胰岛素分泌的调节和对肠促胰岛素的反应依赖于 Rab 家族成员,特别是 Rab3a 和 Rab27a,但不是 Rab3b。我们的结果支持在调节胰岛素分泌方面存在重要的种间差异,其中 RAB3B 是人类胰岛中表达最丰富的同工型。