期刊
ISLETS
卷 2, 期 2, 页码 121-123出版社
TAYLOR & FRANCIS INC
DOI: 10.4161/isl.2.2.10908
关键词
islet-1; pancreas; transcriptional regulation; diabetes
资金
- NIDDK NIH HHS [R01 DK078606-03, P30-DK19525, DK019525, P30-DK050306, DK078606, R01 DK078606] Funding Source: Medline
Recently, we have reported the LIM-homeodoman (HD) transcriptional regulator, Islet-1 (Isl-1,(1)) as a key regulator for pancreatic islets after the secondary transition and into early postnatal stages in mice. Previously, the role of Isl-1 had only been examined during early pancreas development in vivo(2) and cell lines.(3-5) These early studies concluded that Isl-1 is required for the differentiation of early endocrine cells,(2) and hormone gene expression is regulated by Isl-1 in cell culture.(3-5) However, it was not clear from these studies whether the regulation of hormone gene transcription by Isl-1 was a direct transcriptional event. In addition, the function of Isl-1 during the formation of principle hormone producing endocrine cells had not been investigated since Isl-1 null animals die prior to the formation of these cells. Using pancreas-specific inactivation of Isl-1 in mice, we have elucidated the role of Isl-1 during maturation, proliferation and survival of the endocrine pancreas after the secondary transition. We have also identified MafA, a potent Insulin gene regulator, as the first direct target of Isl-1 in beta-cells.
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