EGF receptor in pancreatic β-cell mass regulation

被引:52
作者
Miettinen, Paivi
Ormio, Paivi
Hakonen, Elina
Banerjee, Meenal
Otonkoski, Timo [1 ]
机构
[1] Univ Helsinki, Hosp Children & Adolescents, FIN-00014 Helsinki, Finland
关键词
betacellulin; epidermal growth factor (EGF); ErbB; pancreatic beta-cell; transdifferentiation;
D O I
10.1042/BST0360280
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pancreatic islet development is impaired in mice lacking EGFRs (epidermal growth factor receptors). Even partial tissue-specific attenuation of EGFR signalling in the islets leads to markedly reduced p-cell proliferation and development of diabetes during the first weeks after birth. out of the many EGFR ligands, betacellulin has been specifically associated with positive effects on beta-cell growth, through both increased proliferation and neogenesis. EGFR action is also necessary for the beta-cell mitogenic activity of the gut hormone GLP-1 (glucagon-like peptide 1). Finally, in vitro models demonstrate a central role for EGFR in transdifferentiation of pancreatic acinar and ductal cells into endocrine islet cells. EGFR thus plays an essential role in p-cell mass regulation, but its mechanisms of action remain poorly understood.
引用
收藏
页码:280 / 285
页数:6
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