| Literature DB >> 27587395 |
Zewen Song1,2, Joseph Fusco1, Ray Zimmerman1, Shane Fischbach1, Congde Chen1,3, David Matthew Ricks1, Krishna Prasadan1, Chiyo Shiota1, Xiangwei Xiao4, George K Gittes5.
Abstract
A thorough understanding of the signaling pathways involved in the regulation of β cell proliferation is an important initial step in restoring β cell mass in the diabetic patient. Here, we show that epidermal growth factor receptor 1 (EGFR) was significantly up-regulated in the islets of C57BL/6 mice after 50% partial pancreatectomy (PPx), a model for workload-induced β cell proliferation. Specific deletion of EGFR in the β cells of adult mice impaired β cell proliferation at baseline and after 50% PPx, suggesting that the EGFR signaling pathway plays an essential role in adult β cell proliferation. Further analyses showed that β cell-specific depletion of EGFR resulted in impaired expression of cyclin D1 and impaired suppression of p27 after PPx, both of which enhance β cell proliferation. These data highlight the importance of EGFR signaling and its downstream signaling cascade in postnatal β cell growth.Entities:
Keywords: beta cell (β cell); cell proliferation; cyclin D1; diabetes; epidermal growth factor receptor (EGFR)
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Year: 2016 PMID: 27587395 PMCID: PMC5077199 DOI: 10.1074/jbc.M116.747840
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157