| Literature DB >> 27184845 |
Teruki Dainichi1, Matthew S Hayden2, Sung-Gyoo Park3, Hyunju Oh4, John J Seeley4, Yenkel Grinberg-Bleyer4, Kristen M Beck5, Yoshiki Miyachi6, Kenji Kabashima6, Takashi Hashimoto7, Sankar Ghosh8.
Abstract
Asymmetric cell division (ACD) in a perpendicular orientation promotes cell differentiation and organizes the stratified epithelium. However, the upstream cues regulating ACD have not been identified. Here, we report that phosphoinositide-dependent kinase 1 (PDK1) plays a critical role in establishing ACD in the epithelium. Production of phosphatidyl inositol triphosphate (PIP3) is localized to the apical side of basal cells. Asymmetric recruitment of atypical protein kinase C (aPKC) and partitioning defective (PAR) 3 is impaired in PDK1 conditional knockout (CKO) epidermis. PDK1(CKO) keratinocytes do not undergo calcium-induced activation of aPKC or IGF1-induced activation of AKT and fail to differentiate. PDK1(CKO) epidermis shows decreased expression of Notch, a downstream effector of ACD, and restoration of Notch rescues defective expression of differentiation-induced Notch targets in vitro. We therefore propose that PDK1 signaling regulates the basal-to-suprabasal switch in developing epidermis by acting as both an activator and organizer of ACD and the Notch-dependent differentiation program.Entities:
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Year: 2016 PMID: 27184845 PMCID: PMC4909264 DOI: 10.1016/j.celrep.2016.04.051
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423