| Literature DB >> 29906410 |
Hui Kheng Lim1, Anisa B Rahim1, Vonny Ivon Leo1, Shatarupa Das1, Thiam Chye Lim2, Takeshi Uemura3, Kazuei Igarashi3, John Common1, Leah A Vardy4.
Abstract
Wound healing is a dynamic process involving gene-expression changes that drive re-epithelialization. Here, we describe an essential role for polyamine regulator AMD1 in driving cell migration at the wound edge. The polyamines, putrescine, spermidine, and spermine are small cationic molecules that play essential roles in many cellular processes. We demonstrate that AMD1 is rapidly upregulated following wounding in human skin biopsies. Knockdown of AMD1 with small hairpin RNAs causes a delay in cell migration that is rescued by the addition of spermine. We further show that spermine can promote cell migration in keratinocytes and in human ex vivo wounds, where it significantly increases epithelial tongue migration. Knockdown of AMD1 prevents the upregulation of urokinase-type plasminogen activator/urokinase-type plasminogen activator receptor on wounding and results in a failure in actin cytoskeletal reorganization at the wound edge. We demonstrate that keratinocytes respond to wounding by modulating polyamine regulator AMD1 in order to regulate downstream gene expression and promote cell migration. This article highlights a previously unreported role for the regulation of polyamine levels and ratios in cellular behavior and fate.Entities:
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Year: 2018 PMID: 29906410 DOI: 10.1016/j.jid.2018.05.029
Source DB: PubMed Journal: J Invest Dermatol ISSN: 0022-202X Impact factor: 8.551