| Literature DB >> 29787337 |
D Saxena1, F Mahjour1, A D Findlay2, E A Mously1,3, A Kantarci4, P C Trackman1.
Abstract
Gingival overgrowth is a side effect of certain medications, including calcium channel blockers, cyclosporin A, and phenytoin. Phenytoin-induced gingival overgrowth is fibrotic. Lysyl oxidases are extracellular enzymes that are required for biosynthetic cross-linking of collagens, and members of this enzyme family are upregulated in fibrosis. Previous studies in humans and in a mouse model of phenytoin-induced gingival overgrowth have shown that LOXL2 is elevated in the epithelium and connective tissue in gingival overgrowth tissues and not in normal tissues. Here, using a novel LOXL2 isoform-selective inhibitor and knockdown studies in loss- and gain-of-function studies, we investigated roles for LOXL2 in promoting cultures of human gingival fibroblasts to proliferate and to accumulate collagen. Data indicate that LOXL2 stimulates gingival fibroblast proliferation, likely by a platelet-derived growth factor B receptor-mediated mechanism. Moreover, collagen accumulation was stimulated by LOXL2 enzyme and inhibited by LOXL2 inhibitor or gene knockdown. These studies suggest that LOXL2 could serve as a potential therapeutic target to address oral fibrotic conditions.Entities:
Keywords: cell biology; collagen; extracellular matrix; fibroblasts; matrix biology; receptors
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Year: 2018 PMID: 29787337 PMCID: PMC6151912 DOI: 10.1177/0022034518775971
Source DB: PubMed Journal: J Dent Res ISSN: 0022-0345 Impact factor: 6.116