1 Department of Molecular and Cell Biology, Boston University Henry M. Goldman School of Dental Medicine, Boston, MA, USA.
2 Pharmaxis Ltd, Frenchs Forest NSW, Australia.
J Dent Res. 2018 Oct;97(11):1277-1284. doi: 10.1177/0022034518775971. Epub 2018 May 22.
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.
牙龈增生是某些药物的副作用,包括钙通道阻滞剂、环孢素 A 和苯妥英钠。苯妥英钠引起的牙龈增生是纤维性的。赖氨酰氧化酶是细胞外酶,对于胶原蛋白的生物合成交联是必需的,该酶家族的成员在纤维化中上调。先前在人类和苯妥英钠诱导的牙龈过度生长的小鼠模型中的研究表明,LOXL2 在牙龈过度生长组织的上皮和结缔组织中升高,而在正常组织中不升高。在这里,我们使用一种新型的 LOXL2 同种型选择性抑制剂和基因敲低研究,在基因缺失和功能获得研究中,研究了 LOXL2 在促进人牙龈成纤维细胞增殖和积累胶原蛋白中的作用。数据表明,LOXL2 通过血小板衍生生长因子 B 受体介导的机制刺激牙龈成纤维细胞增殖。此外,胶原的积累被 LOXL2 酶刺激,并被 LOXL2 抑制剂或基因敲低抑制。这些研究表明,LOXL2 可以作为一种潜在的治疗靶点,用于解决口腔纤维性疾病。