| Literature DB >> 30074824 |
Bin Zhao1, Na Xu1, Ran Li1, Feiyan Yu1, Fang Zhang1, Fang Yang1, Xuejun Ge1, Yan Chun Li2, Jie Du1,2.
Abstract
Vitamin D is known to play a protective role in inflammatory diseases. Although the suppressive effect of vitamin D/vitamin D receptor (VDR) signaling has been shown in the context of oral lichen planus (OLP), the molecular basis of its regulatory function remains poorly understood. Herein, we reported that miR-802 overexpression in OLP could aggravate apoptosis of oral keratinocytes by targeting B-cell lymphoma 2 mRNA. In addition, vitamin D/VDR signaling was able to suppress miR-802 expression in LPS-treated or activated CD4+ T cell-stimulated human oral keratinocytes by blocking NF-κB pathways, thereby inhibiting OLP apoptosis. Consistent with the results in vitro, we showed that miR-802 expression was enhanced in oral keratinocytes from VDR-/- mice, and an inverse correlation between VDR and miR-802 was found in human biopsy specimens of OLP. Collectively, our data suggest that vitamin D/VDR signaling suppresses oral keratinocyte apoptosis by targeting miR-802.-Zhao, B., Xu, N., Li, R., Yu, F., Zhang, F., Yang, F., Ge, X., Li, Y. C., Du, J. Vitamin D/VDR signaling suppresses microRNA-802-induced apoptosis of keratinocytes in oral lichen planus.Entities:
Keywords: Bcl2; NF-κB; vitamin D receptor
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Year: 2018 PMID: 30074824 DOI: 10.1096/fj.201801020RRR
Source DB: PubMed Journal: FASEB J ISSN: 0892-6638 Impact factor: 5.191