| Literature DB >> 28816551 |
Dong Zhang1,2, Miaomiao Li1, Yang Dong1, Xinhui Zhang1, Xingyun Liu1, Zhangming Chen1, Yongji Zhu1, Huiming Wang1, Xuwen Liu1, Jialiang Zhu1, Yujun Shen2, Heinrich Korner3, Songcheng Ying1,4, Shengyun Fang2, Yuxian Shen2.
Abstract
Vitamin D supplementation is regarded as a novel approach to treat Alzheimer's disease, but the underlying mechanism remains elusive. The cytokine IL-34 provides strong neuroprotective and survival signals in brain injury and neurodegeneration and could be an immunological mediator for the vitamin D-induced protection. The aim of this study was to investigate whether human IL-34 is up-regulated in neuronal cells by the hormonally active form of vitamin D, 1α,25-dihydroxyvitamin D3 [1α,25(OH)2D3]. We found that IL-34 was detectable in a variety of cell lines and its expression was strongly induced in SH-SY5Y neural cells in a dose- and time-dependent manner by 1α,25(OH)2D3 through the vitamin D receptor (VDR). Furthermore, we identified the core promoter of IL-34 gene and a VDR binding site (CGCCCT) that was required for 1α,25(OH)2D3-induced IL-34 expression. These findings suggest that the induction of IL-34 expression by 1α,25(OH)2D3 may constitute a mechanism that explains the protective function of vitamin D in Alzheimer's disease.Entities:
Keywords: 1α; 25-Dihydroxyvitamin D3; Alzheimer disease; IL-34; expression; neuronal cell
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Year: 2017 PMID: 28816551 DOI: 10.1177/1753425917725391
Source DB: PubMed Journal: Innate Immun ISSN: 1753-4259 Impact factor: 2.680