1α,25-Dihydroxyvitamin D3 up-regulates IL-34 expression in SH-SY5Y neural cells

Author:

Zhang Dong12,Li Miaomiao1,Dong Yang1,Zhang Xinhui1,Liu Xingyun1,Chen Zhangming1,Zhu Yongji1,Wang Huiming1,Liu Xuwen1,Zhu Jialiang1,Shen Yujun2,Korner Heinrich3,Ying Songcheng14,Fang Shengyun2,Shen Yuxian2

Affiliation:

1. Department of Immunology, School of Basic Medical Sciences, Anhui Medical University, Hefei, Anhui Province, P.R. China

2. Biopharmaceutical Research Institute, Anhui Medical University, Hefei, Anhui Province, P.R. China

3. Menzies Institute for Medical Research Tasmania, Hobart, Tasmania, Australia

4. School of Pharmacy, Anhui Medical University, Hefei, Anhui Province, P.R. China

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.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Anhui Province

Publisher

SAGE Publications

Subject

Infectious Diseases,Cell Biology,Molecular Biology,Immunology,Microbiology

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