Age-dependent VDR peak DNA methylation as a mechanism for latitude-dependent multiple sclerosis risk

被引:10
作者
Ong, Lawrence T. C. [1 ,2 ]
Schibeci, Stephen D. [1 ]
Fewings, Nicole L. [1 ]
Booth, David R. [1 ]
Parnell, Grant P. [1 ]
机构
[1] Univ Sydney, Westmead Inst Med Res, Ctr Immunol & Allergy Res, 176 Hawkesbury Rd, Westmead, NSW 2145, Australia
[2] Westmead Hosp, Dept Immunol, Cnr Darcy & Hawkesbury Rds, Westmead, NSW 2145, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
DNA methylation; Calcitriol; Epigenetics; Vitamin D; Myeloid; VDR binding site; VITAMIN-D; PHOSPHATIDYLINOSITOL; 3-KINASE; DIFFERENTIATION; CELLS; POPULATIONS; ENVIRONMENT; PREVALENCE; ACTIVATION; EXPOSURE;
D O I
10.1186/s13072-021-00383-x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background The mechanisms linking UV radiation and vitamin D exposure to the risk of acquiring the latitude and critical period-dependent autoimmune disease, multiple sclerosis, is unclear. We examined the effect of vitamin D on DNA methylation and DNA methylation at vitamin D receptor binding sites in adult and paediatric myeloid cells. This was accomplished through differentiating CD34+ haematopoietic progenitors into CD14+ mononuclear phagocytes, in the presence and absence of calcitriol. Results Few DNA methylation changes occurred in cells treated with calcitriol. However, several VDR-binding sites demonstrated increased DNA methylation in cells of adult origin when compared to cells of paediatric origin. This phenomenon was not observed at other transcription factor binding sites. Genes associated with these sites were enriched for intracellular signalling and cell activation pathways involved in myeloid cell differentiation and adaptive immune system regulation. Conclusion These results suggest vitamin D exposure at critical periods during development may contribute to latitude-related differences in autoimmune disease incidence.
引用
收藏
页数:12
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