Vitamin D3 alleviates inflammation in ulcerative colitis by activating the VDR-NLRP6 signaling pathway

• Published in: Frontiers in immunology 2023-02, Vol.14, p.1135930-1135930
• Main Authors: Gao, Hongliang, Zhou, He, Zhang, Zhiqiang, Gao, Jianshu, Li, Jian, Li, Xinxia
• Format: Article
• Language: English
• Subjects: Animals; ATAC-seq; Cholecalciferol - pharmacology; Colitis, Ulcerative - chemically induced; Colitis, Ulcerative - drug therapy; Immunology; Inflammasomes - metabolism; Inflammation - drug therapy; Mice; NLRP6 inflammasome; Signal Transduction; ulcerative colitis; VD3; VDR; Vitamin D - metabolism
• ISSN: 1664-3224; 1664-3224
• DOI: 10.3389/fimmu.2023.1135930

Inflammation is a key factor in the development of ulcerative colitis (UC). 1,25-dihydroxyvitamin D (1,25(OH) D , VD ), as the major active ingredient of vitamin D and an anti-inflammatory activator, is closely related to the initiation and development of UC, but its regulatory mechanism remains unclear. In this study, we carried out histological and physiological analyses in UC patients and UC mice. RNA sequencing (RNA-seq), assays for transposase-accessible chromatin with high-throughput sequencing (ATAC-seq), chromatin immunoprecipitation (ChIP) assays and protein and mRNA expression were performed to analyze and identify the potential molecular mechanism in UC mice and lipopolysaccharide (LPS)-induced mouse intestinal epithelial cells (MIECs). Moreover, we established nucleotide-binding oligomerization domain (NOD)-like receptor protein mice and siRNA-NLRP6 MIECs to further characterize the role of NLRP6 in anti-inflammation of VD . Our study revealed that VD abolished NOD-like receptor protein 6 (NLRP6) inflammasome activation, suppressing NLRP6, apoptosis-associated speck-like protein (ASC) and Caspase-1 levels the vitamin D receptor (VDR). ChIP and ATAC-seq showed that VDR transcriptionally repressed NLRP6 by binding to vitamin D response elements (VDREs) in the promoter of NLRP6, impairing UC development. Importantly, VD had both preventive and therapeutic effects on the UC mouse model inhibition of NLRP6 inflammasome activation. Our results demonstrated that VD substantially represses inflammation and the development of UC . These findings reveal a new mechanism by which VD affects inflammation in UC by regulating the expression of NLRP6 and show the potential clinical use of VD in autoimmune syndromes or other NLRP6 inflammasome-driven inflammatory diseases.