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A Functional Variant rs3093023 in CCR6 Is Associated With IgA Nephropathy by Regulating Th17 Cells in a North Han Chinese Population

C-C chemokine receptor 6 (CCR6) is a susceptibility gene of various immune-related diseases, which was suggested to be shared with immunoglobulin A nephropathy (IgAN). In this study, we aimed to identify the functional variants. First, we analyzed the associations of CCR6 common and rare variants de...

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Autores principales: Zhang, Yue-miao, Liu, Xing-zi, Zhou, Xu-jie, Liu, Li-jun, Shi, Su-fang, Hou, Ping, Lv, Ji-cheng, Zhang, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7946973/
https://www.ncbi.nlm.nih.gov/pubmed/33717080
http://dx.doi.org/10.3389/fimmu.2021.600598
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author Zhang, Yue-miao
Liu, Xing-zi
Zhou, Xu-jie
Liu, Li-jun
Shi, Su-fang
Hou, Ping
Lv, Ji-cheng
Zhang, Hong
author_facet Zhang, Yue-miao
Liu, Xing-zi
Zhou, Xu-jie
Liu, Li-jun
Shi, Su-fang
Hou, Ping
Lv, Ji-cheng
Zhang, Hong
author_sort Zhang, Yue-miao
collection PubMed
description C-C chemokine receptor 6 (CCR6) is a susceptibility gene of various immune-related diseases, which was suggested to be shared with immunoglobulin A nephropathy (IgAN). In this study, we aimed to identify the functional variants. First, we analyzed the associations of CCR6 common and rare variants detected by multi-platform chips with IgAN susceptibility using imputation and identified 68 significantly associated common variants located in the regulatory region. Among them, rs3093023 showed both statistical significance (rs3093023-A, odds ratio [OR] = 1.15, P = 2.00 × 10(−2)) and the expression quantitative trait loci (eQTL) effect (P = 1.45 × 10(−3)). It was independently replicated (rs3093023-A, OR = 1.18, P = 5.56 × 10(−3)) and the association was reinforced in the meta-analysis (rs3093023-A, OR = 1.17, P = 6.14 × 10(−7)). Although rs3093023 was in a strong linkage disequilibrium with the reported CCR6 functional variant dinucleotide polymorphism, CCR6DNP, the alleles of rs3093023 (G>A) rather than of CCR6DNP were shown differential nuclear protein binding effect by electrophoretic mobility shift assay. The RegulomeDB and JASPAR databases predicted Pou2f1 as the potential transcription factor, which was negatively associated with CCR6 mRNA (r = −0.60, P = 3.94 × 10(−9)). At the mRNA level, the eQTL effect of CCR6 was validated (P = 4.39 × 10(−2)), and CCR6 was positively associated with the expression of CCR4 and IL-17A rather than that of CXCR3 and IFNG. At the protein level, a higher CCR6(+) cell ratio was observed in a risk allele dose-dependent manner in lymphocytes (P = 3.57 × 10(−2)), CD3(+) T cells (P = 4.54 × 10(−2)), and CD4(+) T cells (P = 1.32 × 10(−2)), but not in CD8(+) T cells. Clinical-pathological analysis showed that rs3093023 risk allele was significantly associated with diastolic blood pressure, serum creatinine, and high ratio of tubular atrophy/interstitial fibrosis. Overall, the rs3093023 was prioritized as the function variant in CCR6, which may contribute to IgAN susceptibility by regulating Th17 cells.
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spelling pubmed-79469732021-03-12 A Functional Variant rs3093023 in CCR6 Is Associated With IgA Nephropathy by Regulating Th17 Cells in a North Han Chinese Population Zhang, Yue-miao Liu, Xing-zi Zhou, Xu-jie Liu, Li-jun Shi, Su-fang Hou, Ping Lv, Ji-cheng Zhang, Hong Front Immunol Immunology C-C chemokine receptor 6 (CCR6) is a susceptibility gene of various immune-related diseases, which was suggested to be shared with immunoglobulin A nephropathy (IgAN). In this study, we aimed to identify the functional variants. First, we analyzed the associations of CCR6 common and rare variants detected by multi-platform chips with IgAN susceptibility using imputation and identified 68 significantly associated common variants located in the regulatory region. Among them, rs3093023 showed both statistical significance (rs3093023-A, odds ratio [OR] = 1.15, P = 2.00 × 10(−2)) and the expression quantitative trait loci (eQTL) effect (P = 1.45 × 10(−3)). It was independently replicated (rs3093023-A, OR = 1.18, P = 5.56 × 10(−3)) and the association was reinforced in the meta-analysis (rs3093023-A, OR = 1.17, P = 6.14 × 10(−7)). Although rs3093023 was in a strong linkage disequilibrium with the reported CCR6 functional variant dinucleotide polymorphism, CCR6DNP, the alleles of rs3093023 (G>A) rather than of CCR6DNP were shown differential nuclear protein binding effect by electrophoretic mobility shift assay. The RegulomeDB and JASPAR databases predicted Pou2f1 as the potential transcription factor, which was negatively associated with CCR6 mRNA (r = −0.60, P = 3.94 × 10(−9)). At the mRNA level, the eQTL effect of CCR6 was validated (P = 4.39 × 10(−2)), and CCR6 was positively associated with the expression of CCR4 and IL-17A rather than that of CXCR3 and IFNG. At the protein level, a higher CCR6(+) cell ratio was observed in a risk allele dose-dependent manner in lymphocytes (P = 3.57 × 10(−2)), CD3(+) T cells (P = 4.54 × 10(−2)), and CD4(+) T cells (P = 1.32 × 10(−2)), but not in CD8(+) T cells. Clinical-pathological analysis showed that rs3093023 risk allele was significantly associated with diastolic blood pressure, serum creatinine, and high ratio of tubular atrophy/interstitial fibrosis. Overall, the rs3093023 was prioritized as the function variant in CCR6, which may contribute to IgAN susceptibility by regulating Th17 cells. Frontiers Media S.A. 2021-02-25 /pmc/articles/PMC7946973/ /pubmed/33717080 http://dx.doi.org/10.3389/fimmu.2021.600598 Text en Copyright © 2021 Zhang, Liu, Zhou, Liu, Shi, Hou, Lv and Zhang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Zhang, Yue-miao
Liu, Xing-zi
Zhou, Xu-jie
Liu, Li-jun
Shi, Su-fang
Hou, Ping
Lv, Ji-cheng
Zhang, Hong
A Functional Variant rs3093023 in CCR6 Is Associated With IgA Nephropathy by Regulating Th17 Cells in a North Han Chinese Population
title A Functional Variant rs3093023 in CCR6 Is Associated With IgA Nephropathy by Regulating Th17 Cells in a North Han Chinese Population
title_full A Functional Variant rs3093023 in CCR6 Is Associated With IgA Nephropathy by Regulating Th17 Cells in a North Han Chinese Population
title_fullStr A Functional Variant rs3093023 in CCR6 Is Associated With IgA Nephropathy by Regulating Th17 Cells in a North Han Chinese Population
title_full_unstemmed A Functional Variant rs3093023 in CCR6 Is Associated With IgA Nephropathy by Regulating Th17 Cells in a North Han Chinese Population
title_short A Functional Variant rs3093023 in CCR6 Is Associated With IgA Nephropathy by Regulating Th17 Cells in a North Han Chinese Population
title_sort functional variant rs3093023 in ccr6 is associated with iga nephropathy by regulating th17 cells in a north han chinese population
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7946973/
https://www.ncbi.nlm.nih.gov/pubmed/33717080
http://dx.doi.org/10.3389/fimmu.2021.600598
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