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A Variant in the Nicotinic Acetylcholine Receptor Alpha 3 Subunit Gene Is Associated With Hypertension Risks in Hypogonadic Patients

Ephb6 gene knockout causes hypertension in castrated mice. EPHB6 controls catecholamine secretion by adrenal gland chromaffin cells (AGCCs) in a testosterone-dependent way. Nicotinic acetylcholine receptor (nAChR) is a ligand-gated Ca(2+)/Na(+) channel, and its opening is the first signaling event l...

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Autores principales: Wu, Tao, Wang, Yujia, Shi, Wei, Zhang, Bi-Qi, Raelson, John, Yao, Yu-Mei, Wu, Huan-Dong, Xu, Zao-Xian, Marois-Blanchet, Francois-Christophe, Ledoux, Jonathan, Blunck, Rikard, Sheng, Jian-Zhong, Hu, Shen-Jiang, Luo, Hongyu, Wu, Jiangping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7728919/
https://www.ncbi.nlm.nih.gov/pubmed/33329690
http://dx.doi.org/10.3389/fgene.2020.539862
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author Wu, Tao
Wang, Yujia
Shi, Wei
Zhang, Bi-Qi
Raelson, John
Yao, Yu-Mei
Wu, Huan-Dong
Xu, Zao-Xian
Marois-Blanchet, Francois-Christophe
Ledoux, Jonathan
Blunck, Rikard
Sheng, Jian-Zhong
Hu, Shen-Jiang
Luo, Hongyu
Wu, Jiangping
author_facet Wu, Tao
Wang, Yujia
Shi, Wei
Zhang, Bi-Qi
Raelson, John
Yao, Yu-Mei
Wu, Huan-Dong
Xu, Zao-Xian
Marois-Blanchet, Francois-Christophe
Ledoux, Jonathan
Blunck, Rikard
Sheng, Jian-Zhong
Hu, Shen-Jiang
Luo, Hongyu
Wu, Jiangping
author_sort Wu, Tao
collection PubMed
description Ephb6 gene knockout causes hypertension in castrated mice. EPHB6 controls catecholamine secretion by adrenal gland chromaffin cells (AGCCs) in a testosterone-dependent way. Nicotinic acetylcholine receptor (nAChR) is a ligand-gated Ca(2+)/Na(+) channel, and its opening is the first signaling event leading to catecholamine secretion by AGCCs. There is a possibility that nAChR might be involved in EPHB6 signaling, and thus sequence variants of its subunit genes are associated with hypertension risks. CHRNA3 is the major subunit of nAChR used in human and mouse AGCCs. We conducted a human genetic study to assess the association of CHRNA3 variants with hypertension risks in hypogonadic males. The study cohort included 1,500 hypogonadic Chinese males with (750 patients) or without (750 patients) hypertension. The result revealed that SNV rs3743076 in the fourth intron of CHRNA3 was significantly associated with hypertension risks in the hypogonadic males. We further showed that EPHB6 physically interacted with CHRNA3 in AGCCs, providing a molecular basis for nAChR being in the EPHB6 signaling pathway.
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spelling pubmed-77289192020-12-15 A Variant in the Nicotinic Acetylcholine Receptor Alpha 3 Subunit Gene Is Associated With Hypertension Risks in Hypogonadic Patients Wu, Tao Wang, Yujia Shi, Wei Zhang, Bi-Qi Raelson, John Yao, Yu-Mei Wu, Huan-Dong Xu, Zao-Xian Marois-Blanchet, Francois-Christophe Ledoux, Jonathan Blunck, Rikard Sheng, Jian-Zhong Hu, Shen-Jiang Luo, Hongyu Wu, Jiangping Front Genet Genetics Ephb6 gene knockout causes hypertension in castrated mice. EPHB6 controls catecholamine secretion by adrenal gland chromaffin cells (AGCCs) in a testosterone-dependent way. Nicotinic acetylcholine receptor (nAChR) is a ligand-gated Ca(2+)/Na(+) channel, and its opening is the first signaling event leading to catecholamine secretion by AGCCs. There is a possibility that nAChR might be involved in EPHB6 signaling, and thus sequence variants of its subunit genes are associated with hypertension risks. CHRNA3 is the major subunit of nAChR used in human and mouse AGCCs. We conducted a human genetic study to assess the association of CHRNA3 variants with hypertension risks in hypogonadic males. The study cohort included 1,500 hypogonadic Chinese males with (750 patients) or without (750 patients) hypertension. The result revealed that SNV rs3743076 in the fourth intron of CHRNA3 was significantly associated with hypertension risks in the hypogonadic males. We further showed that EPHB6 physically interacted with CHRNA3 in AGCCs, providing a molecular basis for nAChR being in the EPHB6 signaling pathway. Frontiers Media S.A. 2020-11-27 /pmc/articles/PMC7728919/ /pubmed/33329690 http://dx.doi.org/10.3389/fgene.2020.539862 Text en Copyright © 2020 Wu, Wang, Shi, Zhang, Raelson, Yao, Wu, Xu, Marois-Blanchet, Ledoux, Blunck, Sheng, Hu, Luo and Wu. 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 Genetics
Wu, Tao
Wang, Yujia
Shi, Wei
Zhang, Bi-Qi
Raelson, John
Yao, Yu-Mei
Wu, Huan-Dong
Xu, Zao-Xian
Marois-Blanchet, Francois-Christophe
Ledoux, Jonathan
Blunck, Rikard
Sheng, Jian-Zhong
Hu, Shen-Jiang
Luo, Hongyu
Wu, Jiangping
A Variant in the Nicotinic Acetylcholine Receptor Alpha 3 Subunit Gene Is Associated With Hypertension Risks in Hypogonadic Patients
title A Variant in the Nicotinic Acetylcholine Receptor Alpha 3 Subunit Gene Is Associated With Hypertension Risks in Hypogonadic Patients
title_full A Variant in the Nicotinic Acetylcholine Receptor Alpha 3 Subunit Gene Is Associated With Hypertension Risks in Hypogonadic Patients
title_fullStr A Variant in the Nicotinic Acetylcholine Receptor Alpha 3 Subunit Gene Is Associated With Hypertension Risks in Hypogonadic Patients
title_full_unstemmed A Variant in the Nicotinic Acetylcholine Receptor Alpha 3 Subunit Gene Is Associated With Hypertension Risks in Hypogonadic Patients
title_short A Variant in the Nicotinic Acetylcholine Receptor Alpha 3 Subunit Gene Is Associated With Hypertension Risks in Hypogonadic Patients
title_sort variant in the nicotinic acetylcholine receptor alpha 3 subunit gene is associated with hypertension risks in hypogonadic patients
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7728919/
https://www.ncbi.nlm.nih.gov/pubmed/33329690
http://dx.doi.org/10.3389/fgene.2020.539862
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