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Methylation-reprogrammed CHRM3 results in vascular dysfunction in the human umbilical vein following IVF-ET
Assisted reproductive technology (ART) has been used globally among infertile couples. However, many epidemiological investigations have indicated that ART is associated with a range of long-term adverse health outcomes in offspring, including cardiovascular disease, obesity, and increased plasma li...
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Published in: | Biology of reproduction 2022-04, Vol.106 (4), p.687-698 |
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creator | Shi, Yajun Liu, Jingliu Zhu, Dan Lu, Likui Zhang, Mengshu Li, Weisheng Zeng, Hongtao Yu, Xi Guo, Jun Zhang, Yingying Zhou, Xiuwen Gao, Qinqin Xia, Fei Chen, Youguo Li, Min Sun, Miao |
description | Assisted reproductive technology (ART) has been used globally among infertile couples. However, many epidemiological investigations have indicated that ART is associated with a range of long-term adverse health outcomes in offspring, including cardiovascular disease, obesity, and increased plasma lipid levels. Until now, direct evidence has been limited regarding the pathological changes in vascular function in fetuses with ART. In this study, human umbilical cords were collected from healthy normal pregnancies and in vitro fertilization and embryo transfer (IVF-ET) pregnancies. Vascular functional studies involving acetylcholine (ACh), antagonists of its specific receptors, and L-type calcium channel/PKC-MLC20 phosphorylation pathway specific inhibitors were conducted. Quantitative real-time PCR, Western blotting, and methylation analyses were performed on umbilical vein samples. We found that the umbilical vein constriction induced by ACh in the IVF-ET group was significantly attenuated compared with that in the healthy normal pregnancy group, which was not only associated with the hypermethylation of ACh muscarinic receptor subtype 3 (CHRM3) and decreased expression of CHRM3, PKCβ, and CaV1.2, but was also related to the reduced phosphorylation of MLC20. This study revealed that the hypermethylation of CHRM3, leading to a reduction in CHRM3 expression and downregulation of the CaV1.2/PKC-MLC20 phosphorylation pathway, was responsible for the decreased sensitivity to ACh observed in the umbilical vein under IVF-ET conditions. The hypermethylation of CHRM3 caused by IVF-ET might play an important role in altered vasoconstriction and impact cardiovascular systems in the long run. |
doi_str_mv | 10.1093/biolre/ioab234 |
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However, many epidemiological investigations have indicated that ART is associated with a range of long-term adverse health outcomes in offspring, including cardiovascular disease, obesity, and increased plasma lipid levels. Until now, direct evidence has been limited regarding the pathological changes in vascular function in fetuses with ART. In this study, human umbilical cords were collected from healthy normal pregnancies and in vitro fertilization and embryo transfer (IVF-ET) pregnancies. Vascular functional studies involving acetylcholine (ACh), antagonists of its specific receptors, and L-type calcium channel/PKC-MLC20 phosphorylation pathway specific inhibitors were conducted. Quantitative real-time PCR, Western blotting, and methylation analyses were performed on umbilical vein samples. We found that the umbilical vein constriction induced by ACh in the IVF-ET group was significantly attenuated compared with that in the healthy normal pregnancy group, which was not only associated with the hypermethylation of ACh muscarinic receptor subtype 3 (CHRM3) and decreased expression of CHRM3, PKCβ, and CaV1.2, but was also related to the reduced phosphorylation of MLC20. This study revealed that the hypermethylation of CHRM3, leading to a reduction in CHRM3 expression and downregulation of the CaV1.2/PKC-MLC20 phosphorylation pathway, was responsible for the decreased sensitivity to ACh observed in the umbilical vein under IVF-ET conditions. The hypermethylation of CHRM3 caused by IVF-ET might play an important role in altered vasoconstriction and impact cardiovascular systems in the long run.</description><identifier>ISSN: 0006-3363</identifier><identifier>EISSN: 1529-7268</identifier><identifier>DOI: 10.1093/biolre/ioab234</identifier><identifier>PMID: 34935917</identifier><language>eng</language><publisher>United States: Society for the Study of Reproduction</publisher><subject>Acetylcholine ; Acetylcholine receptors (muscarinic) ; Antagonists ; Calcium channels (L-type) ; Calcium channels (voltage-gated) ; Cardiovascular diseases ; DNA Methylation ; Embryo transfer ; Embryo Transfer - methods ; Epidemiology ; Female ; Fertilization in Vitro - methods ; Fetuses ; human umbilical veins ; Humans ; In vitro fertilization ; L-type calcium channels ; Methylation ; muscarinic receptor subtype 3 ; myosin light chain ; Phosphorylation ; Pregnancy ; Protein kinase C ; protein kinase C β ; Receptor, Muscarinic M3 - metabolism ; Reproductive Techniques, Assisted ; Reproductive technology ; RESEARCH ARTICLE ; Umbilical vein ; Umbilical Veins ; Vasoconstriction ; Veins & arteries ; Western blotting</subject><ispartof>Biology of reproduction, 2022-04, Vol.106 (4), p.687-698</ispartof><rights>The Author(s) 2021. Published by Oxford University Press on behalf of Society for the Study of Reproduction. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com journals.permissions@oup.com</rights><rights>The Author(s) 2021. Published by Oxford University Press on behalf of Society for the Study of Reproduction. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com 2022</rights><rights>The Author(s) 2021. Published by Oxford University Press on behalf of Society for the Study of Reproduction. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.</rights><rights>The Author(s) 2021. Published by Oxford University Press on behalf of Society for the Study of Reproduction. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b394t-561fdafb657600240a421b54d9b397acc5b94df285e788038d73908666e88eb53</citedby><cites>FETCH-LOGICAL-b394t-561fdafb657600240a421b54d9b397acc5b94df285e788038d73908666e88eb53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34935917$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shi, Yajun</creatorcontrib><creatorcontrib>Liu, Jingliu</creatorcontrib><creatorcontrib>Zhu, Dan</creatorcontrib><creatorcontrib>Lu, Likui</creatorcontrib><creatorcontrib>Zhang, Mengshu</creatorcontrib><creatorcontrib>Li, Weisheng</creatorcontrib><creatorcontrib>Zeng, Hongtao</creatorcontrib><creatorcontrib>Yu, Xi</creatorcontrib><creatorcontrib>Guo, Jun</creatorcontrib><creatorcontrib>Zhang, Yingying</creatorcontrib><creatorcontrib>Zhou, Xiuwen</creatorcontrib><creatorcontrib>Gao, Qinqin</creatorcontrib><creatorcontrib>Xia, Fei</creatorcontrib><creatorcontrib>Chen, Youguo</creatorcontrib><creatorcontrib>Li, Min</creatorcontrib><creatorcontrib>Sun, Miao</creatorcontrib><title>Methylation-reprogrammed CHRM3 results in vascular dysfunction in the human umbilical vein following IVF-ET</title><title>Biology of reproduction</title><addtitle>Biol Reprod</addtitle><description>Assisted reproductive technology (ART) has been used globally among infertile couples. However, many epidemiological investigations have indicated that ART is associated with a range of long-term adverse health outcomes in offspring, including cardiovascular disease, obesity, and increased plasma lipid levels. Until now, direct evidence has been limited regarding the pathological changes in vascular function in fetuses with ART. In this study, human umbilical cords were collected from healthy normal pregnancies and in vitro fertilization and embryo transfer (IVF-ET) pregnancies. Vascular functional studies involving acetylcholine (ACh), antagonists of its specific receptors, and L-type calcium channel/PKC-MLC20 phosphorylation pathway specific inhibitors were conducted. Quantitative real-time PCR, Western blotting, and methylation analyses were performed on umbilical vein samples. We found that the umbilical vein constriction induced by ACh in the IVF-ET group was significantly attenuated compared with that in the healthy normal pregnancy group, which was not only associated with the hypermethylation of ACh muscarinic receptor subtype 3 (CHRM3) and decreased expression of CHRM3, PKCβ, and CaV1.2, but was also related to the reduced phosphorylation of MLC20. This study revealed that the hypermethylation of CHRM3, leading to a reduction in CHRM3 expression and downregulation of the CaV1.2/PKC-MLC20 phosphorylation pathway, was responsible for the decreased sensitivity to ACh observed in the umbilical vein under IVF-ET conditions. The hypermethylation of CHRM3 caused by IVF-ET might play an important role in altered vasoconstriction and impact cardiovascular systems in the long run.</description><subject>Acetylcholine</subject><subject>Acetylcholine receptors (muscarinic)</subject><subject>Antagonists</subject><subject>Calcium channels (L-type)</subject><subject>Calcium channels (voltage-gated)</subject><subject>Cardiovascular diseases</subject><subject>DNA Methylation</subject><subject>Embryo transfer</subject><subject>Embryo Transfer - methods</subject><subject>Epidemiology</subject><subject>Female</subject><subject>Fertilization in Vitro - methods</subject><subject>Fetuses</subject><subject>human umbilical veins</subject><subject>Humans</subject><subject>In vitro fertilization</subject><subject>L-type calcium channels</subject><subject>Methylation</subject><subject>muscarinic receptor subtype 3</subject><subject>myosin light chain</subject><subject>Phosphorylation</subject><subject>Pregnancy</subject><subject>Protein kinase C</subject><subject>protein kinase C β</subject><subject>Receptor, Muscarinic M3 - metabolism</subject><subject>Reproductive Techniques, Assisted</subject><subject>Reproductive technology</subject><subject>RESEARCH ARTICLE</subject><subject>Umbilical vein</subject><subject>Umbilical Veins</subject><subject>Vasoconstriction</subject><subject>Veins & arteries</subject><subject>Western blotting</subject><issn>0006-3363</issn><issn>1529-7268</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqFkc1P3DAQxS1EBVvotcfKEpdWasDfsY_VCgoSCAlBr5GdOKzBiRc7Bu1_j1fZ9tALp5FmfvM08x4AXzE6xUjRM-OCj_bMBW0IZXtggTlRVU2E3AcLhJCoKBX0EHxO6QkhzCihB-CQMkW5wvUCPN_YabXxenJhrKJdx_AY9TDYDi4v724ojDZlPyXoRviqU5u9jrDbpD6P7XZl259WFq7yoEeYB-O8a7WHr7YM-uB9eHPjI7z6c1Gd3x-DT732yX7Z1SPwcHF-v7ysrm9_Xy1_XVeGKjZVXOC-070RvBYIEYY0I9hw1qkyr3XbcqNY1xPJbS0lorKrqUJSCGGltIbTI_B91i3fvGSbpmZwqbXe69GGnBoiMKkpk5IU9OQ_9CnkOJbrCsVVcWymTmeqjSGlaPtmHd2g46bBqNnG0MwxNLsYysK3nWw2xct_-F_fC_BjBkJefyz2c2ZLP4z2I_wdOF2ikg</recordid><startdate>20220426</startdate><enddate>20220426</enddate><creator>Shi, Yajun</creator><creator>Liu, Jingliu</creator><creator>Zhu, Dan</creator><creator>Lu, Likui</creator><creator>Zhang, Mengshu</creator><creator>Li, Weisheng</creator><creator>Zeng, Hongtao</creator><creator>Yu, Xi</creator><creator>Guo, Jun</creator><creator>Zhang, Yingying</creator><creator>Zhou, Xiuwen</creator><creator>Gao, Qinqin</creator><creator>Xia, Fei</creator><creator>Chen, Youguo</creator><creator>Li, Min</creator><creator>Sun, Miao</creator><general>Society for the Study of Reproduction</general><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20220426</creationdate><title>Methylation-reprogrammed CHRM3 results in vascular dysfunction in the human umbilical vein following IVF-ET</title><author>Shi, Yajun ; Liu, Jingliu ; Zhu, Dan ; Lu, Likui ; Zhang, Mengshu ; Li, Weisheng ; Zeng, Hongtao ; Yu, Xi ; Guo, Jun ; Zhang, Yingying ; Zhou, Xiuwen ; Gao, Qinqin ; Xia, Fei ; Chen, Youguo ; Li, Min ; Sun, Miao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b394t-561fdafb657600240a421b54d9b397acc5b94df285e788038d73908666e88eb53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Acetylcholine</topic><topic>Acetylcholine receptors (muscarinic)</topic><topic>Antagonists</topic><topic>Calcium channels (L-type)</topic><topic>Calcium channels (voltage-gated)</topic><topic>Cardiovascular diseases</topic><topic>DNA Methylation</topic><topic>Embryo transfer</topic><topic>Embryo Transfer - methods</topic><topic>Epidemiology</topic><topic>Female</topic><topic>Fertilization in Vitro - methods</topic><topic>Fetuses</topic><topic>human umbilical veins</topic><topic>Humans</topic><topic>In vitro fertilization</topic><topic>L-type calcium channels</topic><topic>Methylation</topic><topic>muscarinic receptor subtype 3</topic><topic>myosin light chain</topic><topic>Phosphorylation</topic><topic>Pregnancy</topic><topic>Protein kinase C</topic><topic>protein kinase C β</topic><topic>Receptor, Muscarinic M3 - metabolism</topic><topic>Reproductive Techniques, Assisted</topic><topic>Reproductive technology</topic><topic>RESEARCH ARTICLE</topic><topic>Umbilical vein</topic><topic>Umbilical Veins</topic><topic>Vasoconstriction</topic><topic>Veins & arteries</topic><topic>Western blotting</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shi, Yajun</creatorcontrib><creatorcontrib>Liu, Jingliu</creatorcontrib><creatorcontrib>Zhu, Dan</creatorcontrib><creatorcontrib>Lu, Likui</creatorcontrib><creatorcontrib>Zhang, Mengshu</creatorcontrib><creatorcontrib>Li, Weisheng</creatorcontrib><creatorcontrib>Zeng, Hongtao</creatorcontrib><creatorcontrib>Yu, Xi</creatorcontrib><creatorcontrib>Guo, Jun</creatorcontrib><creatorcontrib>Zhang, Yingying</creatorcontrib><creatorcontrib>Zhou, Xiuwen</creatorcontrib><creatorcontrib>Gao, Qinqin</creatorcontrib><creatorcontrib>Xia, Fei</creatorcontrib><creatorcontrib>Chen, Youguo</creatorcontrib><creatorcontrib>Li, Min</creatorcontrib><creatorcontrib>Sun, Miao</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Biological Science Journals</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biology of reproduction</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shi, Yajun</au><au>Liu, Jingliu</au><au>Zhu, Dan</au><au>Lu, Likui</au><au>Zhang, Mengshu</au><au>Li, Weisheng</au><au>Zeng, Hongtao</au><au>Yu, Xi</au><au>Guo, Jun</au><au>Zhang, Yingying</au><au>Zhou, Xiuwen</au><au>Gao, Qinqin</au><au>Xia, Fei</au><au>Chen, Youguo</au><au>Li, Min</au><au>Sun, Miao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Methylation-reprogrammed CHRM3 results in vascular dysfunction in the human umbilical vein following IVF-ET</atitle><jtitle>Biology of reproduction</jtitle><addtitle>Biol Reprod</addtitle><date>2022-04-26</date><risdate>2022</risdate><volume>106</volume><issue>4</issue><spage>687</spage><epage>698</epage><pages>687-698</pages><issn>0006-3363</issn><eissn>1529-7268</eissn><abstract>Assisted reproductive technology (ART) has been used globally among infertile couples. However, many epidemiological investigations have indicated that ART is associated with a range of long-term adverse health outcomes in offspring, including cardiovascular disease, obesity, and increased plasma lipid levels. Until now, direct evidence has been limited regarding the pathological changes in vascular function in fetuses with ART. In this study, human umbilical cords were collected from healthy normal pregnancies and in vitro fertilization and embryo transfer (IVF-ET) pregnancies. Vascular functional studies involving acetylcholine (ACh), antagonists of its specific receptors, and L-type calcium channel/PKC-MLC20 phosphorylation pathway specific inhibitors were conducted. Quantitative real-time PCR, Western blotting, and methylation analyses were performed on umbilical vein samples. We found that the umbilical vein constriction induced by ACh in the IVF-ET group was significantly attenuated compared with that in the healthy normal pregnancy group, which was not only associated with the hypermethylation of ACh muscarinic receptor subtype 3 (CHRM3) and decreased expression of CHRM3, PKCβ, and CaV1.2, but was also related to the reduced phosphorylation of MLC20. This study revealed that the hypermethylation of CHRM3, leading to a reduction in CHRM3 expression and downregulation of the CaV1.2/PKC-MLC20 phosphorylation pathway, was responsible for the decreased sensitivity to ACh observed in the umbilical vein under IVF-ET conditions. The hypermethylation of CHRM3 caused by IVF-ET might play an important role in altered vasoconstriction and impact cardiovascular systems in the long run.</abstract><cop>United States</cop><pub>Society for the Study of Reproduction</pub><pmid>34935917</pmid><doi>10.1093/biolre/ioab234</doi><tpages>12</tpages></addata></record> |
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subjects | Acetylcholine Acetylcholine receptors (muscarinic) Antagonists Calcium channels (L-type) Calcium channels (voltage-gated) Cardiovascular diseases DNA Methylation Embryo transfer Embryo Transfer - methods Epidemiology Female Fertilization in Vitro - methods Fetuses human umbilical veins Humans In vitro fertilization L-type calcium channels Methylation muscarinic receptor subtype 3 myosin light chain Phosphorylation Pregnancy Protein kinase C protein kinase C β Receptor, Muscarinic M3 - metabolism Reproductive Techniques, Assisted Reproductive technology RESEARCH ARTICLE Umbilical vein Umbilical Veins Vasoconstriction Veins & arteries Western blotting |
title | Methylation-reprogrammed CHRM3 results in vascular dysfunction in the human umbilical vein following IVF-ET |
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