Gestational stress induces the unfolded protein response, resulting in heart defects
Congenital heart disease (CHD) is an enigma. It is the most common human birth defect and yet, even with the application of modern genetic and genomic technologies, only a minority of cases can be explained genetically. This is because environmental stressors also cause CHD. Here we propose a plausi...
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Veröffentlicht in: | Development (Cambridge) 2016-07, Vol.143 (14), p.2561-2572 |
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creator | Shi, Hongjun O'Reilly, Victoria C Moreau, Julie L M Bewes, Therese R Yam, Michelle X Chapman, Bogdan E Grieve, Stuart M Stocker, Roland Graham, Robert M Chapman, Gavin Sparrow, Duncan B Dunwoodie, Sally L |
description | Congenital heart disease (CHD) is an enigma. It is the most common human birth defect and yet, even with the application of modern genetic and genomic technologies, only a minority of cases can be explained genetically. This is because environmental stressors also cause CHD. Here we propose a plausible non-genetic mechanism for induction of CHD by environmental stressors. We show that exposure of mouse embryos to short-term gestational hypoxia induces the most common types of heart defect. This is mediated by the rapid induction of the unfolded protein response (UPR), which profoundly reduces FGF signaling in cardiac progenitor cells of the second heart field. Thus, UPR activation during human pregnancy might be a common cause of CHD. Our findings have far-reaching consequences because the UPR is activated by a myriad of environmental or pathophysiological conditions. Ultimately, our discovery could lead to preventative strategies to reduce the incidence of human CHD. |
doi_str_mv | 10.1242/dev.136820 |
format | Article |
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It is the most common human birth defect and yet, even with the application of modern genetic and genomic technologies, only a minority of cases can be explained genetically. This is because environmental stressors also cause CHD. Here we propose a plausible non-genetic mechanism for induction of CHD by environmental stressors. We show that exposure of mouse embryos to short-term gestational hypoxia induces the most common types of heart defect. This is mediated by the rapid induction of the unfolded protein response (UPR), which profoundly reduces FGF signaling in cardiac progenitor cells of the second heart field. Thus, UPR activation during human pregnancy might be a common cause of CHD. Our findings have far-reaching consequences because the UPR is activated by a myriad of environmental or pathophysiological conditions. Ultimately, our discovery could lead to preventative strategies to reduce the incidence of human CHD.</description><identifier>ISSN: 0950-1991</identifier><identifier>EISSN: 1477-9129</identifier><identifier>DOI: 10.1242/dev.136820</identifier><identifier>PMID: 27436040</identifier><language>eng</language><publisher>England</publisher><subject>Animals ; Apoptosis - drug effects ; Cell Differentiation - drug effects ; Cell Hypoxia - drug effects ; Cell Proliferation - drug effects ; Embryo, Mammalian - drug effects ; Embryo, Mammalian - pathology ; Female ; Fibroblast Growth Factors - metabolism ; Heart Defects, Congenital - etiology ; Heart Defects, Congenital - pathology ; Mice, Inbred C57BL ; Oxygen - pharmacology ; Phenotype ; Pregnancy ; Protein Biosynthesis - drug effects ; Receptor, Fibroblast Growth Factor, Type 1 - metabolism ; Signal Transduction - drug effects ; Stress, Physiological - drug effects ; Unfolded Protein Response - drug effects</subject><ispartof>Development (Cambridge), 2016-07, Vol.143 (14), p.2561-2572</ispartof><rights>2016. 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It is the most common human birth defect and yet, even with the application of modern genetic and genomic technologies, only a minority of cases can be explained genetically. This is because environmental stressors also cause CHD. Here we propose a plausible non-genetic mechanism for induction of CHD by environmental stressors. We show that exposure of mouse embryos to short-term gestational hypoxia induces the most common types of heart defect. This is mediated by the rapid induction of the unfolded protein response (UPR), which profoundly reduces FGF signaling in cardiac progenitor cells of the second heart field. Thus, UPR activation during human pregnancy might be a common cause of CHD. Our findings have far-reaching consequences because the UPR is activated by a myriad of environmental or pathophysiological conditions. Ultimately, our discovery could lead to preventative strategies to reduce the incidence of human CHD.</description><subject>Animals</subject><subject>Apoptosis - drug effects</subject><subject>Cell Differentiation - drug effects</subject><subject>Cell Hypoxia - drug effects</subject><subject>Cell Proliferation - drug effects</subject><subject>Embryo, Mammalian - drug effects</subject><subject>Embryo, Mammalian - pathology</subject><subject>Female</subject><subject>Fibroblast Growth Factors - metabolism</subject><subject>Heart Defects, Congenital - etiology</subject><subject>Heart Defects, Congenital - pathology</subject><subject>Mice, Inbred C57BL</subject><subject>Oxygen - pharmacology</subject><subject>Phenotype</subject><subject>Pregnancy</subject><subject>Protein Biosynthesis - drug effects</subject><subject>Receptor, Fibroblast Growth Factor, Type 1 - metabolism</subject><subject>Signal Transduction - drug effects</subject><subject>Stress, Physiological - drug effects</subject><subject>Unfolded Protein Response - drug effects</subject><issn>0950-1991</issn><issn>1477-9129</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkMtOwzAQRS0EoqWw4QOQlwiR4lf8WKIKClIlNt1Hjj2mQWlSYgeJv8dVC2tWM4szV3cOQteUzCkT7MHD15xyqRk5QVMqlCoMZeYUTYkpSUGNoRN0EeMHIYRLpc7RhCnBJRFkitZLiMmmpu9si2MaIEbcdH50EHHaAB670LcePN4NfYKmw5nY9V2E-_02tqnp3vMB3oAdEvYQwKV4ic6CbSNcHecMrZ-f1ouXYvW2fF08rgrHS5kKa4wTmgettNMCGACvCQXPXJl7ssBq7koQIShVU-2tr53zQdXAlGbM8Rm6PcTmbp9j_qPaNtFB29oO-jFWVFOqlZBE_gMlkihpsqEZujugbuhjHCBUu6HZ2uG7oqTa-66y7-rgO8M3x9yx3oL_Q38F8x_JVnyC</recordid><startdate>20160715</startdate><enddate>20160715</enddate><creator>Shi, Hongjun</creator><creator>O'Reilly, Victoria C</creator><creator>Moreau, Julie L M</creator><creator>Bewes, Therese R</creator><creator>Yam, Michelle X</creator><creator>Chapman, Bogdan E</creator><creator>Grieve, Stuart M</creator><creator>Stocker, Roland</creator><creator>Graham, Robert M</creator><creator>Chapman, Gavin</creator><creator>Sparrow, Duncan B</creator><creator>Dunwoodie, Sally L</creator><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>7X8</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><orcidid>https://orcid.org/0000-0002-2069-7349</orcidid></search><sort><creationdate>20160715</creationdate><title>Gestational stress induces the unfolded protein response, resulting in heart defects</title><author>Shi, Hongjun ; O'Reilly, Victoria C ; Moreau, Julie L M ; Bewes, Therese R ; Yam, Michelle X ; Chapman, Bogdan E ; Grieve, Stuart M ; Stocker, Roland ; Graham, Robert M ; Chapman, Gavin ; Sparrow, Duncan B ; Dunwoodie, Sally L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-a99c483f878c84e2ee3b01ed2c53672f2b3c5e4ff77b18dadbccdf7be27822c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Apoptosis - drug effects</topic><topic>Cell Differentiation - drug effects</topic><topic>Cell Hypoxia - drug effects</topic><topic>Cell Proliferation - drug effects</topic><topic>Embryo, Mammalian - drug effects</topic><topic>Embryo, Mammalian - pathology</topic><topic>Female</topic><topic>Fibroblast Growth Factors - metabolism</topic><topic>Heart Defects, Congenital - etiology</topic><topic>Heart Defects, Congenital - pathology</topic><topic>Mice, Inbred C57BL</topic><topic>Oxygen - pharmacology</topic><topic>Phenotype</topic><topic>Pregnancy</topic><topic>Protein Biosynthesis - drug effects</topic><topic>Receptor, Fibroblast Growth Factor, Type 1 - metabolism</topic><topic>Signal Transduction - drug effects</topic><topic>Stress, Physiological - drug effects</topic><topic>Unfolded Protein Response - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shi, Hongjun</creatorcontrib><creatorcontrib>O'Reilly, Victoria C</creatorcontrib><creatorcontrib>Moreau, Julie L M</creatorcontrib><creatorcontrib>Bewes, Therese R</creatorcontrib><creatorcontrib>Yam, Michelle X</creatorcontrib><creatorcontrib>Chapman, Bogdan E</creatorcontrib><creatorcontrib>Grieve, Stuart M</creatorcontrib><creatorcontrib>Stocker, Roland</creatorcontrib><creatorcontrib>Graham, Robert M</creatorcontrib><creatorcontrib>Chapman, Gavin</creatorcontrib><creatorcontrib>Sparrow, Duncan B</creatorcontrib><creatorcontrib>Dunwoodie, Sally L</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Development (Cambridge)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shi, Hongjun</au><au>O'Reilly, Victoria C</au><au>Moreau, Julie L M</au><au>Bewes, Therese R</au><au>Yam, Michelle X</au><au>Chapman, Bogdan E</au><au>Grieve, Stuart M</au><au>Stocker, Roland</au><au>Graham, Robert M</au><au>Chapman, Gavin</au><au>Sparrow, Duncan B</au><au>Dunwoodie, Sally L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gestational stress induces the unfolded protein response, resulting in heart defects</atitle><jtitle>Development (Cambridge)</jtitle><addtitle>Development</addtitle><date>2016-07-15</date><risdate>2016</risdate><volume>143</volume><issue>14</issue><spage>2561</spage><epage>2572</epage><pages>2561-2572</pages><issn>0950-1991</issn><eissn>1477-9129</eissn><abstract>Congenital heart disease (CHD) is an enigma. It is the most common human birth defect and yet, even with the application of modern genetic and genomic technologies, only a minority of cases can be explained genetically. This is because environmental stressors also cause CHD. Here we propose a plausible non-genetic mechanism for induction of CHD by environmental stressors. We show that exposure of mouse embryos to short-term gestational hypoxia induces the most common types of heart defect. This is mediated by the rapid induction of the unfolded protein response (UPR), which profoundly reduces FGF signaling in cardiac progenitor cells of the second heart field. Thus, UPR activation during human pregnancy might be a common cause of CHD. Our findings have far-reaching consequences because the UPR is activated by a myriad of environmental or pathophysiological conditions. 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subjects | Animals Apoptosis - drug effects Cell Differentiation - drug effects Cell Hypoxia - drug effects Cell Proliferation - drug effects Embryo, Mammalian - drug effects Embryo, Mammalian - pathology Female Fibroblast Growth Factors - metabolism Heart Defects, Congenital - etiology Heart Defects, Congenital - pathology Mice, Inbred C57BL Oxygen - pharmacology Phenotype Pregnancy Protein Biosynthesis - drug effects Receptor, Fibroblast Growth Factor, Type 1 - metabolism Signal Transduction - drug effects Stress, Physiological - drug effects Unfolded Protein Response - drug effects |
title | Gestational stress induces the unfolded protein response, resulting in heart defects |
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