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Soluble fms-like tyrosine kinase-1 and angiotensin2 target calcitonin gene-related peptide family peptides in maternal vascular smooth muscle cells in pregnancy
Calcitonin gene-related peptide (CALCB), adrenomedullin (ADM), and adrenomedullin2 (ADM2) are hypotensive peptides that belong to CALCB family of peptides. Goal of this study was to identify the effect of fms-like tyrosine kinase (sFLT-1) and angiotensin2 (Ang2) on the function of these peptides in...
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Published in: | Biology of reproduction 2021-05, Vol.104 (5), p.1071-1083 |
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description | Calcitonin gene-related peptide (CALCB), adrenomedullin (ADM), and adrenomedullin2 (ADM2) are hypotensive peptides that belong to CALCB family of peptides. Goal of this study was to identify the effect of fms-like tyrosine kinase (sFLT-1) and angiotensin2 (Ang2) on the function of these peptides in OA smooth muscle cells (OASMC) and assess the sensitivity of OA for these peptides in preeclampsia (PE) and normotensive pregnancy. Methods: Peptide function was assessed by Cyclic adenosine monophosphate (cAMP) assays and wire myograph; mRNA expression by Polymerase chain reaction (PCR) and protein-protein interaction by proximity ligation assay and co-immunoprecipitation. Findings: All three peptides increased cAMP synthesis in the order of efficacy CALCB > ADM = ADM2 and vascular endothelial growth factor (VEGF) mRNA in OASMC (P < 0.05); sFLT-1 mediated decrease in cAMP synthesis (P < 0.05) is differentially rescued by all three CALCB family peptides in OASMC (P < 0.005); sFLT-1 decreased receptor activity-modifying protein (RAMP)1 and RAMP2 mRNA expression (P < 0.05); Ang2 decreased the expression of calcitonin-receptor-like receptor and RAMP1 mRNA and desensitized CALCB and ADM2 receptors in OASMC (P < 0.05); sFLT-1 increased RAMP1and Ang2 type 1 receptor (AT1R) interaction in OASMC which is inhibited in presence of all three peptides; and all three peptides relax OA in PE with enhanced ADM2 response (P < 0.05). Conclusion: sFLT-1 and Ang2 impair OASMC mediated functional responses of CALCB family peptides which can be inhibited by respective peptide treatment. The sensitivity of OA for CALCB, ADM, and ADM2-mediated relaxation is retained in PE. Summary sentence sFLT-1 and Ang2 impair smooth muscle cell mediated functional responses of CALCB family peptides which can be inhibited by respective peptide treatment. Graphical Abstract |
doi_str_mv | 10.1093/biolre/ioab026 |
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Goal of this study was to identify the effect of fms-like tyrosine kinase (sFLT-1) and angiotensin2 (Ang2) on the function of these peptides in OA smooth muscle cells (OASMC) and assess the sensitivity of OA for these peptides in preeclampsia (PE) and normotensive pregnancy. Methods: Peptide function was assessed by Cyclic adenosine monophosphate (cAMP) assays and wire myograph; mRNA expression by Polymerase chain reaction (PCR) and protein-protein interaction by proximity ligation assay and co-immunoprecipitation. Findings: All three peptides increased cAMP synthesis in the order of efficacy CALCB > ADM = ADM2 and vascular endothelial growth factor (VEGF) mRNA in OASMC (P < 0.05); sFLT-1 mediated decrease in cAMP synthesis (P < 0.05) is differentially rescued by all three CALCB family peptides in OASMC (P < 0.005); sFLT-1 decreased receptor activity-modifying protein (RAMP)1 and RAMP2 mRNA expression (P < 0.05); Ang2 decreased the expression of calcitonin-receptor-like receptor and RAMP1 mRNA and desensitized CALCB and ADM2 receptors in OASMC (P < 0.05); sFLT-1 increased RAMP1and Ang2 type 1 receptor (AT1R) interaction in OASMC which is inhibited in presence of all three peptides; and all three peptides relax OA in PE with enhanced ADM2 response (P < 0.05). Conclusion: sFLT-1 and Ang2 impair OASMC mediated functional responses of CALCB family peptides which can be inhibited by respective peptide treatment. The sensitivity of OA for CALCB, ADM, and ADM2-mediated relaxation is retained in PE. Summary sentence sFLT-1 and Ang2 impair smooth muscle cell mediated functional responses of CALCB family peptides which can be inhibited by respective peptide treatment. Graphical Abstract]]></description><identifier>ISSN: 0006-3363</identifier><identifier>EISSN: 1529-7268</identifier><identifier>DOI: 10.1093/biolre/ioab026</identifier><identifier>PMID: 33624744</identifier><language>eng</language><publisher>United States: Society for the Study of Reproduction</publisher><subject>Adenylic acid ; angiotensin 2 ; Blood pressure ; Calcitonin Gene-Related Peptide - metabolism ; calcitonin gene-related peptides ; cAMP ; Cyclic adenylic acid ; Female ; Genes ; Genetic research ; Gynecology ; Humans ; Multigene Family ; Muscle, Smooth, Vascular - metabolism ; Myocytes, Smooth Muscle - metabolism ; Obstetrics ; Peptides ; Phenols ; Preeclampsia ; Pregnancy ; Pregnant women ; Protein-protein interactions ; Proteins ; RESEARCH ARTICLE ; RNA ; sFLT-1 ; Smooth muscle ; Tyrosine ; Vascular endothelial growth factor ; Vascular Endothelial Growth Factor Receptor-1 - genetics ; Vascular Endothelial Growth Factor Receptor-1 - metabolism ; vascular smooth muscle cells ; Vesicular Transport Proteins - genetics ; Vesicular Transport Proteins - metabolism</subject><ispartof>Biology of reproduction, 2021-05, Vol.104 (5), p.1071-1083</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 2021</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>COPYRIGHT 2021 Oxford University Press</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><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b556t-43e142910b35cfd5492a0cdab522496a4d783e38aa82a0a477b6b428d3ee99233</citedby><cites>FETCH-LOGICAL-b556t-43e142910b35cfd5492a0cdab522496a4d783e38aa82a0a477b6b428d3ee99233</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33624744$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chauhan, Madhu</creatorcontrib><creatorcontrib>Betancourt, Ancizar</creatorcontrib><creatorcontrib>Balakrishnan, Meena</creatorcontrib><creatorcontrib>Mishra, Akansha</creatorcontrib><creatorcontrib>Fox, Karin</creatorcontrib><creatorcontrib>Belfort, Michael</creatorcontrib><creatorcontrib>Yallampalli, Chandra</creatorcontrib><title>Soluble fms-like tyrosine kinase-1 and angiotensin2 target calcitonin gene-related peptide family peptides in maternal vascular smooth muscle cells in pregnancy</title><title>Biology of reproduction</title><addtitle>Biol Reprod</addtitle><description><![CDATA[Calcitonin gene-related peptide (CALCB), adrenomedullin (ADM), and adrenomedullin2 (ADM2) are hypotensive peptides that belong to CALCB family of peptides. Goal of this study was to identify the effect of fms-like tyrosine kinase (sFLT-1) and angiotensin2 (Ang2) on the function of these peptides in OA smooth muscle cells (OASMC) and assess the sensitivity of OA for these peptides in preeclampsia (PE) and normotensive pregnancy. Methods: Peptide function was assessed by Cyclic adenosine monophosphate (cAMP) assays and wire myograph; mRNA expression by Polymerase chain reaction (PCR) and protein-protein interaction by proximity ligation assay and co-immunoprecipitation. Findings: All three peptides increased cAMP synthesis in the order of efficacy CALCB > ADM = ADM2 and vascular endothelial growth factor (VEGF) mRNA in OASMC (P < 0.05); sFLT-1 mediated decrease in cAMP synthesis (P < 0.05) is differentially rescued by all three CALCB family peptides in OASMC (P < 0.005); sFLT-1 decreased receptor activity-modifying protein (RAMP)1 and RAMP2 mRNA expression (P < 0.05); Ang2 decreased the expression of calcitonin-receptor-like receptor and RAMP1 mRNA and desensitized CALCB and ADM2 receptors in OASMC (P < 0.05); sFLT-1 increased RAMP1and Ang2 type 1 receptor (AT1R) interaction in OASMC which is inhibited in presence of all three peptides; and all three peptides relax OA in PE with enhanced ADM2 response (P < 0.05). Conclusion: sFLT-1 and Ang2 impair OASMC mediated functional responses of CALCB family peptides which can be inhibited by respective peptide treatment. The sensitivity of OA for CALCB, ADM, and ADM2-mediated relaxation is retained in PE. Summary sentence sFLT-1 and Ang2 impair smooth muscle cell mediated functional responses of CALCB family peptides which can be inhibited by respective peptide treatment. Graphical Abstract]]></description><subject>Adenylic acid</subject><subject>angiotensin 2</subject><subject>Blood pressure</subject><subject>Calcitonin Gene-Related Peptide - metabolism</subject><subject>calcitonin gene-related peptides</subject><subject>cAMP</subject><subject>Cyclic adenylic acid</subject><subject>Female</subject><subject>Genes</subject><subject>Genetic research</subject><subject>Gynecology</subject><subject>Humans</subject><subject>Multigene Family</subject><subject>Muscle, Smooth, Vascular - metabolism</subject><subject>Myocytes, Smooth Muscle - metabolism</subject><subject>Obstetrics</subject><subject>Peptides</subject><subject>Phenols</subject><subject>Preeclampsia</subject><subject>Pregnancy</subject><subject>Pregnant women</subject><subject>Protein-protein interactions</subject><subject>Proteins</subject><subject>RESEARCH ARTICLE</subject><subject>RNA</subject><subject>sFLT-1</subject><subject>Smooth muscle</subject><subject>Tyrosine</subject><subject>Vascular endothelial growth factor</subject><subject>Vascular Endothelial Growth Factor Receptor-1 - genetics</subject><subject>Vascular Endothelial Growth Factor Receptor-1 - metabolism</subject><subject>vascular smooth muscle cells</subject><subject>Vesicular Transport Proteins - genetics</subject><subject>Vesicular Transport Proteins - metabolism</subject><issn>0006-3363</issn><issn>1529-7268</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqFkltrFTEQxxdRbK2--igBXxTcNre9vRRK8QYFH9TnMJud3abNJmuSLZxv40c1x3NaLxRKCCEzv_lnZjJF8ZLRY0Y7cdIbbwOeGA895fWj4pBVvCsbXrePi0NKaV0KUYuD4lmMV5QyKbh4WhxkG5eNlIfFz6_err1FMs6xtOYaSdoEH41Dcm0cRCwZATfkPRmf0GUPJwnChIlosNok74wjEzosA1pIOJAFl2SGLAmzsZvbaySZmzMQHFhyA1GvFgKJs_fpksxr1DkLjdb-BpeAkwOnN8-LJyPYiC_251Hx_cP7b-efyosvHz-fn12UfVXVqZQCmeQdo72o9DhUsuNA9QB9xbnsapBD0woULUCbHSCbpq97ydtBIHYdF-KoON3pLms_46DRpQBWLcHMEDbKg1H_epy5VJO_US1jjEuaBd7sBYL_sWJMajZxWw849GtUOQ2R_4OKJqOv_0Ov_LptS6YqwXhHRUv_UBNYVMaNPr-rt6LqrKGsrWTVyUwd30PlNeBstHc4mmy_L0Dnf44Bx7saGVXbmVK7mVL7mcoBr_7uzB1-O0QZeLsD_Lo8LPZux2Z7Tu4h_Bdu9ene</recordid><startdate>20210501</startdate><enddate>20210501</enddate><creator>Chauhan, Madhu</creator><creator>Betancourt, Ancizar</creator><creator>Balakrishnan, Meena</creator><creator>Mishra, Akansha</creator><creator>Fox, Karin</creator><creator>Belfort, Michael</creator><creator>Yallampalli, Chandra</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><scope>5PM</scope></search><sort><creationdate>20210501</creationdate><title>Soluble fms-like tyrosine kinase-1 and angiotensin2 target calcitonin gene-related peptide family peptides in maternal vascular smooth muscle cells in pregnancy</title><author>Chauhan, Madhu ; Betancourt, Ancizar ; Balakrishnan, Meena ; Mishra, Akansha ; Fox, Karin ; Belfort, Michael ; Yallampalli, Chandra</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b556t-43e142910b35cfd5492a0cdab522496a4d783e38aa82a0a477b6b428d3ee99233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adenylic acid</topic><topic>angiotensin 2</topic><topic>Blood pressure</topic><topic>Calcitonin Gene-Related Peptide - metabolism</topic><topic>calcitonin gene-related peptides</topic><topic>cAMP</topic><topic>Cyclic adenylic acid</topic><topic>Female</topic><topic>Genes</topic><topic>Genetic research</topic><topic>Gynecology</topic><topic>Humans</topic><topic>Multigene Family</topic><topic>Muscle, Smooth, Vascular - metabolism</topic><topic>Myocytes, Smooth Muscle - metabolism</topic><topic>Obstetrics</topic><topic>Peptides</topic><topic>Phenols</topic><topic>Preeclampsia</topic><topic>Pregnancy</topic><topic>Pregnant women</topic><topic>Protein-protein interactions</topic><topic>Proteins</topic><topic>RESEARCH ARTICLE</topic><topic>RNA</topic><topic>sFLT-1</topic><topic>Smooth muscle</topic><topic>Tyrosine</topic><topic>Vascular endothelial growth factor</topic><topic>Vascular Endothelial Growth Factor Receptor-1 - genetics</topic><topic>Vascular Endothelial Growth Factor Receptor-1 - metabolism</topic><topic>vascular smooth muscle cells</topic><topic>Vesicular Transport Proteins - genetics</topic><topic>Vesicular Transport Proteins - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chauhan, Madhu</creatorcontrib><creatorcontrib>Betancourt, Ancizar</creatorcontrib><creatorcontrib>Balakrishnan, Meena</creatorcontrib><creatorcontrib>Mishra, Akansha</creatorcontrib><creatorcontrib>Fox, Karin</creatorcontrib><creatorcontrib>Belfort, Michael</creatorcontrib><creatorcontrib>Yallampalli, Chandra</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</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</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>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</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biology of reproduction</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chauhan, Madhu</au><au>Betancourt, Ancizar</au><au>Balakrishnan, Meena</au><au>Mishra, Akansha</au><au>Fox, Karin</au><au>Belfort, Michael</au><au>Yallampalli, Chandra</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Soluble fms-like tyrosine kinase-1 and angiotensin2 target calcitonin gene-related peptide family peptides in maternal vascular smooth muscle cells in pregnancy</atitle><jtitle>Biology of reproduction</jtitle><addtitle>Biol Reprod</addtitle><date>2021-05-01</date><risdate>2021</risdate><volume>104</volume><issue>5</issue><spage>1071</spage><epage>1083</epage><pages>1071-1083</pages><issn>0006-3363</issn><eissn>1529-7268</eissn><abstract><![CDATA[Calcitonin gene-related peptide (CALCB), adrenomedullin (ADM), and adrenomedullin2 (ADM2) are hypotensive peptides that belong to CALCB family of peptides. Goal of this study was to identify the effect of fms-like tyrosine kinase (sFLT-1) and angiotensin2 (Ang2) on the function of these peptides in OA smooth muscle cells (OASMC) and assess the sensitivity of OA for these peptides in preeclampsia (PE) and normotensive pregnancy. Methods: Peptide function was assessed by Cyclic adenosine monophosphate (cAMP) assays and wire myograph; mRNA expression by Polymerase chain reaction (PCR) and protein-protein interaction by proximity ligation assay and co-immunoprecipitation. Findings: All three peptides increased cAMP synthesis in the order of efficacy CALCB > ADM = ADM2 and vascular endothelial growth factor (VEGF) mRNA in OASMC (P < 0.05); sFLT-1 mediated decrease in cAMP synthesis (P < 0.05) is differentially rescued by all three CALCB family peptides in OASMC (P < 0.005); sFLT-1 decreased receptor activity-modifying protein (RAMP)1 and RAMP2 mRNA expression (P < 0.05); Ang2 decreased the expression of calcitonin-receptor-like receptor and RAMP1 mRNA and desensitized CALCB and ADM2 receptors in OASMC (P < 0.05); sFLT-1 increased RAMP1and Ang2 type 1 receptor (AT1R) interaction in OASMC which is inhibited in presence of all three peptides; and all three peptides relax OA in PE with enhanced ADM2 response (P < 0.05). Conclusion: sFLT-1 and Ang2 impair OASMC mediated functional responses of CALCB family peptides which can be inhibited by respective peptide treatment. The sensitivity of OA for CALCB, ADM, and ADM2-mediated relaxation is retained in PE. Summary sentence sFLT-1 and Ang2 impair smooth muscle cell mediated functional responses of CALCB family peptides which can be inhibited by respective peptide treatment. Graphical Abstract]]></abstract><cop>United States</cop><pub>Society for the Study of Reproduction</pub><pmid>33624744</pmid><doi>10.1093/biolre/ioab026</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenylic acid angiotensin 2 Blood pressure Calcitonin Gene-Related Peptide - metabolism calcitonin gene-related peptides cAMP Cyclic adenylic acid Female Genes Genetic research Gynecology Humans Multigene Family Muscle, Smooth, Vascular - metabolism Myocytes, Smooth Muscle - metabolism Obstetrics Peptides Phenols Preeclampsia Pregnancy Pregnant women Protein-protein interactions Proteins RESEARCH ARTICLE RNA sFLT-1 Smooth muscle Tyrosine Vascular endothelial growth factor Vascular Endothelial Growth Factor Receptor-1 - genetics Vascular Endothelial Growth Factor Receptor-1 - metabolism vascular smooth muscle cells Vesicular Transport Proteins - genetics Vesicular Transport Proteins - metabolism |
title | Soluble fms-like tyrosine kinase-1 and angiotensin2 target calcitonin gene-related peptide family peptides in maternal vascular smooth muscle cells in pregnancy |
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