Aortic adaptation to pregnancy: elevated expression of matrix metalloproteinases‐2 and ‐3 in rat gestation
The maternal aorta undergoes substantial functional and structural adaptation in pregnancy. Both aortic diameter and compliance are increased and studies of animal and human gestation indicate that these changes are initiated in early pregnancy and maintained until delivery. The mechanisms underlyin...
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Veröffentlicht in: | Molecular human reproduction 2004-05, Vol.10 (5), p.331-337 |
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description | The maternal aorta undergoes substantial functional and structural adaptation in pregnancy. Both aortic diameter and compliance are increased and studies of animal and human gestation indicate that these changes are initiated in early pregnancy and maintained until delivery. The mechanisms underlying aortic adaptation in normal pregnancy remain largely unknown but matrix metalloproteinase enzymes (MMP) are likely to play a key role. Gene expression of candidate MMP and specific tissue inhibitors of MMP (TIMP) were investigated in non‐pregnant, pregnant (days 7, 14, 21) and postpartum (day 7) rat aorta using real‐time PCR. Of the gene transcripts studied (MMP‐2, ‐3, ‐7, ‐9, ‐12, ‐13, MT1MMP, TIMP‐1, ‐2) in rat aorta, only MMP‐3 was significantly elevated with a 24‐fold increase observed in late gestation compared to virgin control (P = 0.0001). MMP‐2 mRNA appeared constitutively expressed and unchanged at time‐points studied, but MMP‐2 activity as assessed by gelatin zymography suggested further modulation after transcription and/or post‐translation in rat aorta with activity increased in early pregnancy (P < 0.01, compared to virgin control). These data suggest that MMP‐2 and MMP‐3 may contribute to adaptive processes in the maternal rat aorta at different gestations and further support a role for this family of enzymes in physiological vascular remodelling. |
doi_str_mv | 10.1093/humrep/gah045 |
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Both aortic diameter and compliance are increased and studies of animal and human gestation indicate that these changes are initiated in early pregnancy and maintained until delivery. The mechanisms underlying aortic adaptation in normal pregnancy remain largely unknown but matrix metalloproteinase enzymes (MMP) are likely to play a key role. Gene expression of candidate MMP and specific tissue inhibitors of MMP (TIMP) were investigated in non‐pregnant, pregnant (days 7, 14, 21) and postpartum (day 7) rat aorta using real‐time PCR. Of the gene transcripts studied (MMP‐2, ‐3, ‐7, ‐9, ‐12, ‐13, MT1MMP, TIMP‐1, ‐2) in rat aorta, only MMP‐3 was significantly elevated with a 24‐fold increase observed in late gestation compared to virgin control (P = 0.0001). MMP‐2 mRNA appeared constitutively expressed and unchanged at time‐points studied, but MMP‐2 activity as assessed by gelatin zymography suggested further modulation after transcription and/or post‐translation in rat aorta with activity increased in early pregnancy (P < 0.01, compared to virgin control). These data suggest that MMP‐2 and MMP‐3 may contribute to adaptive processes in the maternal rat aorta at different gestations and further support a role for this family of enzymes in physiological vascular remodelling.</description><identifier>ISSN: 1360-9947</identifier><identifier>ISSN: 1460-2407</identifier><identifier>EISSN: 1460-2407</identifier><identifier>DOI: 10.1093/humrep/gah045</identifier><identifier>PMID: 15044600</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Animals ; Aorta - enzymology ; Aorta - physiology ; Biological and medical sciences ; Embryology: invertebrates and vertebrates. Teratology ; Female ; Fundamental and applied biological sciences. Psychology ; Humans ; Key words: aorta/MMP/pregnancy/rat/TIMP ; Matrix Metalloproteinase 2 - genetics ; Matrix Metalloproteinase 2 - metabolism ; Matrix Metalloproteinase 3 - genetics ; Matrix Metalloproteinase 3 - metabolism ; Pregnancy ; Pregnancy, Animal ; Rats ; Rats, Sprague-Dawley</subject><ispartof>Molecular human reproduction, 2004-05, Vol.10 (5), p.331-337</ispartof><rights>2005 INIST-CNRS</rights><rights>Copyright Oxford University Press(England) May 2004</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c454t-b9aa71bb4d8b506a928a46ba9d84a8e3aba6d5e858204c0a84e6d549e5c446c03</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16270181$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15044600$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kelly, B.A.</creatorcontrib><creatorcontrib>Bond, B.C.</creatorcontrib><creatorcontrib>Poston, L.</creatorcontrib><title>Aortic adaptation to pregnancy: elevated expression of matrix metalloproteinases‐2 and ‐3 in rat gestation</title><title>Molecular human reproduction</title><addtitle>Mol. Hum. Reprod</addtitle><description>The maternal aorta undergoes substantial functional and structural adaptation in pregnancy. Both aortic diameter and compliance are increased and studies of animal and human gestation indicate that these changes are initiated in early pregnancy and maintained until delivery. The mechanisms underlying aortic adaptation in normal pregnancy remain largely unknown but matrix metalloproteinase enzymes (MMP) are likely to play a key role. Gene expression of candidate MMP and specific tissue inhibitors of MMP (TIMP) were investigated in non‐pregnant, pregnant (days 7, 14, 21) and postpartum (day 7) rat aorta using real‐time PCR. Of the gene transcripts studied (MMP‐2, ‐3, ‐7, ‐9, ‐12, ‐13, MT1MMP, TIMP‐1, ‐2) in rat aorta, only MMP‐3 was significantly elevated with a 24‐fold increase observed in late gestation compared to virgin control (P = 0.0001). MMP‐2 mRNA appeared constitutively expressed and unchanged at time‐points studied, but MMP‐2 activity as assessed by gelatin zymography suggested further modulation after transcription and/or post‐translation in rat aorta with activity increased in early pregnancy (P < 0.01, compared to virgin control). These data suggest that MMP‐2 and MMP‐3 may contribute to adaptive processes in the maternal rat aorta at different gestations and further support a role for this family of enzymes in physiological vascular remodelling.</description><subject>Animals</subject><subject>Aorta - enzymology</subject><subject>Aorta - physiology</subject><subject>Biological and medical sciences</subject><subject>Embryology: invertebrates and vertebrates. Teratology</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Key words: aorta/MMP/pregnancy/rat/TIMP</subject><subject>Matrix Metalloproteinase 2 - genetics</subject><subject>Matrix Metalloproteinase 2 - metabolism</subject><subject>Matrix Metalloproteinase 3 - genetics</subject><subject>Matrix Metalloproteinase 3 - metabolism</subject><subject>Pregnancy</subject><subject>Pregnancy, Animal</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><issn>1360-9947</issn><issn>1460-2407</issn><issn>1460-2407</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU9rFTEUxQex2FpdupUg6G5s_k4Sd_WhraXgpkJxE-5k7nudOv9MMvK68yP4GftJmjIPH7hxlZPkxzn3coriFaPvGbXi5GbuA04nG7ihUj0pjpisaMkl1U-zFllbK_Vh8TzGW0qZ5so8Kw6ZojJz9KgYTseQWk-ggSlBaseBpJFMATcDDP7uA8EOf0HChuA2v8b4SIxr0kMK7Zb0mKDrximMCdsBIsb73384gaEhWQjSDiRAIhuMi_mL4mANXcSXu_O4-Pb509XqvLz8evZldXpZeqlkKmsLoFldy8bUilZguQFZ1WAbI8GggBqqRqFRhlPpKRiJ-S4tKp_38lQcF-8W3zzZzzmnu76NHrsOBhzn6DQzOaiS_wWzvxTaigy--Qe8Hecw5CUc54pTzS3PULlAPowxBly7KbQ9hDvHqHusyy11uaWuzL_emc51j82e3vWTgbc7AKKHbh1yKW3ccxXXlBm2D25jwu3ffwg_XKWFVu78-rtbiY_XV_qicmfiAZ4JsVU</recordid><startdate>20040501</startdate><enddate>20040501</enddate><creator>Kelly, B.A.</creator><creator>Bond, B.C.</creator><creator>Poston, L.</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>BSCLL</scope><scope>IQODW</scope><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>7QP</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20040501</creationdate><title>Aortic adaptation to pregnancy: elevated expression of matrix metalloproteinases‐2 and ‐3 in rat gestation</title><author>Kelly, B.A. ; Bond, B.C. ; Poston, L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c454t-b9aa71bb4d8b506a928a46ba9d84a8e3aba6d5e858204c0a84e6d549e5c446c03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Aorta - enzymology</topic><topic>Aorta - physiology</topic><topic>Biological and medical sciences</topic><topic>Embryology: invertebrates and vertebrates. Teratology</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Key words: aorta/MMP/pregnancy/rat/TIMP</topic><topic>Matrix Metalloproteinase 2 - genetics</topic><topic>Matrix Metalloproteinase 2 - metabolism</topic><topic>Matrix Metalloproteinase 3 - genetics</topic><topic>Matrix Metalloproteinase 3 - metabolism</topic><topic>Pregnancy</topic><topic>Pregnancy, Animal</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kelly, B.A.</creatorcontrib><creatorcontrib>Bond, B.C.</creatorcontrib><creatorcontrib>Poston, L.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular human reproduction</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kelly, B.A.</au><au>Bond, B.C.</au><au>Poston, L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Aortic adaptation to pregnancy: elevated expression of matrix metalloproteinases‐2 and ‐3 in rat gestation</atitle><jtitle>Molecular human reproduction</jtitle><addtitle>Mol. Hum. Reprod</addtitle><date>2004-05-01</date><risdate>2004</risdate><volume>10</volume><issue>5</issue><spage>331</spage><epage>337</epage><pages>331-337</pages><issn>1360-9947</issn><issn>1460-2407</issn><eissn>1460-2407</eissn><abstract>The maternal aorta undergoes substantial functional and structural adaptation in pregnancy. Both aortic diameter and compliance are increased and studies of animal and human gestation indicate that these changes are initiated in early pregnancy and maintained until delivery. The mechanisms underlying aortic adaptation in normal pregnancy remain largely unknown but matrix metalloproteinase enzymes (MMP) are likely to play a key role. Gene expression of candidate MMP and specific tissue inhibitors of MMP (TIMP) were investigated in non‐pregnant, pregnant (days 7, 14, 21) and postpartum (day 7) rat aorta using real‐time PCR. Of the gene transcripts studied (MMP‐2, ‐3, ‐7, ‐9, ‐12, ‐13, MT1MMP, TIMP‐1, ‐2) in rat aorta, only MMP‐3 was significantly elevated with a 24‐fold increase observed in late gestation compared to virgin control (P = 0.0001). MMP‐2 mRNA appeared constitutively expressed and unchanged at time‐points studied, but MMP‐2 activity as assessed by gelatin zymography suggested further modulation after transcription and/or post‐translation in rat aorta with activity increased in early pregnancy (P < 0.01, compared to virgin control). These data suggest that MMP‐2 and MMP‐3 may contribute to adaptive processes in the maternal rat aorta at different gestations and further support a role for this family of enzymes in physiological vascular remodelling.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>15044600</pmid><doi>10.1093/humrep/gah045</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Aorta - enzymology Aorta - physiology Biological and medical sciences Embryology: invertebrates and vertebrates. Teratology Female Fundamental and applied biological sciences. Psychology Humans Key words: aorta/MMP/pregnancy/rat/TIMP Matrix Metalloproteinase 2 - genetics Matrix Metalloproteinase 2 - metabolism Matrix Metalloproteinase 3 - genetics Matrix Metalloproteinase 3 - metabolism Pregnancy Pregnancy, Animal Rats Rats, Sprague-Dawley |
title | Aortic adaptation to pregnancy: elevated expression of matrix metalloproteinases‐2 and ‐3 in rat gestation |
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