Proliferating Cell Nuclear Antigen in Developing and Adult Rat Cardiac Muscle Cells

During early development, rat cardiac muscle cells actively proliferate. Shortly after birth, division of cardiac muscle cells ceases, whereas DNA synthesis continues for approximately 2 weeks at a progressively diminishing rate. Little DNA synthesis or cell division occurs in adult cardiocytes. Thu...

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Veröffentlicht in:Circulation research 1991-11, Vol.69 (5), p.1353-1360
Hauptverfasser: Marino, Thomas A, Haldar, Subrata, Williamson, Eileen C, Beaverson, Katherine, Walter, Ruth Anne, Marino, Deborah R, Beatty, Christine, Lipson, Kenneth E
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container_end_page 1360
container_issue 5
container_start_page 1353
container_title Circulation research
container_volume 69
creator Marino, Thomas A
Haldar, Subrata
Williamson, Eileen C
Beaverson, Katherine
Walter, Ruth Anne
Marino, Deborah R
Beatty, Christine
Lipson, Kenneth E
description During early development, rat cardiac muscle cells actively proliferate. Shortly after birth, division of cardiac muscle cells ceases, whereas DNA synthesis continues for approximately 2 weeks at a progressively diminishing rate. Little DNA synthesis or cell division occurs in adult cardiocytes. Thus, developing cardiac muscle cells are an ideal system in which to examine the expression of cell cycle-regulated genes during development. We chose to examine proliferating cell nuclear antigen (PCNA), a gene expressed at the GI/S phase boundary of the cell cycle. Northern blots of RNA from cardiac muscle cells from 18 -day-old rat fetuses and from day 0, 5, and 14 neonatal as well as adult rat hearts revealed that the PCNA mRNA was found in cardiac muscle cells from all ages. However, because it was possible that this was a result of fibroblast PCNA gene expression, we used reverse transcription followed by polymerase chain reaction to see if it was possible to detect the message for PCNA in cardiac muscle cells from all ages. Because of the great sensitivity of this technique, RNA was recovered from 25 isolated adult cardiac muscle cells. Polymerase chain reaction amplification products for PCNA produced from the RNA isolated from these cells conclusively demonstrated that mRNA for this gene, which normally is associated with proliferating cells, is expressed in adult cardiac muscle cells that no longer divide. Furthermore, Western blot analysis demonstrated that the PCNA protein was found only in embryonic and neonatal cells and not in adult rat cardiac muscle cells. Therefore, it might be inferred from these data that PCNA might be regulated at the posttranscriptional level in adult cardiac muscle cells. (Circulation Research 1991;69:1353–1360)
doi_str_mv 10.1161/01.res.69.5.1353
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Shortly after birth, division of cardiac muscle cells ceases, whereas DNA synthesis continues for approximately 2 weeks at a progressively diminishing rate. Little DNA synthesis or cell division occurs in adult cardiocytes. Thus, developing cardiac muscle cells are an ideal system in which to examine the expression of cell cycle-regulated genes during development. We chose to examine proliferating cell nuclear antigen (PCNA), a gene expressed at the GI/S phase boundary of the cell cycle. Northern blots of RNA from cardiac muscle cells from 18 -day-old rat fetuses and from day 0, 5, and 14 neonatal as well as adult rat hearts revealed that the PCNA mRNA was found in cardiac muscle cells from all ages. However, because it was possible that this was a result of fibroblast PCNA gene expression, we used reverse transcription followed by polymerase chain reaction to see if it was possible to detect the message for PCNA in cardiac muscle cells from all ages. Because of the great sensitivity of this technique, RNA was recovered from 25 isolated adult cardiac muscle cells. Polymerase chain reaction amplification products for PCNA produced from the RNA isolated from these cells conclusively demonstrated that mRNA for this gene, which normally is associated with proliferating cells, is expressed in adult cardiac muscle cells that no longer divide. Furthermore, Western blot analysis demonstrated that the PCNA protein was found only in embryonic and neonatal cells and not in adult rat cardiac muscle cells. Therefore, it might be inferred from these data that PCNA might be regulated at the posttranscriptional level in adult cardiac muscle cells. 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Psychology ; Heart ; Heart - embryology ; Heart - growth &amp; development ; Immunoblotting ; Myocardium - cytology ; Myocardium - immunology ; Nuclear Proteins - analysis ; Nuclear Proteins - genetics ; Polymerase Chain Reaction ; Proliferating Cell Nuclear Antigen ; Rats ; RNA - analysis ; RNA, Antisense - analysis ; Transcription, Genetic ; Vertebrates: cardiovascular system</subject><ispartof>Circulation research, 1991-11, Vol.69 (5), p.1353-1360</ispartof><rights>1991 American Heart Association, Inc.</rights><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5138-6212b021c8497c095513cbc6e9b2e510391310629d297ce7d6246432cc43225c3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,3688,27926,27927</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=5058736$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1718625$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Marino, Thomas A</creatorcontrib><creatorcontrib>Haldar, Subrata</creatorcontrib><creatorcontrib>Williamson, Eileen C</creatorcontrib><creatorcontrib>Beaverson, Katherine</creatorcontrib><creatorcontrib>Walter, Ruth Anne</creatorcontrib><creatorcontrib>Marino, Deborah R</creatorcontrib><creatorcontrib>Beatty, Christine</creatorcontrib><creatorcontrib>Lipson, Kenneth E</creatorcontrib><title>Proliferating Cell Nuclear Antigen in Developing and Adult Rat Cardiac Muscle Cells</title><title>Circulation research</title><addtitle>Circ Res</addtitle><description>During early development, rat cardiac muscle cells actively proliferate. Shortly after birth, division of cardiac muscle cells ceases, whereas DNA synthesis continues for approximately 2 weeks at a progressively diminishing rate. Little DNA synthesis or cell division occurs in adult cardiocytes. Thus, developing cardiac muscle cells are an ideal system in which to examine the expression of cell cycle-regulated genes during development. We chose to examine proliferating cell nuclear antigen (PCNA), a gene expressed at the GI/S phase boundary of the cell cycle. Northern blots of RNA from cardiac muscle cells from 18 -day-old rat fetuses and from day 0, 5, and 14 neonatal as well as adult rat hearts revealed that the PCNA mRNA was found in cardiac muscle cells from all ages. However, because it was possible that this was a result of fibroblast PCNA gene expression, we used reverse transcription followed by polymerase chain reaction to see if it was possible to detect the message for PCNA in cardiac muscle cells from all ages. Because of the great sensitivity of this technique, RNA was recovered from 25 isolated adult cardiac muscle cells. Polymerase chain reaction amplification products for PCNA produced from the RNA isolated from these cells conclusively demonstrated that mRNA for this gene, which normally is associated with proliferating cells, is expressed in adult cardiac muscle cells that no longer divide. Furthermore, Western blot analysis demonstrated that the PCNA protein was found only in embryonic and neonatal cells and not in adult rat cardiac muscle cells. Therefore, it might be inferred from these data that PCNA might be regulated at the posttranscriptional level in adult cardiac muscle cells. (Circulation Research 1991;69:1353–1360)</description><subject>Animals</subject><subject>Animals, Newborn - growth &amp; development</subject><subject>Animals, Newborn - immunology</subject><subject>Biological and medical sciences</subject><subject>Blotting, Northern</subject><subject>Embryonic and Fetal Development</subject><subject>Fetus - immunology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Heart</subject><subject>Heart - embryology</subject><subject>Heart - growth &amp; development</subject><subject>Immunoblotting</subject><subject>Myocardium - cytology</subject><subject>Myocardium - immunology</subject><subject>Nuclear Proteins - analysis</subject><subject>Nuclear Proteins - genetics</subject><subject>Polymerase Chain Reaction</subject><subject>Proliferating Cell Nuclear Antigen</subject><subject>Rats</subject><subject>RNA - analysis</subject><subject>RNA, Antisense - analysis</subject><subject>Transcription, Genetic</subject><subject>Vertebrates: cardiovascular system</subject><issn>0009-7330</issn><issn>1524-4571</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkc1P3DAQxa2qFV2g914q-VBxSzpjx058XG2hVKIF8XG2vM4spHiTrZ2A-t_j7a7gYFsz7_dGo2fGPiOUiBq_AZaRUqlNqUqUSr5jM1SiKipV43s2AwBT1FLCR3aY0h8ArKQwB-wAa2y0UDN2cxWH0K0ourHr7_mCQuC_Jx_IRT7vx-6eet71_Ds9URg2W8T1LZ-3Uxj5tRv5wsW2c57_mlI2_fenY_Zh5UKiT_v3iN2dnd4uzouLyx8_F_OLwiuUTaEFiiUI9E1lag9G5a5fek1mKUghSIMSQQvTiqxT3WpR6by_9_kSyssjdrKbu4nD34nSaNdd8nkD19MwJVuLqpJG1BmEHejjkFKkld3Ebu3iP4tgtzlaQHt9emO1scpuc8yWL_vZ03JN7ZthF1zWv-51l7wLq-h636VXTIFqaqkzVu2w5yGMFNNjmJ4p2gdyYXyw-XtAAooCjUHEXBX5YCNfAPVvh-Q</recordid><startdate>199111</startdate><enddate>199111</enddate><creator>Marino, Thomas A</creator><creator>Haldar, Subrata</creator><creator>Williamson, Eileen C</creator><creator>Beaverson, Katherine</creator><creator>Walter, Ruth Anne</creator><creator>Marino, Deborah R</creator><creator>Beatty, Christine</creator><creator>Lipson, Kenneth E</creator><general>American Heart Association, Inc</general><general>Lippincott</general><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>7X8</scope></search><sort><creationdate>199111</creationdate><title>Proliferating Cell Nuclear Antigen in Developing and Adult Rat Cardiac Muscle Cells</title><author>Marino, Thomas A ; Haldar, Subrata ; Williamson, Eileen C ; Beaverson, Katherine ; Walter, Ruth Anne ; Marino, Deborah R ; Beatty, Christine ; Lipson, Kenneth E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5138-6212b021c8497c095513cbc6e9b2e510391310629d297ce7d6246432cc43225c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Animals</topic><topic>Animals, Newborn - growth &amp; development</topic><topic>Animals, Newborn - immunology</topic><topic>Biological and medical sciences</topic><topic>Blotting, Northern</topic><topic>Embryonic and Fetal Development</topic><topic>Fetus - immunology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Heart</topic><topic>Heart - embryology</topic><topic>Heart - growth &amp; development</topic><topic>Immunoblotting</topic><topic>Myocardium - cytology</topic><topic>Myocardium - immunology</topic><topic>Nuclear Proteins - analysis</topic><topic>Nuclear Proteins - genetics</topic><topic>Polymerase Chain Reaction</topic><topic>Proliferating Cell Nuclear Antigen</topic><topic>Rats</topic><topic>RNA - analysis</topic><topic>RNA, Antisense - analysis</topic><topic>Transcription, Genetic</topic><topic>Vertebrates: cardiovascular system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Marino, Thomas A</creatorcontrib><creatorcontrib>Haldar, Subrata</creatorcontrib><creatorcontrib>Williamson, Eileen C</creatorcontrib><creatorcontrib>Beaverson, Katherine</creatorcontrib><creatorcontrib>Walter, Ruth Anne</creatorcontrib><creatorcontrib>Marino, Deborah R</creatorcontrib><creatorcontrib>Beatty, Christine</creatorcontrib><creatorcontrib>Lipson, Kenneth E</creatorcontrib><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>MEDLINE - Academic</collection><jtitle>Circulation research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Marino, Thomas A</au><au>Haldar, Subrata</au><au>Williamson, Eileen C</au><au>Beaverson, Katherine</au><au>Walter, Ruth Anne</au><au>Marino, Deborah R</au><au>Beatty, Christine</au><au>Lipson, Kenneth E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Proliferating Cell Nuclear Antigen in Developing and Adult Rat Cardiac Muscle Cells</atitle><jtitle>Circulation research</jtitle><addtitle>Circ Res</addtitle><date>1991-11</date><risdate>1991</risdate><volume>69</volume><issue>5</issue><spage>1353</spage><epage>1360</epage><pages>1353-1360</pages><issn>0009-7330</issn><eissn>1524-4571</eissn><coden>CIRUAL</coden><abstract>During early development, rat cardiac muscle cells actively proliferate. Shortly after birth, division of cardiac muscle cells ceases, whereas DNA synthesis continues for approximately 2 weeks at a progressively diminishing rate. Little DNA synthesis or cell division occurs in adult cardiocytes. Thus, developing cardiac muscle cells are an ideal system in which to examine the expression of cell cycle-regulated genes during development. We chose to examine proliferating cell nuclear antigen (PCNA), a gene expressed at the GI/S phase boundary of the cell cycle. Northern blots of RNA from cardiac muscle cells from 18 -day-old rat fetuses and from day 0, 5, and 14 neonatal as well as adult rat hearts revealed that the PCNA mRNA was found in cardiac muscle cells from all ages. However, because it was possible that this was a result of fibroblast PCNA gene expression, we used reverse transcription followed by polymerase chain reaction to see if it was possible to detect the message for PCNA in cardiac muscle cells from all ages. Because of the great sensitivity of this technique, RNA was recovered from 25 isolated adult cardiac muscle cells. Polymerase chain reaction amplification products for PCNA produced from the RNA isolated from these cells conclusively demonstrated that mRNA for this gene, which normally is associated with proliferating cells, is expressed in adult cardiac muscle cells that no longer divide. Furthermore, Western blot analysis demonstrated that the PCNA protein was found only in embryonic and neonatal cells and not in adult rat cardiac muscle cells. Therefore, it might be inferred from these data that PCNA might be regulated at the posttranscriptional level in adult cardiac muscle cells. (Circulation Research 1991;69:1353–1360)</abstract><cop>Hagerstown, MD</cop><pub>American Heart Association, Inc</pub><pmid>1718625</pmid><doi>10.1161/01.res.69.5.1353</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; American Heart Association; Journals@Ovid Complete
subjects Animals
Animals, Newborn - growth & development
Animals, Newborn - immunology
Biological and medical sciences
Blotting, Northern
Embryonic and Fetal Development
Fetus - immunology
Fundamental and applied biological sciences. Psychology
Heart
Heart - embryology
Heart - growth & development
Immunoblotting
Myocardium - cytology
Myocardium - immunology
Nuclear Proteins - analysis
Nuclear Proteins - genetics
Polymerase Chain Reaction
Proliferating Cell Nuclear Antigen
Rats
RNA - analysis
RNA, Antisense - analysis
Transcription, Genetic
Vertebrates: cardiovascular system
title Proliferating Cell Nuclear Antigen in Developing and Adult Rat Cardiac Muscle Cells
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