Effects of platelet‐derived growth factor‐AA and ‐BB on embryonic cardiac development
Several studies have shown that disruption of the normal expression patterns of platelet‐derived growth factor (PDGF) ligands and receptors during development results in gross cardiac defects and embryonic or neonatal death. However, little is known about the specific role that PDGF plays in the dif...
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Veröffentlicht in: | The anatomical record. Part A, Discoveries in molecular, cellular, and evolutionary biology Discoveries in molecular, cellular, and evolutionary biology, 2003-05, Vol.272A (1), p.424-433 |
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container_title | The anatomical record. Part A, Discoveries in molecular, cellular, and evolutionary biology |
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creator | Price, Robert L. Haley, Stephen T. Bullard, Tara A. Goldsmith, Edie C. Simpson, David G. Thielen, Thomas E. Yost, Michael J. Terracio, Louis |
description | Several studies have shown that disruption of the normal expression patterns of platelet‐derived growth factor (PDGF) ligands and receptors during development results in gross cardiac defects and embryonic or neonatal death. However, little is known about the specific role that PDGF plays in the differentiation of cardiac myocytes. In experiments complementing studies that utilized naturally‐occurring Patch mice lacking the PDGFr α, or knockout animals lacking a PDGF ligand or receptor, we used rat and mouse whole‐embryo culture (WEC) techniques to increase the exposure of embryos to the PDGF‐AA or ‐BB ligands. Following a 48‐hr culture period, we analyzed heart growth and cardiac myocyte differentiation. Exposure of rat embryos to 50 ng/ml of PDGF‐AA resulted in a 42% increase in total protein levels in the heart, but did not result in a significant increase in heart growth, as determined by measurements of the atrioventricular length and the left ventricular length and width. Exposure of embryos to 50 ng/ml of PDGF‐BB resulted in a 77% increase in total protein levels and a significant (P < 0.05) 8–15% increase in the measured heart parameters. Although a comparison of control and PDGF‐AA‐treated embryos showed no increase in the overall size of the heart, confocal microscopy showed an increase in the size and number of myofibrillar bundles in the developing myocardium. In addition, transmission electron microscopy (TEM) revealed an increase in the presence of sarcomeres, indicating that myofibrils were more highly differentiated in these areas of the treated embryos. In PDGF‐BB‐treated embryos, the compact zone of the myocardium was thicker and, as shown by confocal microscopy and TEM, f‐actin and well‐developed sarcomeres were more prevalent, indicating that the myofibrils were more differentiated in the treated embryos than in the control embryos. These studies indicate that increased exposure of embryonic hearts to PDGF‐AA or ‐BB increases the rate of myocardial development. Anat Rec Part A 272A:424–433, 2003. © 2003 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/ar.a.10054 |
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However, little is known about the specific role that PDGF plays in the differentiation of cardiac myocytes. In experiments complementing studies that utilized naturally‐occurring Patch mice lacking the PDGFr α, or knockout animals lacking a PDGF ligand or receptor, we used rat and mouse whole‐embryo culture (WEC) techniques to increase the exposure of embryos to the PDGF‐AA or ‐BB ligands. Following a 48‐hr culture period, we analyzed heart growth and cardiac myocyte differentiation. Exposure of rat embryos to 50 ng/ml of PDGF‐AA resulted in a 42% increase in total protein levels in the heart, but did not result in a significant increase in heart growth, as determined by measurements of the atrioventricular length and the left ventricular length and width. Exposure of embryos to 50 ng/ml of PDGF‐BB resulted in a 77% increase in total protein levels and a significant (P < 0.05) 8–15% increase in the measured heart parameters. Although a comparison of control and PDGF‐AA‐treated embryos showed no increase in the overall size of the heart, confocal microscopy showed an increase in the size and number of myofibrillar bundles in the developing myocardium. In addition, transmission electron microscopy (TEM) revealed an increase in the presence of sarcomeres, indicating that myofibrils were more highly differentiated in these areas of the treated embryos. In PDGF‐BB‐treated embryos, the compact zone of the myocardium was thicker and, as shown by confocal microscopy and TEM, f‐actin and well‐developed sarcomeres were more prevalent, indicating that the myofibrils were more differentiated in the treated embryos than in the control embryos. These studies indicate that increased exposure of embryonic hearts to PDGF‐AA or ‐BB increases the rate of myocardial development. Anat Rec Part A 272A:424–433, 2003. © 2003 Wiley‐Liss, Inc.</description><identifier>ISSN: 1552-4884</identifier><identifier>EISSN: 1552-4892</identifier><identifier>DOI: 10.1002/ar.a.10054</identifier><identifier>PMID: 12704700</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animals ; cardiac development ; Cell Differentiation - drug effects ; Cell Differentiation - physiology ; confocal microscopy ; electron microscopy ; Female ; Heart - drug effects ; Heart - embryology ; Heart Defects, Congenital - chemically induced ; Heart Defects, Congenital - metabolism ; Heart Defects, Congenital - physiopathology ; Mice ; Mice, Inbred C57BL ; Microscopy, Electron ; Muscle Cells - drug effects ; Muscle Cells - metabolism ; Muscle Cells - ultrastructure ; Myocardium - metabolism ; Myocardium - ultrastructure ; myofibrillogenesis ; Myofibrils - drug effects ; Myofibrils - metabolism ; Myofibrils - ultrastructure ; Platelet-Derived Growth Factor - metabolism ; Platelet-Derived Growth Factor - pharmacology ; platelet‐derived growth factor ; Proto-Oncogene Proteins c-sis ; Rats ; Rats, Sprague-Dawley ; Receptor, Platelet-Derived Growth Factor alpha - metabolism ; Receptor, Platelet-Derived Growth Factor beta - metabolism ; Sarcomeres - drug effects ; Sarcomeres - metabolism ; Sarcomeres - ultrastructure</subject><ispartof>The anatomical record. Part A, Discoveries in molecular, cellular, and evolutionary biology, 2003-05, Vol.272A (1), p.424-433</ispartof><rights>Copyright © 2003 Wiley‐Liss, Inc.</rights><rights>Copyright 2003 Wiley-Liss, Inc.</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3594-bc6314c17d3b9d942e44da73e7614d3f7a492d5b74cf106ffb84ea6dd16cb4703</citedby><cites>FETCH-LOGICAL-c3594-bc6314c17d3b9d942e44da73e7614d3f7a492d5b74cf106ffb84ea6dd16cb4703</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Far.a.10054$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Far.a.10054$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,1428,27905,27906,45555,45556,46390,46814</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12704700$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Price, Robert L.</creatorcontrib><creatorcontrib>Haley, Stephen T.</creatorcontrib><creatorcontrib>Bullard, Tara A.</creatorcontrib><creatorcontrib>Goldsmith, Edie C.</creatorcontrib><creatorcontrib>Simpson, David G.</creatorcontrib><creatorcontrib>Thielen, Thomas E.</creatorcontrib><creatorcontrib>Yost, Michael J.</creatorcontrib><creatorcontrib>Terracio, Louis</creatorcontrib><title>Effects of platelet‐derived growth factor‐AA and ‐BB on embryonic cardiac development</title><title>The anatomical record. Part A, Discoveries in molecular, cellular, and evolutionary biology</title><addtitle>Anat Rec A Discov Mol Cell Evol Biol</addtitle><description>Several studies have shown that disruption of the normal expression patterns of platelet‐derived growth factor (PDGF) ligands and receptors during development results in gross cardiac defects and embryonic or neonatal death. However, little is known about the specific role that PDGF plays in the differentiation of cardiac myocytes. In experiments complementing studies that utilized naturally‐occurring Patch mice lacking the PDGFr α, or knockout animals lacking a PDGF ligand or receptor, we used rat and mouse whole‐embryo culture (WEC) techniques to increase the exposure of embryos to the PDGF‐AA or ‐BB ligands. Following a 48‐hr culture period, we analyzed heart growth and cardiac myocyte differentiation. Exposure of rat embryos to 50 ng/ml of PDGF‐AA resulted in a 42% increase in total protein levels in the heart, but did not result in a significant increase in heart growth, as determined by measurements of the atrioventricular length and the left ventricular length and width. Exposure of embryos to 50 ng/ml of PDGF‐BB resulted in a 77% increase in total protein levels and a significant (P < 0.05) 8–15% increase in the measured heart parameters. Although a comparison of control and PDGF‐AA‐treated embryos showed no increase in the overall size of the heart, confocal microscopy showed an increase in the size and number of myofibrillar bundles in the developing myocardium. In addition, transmission electron microscopy (TEM) revealed an increase in the presence of sarcomeres, indicating that myofibrils were more highly differentiated in these areas of the treated embryos. In PDGF‐BB‐treated embryos, the compact zone of the myocardium was thicker and, as shown by confocal microscopy and TEM, f‐actin and well‐developed sarcomeres were more prevalent, indicating that the myofibrils were more differentiated in the treated embryos than in the control embryos. These studies indicate that increased exposure of embryonic hearts to PDGF‐AA or ‐BB increases the rate of myocardial development. Anat Rec Part A 272A:424–433, 2003. © 2003 Wiley‐Liss, Inc.</description><subject>Animals</subject><subject>cardiac development</subject><subject>Cell Differentiation - drug effects</subject><subject>Cell Differentiation - physiology</subject><subject>confocal microscopy</subject><subject>electron microscopy</subject><subject>Female</subject><subject>Heart - drug effects</subject><subject>Heart - embryology</subject><subject>Heart Defects, Congenital - chemically induced</subject><subject>Heart Defects, Congenital - metabolism</subject><subject>Heart Defects, Congenital - physiopathology</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Microscopy, Electron</subject><subject>Muscle Cells - drug effects</subject><subject>Muscle Cells - metabolism</subject><subject>Muscle Cells - ultrastructure</subject><subject>Myocardium - metabolism</subject><subject>Myocardium - ultrastructure</subject><subject>myofibrillogenesis</subject><subject>Myofibrils - drug effects</subject><subject>Myofibrils - metabolism</subject><subject>Myofibrils - ultrastructure</subject><subject>Platelet-Derived Growth Factor - metabolism</subject><subject>Platelet-Derived Growth Factor - pharmacology</subject><subject>platelet‐derived growth factor</subject><subject>Proto-Oncogene Proteins c-sis</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptor, Platelet-Derived Growth Factor alpha - metabolism</subject><subject>Receptor, Platelet-Derived Growth Factor beta - metabolism</subject><subject>Sarcomeres - drug effects</subject><subject>Sarcomeres - metabolism</subject><subject>Sarcomeres - ultrastructure</subject><issn>1552-4884</issn><issn>1552-4892</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtKw0AUhgdRbL1sfACZtZB2JplkmmVa6gUKgujKxTCXMxpJMmESW7rzEXxGn8SpKbpzdT4OHz_8P0IXlEwoIfFU-oncUcoO0JimaRyxWR4f_vKMjdBJ170FNyOMH6MRjXkAQsboeWkt6L7DzuK2kj1U0H99fBrw5RoMfvFu079iK3XvfPgXBZaNwYHmc-waDLXyW9eUGmvpTSk1NrCGyrU1NP0ZOrKy6uB8f0_R0_XycXEbre5v7hbFKtJJmrNI6SyhTFNuEpWbnMXAmJE8AZ5RZhLLJctjkyrOtKUks1bNGMjMGJppFVokp-hqyNXedZ0HK1pf1tJvBSVit5CQXkjxs1CQLwe5fVc1mD91P0kQpoOwKSvY_hMlioch8huKqXMt</recordid><startdate>200305</startdate><enddate>200305</enddate><creator>Price, Robert L.</creator><creator>Haley, Stephen T.</creator><creator>Bullard, Tara A.</creator><creator>Goldsmith, Edie C.</creator><creator>Simpson, David G.</creator><creator>Thielen, Thomas E.</creator><creator>Yost, Michael J.</creator><creator>Terracio, Louis</creator><general>Wiley Subscription Services, Inc., A Wiley Company</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></search><sort><creationdate>200305</creationdate><title>Effects of platelet‐derived growth factor‐AA and ‐BB on embryonic cardiac development</title><author>Price, Robert L. ; Haley, Stephen T. ; Bullard, Tara A. ; Goldsmith, Edie C. ; Simpson, David G. ; Thielen, Thomas E. ; Yost, Michael J. ; Terracio, Louis</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3594-bc6314c17d3b9d942e44da73e7614d3f7a492d5b74cf106ffb84ea6dd16cb4703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Animals</topic><topic>cardiac development</topic><topic>Cell Differentiation - drug effects</topic><topic>Cell Differentiation - physiology</topic><topic>confocal microscopy</topic><topic>electron microscopy</topic><topic>Female</topic><topic>Heart - drug effects</topic><topic>Heart - embryology</topic><topic>Heart Defects, Congenital - chemically induced</topic><topic>Heart Defects, Congenital - metabolism</topic><topic>Heart Defects, Congenital - physiopathology</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Microscopy, Electron</topic><topic>Muscle Cells - drug effects</topic><topic>Muscle Cells - metabolism</topic><topic>Muscle Cells - ultrastructure</topic><topic>Myocardium - metabolism</topic><topic>Myocardium - ultrastructure</topic><topic>myofibrillogenesis</topic><topic>Myofibrils - drug effects</topic><topic>Myofibrils - metabolism</topic><topic>Myofibrils - ultrastructure</topic><topic>Platelet-Derived Growth Factor - metabolism</topic><topic>Platelet-Derived Growth Factor - pharmacology</topic><topic>platelet‐derived growth factor</topic><topic>Proto-Oncogene Proteins c-sis</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptor, Platelet-Derived Growth Factor alpha - metabolism</topic><topic>Receptor, Platelet-Derived Growth Factor beta - metabolism</topic><topic>Sarcomeres - drug effects</topic><topic>Sarcomeres - metabolism</topic><topic>Sarcomeres - ultrastructure</topic><toplevel>online_resources</toplevel><creatorcontrib>Price, Robert L.</creatorcontrib><creatorcontrib>Haley, Stephen T.</creatorcontrib><creatorcontrib>Bullard, Tara A.</creatorcontrib><creatorcontrib>Goldsmith, Edie C.</creatorcontrib><creatorcontrib>Simpson, David G.</creatorcontrib><creatorcontrib>Thielen, Thomas E.</creatorcontrib><creatorcontrib>Yost, Michael J.</creatorcontrib><creatorcontrib>Terracio, Louis</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>The anatomical record. Part A, Discoveries in molecular, cellular, and evolutionary biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Price, Robert L.</au><au>Haley, Stephen T.</au><au>Bullard, Tara A.</au><au>Goldsmith, Edie C.</au><au>Simpson, David G.</au><au>Thielen, Thomas E.</au><au>Yost, Michael J.</au><au>Terracio, Louis</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of platelet‐derived growth factor‐AA and ‐BB on embryonic cardiac development</atitle><jtitle>The anatomical record. Part A, Discoveries in molecular, cellular, and evolutionary biology</jtitle><addtitle>Anat Rec A Discov Mol Cell Evol Biol</addtitle><date>2003-05</date><risdate>2003</risdate><volume>272A</volume><issue>1</issue><spage>424</spage><epage>433</epage><pages>424-433</pages><issn>1552-4884</issn><eissn>1552-4892</eissn><abstract>Several studies have shown that disruption of the normal expression patterns of platelet‐derived growth factor (PDGF) ligands and receptors during development results in gross cardiac defects and embryonic or neonatal death. However, little is known about the specific role that PDGF plays in the differentiation of cardiac myocytes. In experiments complementing studies that utilized naturally‐occurring Patch mice lacking the PDGFr α, or knockout animals lacking a PDGF ligand or receptor, we used rat and mouse whole‐embryo culture (WEC) techniques to increase the exposure of embryos to the PDGF‐AA or ‐BB ligands. Following a 48‐hr culture period, we analyzed heart growth and cardiac myocyte differentiation. Exposure of rat embryos to 50 ng/ml of PDGF‐AA resulted in a 42% increase in total protein levels in the heart, but did not result in a significant increase in heart growth, as determined by measurements of the atrioventricular length and the left ventricular length and width. Exposure of embryos to 50 ng/ml of PDGF‐BB resulted in a 77% increase in total protein levels and a significant (P < 0.05) 8–15% increase in the measured heart parameters. Although a comparison of control and PDGF‐AA‐treated embryos showed no increase in the overall size of the heart, confocal microscopy showed an increase in the size and number of myofibrillar bundles in the developing myocardium. In addition, transmission electron microscopy (TEM) revealed an increase in the presence of sarcomeres, indicating that myofibrils were more highly differentiated in these areas of the treated embryos. In PDGF‐BB‐treated embryos, the compact zone of the myocardium was thicker and, as shown by confocal microscopy and TEM, f‐actin and well‐developed sarcomeres were more prevalent, indicating that the myofibrils were more differentiated in the treated embryos than in the control embryos. These studies indicate that increased exposure of embryonic hearts to PDGF‐AA or ‐BB increases the rate of myocardial development. Anat Rec Part A 272A:424–433, 2003. © 2003 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>12704700</pmid><doi>10.1002/ar.a.10054</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals cardiac development Cell Differentiation - drug effects Cell Differentiation - physiology confocal microscopy electron microscopy Female Heart - drug effects Heart - embryology Heart Defects, Congenital - chemically induced Heart Defects, Congenital - metabolism Heart Defects, Congenital - physiopathology Mice Mice, Inbred C57BL Microscopy, Electron Muscle Cells - drug effects Muscle Cells - metabolism Muscle Cells - ultrastructure Myocardium - metabolism Myocardium - ultrastructure myofibrillogenesis Myofibrils - drug effects Myofibrils - metabolism Myofibrils - ultrastructure Platelet-Derived Growth Factor - metabolism Platelet-Derived Growth Factor - pharmacology platelet‐derived growth factor Proto-Oncogene Proteins c-sis Rats Rats, Sprague-Dawley Receptor, Platelet-Derived Growth Factor alpha - metabolism Receptor, Platelet-Derived Growth Factor beta - metabolism Sarcomeres - drug effects Sarcomeres - metabolism Sarcomeres - ultrastructure |
title | Effects of platelet‐derived growth factor‐AA and ‐BB on embryonic cardiac development |
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