Regulation of Muscle Growth by Multiple Ligands Signaling through Activin Type II Receptors
Myostatin is a secreted protein that normally functions as a negative regulator of muscle growth. Agents capable of blocking the myostatin signaling pathway could have important applications for treating human muscle degenerative diseases as well as for enhancing livestock production. Here we descri...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 2005-12, Vol.102 (50), p.18117-18122 |
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creator | Lee, Se-Jin Lori A. Reed Davies, Monique V. Stefan Girgenrath Mary E. P. Goad Tomkinson, Kathy N. Wright, Jill F. Christopher Barker Gregory Ehrmantraut James Holmstrom Betty Trowell Barry Gertz Jiang, Man-Shiow Sebald, Suzanne M. Matzuk, Martin Li, En Li-fang Liang Edwin Quattlebaum Ronald L. Stotish Wolfman, Neil M. |
description | Myostatin is a secreted protein that normally functions as a negative regulator of muscle growth. Agents capable of blocking the myostatin signaling pathway could have important applications for treating human muscle degenerative diseases as well as for enhancing livestock production. Here we describe a potent myostatin inhibitor, a soluble form of the activin type MB receptor (ACVR2B), which can cause dramatic increases in muscle mass (up to 60% in 2 weeks) when injected into wild-type mice. Furthermore, we show that the effect of the soluble receptor is attenuated but not eliminated in Mstn-/-mice, suggesting that at least one other ligand in addition to myostatin normally functions to limit muscle growth. Finally, we provide genetic evidence that these ligands signal through both activin type II receptors, ACVR2 and ACVR2B, to regulate muscle growth in vivo. |
doi_str_mv | 10.1073/pnas.0505996102 |
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Reed ; Davies, Monique V. ; Stefan Girgenrath ; Mary E. P. Goad ; Tomkinson, Kathy N. ; Wright, Jill F. ; Christopher Barker ; Gregory Ehrmantraut ; James Holmstrom ; Betty Trowell ; Barry Gertz ; Jiang, Man-Shiow ; Sebald, Suzanne M. ; Matzuk, Martin ; Li, En ; Li-fang Liang ; Edwin Quattlebaum ; Ronald L. Stotish ; Wolfman, Neil M.</creator><creatorcontrib>Lee, Se-Jin ; Lori A. Reed ; Davies, Monique V. ; Stefan Girgenrath ; Mary E. P. Goad ; Tomkinson, Kathy N. ; Wright, Jill F. ; Christopher Barker ; Gregory Ehrmantraut ; James Holmstrom ; Betty Trowell ; Barry Gertz ; Jiang, Man-Shiow ; Sebald, Suzanne M. ; Matzuk, Martin ; Li, En ; Li-fang Liang ; Edwin Quattlebaum ; Ronald L. Stotish ; Wolfman, Neil M.</creatorcontrib><description>Myostatin is a secreted protein that normally functions as a negative regulator of muscle growth. Agents capable of blocking the myostatin signaling pathway could have important applications for treating human muscle degenerative diseases as well as for enhancing livestock production. Here we describe a potent myostatin inhibitor, a soluble form of the activin type MB receptor (ACVR2B), which can cause dramatic increases in muscle mass (up to 60% in 2 weeks) when injected into wild-type mice. Furthermore, we show that the effect of the soluble receptor is attenuated but not eliminated in Mstn-/-mice, suggesting that at least one other ligand in addition to myostatin normally functions to limit muscle growth. Finally, we provide genetic evidence that these ligands signal through both activin type II receptors, ACVR2 and ACVR2B, to regulate muscle growth in vivo.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.0505996102</identifier><identifier>PMID: 16330774</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Activin Receptors, Type II - genetics ; Activin Receptors, Type II - metabolism ; Activin Receptors, Type II - pharmacology ; Animals ; Biological Sciences ; Disease models ; Gene expression regulation ; Hypertrophy ; Ligands ; Livestock ; Medical research ; Mice ; Mice, Knockout ; Muscle fibers ; Muscle, Skeletal - drug effects ; Muscle, Skeletal - growth & development ; Muscles ; Muscular system ; Myostatin ; Organ Size ; P values ; Proteins ; Receptors ; Signal transduction ; Signal Transduction - physiology ; Statistical significance ; Transforming Growth Factor beta - antagonists & inhibitors</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2005-12, Vol.102 (50), p.18117-18122</ispartof><rights>Copyright 2005 National Academy of Sciences of the United States of America</rights><rights>Copyright National Academy of Sciences Dec 13, 2005</rights><rights>Copyright © 2005, The National Academy of Sciences 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c595t-aef945da3de17f4c996b9c0bbea790957d20507611dc13976b67e4b082f62a403</citedby><cites>FETCH-LOGICAL-c595t-aef945da3de17f4c996b9c0bbea790957d20507611dc13976b67e4b082f62a403</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/102/50.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/4152737$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/4152737$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,723,776,780,799,881,27901,27902,53766,53768,57992,58225</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16330774$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Se-Jin</creatorcontrib><creatorcontrib>Lori A. Reed</creatorcontrib><creatorcontrib>Davies, Monique V.</creatorcontrib><creatorcontrib>Stefan Girgenrath</creatorcontrib><creatorcontrib>Mary E. P. Goad</creatorcontrib><creatorcontrib>Tomkinson, Kathy N.</creatorcontrib><creatorcontrib>Wright, Jill F.</creatorcontrib><creatorcontrib>Christopher Barker</creatorcontrib><creatorcontrib>Gregory Ehrmantraut</creatorcontrib><creatorcontrib>James Holmstrom</creatorcontrib><creatorcontrib>Betty Trowell</creatorcontrib><creatorcontrib>Barry Gertz</creatorcontrib><creatorcontrib>Jiang, Man-Shiow</creatorcontrib><creatorcontrib>Sebald, Suzanne M.</creatorcontrib><creatorcontrib>Matzuk, Martin</creatorcontrib><creatorcontrib>Li, En</creatorcontrib><creatorcontrib>Li-fang Liang</creatorcontrib><creatorcontrib>Edwin Quattlebaum</creatorcontrib><creatorcontrib>Ronald L. Stotish</creatorcontrib><creatorcontrib>Wolfman, Neil M.</creatorcontrib><title>Regulation of Muscle Growth by Multiple Ligands Signaling through Activin Type II Receptors</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Myostatin is a secreted protein that normally functions as a negative regulator of muscle growth. Agents capable of blocking the myostatin signaling pathway could have important applications for treating human muscle degenerative diseases as well as for enhancing livestock production. Here we describe a potent myostatin inhibitor, a soluble form of the activin type MB receptor (ACVR2B), which can cause dramatic increases in muscle mass (up to 60% in 2 weeks) when injected into wild-type mice. Furthermore, we show that the effect of the soluble receptor is attenuated but not eliminated in Mstn-/-mice, suggesting that at least one other ligand in addition to myostatin normally functions to limit muscle growth. Finally, we provide genetic evidence that these ligands signal through both activin type II receptors, ACVR2 and ACVR2B, to regulate muscle growth in vivo.</description><subject>Activin Receptors, Type II - genetics</subject><subject>Activin Receptors, Type II - metabolism</subject><subject>Activin Receptors, Type II - pharmacology</subject><subject>Animals</subject><subject>Biological Sciences</subject><subject>Disease models</subject><subject>Gene expression regulation</subject><subject>Hypertrophy</subject><subject>Ligands</subject><subject>Livestock</subject><subject>Medical research</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Muscle fibers</subject><subject>Muscle, Skeletal - drug effects</subject><subject>Muscle, Skeletal - growth & development</subject><subject>Muscles</subject><subject>Muscular system</subject><subject>Myostatin</subject><subject>Organ Size</subject><subject>P values</subject><subject>Proteins</subject><subject>Receptors</subject><subject>Signal transduction</subject><subject>Signal Transduction - physiology</subject><subject>Statistical significance</subject><subject>Transforming Growth Factor beta - antagonists & inhibitors</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc-LEzEUx4Mobq2evYgED4KH7ubXJJOLsCy6FirCup48hEwmM01JJ7NJZrX_vSktW_Wyp8DL5314730BeI3ROUaCXoyDTueoQpWUHCPyBMwwknjBmURPwQwhIhY1I-wMvEhpgxCSVY2egzPMKUVCsBn4eWP7yevswgBDB79OyXgLr2P4ldew2ZWCz24spZXr9dAm-N31g_Zu6GFexzD1a3hpsrt3A7zdjRYul_DGGjvmENNL8KzTPtlXx3cOfnz-dHv1ZbH6dr28ulwtTCWrvNC2k6xqNW0tFh0zZZVGGtQ0VgtZJhYtKRsKjnFrMJWCN1xY1qCadJxohugcfDx4x6nZ2tbYIUft1RjdVsedCtqpf38Gt1Z9uFeYIi4kLYL3R0EMd5NNWW1dMtZ7PdgwJcXrWvIak0dBLFhR0j347j9wE6ZYDpcUQZjUvCrYHFwcIBNDStF2DyNjpPbxqn286hRv6Xj796Yn_phnAeAR2HeedERVRVljLAry4RFEdZP32f7OhX1zYDepBPoAM1wRQQX9AyJBwwg</recordid><startdate>20051213</startdate><enddate>20051213</enddate><creator>Lee, Se-Jin</creator><creator>Lori A. Reed</creator><creator>Davies, Monique V.</creator><creator>Stefan Girgenrath</creator><creator>Mary E. P. Goad</creator><creator>Tomkinson, Kathy N.</creator><creator>Wright, Jill F.</creator><creator>Christopher Barker</creator><creator>Gregory Ehrmantraut</creator><creator>James Holmstrom</creator><creator>Betty Trowell</creator><creator>Barry Gertz</creator><creator>Jiang, Man-Shiow</creator><creator>Sebald, Suzanne M.</creator><creator>Matzuk, Martin</creator><creator>Li, En</creator><creator>Li-fang Liang</creator><creator>Edwin Quattlebaum</creator><creator>Ronald L. Stotish</creator><creator>Wolfman, Neil M.</creator><general>National Academy of Sciences</general><general>National Acad Sciences</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>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20051213</creationdate><title>Regulation of Muscle Growth by Multiple Ligands Signaling through Activin Type II Receptors</title><author>Lee, Se-Jin ; Lori A. Reed ; Davies, Monique V. ; Stefan Girgenrath ; Mary E. P. Goad ; Tomkinson, Kathy N. ; Wright, Jill F. ; Christopher Barker ; Gregory Ehrmantraut ; James Holmstrom ; Betty Trowell ; Barry Gertz ; Jiang, Man-Shiow ; Sebald, Suzanne M. ; Matzuk, Martin ; Li, En ; Li-fang Liang ; Edwin Quattlebaum ; Ronald L. 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Reed</au><au>Davies, Monique V.</au><au>Stefan Girgenrath</au><au>Mary E. P. Goad</au><au>Tomkinson, Kathy N.</au><au>Wright, Jill F.</au><au>Christopher Barker</au><au>Gregory Ehrmantraut</au><au>James Holmstrom</au><au>Betty Trowell</au><au>Barry Gertz</au><au>Jiang, Man-Shiow</au><au>Sebald, Suzanne M.</au><au>Matzuk, Martin</au><au>Li, En</au><au>Li-fang Liang</au><au>Edwin Quattlebaum</au><au>Ronald L. 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Here we describe a potent myostatin inhibitor, a soluble form of the activin type MB receptor (ACVR2B), which can cause dramatic increases in muscle mass (up to 60% in 2 weeks) when injected into wild-type mice. Furthermore, we show that the effect of the soluble receptor is attenuated but not eliminated in Mstn-/-mice, suggesting that at least one other ligand in addition to myostatin normally functions to limit muscle growth. Finally, we provide genetic evidence that these ligands signal through both activin type II receptors, ACVR2 and ACVR2B, to regulate muscle growth in vivo.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>16330774</pmid><doi>10.1073/pnas.0505996102</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Activin Receptors, Type II - genetics Activin Receptors, Type II - metabolism Activin Receptors, Type II - pharmacology Animals Biological Sciences Disease models Gene expression regulation Hypertrophy Ligands Livestock Medical research Mice Mice, Knockout Muscle fibers Muscle, Skeletal - drug effects Muscle, Skeletal - growth & development Muscles Muscular system Myostatin Organ Size P values Proteins Receptors Signal transduction Signal Transduction - physiology Statistical significance Transforming Growth Factor beta - antagonists & inhibitors |
title | Regulation of Muscle Growth by Multiple Ligands Signaling through Activin Type II Receptors |
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