The pesticide methoxychlor decreases myotube formation in cell culture by slowing myoblast proliferation
We studied the effect of the estrogenic pesticide methoxychlor (MXC) on skeletal muscle development using C2C12 cell culture. Myoblast cultures were exposed to various concentrations of MXC at various times during the process of myoblast fusion into myotubes. We observed that MXC exposure decreased...
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Veröffentlicht in: | Toxicology in vitro 2007-08, Vol.21 (5), p.770-781 |
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description | We studied the effect of the estrogenic pesticide methoxychlor (MXC) on skeletal muscle development using C2C12 cell culture. Myoblast cultures were exposed to various concentrations of MXC at various times during the process of myoblast fusion into myotubes. We observed that MXC exposure decreased myotube formation. In addition, we observed myoblasts with cytoplasmic vacuoles in cultures exposed to MXC. Because cytoplasmic vacuoles can be characteristic of cell death, apoptosis assays and trypan blue exclusion assays were performed. We found no difference in the frequency of apoptosis or in the frequency of cell death for cultures exposed to MXC and untreated cultures. Collectively, these results indicate that MXC exposure decreases myotube formation without causing cell death. In contrast, when cell proliferation was assessed, untreated cultures had a myoblast proliferation rate 50% greater than cultures exposed to MXC. We conclude that MXC decreases myotube formation at least in part by slowing myoblast proliferation. Furthermore, we suggest that direct exposure to MXC could affect skeletal muscle development in animals or humans, in addition to the defects in reproductive development that have previously been reported. |
doi_str_mv | 10.1016/j.tiv.2007.01.007 |
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Myoblast cultures were exposed to various concentrations of MXC at various times during the process of myoblast fusion into myotubes. We observed that MXC exposure decreased myotube formation. In addition, we observed myoblasts with cytoplasmic vacuoles in cultures exposed to MXC. Because cytoplasmic vacuoles can be characteristic of cell death, apoptosis assays and trypan blue exclusion assays were performed. We found no difference in the frequency of apoptosis or in the frequency of cell death for cultures exposed to MXC and untreated cultures. Collectively, these results indicate that MXC exposure decreases myotube formation without causing cell death. In contrast, when cell proliferation was assessed, untreated cultures had a myoblast proliferation rate 50% greater than cultures exposed to MXC. We conclude that MXC decreases myotube formation at least in part by slowing myoblast proliferation. Furthermore, we suggest that direct exposure to MXC could affect skeletal muscle development in animals or humans, in addition to the defects in reproductive development that have previously been reported.</description><identifier>ISSN: 0887-2333</identifier><identifier>EISSN: 1879-3177</identifier><identifier>DOI: 10.1016/j.tiv.2007.01.007</identifier><identifier>PMID: 17314029</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Agrin - pharmacology ; Animals ; Apoptosis - drug effects ; C2C12 muscle cells ; Cell Line ; Cell proliferation ; Cell Proliferation - drug effects ; Cell Survival - drug effects ; Cells, Cultured ; Depression, Chemical ; Insecticides - toxicity ; Methoxychlor ; Methoxychlor - toxicity ; Mice ; Muscle Fibers, Skeletal - drug effects ; Muscle Fibers, Skeletal - ultrastructure ; Myoblasts ; Myoblasts - drug effects ; Myoblasts - ultrastructure ; Myotubes ; Receptors, Cholinergic - drug effects ; Receptors, Cholinergic - metabolism ; Trypan Blue</subject><ispartof>Toxicology in vitro, 2007-08, Vol.21 (5), p.770-781</ispartof><rights>2007 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c382t-c4338ab50e573d9c5b84847ba3a8314b663d5bf8ae510f1fa4e45f0b2952bb183</citedby><cites>FETCH-LOGICAL-c382t-c4338ab50e573d9c5b84847ba3a8314b663d5bf8ae510f1fa4e45f0b2952bb183</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.tiv.2007.01.007$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17314029$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Steffens, Bradley W.</creatorcontrib><creatorcontrib>Batia, Lyn M.</creatorcontrib><creatorcontrib>Baarson, Chad J.</creatorcontrib><creatorcontrib>Choi, Chang-Kun Charles</creatorcontrib><creatorcontrib>Grow, Wade A.</creatorcontrib><title>The pesticide methoxychlor decreases myotube formation in cell culture by slowing myoblast proliferation</title><title>Toxicology in vitro</title><addtitle>Toxicol In Vitro</addtitle><description>We studied the effect of the estrogenic pesticide methoxychlor (MXC) on skeletal muscle development using C2C12 cell culture. Myoblast cultures were exposed to various concentrations of MXC at various times during the process of myoblast fusion into myotubes. We observed that MXC exposure decreased myotube formation. In addition, we observed myoblasts with cytoplasmic vacuoles in cultures exposed to MXC. Because cytoplasmic vacuoles can be characteristic of cell death, apoptosis assays and trypan blue exclusion assays were performed. We found no difference in the frequency of apoptosis or in the frequency of cell death for cultures exposed to MXC and untreated cultures. Collectively, these results indicate that MXC exposure decreases myotube formation without causing cell death. In contrast, when cell proliferation was assessed, untreated cultures had a myoblast proliferation rate 50% greater than cultures exposed to MXC. We conclude that MXC decreases myotube formation at least in part by slowing myoblast proliferation. Furthermore, we suggest that direct exposure to MXC could affect skeletal muscle development in animals or humans, in addition to the defects in reproductive development that have previously been reported.</description><subject>Agrin - pharmacology</subject><subject>Animals</subject><subject>Apoptosis - drug effects</subject><subject>C2C12 muscle cells</subject><subject>Cell Line</subject><subject>Cell proliferation</subject><subject>Cell Proliferation - drug effects</subject><subject>Cell Survival - drug effects</subject><subject>Cells, Cultured</subject><subject>Depression, Chemical</subject><subject>Insecticides - toxicity</subject><subject>Methoxychlor</subject><subject>Methoxychlor - toxicity</subject><subject>Mice</subject><subject>Muscle Fibers, Skeletal - drug effects</subject><subject>Muscle Fibers, Skeletal - ultrastructure</subject><subject>Myoblasts</subject><subject>Myoblasts - drug effects</subject><subject>Myoblasts - ultrastructure</subject><subject>Myotubes</subject><subject>Receptors, Cholinergic - drug effects</subject><subject>Receptors, Cholinergic - metabolism</subject><subject>Trypan Blue</subject><issn>0887-2333</issn><issn>1879-3177</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kDFP5DAUhC0Egj3gB9AgV3TJPcfJ2hHVCR3cSUg0UFu288J6lcSL7XDsvz8vuxId1TTfzJs3hFwxKBmw5c91mdx7WQGIEliZ5YgsmBRtwZkQx2QBUoqi4pyfkR8xrgGgkRWckjMmOKuhahdk9bxCusGYnHUd0hHTyn9s7WrwgXZoA-qIkY5bn2aDtPdh1Mn5ibqJWhwGauchzQGp2dI4-H9uet3BZtAx0U3wg-sxfDouyEmvh4iXBz0nL_e_n-_-FI9PD3_vfj0WlssqFbbmXGrTADaCd61tjKxlLYzmWubOZrnkXWN6qbFh0LNe11g3PZiqbSpjmOTn5Gafm6-_zfkxNbq4q6on9HNUea22ZUvIINuDNvgYA_ZqE9yow1YxULt51VrleXcGoYCpLNlzfQifzYjdl-OwZwZu9wDmF98dBhWtw8li5wLapDrvvon_D5lHjYQ</recordid><startdate>20070801</startdate><enddate>20070801</enddate><creator>Steffens, Bradley W.</creator><creator>Batia, Lyn M.</creator><creator>Baarson, Chad J.</creator><creator>Choi, Chang-Kun Charles</creator><creator>Grow, Wade A.</creator><general>Elsevier Ltd</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>7QO</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20070801</creationdate><title>The pesticide methoxychlor decreases myotube formation in cell culture by slowing myoblast proliferation</title><author>Steffens, Bradley W. ; Batia, Lyn M. ; Baarson, Chad J. ; Choi, Chang-Kun Charles ; Grow, Wade A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c382t-c4338ab50e573d9c5b84847ba3a8314b663d5bf8ae510f1fa4e45f0b2952bb183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Agrin - pharmacology</topic><topic>Animals</topic><topic>Apoptosis - drug effects</topic><topic>C2C12 muscle cells</topic><topic>Cell Line</topic><topic>Cell proliferation</topic><topic>Cell Proliferation - drug effects</topic><topic>Cell Survival - drug effects</topic><topic>Cells, Cultured</topic><topic>Depression, Chemical</topic><topic>Insecticides - toxicity</topic><topic>Methoxychlor</topic><topic>Methoxychlor - toxicity</topic><topic>Mice</topic><topic>Muscle Fibers, Skeletal - drug effects</topic><topic>Muscle Fibers, Skeletal - ultrastructure</topic><topic>Myoblasts</topic><topic>Myoblasts - drug effects</topic><topic>Myoblasts - ultrastructure</topic><topic>Myotubes</topic><topic>Receptors, Cholinergic - drug effects</topic><topic>Receptors, Cholinergic - metabolism</topic><topic>Trypan Blue</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Steffens, Bradley W.</creatorcontrib><creatorcontrib>Batia, Lyn M.</creatorcontrib><creatorcontrib>Baarson, Chad J.</creatorcontrib><creatorcontrib>Choi, Chang-Kun Charles</creatorcontrib><creatorcontrib>Grow, Wade A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Toxicology in vitro</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Steffens, Bradley W.</au><au>Batia, Lyn M.</au><au>Baarson, Chad J.</au><au>Choi, Chang-Kun Charles</au><au>Grow, Wade A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The pesticide methoxychlor decreases myotube formation in cell culture by slowing myoblast proliferation</atitle><jtitle>Toxicology in vitro</jtitle><addtitle>Toxicol In Vitro</addtitle><date>2007-08-01</date><risdate>2007</risdate><volume>21</volume><issue>5</issue><spage>770</spage><epage>781</epage><pages>770-781</pages><issn>0887-2333</issn><eissn>1879-3177</eissn><abstract>We studied the effect of the estrogenic pesticide methoxychlor (MXC) on skeletal muscle development using C2C12 cell culture. Myoblast cultures were exposed to various concentrations of MXC at various times during the process of myoblast fusion into myotubes. We observed that MXC exposure decreased myotube formation. In addition, we observed myoblasts with cytoplasmic vacuoles in cultures exposed to MXC. Because cytoplasmic vacuoles can be characteristic of cell death, apoptosis assays and trypan blue exclusion assays were performed. We found no difference in the frequency of apoptosis or in the frequency of cell death for cultures exposed to MXC and untreated cultures. Collectively, these results indicate that MXC exposure decreases myotube formation without causing cell death. In contrast, when cell proliferation was assessed, untreated cultures had a myoblast proliferation rate 50% greater than cultures exposed to MXC. We conclude that MXC decreases myotube formation at least in part by slowing myoblast proliferation. Furthermore, we suggest that direct exposure to MXC could affect skeletal muscle development in animals or humans, in addition to the defects in reproductive development that have previously been reported.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>17314029</pmid><doi>10.1016/j.tiv.2007.01.007</doi><tpages>12</tpages></addata></record> |
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subjects | Agrin - pharmacology Animals Apoptosis - drug effects C2C12 muscle cells Cell Line Cell proliferation Cell Proliferation - drug effects Cell Survival - drug effects Cells, Cultured Depression, Chemical Insecticides - toxicity Methoxychlor Methoxychlor - toxicity Mice Muscle Fibers, Skeletal - drug effects Muscle Fibers, Skeletal - ultrastructure Myoblasts Myoblasts - drug effects Myoblasts - ultrastructure Myotubes Receptors, Cholinergic - drug effects Receptors, Cholinergic - metabolism Trypan Blue |
title | The pesticide methoxychlor decreases myotube formation in cell culture by slowing myoblast proliferation |
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