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Reversal of Muscle Differentiation During Urodele Limb Regeneration
Recent studies suggest that maintenance of the differentiated state requires continuous regulation. Limb regeneration in urodele amphibians provides a context in which to address this issue, as limb regeneration may involve the dedifferentiation of multinucleate myotubes to yield mononucleate blaste...
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Published in: | Proceedings of the National Academy of Sciences - PNAS 1993-08, Vol.90 (15), p.7230-7234 |
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creator | Lo, Donald C. Allen, Francesca Brockes, Jeremy P. |
description | Recent studies suggest that maintenance of the differentiated state requires continuous regulation. Limb regeneration in urodele amphibians provides a context in which to address this issue, as limb regeneration may involve the dedifferentiation of multinucleate myotubes to yield mononucleate blastemal cells, which then proliferate and contribute to regenerate tissues. To evaluate this possibility, cultured newt limb myotubes were selectively microinjected with the lineage tracer rhodamine-dextran and introduced into regenerating limbs. In culture, such labeled myotubes were stable after 6-8 weeks, and transfer of the tracer to mononucleate cells was not observed. In contrast, after implantation of labeled myotubes under the wound epidermis of limb blastemas, strongly labeled mononucleate cells were observed after 1 week. These cells could be double-labeled with the cytoplasmic lineage tracer and [3H]thymidine that had been incorporated into the nuclei of implanted myotubes. The number of labeled mononucleate cells increased significantly by 2-3 weeks after implantation, indicating that these cells proliferated. Although the fate of these cells at later times was uncertain, we provide evidence consistent with their subsequent differentiation. These results demonstrate reversal in the mononucleate-to-multinucleate transition of vertebrate myogenesis. |
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Limb regeneration in urodele amphibians provides a context in which to address this issue, as limb regeneration may involve the dedifferentiation of multinucleate myotubes to yield mononucleate blastemal cells, which then proliferate and contribute to regenerate tissues. To evaluate this possibility, cultured newt limb myotubes were selectively microinjected with the lineage tracer rhodamine-dextran and introduced into regenerating limbs. In culture, such labeled myotubes were stable after 6-8 weeks, and transfer of the tracer to mononucleate cells was not observed. In contrast, after implantation of labeled myotubes under the wound epidermis of limb blastemas, strongly labeled mononucleate cells were observed after 1 week. These cells could be double-labeled with the cytoplasmic lineage tracer and [3H]thymidine that had been incorporated into the nuclei of implanted myotubes. The number of labeled mononucleate cells increased significantly by 2-3 weeks after implantation, indicating that these cells proliferated. Although the fate of these cells at later times was uncertain, we provide evidence consistent with their subsequent differentiation. These results demonstrate reversal in the mononucleate-to-multinucleate transition of vertebrate myogenesis.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.90.15.7230</identifier><identifier>PMID: 8346239</identifier><identifier>CODEN: PNASA6</identifier><language>eng</language><publisher>Washington, DC: National Academy of Sciences of the United States of America</publisher><subject>Animal reproduction ; Animals ; Biological and medical sciences ; Cartilage ; Cell culture techniques ; Cell Differentiation ; Cell growth ; Cell lines ; Cell nucleus ; Chondrocytes ; Cultured cells ; Degeneration. Regeneration. Wound healing. Graft ; Epidermal cells ; Extremities - anatomy & histology ; Fundamental and applied biological sciences. Psychology ; Microinjections ; Muscle fibers ; Muscles - cytology ; Muscular system ; Regeneration ; Reptiles & amphibians ; Salamandridae - physiology ; Triturus ; Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1993-08, Vol.90 (15), p.7230-7234</ispartof><rights>Copyright 1993 The National Academy of Sciences of the United States of America</rights><rights>1993 INIST-CNRS</rights><rights>Copyright National Academy of Sciences Aug 1, 1993</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c615t-c5736f3b171ea94221e8a632ca8701ef4f90b40fba6f39647684e709b02661c83</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/90/15.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/2362686$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/2362686$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,724,777,781,882,27905,27906,53772,53774,58219,58452</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4898850$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8346239$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lo, Donald C.</creatorcontrib><creatorcontrib>Allen, Francesca</creatorcontrib><creatorcontrib>Brockes, Jeremy P.</creatorcontrib><title>Reversal of Muscle Differentiation During Urodele Limb Regeneration</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Recent studies suggest that maintenance of the differentiated state requires continuous regulation. Limb regeneration in urodele amphibians provides a context in which to address this issue, as limb regeneration may involve the dedifferentiation of multinucleate myotubes to yield mononucleate blastemal cells, which then proliferate and contribute to regenerate tissues. To evaluate this possibility, cultured newt limb myotubes were selectively microinjected with the lineage tracer rhodamine-dextran and introduced into regenerating limbs. In culture, such labeled myotubes were stable after 6-8 weeks, and transfer of the tracer to mononucleate cells was not observed. In contrast, after implantation of labeled myotubes under the wound epidermis of limb blastemas, strongly labeled mononucleate cells were observed after 1 week. These cells could be double-labeled with the cytoplasmic lineage tracer and [3H]thymidine that had been incorporated into the nuclei of implanted myotubes. The number of labeled mononucleate cells increased significantly by 2-3 weeks after implantation, indicating that these cells proliferated. Although the fate of these cells at later times was uncertain, we provide evidence consistent with their subsequent differentiation. These results demonstrate reversal in the mononucleate-to-multinucleate transition of vertebrate myogenesis.</description><subject>Animal reproduction</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cartilage</subject><subject>Cell culture techniques</subject><subject>Cell Differentiation</subject><subject>Cell growth</subject><subject>Cell lines</subject><subject>Cell nucleus</subject><subject>Chondrocytes</subject><subject>Cultured cells</subject><subject>Degeneration. Regeneration. Wound healing. Graft</subject><subject>Epidermal cells</subject><subject>Extremities - anatomy & histology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Microinjections</subject><subject>Muscle fibers</subject><subject>Muscles - cytology</subject><subject>Muscular system</subject><subject>Regeneration</subject><subject>Reptiles & amphibians</subject><subject>Salamandridae - physiology</subject><subject>Triturus</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><recordid>eNqFkUuLFDEUhYMoY8_o2o1KMYiuqufmUXmAG-nxBS3C4KxDKpO0aaorbVI16L83ZZftY6GrcDnfuY8chB5hWGIQ9GLfm7xUpWiWglC4gxYYFK45U3AXLQCIqCUj7D46zXkLAKqRcIJOJGWcULVAqyt361I2XRV99WHMtnPVZfDeJdcPwQwh9tXlmEK_qa5TvHFFXoddW125jetd-gE8QPe86bJ7OL9n6PrN60-rd_X649v3q1fr2nLcDLVtBOWetlhgZxQjBDtpOCXWSAHYeeYVtAx8awqlOBNcMidAtUA4x1bSM_Ty0Hc_tjt3Y8uGyXR6n8LOpG86mqD_VPrwWW_irWYCYyj257M9xS-jy4PehWxd15nexTFr0UglG4X_C2LOQSmgBTz_C9zGMfXlDzQBTDjGdBp7cYBsijkn548LY9BThnrKUKtSNHrKsDie_H7nkZ9DK_qzWTfZms4n09uQjxgrZ8hmavNixqb-P9Vfc7Qfu25wX4dCPv0nWYDHB2Cbh5iOBKGccMnpd1_yxSw</recordid><startdate>19930801</startdate><enddate>19930801</enddate><creator>Lo, Donald C.</creator><creator>Allen, Francesca</creator><creator>Brockes, Jeremy P.</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</general><general>National Academy of Sciences</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>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>19930801</creationdate><title>Reversal of Muscle Differentiation During Urodele Limb Regeneration</title><author>Lo, Donald C. ; Allen, Francesca ; Brockes, Jeremy P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c615t-c5736f3b171ea94221e8a632ca8701ef4f90b40fba6f39647684e709b02661c83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Animal reproduction</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cartilage</topic><topic>Cell culture techniques</topic><topic>Cell Differentiation</topic><topic>Cell growth</topic><topic>Cell lines</topic><topic>Cell nucleus</topic><topic>Chondrocytes</topic><topic>Cultured cells</topic><topic>Degeneration. Regeneration. Wound healing. Graft</topic><topic>Epidermal cells</topic><topic>Extremities - anatomy & histology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Microinjections</topic><topic>Muscle fibers</topic><topic>Muscles - cytology</topic><topic>Muscular system</topic><topic>Regeneration</topic><topic>Reptiles & amphibians</topic><topic>Salamandridae - physiology</topic><topic>Triturus</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lo, Donald C.</creatorcontrib><creatorcontrib>Allen, Francesca</creatorcontrib><creatorcontrib>Brockes, Jeremy P.</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>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lo, Donald C.</au><au>Allen, Francesca</au><au>Brockes, Jeremy P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reversal of Muscle Differentiation During Urodele Limb Regeneration</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1993-08-01</date><risdate>1993</risdate><volume>90</volume><issue>15</issue><spage>7230</spage><epage>7234</epage><pages>7230-7234</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><coden>PNASA6</coden><abstract>Recent studies suggest that maintenance of the differentiated state requires continuous regulation. Limb regeneration in urodele amphibians provides a context in which to address this issue, as limb regeneration may involve the dedifferentiation of multinucleate myotubes to yield mononucleate blastemal cells, which then proliferate and contribute to regenerate tissues. To evaluate this possibility, cultured newt limb myotubes were selectively microinjected with the lineage tracer rhodamine-dextran and introduced into regenerating limbs. In culture, such labeled myotubes were stable after 6-8 weeks, and transfer of the tracer to mononucleate cells was not observed. In contrast, after implantation of labeled myotubes under the wound epidermis of limb blastemas, strongly labeled mononucleate cells were observed after 1 week. These cells could be double-labeled with the cytoplasmic lineage tracer and [3H]thymidine that had been incorporated into the nuclei of implanted myotubes. The number of labeled mononucleate cells increased significantly by 2-3 weeks after implantation, indicating that these cells proliferated. Although the fate of these cells at later times was uncertain, we provide evidence consistent with their subsequent differentiation. These results demonstrate reversal in the mononucleate-to-multinucleate transition of vertebrate myogenesis.</abstract><cop>Washington, DC</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>8346239</pmid><doi>10.1073/pnas.90.15.7230</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animal reproduction Animals Biological and medical sciences Cartilage Cell culture techniques Cell Differentiation Cell growth Cell lines Cell nucleus Chondrocytes Cultured cells Degeneration. Regeneration. Wound healing. Graft Epidermal cells Extremities - anatomy & histology Fundamental and applied biological sciences. Psychology Microinjections Muscle fibers Muscles - cytology Muscular system Regeneration Reptiles & amphibians Salamandridae - physiology Triturus Vertebrates: anatomy and physiology, studies on body, several organs or systems |
title | Reversal of Muscle Differentiation During Urodele Limb Regeneration |
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