Neural crest-derived cells with stem cell features can be traced back to multiple lineages in the adult skin
Given their accessibility, multipotent skin-derived cells might be useful for future cell replacement therapies. We describe the isolation of multipotent stem cell-like cells from the adult trunk skin of mice and humans that express the neural crest stem cell markers p75 and Sox10 and display extens...
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Veröffentlicht in: | The Journal of cell biology 2006-12, Vol.175 (6), p.1005-1015 |
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creator | Wong, Christine E Paratore, Christian Dours-Zimmermann, María T Rochat, Ariane Pietri, Thomas Suter, Ueli Zimmermann, Dieter R Dufour, Sylvie Thiery, Jean Paul Meijer, Dies Beermann, Friedrich Barrandon, Yann Sommer, Lukas |
description | Given their accessibility, multipotent skin-derived cells might be useful for future cell replacement therapies. We describe the isolation of multipotent stem cell-like cells from the adult trunk skin of mice and humans that express the neural crest stem cell markers p75 and Sox10 and display extensive self-renewal capacity in sphere cultures. To determine the origin of these cells, we genetically mapped the fate of neural crest cells in face and trunk skin of mouse. In whisker follicles of the face, many mesenchymal structures are neural crest derived and appear to contain cells with sphere-forming potential. In the trunk skin, however, sphere-forming neural crest-derived cells are restricted to the glial and melanocyte lineages. Thus, self-renewing cells in the adult skin can be obtained from several neural crest derivatives, and these are of distinct nature in face and trunk skin. These findings are relevant for the design of therapeutic strategies because the potential of stem and progenitor cells in vivo likely depends on their nature and origin. |
doi_str_mv | 10.1083/jcb.200606062 |
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We describe the isolation of multipotent stem cell-like cells from the adult trunk skin of mice and humans that express the neural crest stem cell markers p75 and Sox10 and display extensive self-renewal capacity in sphere cultures. To determine the origin of these cells, we genetically mapped the fate of neural crest cells in face and trunk skin of mouse. In whisker follicles of the face, many mesenchymal structures are neural crest derived and appear to contain cells with sphere-forming potential. In the trunk skin, however, sphere-forming neural crest-derived cells are restricted to the glial and melanocyte lineages. Thus, self-renewing cells in the adult skin can be obtained from several neural crest derivatives, and these are of distinct nature in face and trunk skin. These findings are relevant for the design of therapeutic strategies because the potential of stem and progenitor cells in vivo likely depends on their nature and origin.</description><identifier>ISSN: 0021-9525</identifier><identifier>EISSN: 1540-8140</identifier><identifier>DOI: 10.1083/jcb.200606062</identifier><identifier>PMID: 17158956</identifier><identifier>CODEN: JCLBA3</identifier><language>eng</language><publisher>United States: The Rockefeller University Press</publisher><subject>Adipocytes - cytology ; Adipocytes - metabolism ; Adult ; Adult stem cells ; Animals ; Cell Differentiation ; Cell Lineage ; Cells, Cultured ; Cellular biology ; DNA-Binding Proteins - metabolism ; Face ; Female ; Fluorescent Antibody Technique ; Genomics ; Hair Follicle - cytology ; Hair Follicle - physiology ; High Mobility Group Proteins - metabolism ; Humans ; Male ; Mapping ; Melanocytes ; Melanocytes - cytology ; Melanocytes - physiology ; Mesenchymal stem cells ; Mice ; Mice, Inbred C57BL ; Middle Aged ; Multipotent stem cells ; Multipotent Stem Cells - cytology ; Multipotent Stem Cells - physiology ; Neural crest ; Neural Crest - cytology ; Neural Crest - physiology ; Neural stem cells ; Neuroglia - cytology ; Neuroglia - physiology ; Neurons ; Skin ; Skin - cytology ; SOXE Transcription Factors ; Stem cells ; Transcription Factors - metabolism</subject><ispartof>The Journal of cell biology, 2006-12, Vol.175 (6), p.1005-1015</ispartof><rights>Copyright 2006 The Rockefeller University Press</rights><rights>Copyright Rockefeller University Press Dec 18, 2006</rights><rights>Copyright © 2006, The Rockefeller University Press 2006</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c457t-2b641b7620a3370811d4f85252cede0a048ee89866a7639ff2abebb8452038293</citedby><cites>FETCH-LOGICAL-c457t-2b641b7620a3370811d4f85252cede0a048ee89866a7639ff2abebb8452038293</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27915,27916</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17158956$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wong, Christine E</creatorcontrib><creatorcontrib>Paratore, Christian</creatorcontrib><creatorcontrib>Dours-Zimmermann, María T</creatorcontrib><creatorcontrib>Rochat, Ariane</creatorcontrib><creatorcontrib>Pietri, Thomas</creatorcontrib><creatorcontrib>Suter, Ueli</creatorcontrib><creatorcontrib>Zimmermann, Dieter R</creatorcontrib><creatorcontrib>Dufour, Sylvie</creatorcontrib><creatorcontrib>Thiery, Jean Paul</creatorcontrib><creatorcontrib>Meijer, Dies</creatorcontrib><creatorcontrib>Beermann, Friedrich</creatorcontrib><creatorcontrib>Barrandon, Yann</creatorcontrib><creatorcontrib>Sommer, Lukas</creatorcontrib><title>Neural crest-derived cells with stem cell features can be traced back to multiple lineages in the adult skin</title><title>The Journal of cell biology</title><addtitle>J Cell Biol</addtitle><description>Given their accessibility, multipotent skin-derived cells might be useful for future cell replacement therapies. We describe the isolation of multipotent stem cell-like cells from the adult trunk skin of mice and humans that express the neural crest stem cell markers p75 and Sox10 and display extensive self-renewal capacity in sphere cultures. To determine the origin of these cells, we genetically mapped the fate of neural crest cells in face and trunk skin of mouse. In whisker follicles of the face, many mesenchymal structures are neural crest derived and appear to contain cells with sphere-forming potential. In the trunk skin, however, sphere-forming neural crest-derived cells are restricted to the glial and melanocyte lineages. Thus, self-renewing cells in the adult skin can be obtained from several neural crest derivatives, and these are of distinct nature in face and trunk skin. These findings are relevant for the design of therapeutic strategies because the potential of stem and progenitor cells in vivo likely depends on their nature and origin.</description><subject>Adipocytes - cytology</subject><subject>Adipocytes - metabolism</subject><subject>Adult</subject><subject>Adult stem cells</subject><subject>Animals</subject><subject>Cell Differentiation</subject><subject>Cell Lineage</subject><subject>Cells, Cultured</subject><subject>Cellular biology</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>Face</subject><subject>Female</subject><subject>Fluorescent Antibody Technique</subject><subject>Genomics</subject><subject>Hair Follicle - cytology</subject><subject>Hair Follicle - physiology</subject><subject>High Mobility Group Proteins - metabolism</subject><subject>Humans</subject><subject>Male</subject><subject>Mapping</subject><subject>Melanocytes</subject><subject>Melanocytes - cytology</subject><subject>Melanocytes - physiology</subject><subject>Mesenchymal stem cells</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Middle Aged</subject><subject>Multipotent stem cells</subject><subject>Multipotent Stem Cells - cytology</subject><subject>Multipotent Stem Cells - physiology</subject><subject>Neural crest</subject><subject>Neural Crest - cytology</subject><subject>Neural Crest - physiology</subject><subject>Neural stem cells</subject><subject>Neuroglia - cytology</subject><subject>Neuroglia - physiology</subject><subject>Neurons</subject><subject>Skin</subject><subject>Skin - cytology</subject><subject>SOXE Transcription Factors</subject><subject>Stem cells</subject><subject>Transcription Factors - metabolism</subject><issn>0021-9525</issn><issn>1540-8140</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkUtv1DAUhS1ERYeBJTsEFgt2KdfPOBskVPGoVMECurac5GbG0zwG2ynqv8dhRlNAXljW-XR87j2EvGBwwcCId7umvuAAejn8EVkxJaEwTMJjsgLgrKgUV-fkaYw7AJClFE_IOSuZMpXSK9J_xTm4njYBYypaDP4OW9pg30f6y6ctjQmHP2_aoUtzxmjjRlojTcE1ma1dc0vTRIe5T37fI-39iG6TOT_StEXq2qzQeOvHZ-Ssc33E58d7TW4-ffxx-aW4_vb56vLDddFIVaaC11qyutQcnBAlGMZa2Zk8Bs__ITiQBtFURmtXalF1HXc11rWRioMwvBJr8v7gu5_rAdsGx5y1t_vgBxfu7eS8_VcZ_dZupjvLQcsSFoO3R4Mw_ZzzZuzg47IEN-I0R6sN1wz0Ar75D9xNcxjzcJbnJYOURmWoOEBNmGIM2J2SMLBLiTaXaE8lZv7V3_Ef6GNrGXh5AHYxTeGkS6Y4z3Zr8vogd26ybhN8tDffOTABjHFhKhC_AWGLqrM</recordid><startdate>20061218</startdate><enddate>20061218</enddate><creator>Wong, Christine E</creator><creator>Paratore, Christian</creator><creator>Dours-Zimmermann, María T</creator><creator>Rochat, Ariane</creator><creator>Pietri, Thomas</creator><creator>Suter, Ueli</creator><creator>Zimmermann, Dieter R</creator><creator>Dufour, Sylvie</creator><creator>Thiery, Jean Paul</creator><creator>Meijer, Dies</creator><creator>Beermann, Friedrich</creator><creator>Barrandon, Yann</creator><creator>Sommer, Lukas</creator><general>The Rockefeller University Press</general><general>Rockefeller University Press</general><scope>FBQ</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>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TM</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>20061218</creationdate><title>Neural crest-derived cells with stem cell features can be traced back to multiple lineages in the adult skin</title><author>Wong, Christine E ; Paratore, Christian ; Dours-Zimmermann, María T ; Rochat, Ariane ; Pietri, Thomas ; Suter, Ueli ; Zimmermann, Dieter R ; Dufour, Sylvie ; Thiery, Jean Paul ; Meijer, Dies ; Beermann, Friedrich ; Barrandon, Yann ; Sommer, Lukas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c457t-2b641b7620a3370811d4f85252cede0a048ee89866a7639ff2abebb8452038293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adipocytes - cytology</topic><topic>Adipocytes - metabolism</topic><topic>Adult</topic><topic>Adult stem cells</topic><topic>Animals</topic><topic>Cell Differentiation</topic><topic>Cell Lineage</topic><topic>Cells, Cultured</topic><topic>Cellular biology</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>Face</topic><topic>Female</topic><topic>Fluorescent Antibody Technique</topic><topic>Genomics</topic><topic>Hair Follicle - cytology</topic><topic>Hair Follicle - physiology</topic><topic>High Mobility Group Proteins - metabolism</topic><topic>Humans</topic><topic>Male</topic><topic>Mapping</topic><topic>Melanocytes</topic><topic>Melanocytes - cytology</topic><topic>Melanocytes - physiology</topic><topic>Mesenchymal stem cells</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Middle Aged</topic><topic>Multipotent stem cells</topic><topic>Multipotent Stem Cells - cytology</topic><topic>Multipotent Stem Cells - physiology</topic><topic>Neural crest</topic><topic>Neural Crest - cytology</topic><topic>Neural Crest - physiology</topic><topic>Neural stem cells</topic><topic>Neuroglia - cytology</topic><topic>Neuroglia - physiology</topic><topic>Neurons</topic><topic>Skin</topic><topic>Skin - cytology</topic><topic>SOXE Transcription Factors</topic><topic>Stem cells</topic><topic>Transcription Factors - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wong, Christine E</creatorcontrib><creatorcontrib>Paratore, Christian</creatorcontrib><creatorcontrib>Dours-Zimmermann, María T</creatorcontrib><creatorcontrib>Rochat, Ariane</creatorcontrib><creatorcontrib>Pietri, Thomas</creatorcontrib><creatorcontrib>Suter, Ueli</creatorcontrib><creatorcontrib>Zimmermann, Dieter R</creatorcontrib><creatorcontrib>Dufour, Sylvie</creatorcontrib><creatorcontrib>Thiery, Jean Paul</creatorcontrib><creatorcontrib>Meijer, Dies</creatorcontrib><creatorcontrib>Beermann, Friedrich</creatorcontrib><creatorcontrib>Barrandon, Yann</creatorcontrib><creatorcontrib>Sommer, Lukas</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids 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>The Journal of cell biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wong, Christine E</au><au>Paratore, Christian</au><au>Dours-Zimmermann, María T</au><au>Rochat, Ariane</au><au>Pietri, Thomas</au><au>Suter, Ueli</au><au>Zimmermann, Dieter R</au><au>Dufour, Sylvie</au><au>Thiery, Jean Paul</au><au>Meijer, Dies</au><au>Beermann, Friedrich</au><au>Barrandon, Yann</au><au>Sommer, Lukas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neural crest-derived cells with stem cell features can be traced back to multiple lineages in the adult skin</atitle><jtitle>The Journal of cell biology</jtitle><addtitle>J Cell Biol</addtitle><date>2006-12-18</date><risdate>2006</risdate><volume>175</volume><issue>6</issue><spage>1005</spage><epage>1015</epage><pages>1005-1015</pages><issn>0021-9525</issn><eissn>1540-8140</eissn><coden>JCLBA3</coden><abstract>Given their accessibility, multipotent skin-derived cells might be useful for future cell replacement therapies. We describe the isolation of multipotent stem cell-like cells from the adult trunk skin of mice and humans that express the neural crest stem cell markers p75 and Sox10 and display extensive self-renewal capacity in sphere cultures. To determine the origin of these cells, we genetically mapped the fate of neural crest cells in face and trunk skin of mouse. In whisker follicles of the face, many mesenchymal structures are neural crest derived and appear to contain cells with sphere-forming potential. In the trunk skin, however, sphere-forming neural crest-derived cells are restricted to the glial and melanocyte lineages. Thus, self-renewing cells in the adult skin can be obtained from several neural crest derivatives, and these are of distinct nature in face and trunk skin. These findings are relevant for the design of therapeutic strategies because the potential of stem and progenitor cells in vivo likely depends on their nature and origin.</abstract><cop>United States</cop><pub>The Rockefeller University Press</pub><pmid>17158956</pmid><doi>10.1083/jcb.200606062</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adipocytes - cytology Adipocytes - metabolism Adult Adult stem cells Animals Cell Differentiation Cell Lineage Cells, Cultured Cellular biology DNA-Binding Proteins - metabolism Face Female Fluorescent Antibody Technique Genomics Hair Follicle - cytology Hair Follicle - physiology High Mobility Group Proteins - metabolism Humans Male Mapping Melanocytes Melanocytes - cytology Melanocytes - physiology Mesenchymal stem cells Mice Mice, Inbred C57BL Middle Aged Multipotent stem cells Multipotent Stem Cells - cytology Multipotent Stem Cells - physiology Neural crest Neural Crest - cytology Neural Crest - physiology Neural stem cells Neuroglia - cytology Neuroglia - physiology Neurons Skin Skin - cytology SOXE Transcription Factors Stem cells Transcription Factors - metabolism |
title | Neural crest-derived cells with stem cell features can be traced back to multiple lineages in the adult skin |
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