Schwann Cells Can Be Reprogrammed to Multipotency by Culture
Adult neural crest related-stem cells persist in adulthood, making them an ideal and easily accessible source of multipotent cells for potential clinical use. Recently, we reported the presence of neural crest-related stem cells within adult palatal ridges, thus raising the question of their localiz...
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creator | Widera, Darius Heimann, Peter Zander, Christin Imielski, Yvonne Heidbreder, Meike Heilemann, Mike Kaltschmidt, Christian Kaltschmidt, Barbara |
description | Adult neural crest related-stem cells persist in adulthood, making them an ideal and easily accessible source of multipotent cells for potential clinical use. Recently, we reported the presence of neural crest-related stem cells within adult palatal ridges, thus raising the question of their localization in their endogenous niche. Using immunocytochemistry, reverse transcription
–
polymerase chain reaction, and correlative fluorescence and transmission electron microscopy, we identified myelinating Schwann cells within palatal ridges as a putative neural crest stem cell source. Palatal Schwann cells expressed nestin, p75
NTR
, and S100. Correlative fluorescence and transmission electron microscopy revealed the exclusive nestin expression within myelinating Schwann cells. Palatal neural crest stem cells and nestin-positive Schwann cells isolated from adult sciatic nerves were able to grow under serum-free conditions as neurospheres in presence of FGF-2 and EGF. Spheres of palatal and sciatic origin showed overlapping expression pattern of neural crest stem cell and Schwann cell markers. Expression of the pluripotency factors Sox2, Klf4, c-Myc, Oct4, the NF-κB subunits p65, p50, and the NF-κB-inhibitor IκB-β were up-regulated in conventionally cultivated sciatic nerve Schwann cells and in neurosphere cultures. Finally, neurospheres of palatal and sciatic origin were able to differentiate into ectodermal, mesodermal, and endodermal cell types emphasizing their multipotency. Taken together, we show that nestin-positive myelinating Schwann cells can be reprogrammed into multipotent adult neural crest stem cells under appropriate culture conditions. |
doi_str_mv | 10.1089/scd.2010.0525 |
format | Article |
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–
polymerase chain reaction, and correlative fluorescence and transmission electron microscopy, we identified myelinating Schwann cells within palatal ridges as a putative neural crest stem cell source. Palatal Schwann cells expressed nestin, p75
NTR
, and S100. Correlative fluorescence and transmission electron microscopy revealed the exclusive nestin expression within myelinating Schwann cells. Palatal neural crest stem cells and nestin-positive Schwann cells isolated from adult sciatic nerves were able to grow under serum-free conditions as neurospheres in presence of FGF-2 and EGF. Spheres of palatal and sciatic origin showed overlapping expression pattern of neural crest stem cell and Schwann cell markers. Expression of the pluripotency factors Sox2, Klf4, c-Myc, Oct4, the NF-κB subunits p65, p50, and the NF-κB-inhibitor IκB-β were up-regulated in conventionally cultivated sciatic nerve Schwann cells and in neurosphere cultures. Finally, neurospheres of palatal and sciatic origin were able to differentiate into ectodermal, mesodermal, and endodermal cell types emphasizing their multipotency. Taken together, we show that nestin-positive myelinating Schwann cells can be reprogrammed into multipotent adult neural crest stem cells under appropriate culture conditions.</description><identifier>ISSN: 1547-3287</identifier><identifier>EISSN: 1557-8534</identifier><identifier>DOI: 10.1089/scd.2010.0525</identifier><identifier>PMID: 21466279</identifier><language>eng</language><publisher>United States: Mary Ann Liebert, Inc</publisher><subject>Animals ; Cell Aggregation ; Cell Culture Techniques - methods ; Cell Differentiation ; Cell Separation ; Cells, Cultured ; Cellular Reprogramming ; Clone Cells ; Intermediate Filament Proteins - metabolism ; Intermediate Filament Proteins - ultrastructure ; Ki-67 Antigen - metabolism ; Mucous Membrane - cytology ; Multipotent Stem Cells - cytology ; Multipotent Stem Cells - metabolism ; Myelin Proteins - metabolism ; Myelin Sheath - metabolism ; Myelin Sheath - ultrastructure ; Nerve Fibers - metabolism ; Nerve Tissue Proteins - metabolism ; Nerve Tissue Proteins - ultrastructure ; Nestin ; Neural Crest - cytology ; Neural Stem Cells - cytology ; Neural Stem Cells - metabolism ; NF-kappa B - metabolism ; Original Research Reports ; Palate - cytology ; Pluripotent Stem Cells - cytology ; Pluripotent Stem Cells - metabolism ; Rats ; Receptors, Nerve Growth Factor - metabolism ; S100 Proteins - metabolism ; Schwann Cells - cytology ; Schwann Cells - metabolism ; Schwann Cells - ultrastructure ; Sciatic Nerve - cytology ; Sciatic Nerve - metabolism ; Synapses - metabolism</subject><ispartof>Stem cells and development, 2011-12, Vol.20 (12), p.253-2064</ispartof><rights>2011, Mary Ann Liebert, Inc.</rights><rights>Copyright 2011, Mary Ann Liebert, Inc. 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c430t-39fab1c023deefd99a0d966fa94395e2c63aff6d34f6ae78733baa9531ce82483</citedby><cites>FETCH-LOGICAL-c430t-39fab1c023deefd99a0d966fa94395e2c63aff6d34f6ae78733baa9531ce82483</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21466279$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Widera, Darius</creatorcontrib><creatorcontrib>Heimann, Peter</creatorcontrib><creatorcontrib>Zander, Christin</creatorcontrib><creatorcontrib>Imielski, Yvonne</creatorcontrib><creatorcontrib>Heidbreder, Meike</creatorcontrib><creatorcontrib>Heilemann, Mike</creatorcontrib><creatorcontrib>Kaltschmidt, Christian</creatorcontrib><creatorcontrib>Kaltschmidt, Barbara</creatorcontrib><title>Schwann Cells Can Be Reprogrammed to Multipotency by Culture</title><title>Stem cells and development</title><addtitle>Stem Cells Dev</addtitle><description>Adult neural crest related-stem cells persist in adulthood, making them an ideal and easily accessible source of multipotent cells for potential clinical use. Recently, we reported the presence of neural crest-related stem cells within adult palatal ridges, thus raising the question of their localization in their endogenous niche. Using immunocytochemistry, reverse transcription
–
polymerase chain reaction, and correlative fluorescence and transmission electron microscopy, we identified myelinating Schwann cells within palatal ridges as a putative neural crest stem cell source. Palatal Schwann cells expressed nestin, p75
NTR
, and S100. Correlative fluorescence and transmission electron microscopy revealed the exclusive nestin expression within myelinating Schwann cells. Palatal neural crest stem cells and nestin-positive Schwann cells isolated from adult sciatic nerves were able to grow under serum-free conditions as neurospheres in presence of FGF-2 and EGF. Spheres of palatal and sciatic origin showed overlapping expression pattern of neural crest stem cell and Schwann cell markers. Expression of the pluripotency factors Sox2, Klf4, c-Myc, Oct4, the NF-κB subunits p65, p50, and the NF-κB-inhibitor IκB-β were up-regulated in conventionally cultivated sciatic nerve Schwann cells and in neurosphere cultures. Finally, neurospheres of palatal and sciatic origin were able to differentiate into ectodermal, mesodermal, and endodermal cell types emphasizing their multipotency. Taken together, we show that nestin-positive myelinating Schwann cells can be reprogrammed into multipotent adult neural crest stem cells under appropriate culture conditions.</description><subject>Animals</subject><subject>Cell Aggregation</subject><subject>Cell Culture Techniques - methods</subject><subject>Cell Differentiation</subject><subject>Cell Separation</subject><subject>Cells, Cultured</subject><subject>Cellular Reprogramming</subject><subject>Clone Cells</subject><subject>Intermediate Filament Proteins - metabolism</subject><subject>Intermediate Filament Proteins - ultrastructure</subject><subject>Ki-67 Antigen - metabolism</subject><subject>Mucous Membrane - cytology</subject><subject>Multipotent Stem Cells - cytology</subject><subject>Multipotent Stem Cells - metabolism</subject><subject>Myelin Proteins - metabolism</subject><subject>Myelin Sheath - metabolism</subject><subject>Myelin Sheath - ultrastructure</subject><subject>Nerve Fibers - metabolism</subject><subject>Nerve Tissue Proteins - metabolism</subject><subject>Nerve Tissue Proteins - ultrastructure</subject><subject>Nestin</subject><subject>Neural Crest - cytology</subject><subject>Neural Stem Cells - cytology</subject><subject>Neural Stem Cells - metabolism</subject><subject>NF-kappa B - metabolism</subject><subject>Original Research Reports</subject><subject>Palate - cytology</subject><subject>Pluripotent Stem Cells - cytology</subject><subject>Pluripotent Stem Cells - metabolism</subject><subject>Rats</subject><subject>Receptors, Nerve Growth Factor - metabolism</subject><subject>S100 Proteins - metabolism</subject><subject>Schwann Cells - cytology</subject><subject>Schwann Cells - metabolism</subject><subject>Schwann Cells - ultrastructure</subject><subject>Sciatic Nerve - cytology</subject><subject>Sciatic Nerve - metabolism</subject><subject>Synapses - metabolism</subject><issn>1547-3287</issn><issn>1557-8534</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMtLxDAQh4Morq4evUpvnrqmSZo2IIIWX7Ai-DiHNJ3sVvoyaZX9703ZddGTp2QyH7_MfAidRHgW4VScO13MCPYVjkm8gw6iOE7CNKZsd7yzJKQkTSbo0Ll3jAknKdtHExIxzkkiDtDFi15-qaYJMqgqF2SqCa4heIbOtgur6hqKoG-Dx6Hqy67todGrIF8Fma8HC0doz6jKwfHmnKK325vX7D6cP909ZFfzUDOK-5AKo_JIY0ILAFMIoXAhODdKMCpiIJpTZQwvKDNcQZImlOZKiZhGGlLCUjpFl-vcbsj9RBqa3qpKdraslV3JVpXyb6cpl3LRfkpKSIw58wFnmwDbfgzgelmXTvuNVQPt4KTACaY89dqmKFyT2rbOWTDbXyIsR-HSC5ejcDkK9_zp79G29I9hD9A1MD570VUJOdj-n9hvXP6OGg</recordid><startdate>20111201</startdate><enddate>20111201</enddate><creator>Widera, Darius</creator><creator>Heimann, Peter</creator><creator>Zander, Christin</creator><creator>Imielski, Yvonne</creator><creator>Heidbreder, Meike</creator><creator>Heilemann, Mike</creator><creator>Kaltschmidt, Christian</creator><creator>Kaltschmidt, Barbara</creator><general>Mary Ann Liebert, Inc</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20111201</creationdate><title>Schwann Cells Can Be Reprogrammed to Multipotency by Culture</title><author>Widera, Darius ; Heimann, Peter ; Zander, Christin ; Imielski, Yvonne ; Heidbreder, Meike ; Heilemann, Mike ; Kaltschmidt, Christian ; Kaltschmidt, Barbara</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c430t-39fab1c023deefd99a0d966fa94395e2c63aff6d34f6ae78733baa9531ce82483</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Cell Aggregation</topic><topic>Cell Culture Techniques - methods</topic><topic>Cell Differentiation</topic><topic>Cell Separation</topic><topic>Cells, Cultured</topic><topic>Cellular Reprogramming</topic><topic>Clone Cells</topic><topic>Intermediate Filament Proteins - metabolism</topic><topic>Intermediate Filament Proteins - ultrastructure</topic><topic>Ki-67 Antigen - metabolism</topic><topic>Mucous Membrane - cytology</topic><topic>Multipotent Stem Cells - cytology</topic><topic>Multipotent Stem Cells - metabolism</topic><topic>Myelin Proteins - metabolism</topic><topic>Myelin Sheath - metabolism</topic><topic>Myelin Sheath - ultrastructure</topic><topic>Nerve Fibers - metabolism</topic><topic>Nerve Tissue Proteins - metabolism</topic><topic>Nerve Tissue Proteins - ultrastructure</topic><topic>Nestin</topic><topic>Neural Crest - cytology</topic><topic>Neural Stem Cells - cytology</topic><topic>Neural Stem Cells - metabolism</topic><topic>NF-kappa B - metabolism</topic><topic>Original Research Reports</topic><topic>Palate - cytology</topic><topic>Pluripotent Stem Cells - cytology</topic><topic>Pluripotent Stem Cells - metabolism</topic><topic>Rats</topic><topic>Receptors, Nerve Growth Factor - metabolism</topic><topic>S100 Proteins - metabolism</topic><topic>Schwann Cells - cytology</topic><topic>Schwann Cells - metabolism</topic><topic>Schwann Cells - ultrastructure</topic><topic>Sciatic Nerve - cytology</topic><topic>Sciatic Nerve - metabolism</topic><topic>Synapses - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Widera, Darius</creatorcontrib><creatorcontrib>Heimann, Peter</creatorcontrib><creatorcontrib>Zander, Christin</creatorcontrib><creatorcontrib>Imielski, Yvonne</creatorcontrib><creatorcontrib>Heidbreder, Meike</creatorcontrib><creatorcontrib>Heilemann, Mike</creatorcontrib><creatorcontrib>Kaltschmidt, Christian</creatorcontrib><creatorcontrib>Kaltschmidt, Barbara</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Stem cells and development</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Widera, Darius</au><au>Heimann, Peter</au><au>Zander, Christin</au><au>Imielski, Yvonne</au><au>Heidbreder, Meike</au><au>Heilemann, Mike</au><au>Kaltschmidt, Christian</au><au>Kaltschmidt, Barbara</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Schwann Cells Can Be Reprogrammed to Multipotency by Culture</atitle><jtitle>Stem cells and development</jtitle><addtitle>Stem Cells Dev</addtitle><date>2011-12-01</date><risdate>2011</risdate><volume>20</volume><issue>12</issue><spage>253</spage><epage>2064</epage><pages>253-2064</pages><issn>1547-3287</issn><eissn>1557-8534</eissn><abstract>Adult neural crest related-stem cells persist in adulthood, making them an ideal and easily accessible source of multipotent cells for potential clinical use. Recently, we reported the presence of neural crest-related stem cells within adult palatal ridges, thus raising the question of their localization in their endogenous niche. Using immunocytochemistry, reverse transcription
–
polymerase chain reaction, and correlative fluorescence and transmission electron microscopy, we identified myelinating Schwann cells within palatal ridges as a putative neural crest stem cell source. Palatal Schwann cells expressed nestin, p75
NTR
, and S100. Correlative fluorescence and transmission electron microscopy revealed the exclusive nestin expression within myelinating Schwann cells. Palatal neural crest stem cells and nestin-positive Schwann cells isolated from adult sciatic nerves were able to grow under serum-free conditions as neurospheres in presence of FGF-2 and EGF. Spheres of palatal and sciatic origin showed overlapping expression pattern of neural crest stem cell and Schwann cell markers. Expression of the pluripotency factors Sox2, Klf4, c-Myc, Oct4, the NF-κB subunits p65, p50, and the NF-κB-inhibitor IκB-β were up-regulated in conventionally cultivated sciatic nerve Schwann cells and in neurosphere cultures. Finally, neurospheres of palatal and sciatic origin were able to differentiate into ectodermal, mesodermal, and endodermal cell types emphasizing their multipotency. Taken together, we show that nestin-positive myelinating Schwann cells can be reprogrammed into multipotent adult neural crest stem cells under appropriate culture conditions.</abstract><cop>United States</cop><pub>Mary Ann Liebert, Inc</pub><pmid>21466279</pmid><doi>10.1089/scd.2010.0525</doi><tpages>1812</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Cell Aggregation Cell Culture Techniques - methods Cell Differentiation Cell Separation Cells, Cultured Cellular Reprogramming Clone Cells Intermediate Filament Proteins - metabolism Intermediate Filament Proteins - ultrastructure Ki-67 Antigen - metabolism Mucous Membrane - cytology Multipotent Stem Cells - cytology Multipotent Stem Cells - metabolism Myelin Proteins - metabolism Myelin Sheath - metabolism Myelin Sheath - ultrastructure Nerve Fibers - metabolism Nerve Tissue Proteins - metabolism Nerve Tissue Proteins - ultrastructure Nestin Neural Crest - cytology Neural Stem Cells - cytology Neural Stem Cells - metabolism NF-kappa B - metabolism Original Research Reports Palate - cytology Pluripotent Stem Cells - cytology Pluripotent Stem Cells - metabolism Rats Receptors, Nerve Growth Factor - metabolism S100 Proteins - metabolism Schwann Cells - cytology Schwann Cells - metabolism Schwann Cells - ultrastructure Sciatic Nerve - cytology Sciatic Nerve - metabolism Synapses - metabolism |
title | Schwann Cells Can Be Reprogrammed to Multipotency by Culture |
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