Response of Schwann cells to mitogens in vitro is determined by pre-exposure to serum, time in vitro, and developmental age
We compared the mitogenic response of Schwann cells freshly isolated from adult, neonatal, and embryonic nerves, and compared these cells with cells that had been cultured in serum for 5 days. DNA synthesis in response to growth factors was measured using bromodeoxyuridine and immunocytochemistry. F...
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description | We compared the mitogenic response of Schwann cells freshly isolated from adult, neonatal, and embryonic nerves, and compared these cells with cells that had been cultured in serum for 5 days. DNA synthesis in response to growth factors was measured using bromodeoxyuridine and immunocytochemistry. Freshly isolated adult Schwann cells were unresponsive to growth factors with or without forskolin to elevate intracellular cAMP levels. After 5 days of culture in serum, or alternatively in defined medium containing fibroblast growth factor 2 plus forskolin, or neu‐differentiation factor β2, adult cells were responsive to mitogens, whereas cells cultured in defined medium alone remained unresponsive. Serum also increased expression of type 1 fibroblast growth factor receptor. Freshly isolated embryonic and neonatal Schwann cells in contrast responded to growth factors even in the absence of forskolin. This responsiveness changed with time in culture. Neonatal cells cultured for 5 days in defined medium in the presence or absence of serum no longer responded to FGF alone, but required forskolin for a mitogenic response. Thus, the response of freshly isolated cells to mitogens is developmentally regulated; extrinsic signals are required to render adult cells responsive to mitogens; and with time in culture, neonatal cells develop a requirement for cAMP elevation for mitogenic response. GLIA 20:219–230, 1997. © 1997 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/(SICI)1098-1136(199707)20:3<219::AID-GLIA6>3.0.CO;2-2 |
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DNA synthesis in response to growth factors was measured using bromodeoxyuridine and immunocytochemistry. Freshly isolated adult Schwann cells were unresponsive to growth factors with or without forskolin to elevate intracellular cAMP levels. After 5 days of culture in serum, or alternatively in defined medium containing fibroblast growth factor 2 plus forskolin, or neu‐differentiation factor β2, adult cells were responsive to mitogens, whereas cells cultured in defined medium alone remained unresponsive. Serum also increased expression of type 1 fibroblast growth factor receptor. Freshly isolated embryonic and neonatal Schwann cells in contrast responded to growth factors even in the absence of forskolin. This responsiveness changed with time in culture. Neonatal cells cultured for 5 days in defined medium in the presence or absence of serum no longer responded to FGF alone, but required forskolin for a mitogenic response. Thus, the response of freshly isolated cells to mitogens is developmentally regulated; extrinsic signals are required to render adult cells responsive to mitogens; and with time in culture, neonatal cells develop a requirement for cAMP elevation for mitogenic response. GLIA 20:219–230, 1997. © 1997 Wiley‐Liss, Inc.</description><identifier>ISSN: 0894-1491</identifier><identifier>EISSN: 1098-1136</identifier><identifier>DOI: 10.1002/(SICI)1098-1136(199707)20:3<219::AID-GLIA6>3.0.CO;2-2</identifier><identifier>PMID: 9215731</identifier><identifier>CODEN: GLIAEJ</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Inc</publisher><subject>adult ; Animals ; Animals, Newborn ; Biological and medical sciences ; Blood ; Cells, Cultured ; Cellular Senescence - physiology ; Colforsin - pharmacology ; DNA - biosynthesis ; DNA synthesis ; FGF ; Fibroblast Growth Factor 2 - pharmacology ; Fundamental and applied biological sciences. Psychology ; Glycoproteins - pharmacology ; Isolated neuron and nerve. Neuroglia ; Mitogens - pharmacology ; Nerve Growth Factors - pharmacology ; Neuregulins ; PDGF ; Platelet-Derived Growth Factor - pharmacology ; Rabbits ; Rats ; Receptor Protein-Tyrosine Kinases ; Receptor, Fibroblast Growth Factor, Type 1 ; Receptors, Fibroblast Growth Factor - biosynthesis ; Schwann Cells - drug effects ; Schwann Cells - physiology ; Vertebrates: nervous system and sense organs</subject><ispartof>Glia, 1997-07, Vol.20 (3), p.219-230</ispartof><rights>Copyright © 1997 Wiley‐Liss, Inc.</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4616-733247c451e814f903727b4dff6c886081a35fb931c91c6f391b8c6e0e9c940a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2F%28SICI%291098-1136%28199707%2920%3A3%3C219%3A%3AAID-GLIA6%3E3.0.CO%3B2-2$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2F%28SICI%291098-1136%28199707%2920%3A3%3C219%3A%3AAID-GLIA6%3E3.0.CO%3B2-2$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2789704$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9215731$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dong, Ziping</creatorcontrib><creatorcontrib>Dean, Charlotte</creatorcontrib><creatorcontrib>Walters, Jean E.</creatorcontrib><creatorcontrib>Mirsky, Rhona</creatorcontrib><creatorcontrib>Jessen, Kristján R.</creatorcontrib><title>Response of Schwann cells to mitogens in vitro is determined by pre-exposure to serum, time in vitro, and developmental age</title><title>Glia</title><addtitle>Glia</addtitle><description>We compared the mitogenic response of Schwann cells freshly isolated from adult, neonatal, and embryonic nerves, and compared these cells with cells that had been cultured in serum for 5 days. DNA synthesis in response to growth factors was measured using bromodeoxyuridine and immunocytochemistry. Freshly isolated adult Schwann cells were unresponsive to growth factors with or without forskolin to elevate intracellular cAMP levels. After 5 days of culture in serum, or alternatively in defined medium containing fibroblast growth factor 2 plus forskolin, or neu‐differentiation factor β2, adult cells were responsive to mitogens, whereas cells cultured in defined medium alone remained unresponsive. Serum also increased expression of type 1 fibroblast growth factor receptor. Freshly isolated embryonic and neonatal Schwann cells in contrast responded to growth factors even in the absence of forskolin. This responsiveness changed with time in culture. Neonatal cells cultured for 5 days in defined medium in the presence or absence of serum no longer responded to FGF alone, but required forskolin for a mitogenic response. Thus, the response of freshly isolated cells to mitogens is developmentally regulated; extrinsic signals are required to render adult cells responsive to mitogens; and with time in culture, neonatal cells develop a requirement for cAMP elevation for mitogenic response. GLIA 20:219–230, 1997. © 1997 Wiley‐Liss, Inc.</description><subject>adult</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Biological and medical sciences</subject><subject>Blood</subject><subject>Cells, Cultured</subject><subject>Cellular Senescence - physiology</subject><subject>Colforsin - pharmacology</subject><subject>DNA - biosynthesis</subject><subject>DNA synthesis</subject><subject>FGF</subject><subject>Fibroblast Growth Factor 2 - pharmacology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Glycoproteins - pharmacology</subject><subject>Isolated neuron and nerve. Neuroglia</subject><subject>Mitogens - pharmacology</subject><subject>Nerve Growth Factors - pharmacology</subject><subject>Neuregulins</subject><subject>PDGF</subject><subject>Platelet-Derived Growth Factor - pharmacology</subject><subject>Rabbits</subject><subject>Rats</subject><subject>Receptor Protein-Tyrosine Kinases</subject><subject>Receptor, Fibroblast Growth Factor, Type 1</subject><subject>Receptors, Fibroblast Growth Factor - biosynthesis</subject><subject>Schwann Cells - drug effects</subject><subject>Schwann Cells - physiology</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0894-1491</issn><issn>1098-1136</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkd1v0zAUxSMEGmPwJyD5AaFNWoqv7cRx-ZCqwkpFRSU26KPlujcjkC_sdFvFP49Dq7yAtCfLvuccn6tfFL0FOgJK2avTy_l0fgZUZTEAT09BKUnlGaNj_oaBGo8n8_fxbDGfpO_4iI6my9csZg-i48HxMDqmmRIxCAWPoyfe_6AUwkUeRUeKQSI5HEe_v6Bvm9ojaXJyab_fmromFsvSk64hVdE111h7UtTkpuhcQwpPNtihq4oaN2S9I63DGO_axm8d9haPbludk66ocHCdE1Nvgu8Gy6atsO5MScw1Po0e5ab0-OxwnkRfLz5cTT_Gi-VsPp0sYitSSGPJORPSigQwA5EryiWTa7HJ89RmWUozMDzJ14qDVWDTnCtYZzZFisoqQQ0_iV7uc1vX_Nqi73RV-H5HU2Oz9VoqoBml2b1CSIXIkjThQ1PrGu8d5rp1RWXcTgPVPT2te3q6Z6F7FnpPTzOquQ70tA709F964YHq6VIzzULu80OB7brCzZB6wBXmLw5z460pc2dqW_hBxmQWfhFB9m0vuy1K3P3T7Z5q_2u2fwjB8T648B3eDcHG_dSp5DLRq88zvfo0W8GFuAr7_AEdWtCS</recordid><startdate>199707</startdate><enddate>199707</enddate><creator>Dong, Ziping</creator><creator>Dean, Charlotte</creator><creator>Walters, Jean E.</creator><creator>Mirsky, Rhona</creator><creator>Jessen, Kristján R.</creator><general>John Wiley & Sons, Inc</general><general>Wiley-Liss</general><scope>BSCLL</scope><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>7TK</scope><scope>7X8</scope></search><sort><creationdate>199707</creationdate><title>Response of Schwann cells to mitogens in vitro is determined by pre-exposure to serum, time in vitro, and developmental age</title><author>Dong, Ziping ; Dean, Charlotte ; Walters, Jean E. ; Mirsky, Rhona ; Jessen, Kristján R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4616-733247c451e814f903727b4dff6c886081a35fb931c91c6f391b8c6e0e9c940a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>adult</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Biological and medical sciences</topic><topic>Blood</topic><topic>Cells, Cultured</topic><topic>Cellular Senescence - physiology</topic><topic>Colforsin - pharmacology</topic><topic>DNA - biosynthesis</topic><topic>DNA synthesis</topic><topic>FGF</topic><topic>Fibroblast Growth Factor 2 - pharmacology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glycoproteins - pharmacology</topic><topic>Isolated neuron and nerve. Neuroglia</topic><topic>Mitogens - pharmacology</topic><topic>Nerve Growth Factors - pharmacology</topic><topic>Neuregulins</topic><topic>PDGF</topic><topic>Platelet-Derived Growth Factor - pharmacology</topic><topic>Rabbits</topic><topic>Rats</topic><topic>Receptor Protein-Tyrosine Kinases</topic><topic>Receptor, Fibroblast Growth Factor, Type 1</topic><topic>Receptors, Fibroblast Growth Factor - biosynthesis</topic><topic>Schwann Cells - drug effects</topic><topic>Schwann Cells - physiology</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dong, Ziping</creatorcontrib><creatorcontrib>Dean, Charlotte</creatorcontrib><creatorcontrib>Walters, Jean E.</creatorcontrib><creatorcontrib>Mirsky, Rhona</creatorcontrib><creatorcontrib>Jessen, Kristján R.</creatorcontrib><collection>Istex</collection><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>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Glia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dong, Ziping</au><au>Dean, Charlotte</au><au>Walters, Jean E.</au><au>Mirsky, Rhona</au><au>Jessen, Kristján R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Response of Schwann cells to mitogens in vitro is determined by pre-exposure to serum, time in vitro, and developmental age</atitle><jtitle>Glia</jtitle><addtitle>Glia</addtitle><date>1997-07</date><risdate>1997</risdate><volume>20</volume><issue>3</issue><spage>219</spage><epage>230</epage><pages>219-230</pages><issn>0894-1491</issn><eissn>1098-1136</eissn><coden>GLIAEJ</coden><abstract>We compared the mitogenic response of Schwann cells freshly isolated from adult, neonatal, and embryonic nerves, and compared these cells with cells that had been cultured in serum for 5 days. DNA synthesis in response to growth factors was measured using bromodeoxyuridine and immunocytochemistry. Freshly isolated adult Schwann cells were unresponsive to growth factors with or without forskolin to elevate intracellular cAMP levels. After 5 days of culture in serum, or alternatively in defined medium containing fibroblast growth factor 2 plus forskolin, or neu‐differentiation factor β2, adult cells were responsive to mitogens, whereas cells cultured in defined medium alone remained unresponsive. Serum also increased expression of type 1 fibroblast growth factor receptor. Freshly isolated embryonic and neonatal Schwann cells in contrast responded to growth factors even in the absence of forskolin. This responsiveness changed with time in culture. Neonatal cells cultured for 5 days in defined medium in the presence or absence of serum no longer responded to FGF alone, but required forskolin for a mitogenic response. Thus, the response of freshly isolated cells to mitogens is developmentally regulated; extrinsic signals are required to render adult cells responsive to mitogens; and with time in culture, neonatal cells develop a requirement for cAMP elevation for mitogenic response. GLIA 20:219–230, 1997. © 1997 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><pmid>9215731</pmid><doi>10.1002/(SICI)1098-1136(199707)20:3<219::AID-GLIA6>3.0.CO;2-2</doi><tpages>12</tpages></addata></record> |
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subjects | adult Animals Animals, Newborn Biological and medical sciences Blood Cells, Cultured Cellular Senescence - physiology Colforsin - pharmacology DNA - biosynthesis DNA synthesis FGF Fibroblast Growth Factor 2 - pharmacology Fundamental and applied biological sciences. Psychology Glycoproteins - pharmacology Isolated neuron and nerve. Neuroglia Mitogens - pharmacology Nerve Growth Factors - pharmacology Neuregulins PDGF Platelet-Derived Growth Factor - pharmacology Rabbits Rats Receptor Protein-Tyrosine Kinases Receptor, Fibroblast Growth Factor, Type 1 Receptors, Fibroblast Growth Factor - biosynthesis Schwann Cells - drug effects Schwann Cells - physiology Vertebrates: nervous system and sense organs |
title | Response of Schwann cells to mitogens in vitro is determined by pre-exposure to serum, time in vitro, and developmental age |
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