Galactocerebroside Is Expressed by Non-Myelin-Forming Schwann Cells in Situ
Interest in the glycosphingolipid galactocerebroside (GC) is based on the consensus that in the nervous system it is expressed only by myelin-forming Schwann cells and oligodendrocytes, and that it has a specific role in the elaboration of myelin sheaths. We have investigated GC distribution in two...
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Veröffentlicht in: | The Journal of cell biology 1985-09, Vol.101 (3), p.1135-1143 |
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description | Interest in the glycosphingolipid galactocerebroside (GC) is based on the consensus that in the nervous system it is expressed only by myelin-forming Schwann cells and oligodendrocytes, and that it has a specific role in the elaboration of myelin sheaths. We have investigated GC distribution in two rat nerves--the sciatic, containing a mixture of myelinated and non-myelinated axons, and the cervical sympathetic trunk, in which > 99% of axons are non-myelinated. Immunohistochemical experiments using mono- and polyclonal GC antibodies were carried out on teased nerves and cultured Schwann cells, and GC synthesis was assayed biochemically. Unexpectedly, we found that mature non-myelin-forming Schwann cells in situ and in short-term cultures express unambiguous GC immuno-reactivity, comparable in intensity to that of myelinated fibers or myelin-forming cells in short-term cultures. GC synthesis was also detected in both sympathetic trunks and sciatic nerves. In the developing sympathetic trunk, GC was first seen at day 19 in utero, the number of GC-positive cells rising to ∼95% at postnatal day 10. In contrast, the time course of GC appearance in the sciatic nerve shows two separate phases of increase, between day 18 in utero and postnatal day 1, and between postnatal days 20 and 35, at which stage ∼94% of the cells express GC. These time courses suggest that Schwann cells, irrespective of subsequent differentiation pathway, start expressing GC at about the same time as cell division stops. We suggest that GC is a ubiquitous component of mature Schwann cell membranes in situ. Therefore, the role of GC needs to be reevaluated, since its function is clearly not restricted to events involved in myelination. |
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We have investigated GC distribution in two rat nerves--the sciatic, containing a mixture of myelinated and non-myelinated axons, and the cervical sympathetic trunk, in which > 99% of axons are non-myelinated. Immunohistochemical experiments using mono- and polyclonal GC antibodies were carried out on teased nerves and cultured Schwann cells, and GC synthesis was assayed biochemically. Unexpectedly, we found that mature non-myelin-forming Schwann cells in situ and in short-term cultures express unambiguous GC immuno-reactivity, comparable in intensity to that of myelinated fibers or myelin-forming cells in short-term cultures. GC synthesis was also detected in both sympathetic trunks and sciatic nerves. In the developing sympathetic trunk, GC was first seen at day 19 in utero, the number of GC-positive cells rising to ∼95% at postnatal day 10. In contrast, the time course of GC appearance in the sciatic nerve shows two separate phases of increase, between day 18 in utero and postnatal day 1, and between postnatal days 20 and 35, at which stage ∼94% of the cells express GC. These time courses suggest that Schwann cells, irrespective of subsequent differentiation pathway, start expressing GC at about the same time as cell division stops. We suggest that GC is a ubiquitous component of mature Schwann cell membranes in situ. Therefore, the role of GC needs to be reevaluated, since its function is clearly not restricted to events involved in myelination.</description><identifier>ISSN: 0021-9525</identifier><identifier>EISSN: 1540-8140</identifier><identifier>DOI: 10.1083/jcb.101.3.1135</identifier><identifier>PMID: 3897245</identifier><identifier>CODEN: JCLBA3</identifier><language>eng</language><publisher>New York, NY: Rockefeller University Press</publisher><subject>Animals ; Antibodies ; Antibodies, Monoclonal ; Applied sciences ; Axons ; Biological and medical sciences ; Cells ; Cells, Cultured ; Cerebrosides - metabolism ; Cultured cells ; Exact sciences and technology ; Fluorescent Antibody Technique ; Fundamental and applied biological sciences. Psychology ; Galactosylceramides - metabolism ; Isolated neuron and nerve. Neuroglia ; Myelin ; Myelin Sheath - metabolism ; Nerves ; Neuroglia ; Oligodendroglia ; Other techniques and industries ; Rats ; Schwann cells ; Schwann Cells - metabolism ; Sciatic nerve ; Sympathetic Nervous System - cytology ; Vertebrates: nervous system and sense organs</subject><ispartof>The Journal of cell biology, 1985-09, Vol.101 (3), p.1135-1143</ispartof><rights>Copyright 1985 The Rockefeller University Press</rights><rights>1987 INIST-CNRS</rights><rights>1986 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4455-426eb79156d34c8a5f111214703bf687ed6b932ac866d6f6d55002a00f663e193</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7974239$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8770018$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3897245$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jessen, Kristjan R.</creatorcontrib><creatorcontrib>Morgan, Louise</creatorcontrib><creatorcontrib>Brammer, Michael</creatorcontrib><creatorcontrib>Mirsky, Rhona</creatorcontrib><title>Galactocerebroside Is Expressed by Non-Myelin-Forming Schwann Cells in Situ</title><title>The Journal of cell biology</title><addtitle>J Cell Biol</addtitle><description>Interest in the glycosphingolipid galactocerebroside (GC) is based on the consensus that in the nervous system it is expressed only by myelin-forming Schwann cells and oligodendrocytes, and that it has a specific role in the elaboration of myelin sheaths. We have investigated GC distribution in two rat nerves--the sciatic, containing a mixture of myelinated and non-myelinated axons, and the cervical sympathetic trunk, in which > 99% of axons are non-myelinated. Immunohistochemical experiments using mono- and polyclonal GC antibodies were carried out on teased nerves and cultured Schwann cells, and GC synthesis was assayed biochemically. Unexpectedly, we found that mature non-myelin-forming Schwann cells in situ and in short-term cultures express unambiguous GC immuno-reactivity, comparable in intensity to that of myelinated fibers or myelin-forming cells in short-term cultures. GC synthesis was also detected in both sympathetic trunks and sciatic nerves. In the developing sympathetic trunk, GC was first seen at day 19 in utero, the number of GC-positive cells rising to ∼95% at postnatal day 10. In contrast, the time course of GC appearance in the sciatic nerve shows two separate phases of increase, between day 18 in utero and postnatal day 1, and between postnatal days 20 and 35, at which stage ∼94% of the cells express GC. These time courses suggest that Schwann cells, irrespective of subsequent differentiation pathway, start expressing GC at about the same time as cell division stops. We suggest that GC is a ubiquitous component of mature Schwann cell membranes in situ. Therefore, the role of GC needs to be reevaluated, since its function is clearly not restricted to events involved in myelination.</description><subject>Animals</subject><subject>Antibodies</subject><subject>Antibodies, Monoclonal</subject><subject>Applied sciences</subject><subject>Axons</subject><subject>Biological and medical sciences</subject><subject>Cells</subject><subject>Cells, Cultured</subject><subject>Cerebrosides - metabolism</subject><subject>Cultured cells</subject><subject>Exact sciences and technology</subject><subject>Fluorescent Antibody Technique</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Galactosylceramides - metabolism</subject><subject>Isolated neuron and nerve. Neuroglia</subject><subject>Myelin</subject><subject>Myelin Sheath - metabolism</subject><subject>Nerves</subject><subject>Neuroglia</subject><subject>Oligodendroglia</subject><subject>Other techniques and industries</subject><subject>Rats</subject><subject>Schwann cells</subject><subject>Schwann Cells - metabolism</subject><subject>Sciatic nerve</subject><subject>Sympathetic Nervous System - cytology</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0021-9525</issn><issn>1540-8140</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1985</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1PGzEQhi1URFPKlROV9oB62-Dx914qoQgo4qMH2rPl9XrB0cZO7Q1t_n0dJUrbEyePNM-8nnkQOgU8Bazoxdy2pYApnQJQfoAmwBmuFTD8Dk0wJlA3nPD36EPOc4wxk4weoSOqGkkYn6C7GzMYO0brkmtTzL5z1W2urn4vk8vZdVW7rh5jqB_WbvChvo5p4cNz9WRffpkQqpkbhlz5UD35cfURHfZmyO5k9x6jH9dX32df6_tvN7ezy_vaMsZ5zYhwrWyAi44yqwzvAYAAk5i2vVDSdaJtKDFWCdGJXnSclzsMxr0Q1EFDj9GXbe5y1S5cZ10Ykxn0MvmFSWsdjdf_d4J_0c_xVZOiSDJcAj7vAlL8uXJ51AufbTnFBBdXWUtBFKGCFHC6BW1Rk5Pr958A1hv9uugvBWiqN_rLwKd_V9vjO9-lf77rm2zN0CcTrM97TEmJMai3MNlIRuhGxNkWm-cxpr-7CQDOFf0De4Wiyw</recordid><startdate>19850901</startdate><enddate>19850901</enddate><creator>Jessen, Kristjan R.</creator><creator>Morgan, Louise</creator><creator>Brammer, Michael</creator><creator>Mirsky, Rhona</creator><general>Rockefeller University Press</general><general>The Rockefeller University Press</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>19850901</creationdate><title>Galactocerebroside Is Expressed by Non-Myelin-Forming Schwann Cells in Situ</title><author>Jessen, Kristjan R. ; Morgan, Louise ; Brammer, Michael ; Mirsky, Rhona</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4455-426eb79156d34c8a5f111214703bf687ed6b932ac866d6f6d55002a00f663e193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1985</creationdate><topic>Animals</topic><topic>Antibodies</topic><topic>Antibodies, Monoclonal</topic><topic>Applied sciences</topic><topic>Axons</topic><topic>Biological and medical sciences</topic><topic>Cells</topic><topic>Cells, Cultured</topic><topic>Cerebrosides - metabolism</topic><topic>Cultured cells</topic><topic>Exact sciences and technology</topic><topic>Fluorescent Antibody Technique</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Galactosylceramides - metabolism</topic><topic>Isolated neuron and nerve. Neuroglia</topic><topic>Myelin</topic><topic>Myelin Sheath - metabolism</topic><topic>Nerves</topic><topic>Neuroglia</topic><topic>Oligodendroglia</topic><topic>Other techniques and industries</topic><topic>Rats</topic><topic>Schwann cells</topic><topic>Schwann Cells - metabolism</topic><topic>Sciatic nerve</topic><topic>Sympathetic Nervous System - cytology</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jessen, Kristjan R.</creatorcontrib><creatorcontrib>Morgan, Louise</creatorcontrib><creatorcontrib>Brammer, Michael</creatorcontrib><creatorcontrib>Mirsky, Rhona</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>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>Jessen, Kristjan R.</au><au>Morgan, Louise</au><au>Brammer, Michael</au><au>Mirsky, Rhona</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Galactocerebroside Is Expressed by Non-Myelin-Forming Schwann Cells in Situ</atitle><jtitle>The Journal of cell biology</jtitle><addtitle>J Cell Biol</addtitle><date>1985-09-01</date><risdate>1985</risdate><volume>101</volume><issue>3</issue><spage>1135</spage><epage>1143</epage><pages>1135-1143</pages><issn>0021-9525</issn><eissn>1540-8140</eissn><coden>JCLBA3</coden><abstract>Interest in the glycosphingolipid galactocerebroside (GC) is based on the consensus that in the nervous system it is expressed only by myelin-forming Schwann cells and oligodendrocytes, and that it has a specific role in the elaboration of myelin sheaths. We have investigated GC distribution in two rat nerves--the sciatic, containing a mixture of myelinated and non-myelinated axons, and the cervical sympathetic trunk, in which > 99% of axons are non-myelinated. Immunohistochemical experiments using mono- and polyclonal GC antibodies were carried out on teased nerves and cultured Schwann cells, and GC synthesis was assayed biochemically. Unexpectedly, we found that mature non-myelin-forming Schwann cells in situ and in short-term cultures express unambiguous GC immuno-reactivity, comparable in intensity to that of myelinated fibers or myelin-forming cells in short-term cultures. GC synthesis was also detected in both sympathetic trunks and sciatic nerves. In the developing sympathetic trunk, GC was first seen at day 19 in utero, the number of GC-positive cells rising to ∼95% at postnatal day 10. In contrast, the time course of GC appearance in the sciatic nerve shows two separate phases of increase, between day 18 in utero and postnatal day 1, and between postnatal days 20 and 35, at which stage ∼94% of the cells express GC. These time courses suggest that Schwann cells, irrespective of subsequent differentiation pathway, start expressing GC at about the same time as cell division stops. We suggest that GC is a ubiquitous component of mature Schwann cell membranes in situ. Therefore, the role of GC needs to be reevaluated, since its function is clearly not restricted to events involved in myelination.</abstract><cop>New York, NY</cop><pub>Rockefeller University Press</pub><pmid>3897245</pmid><doi>10.1083/jcb.101.3.1135</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antibodies Antibodies, Monoclonal Applied sciences Axons Biological and medical sciences Cells Cells, Cultured Cerebrosides - metabolism Cultured cells Exact sciences and technology Fluorescent Antibody Technique Fundamental and applied biological sciences. Psychology Galactosylceramides - metabolism Isolated neuron and nerve. Neuroglia Myelin Myelin Sheath - metabolism Nerves Neuroglia Oligodendroglia Other techniques and industries Rats Schwann cells Schwann Cells - metabolism Sciatic nerve Sympathetic Nervous System - cytology Vertebrates: nervous system and sense organs |
title | Galactocerebroside Is Expressed by Non-Myelin-Forming Schwann Cells in Situ |
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