Neurite extension by peripheral and central nervous system neurons in response to substratum-bound fibronectin and laminin
Dissociated neurons from embryonic chick dorsal root and sympathetic ganglia (peripheral neurons) and from spinal cord and retina (central nervous system neurons) were cultured on plastic substrata treated with purified fibronectin and laminin. Both central and peripheral neurons attached to and ext...
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Veröffentlicht in: | Developmental biology 1983-07, Vol.98 (1), p.212-220 |
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creator | Rogers, Sherry L. Letourneau, Paul C. Palm, Sally L. McCarthy, James Furcht, Leo T. |
description | Dissociated neurons from embryonic chick dorsal root and sympathetic ganglia (peripheral neurons) and from spinal cord and retina (central nervous system neurons) were cultured on plastic substrata treated with purified fibronectin and laminin. Both central and peripheral neurons attached to and extended neurites on laminin. In contrast, only peripheral neurons initiated neurites on fibronectin; central neurons cultured under identical conditions aggregated into clusters and did not extend neurites. Neurite length, number of neurites initiated, and extent of neurite branching on fibronectin- and laminin-treated substrata were evaluated and compared with similar measurements of neuronal response to poly-
l-lysine-treated plastic. Poly-
l-lysine provides an adhesive surface for neurite elongation, but fibronectin and laminin appear to promote more rapid neurite elongation. Our observations suggest that neuronal interaction with these glycoproteins may involve neuron-specific cell surface components. These responses to laminin and fibronectin
in vitro may be related to the presence or absence of these glycoproteins in specific extracellular environments during specific developmental stages. |
doi_str_mv | 10.1016/0012-1606(83)90350-0 |
format | Article |
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l-lysine-treated plastic. Poly-
l-lysine provides an adhesive surface for neurite elongation, but fibronectin and laminin appear to promote more rapid neurite elongation. Our observations suggest that neuronal interaction with these glycoproteins may involve neuron-specific cell surface components. These responses to laminin and fibronectin
in vitro may be related to the presence or absence of these glycoproteins in specific extracellular environments during specific developmental stages.</description><identifier>ISSN: 0012-1606</identifier><identifier>EISSN: 1095-564X</identifier><identifier>DOI: 10.1016/0012-1606(83)90350-0</identifier><identifier>PMID: 6862106</identifier><identifier>CODEN: DEBIAO</identifier><language>eng</language><publisher>Amsterdam: Elsevier Inc</publisher><subject>Animals ; Biological and medical sciences ; Cell Aggregation - drug effects ; Cell differentiation, maturation, development, hematopoiesis ; Cell physiology ; central nervous system ; Chick Embryo ; chick embryos ; fibronectin ; Fibronectins - pharmacology ; Fundamental and applied biological sciences. Psychology ; Ganglia, Spinal - cytology ; Ganglia, Sympathetic - cytology ; Glycoproteins - pharmacology ; Laminin ; Mice ; Molecular and cellular biology ; neurites ; neurons ; Neurons - cytology ; Neurons - drug effects ; peripheral nervous system ; Rabbits ; Retinal Ganglion Cells - cytology ; Spinal Cord - cytology</subject><ispartof>Developmental biology, 1983-07, Vol.98 (1), p.212-220</ispartof><rights>1983</rights><rights>1984 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c483t-c3ccc3279c6f3c16471499ab168f46e4b36a7c4330f02d37a12a92dd16104cb63</citedby><cites>FETCH-LOGICAL-c483t-c3ccc3279c6f3c16471499ab168f46e4b36a7c4330f02d37a12a92dd16104cb63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0012-1606(83)90350-0$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=9457178$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6862106$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rogers, Sherry L.</creatorcontrib><creatorcontrib>Letourneau, Paul C.</creatorcontrib><creatorcontrib>Palm, Sally L.</creatorcontrib><creatorcontrib>McCarthy, James</creatorcontrib><creatorcontrib>Furcht, Leo T.</creatorcontrib><title>Neurite extension by peripheral and central nervous system neurons in response to substratum-bound fibronectin and laminin</title><title>Developmental biology</title><addtitle>Dev Biol</addtitle><description>Dissociated neurons from embryonic chick dorsal root and sympathetic ganglia (peripheral neurons) and from spinal cord and retina (central nervous system neurons) were cultured on plastic substrata treated with purified fibronectin and laminin. Both central and peripheral neurons attached to and extended neurites on laminin. In contrast, only peripheral neurons initiated neurites on fibronectin; central neurons cultured under identical conditions aggregated into clusters and did not extend neurites. Neurite length, number of neurites initiated, and extent of neurite branching on fibronectin- and laminin-treated substrata were evaluated and compared with similar measurements of neuronal response to poly-
l-lysine-treated plastic. Poly-
l-lysine provides an adhesive surface for neurite elongation, but fibronectin and laminin appear to promote more rapid neurite elongation. Our observations suggest that neuronal interaction with these glycoproteins may involve neuron-specific cell surface components. These responses to laminin and fibronectin
in vitro may be related to the presence or absence of these glycoproteins in specific extracellular environments during specific developmental stages.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cell Aggregation - drug effects</subject><subject>Cell differentiation, maturation, development, hematopoiesis</subject><subject>Cell physiology</subject><subject>central nervous system</subject><subject>Chick Embryo</subject><subject>chick embryos</subject><subject>fibronectin</subject><subject>Fibronectins - pharmacology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Ganglia, Spinal - cytology</subject><subject>Ganglia, Sympathetic - cytology</subject><subject>Glycoproteins - pharmacology</subject><subject>Laminin</subject><subject>Mice</subject><subject>Molecular and cellular biology</subject><subject>neurites</subject><subject>neurons</subject><subject>Neurons - cytology</subject><subject>Neurons - drug effects</subject><subject>peripheral nervous system</subject><subject>Rabbits</subject><subject>Retinal Ganglion Cells - cytology</subject><subject>Spinal Cord - cytology</subject><issn>0012-1606</issn><issn>1095-564X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1983</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcGL1TAQxoMo69vV_0AhB1n00HXSSdP2IsjiqrC4FwVvIU2nGGnTmqSLb_96U9_jHfWUCfP7hpnvY-yFgCsBQr0FEGUhFKjXDb5pASso4BHbCWirolLy-2O2OyFP2XmMPwEAmwbP2JlqVClA7djDF1qDS8TpdyIf3ex5t-cLBbf8oGBGbnzPLfm01Z7C_bxGHvcx0ZS_a5h95M7zQHHJJfE087h2MeNpnYpuXrN8cF3myKYMbuNGMznv_DP2ZDBjpOfH94J9u_nw9fpTcXv38fP1-9vCygZTYdFai2XdWjWgFUrWQrat6YRqBqlIdqhMbSUiDFD2WBtRmrbse6EESNspvGCXh7lLmH-tFJOeXLQ0jsZTvkY3UJU1YvNfUMgSEUWdQXkAbZhjDDToJbjJhL0WoLds9Ga83ozXDeq_2WjIspfH-Ws3UX8SHcPI_VfHvonWjEMw3rp4wlpZ1aLe1nx3wCibdu8o6GgdeUu9C9lk3c_u33v8AU6urHM</recordid><startdate>198307</startdate><enddate>198307</enddate><creator>Rogers, Sherry L.</creator><creator>Letourneau, Paul C.</creator><creator>Palm, Sally L.</creator><creator>McCarthy, James</creator><creator>Furcht, Leo T.</creator><general>Elsevier Inc</general><general>Elsevier</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>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>M7Z</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>198307</creationdate><title>Neurite extension by peripheral and central nervous system neurons in response to substratum-bound fibronectin and laminin</title><author>Rogers, Sherry L. ; Letourneau, Paul C. ; Palm, Sally L. ; McCarthy, James ; Furcht, Leo T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c483t-c3ccc3279c6f3c16471499ab168f46e4b36a7c4330f02d37a12a92dd16104cb63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1983</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cell Aggregation - drug effects</topic><topic>Cell differentiation, maturation, development, hematopoiesis</topic><topic>Cell physiology</topic><topic>central nervous system</topic><topic>Chick Embryo</topic><topic>chick embryos</topic><topic>fibronectin</topic><topic>Fibronectins - pharmacology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Ganglia, Spinal - cytology</topic><topic>Ganglia, Sympathetic - cytology</topic><topic>Glycoproteins - pharmacology</topic><topic>Laminin</topic><topic>Mice</topic><topic>Molecular and cellular biology</topic><topic>neurites</topic><topic>neurons</topic><topic>Neurons - cytology</topic><topic>Neurons - drug effects</topic><topic>peripheral nervous system</topic><topic>Rabbits</topic><topic>Retinal Ganglion Cells - cytology</topic><topic>Spinal Cord - cytology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rogers, Sherry L.</creatorcontrib><creatorcontrib>Letourneau, Paul C.</creatorcontrib><creatorcontrib>Palm, Sally L.</creatorcontrib><creatorcontrib>McCarthy, James</creatorcontrib><creatorcontrib>Furcht, Leo T.</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>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Developmental biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rogers, Sherry L.</au><au>Letourneau, Paul C.</au><au>Palm, Sally L.</au><au>McCarthy, James</au><au>Furcht, Leo T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neurite extension by peripheral and central nervous system neurons in response to substratum-bound fibronectin and laminin</atitle><jtitle>Developmental biology</jtitle><addtitle>Dev Biol</addtitle><date>1983-07</date><risdate>1983</risdate><volume>98</volume><issue>1</issue><spage>212</spage><epage>220</epage><pages>212-220</pages><issn>0012-1606</issn><eissn>1095-564X</eissn><coden>DEBIAO</coden><abstract>Dissociated neurons from embryonic chick dorsal root and sympathetic ganglia (peripheral neurons) and from spinal cord and retina (central nervous system neurons) were cultured on plastic substrata treated with purified fibronectin and laminin. Both central and peripheral neurons attached to and extended neurites on laminin. In contrast, only peripheral neurons initiated neurites on fibronectin; central neurons cultured under identical conditions aggregated into clusters and did not extend neurites. Neurite length, number of neurites initiated, and extent of neurite branching on fibronectin- and laminin-treated substrata were evaluated and compared with similar measurements of neuronal response to poly-
l-lysine-treated plastic. Poly-
l-lysine provides an adhesive surface for neurite elongation, but fibronectin and laminin appear to promote more rapid neurite elongation. Our observations suggest that neuronal interaction with these glycoproteins may involve neuron-specific cell surface components. These responses to laminin and fibronectin
in vitro may be related to the presence or absence of these glycoproteins in specific extracellular environments during specific developmental stages.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>6862106</pmid><doi>10.1016/0012-1606(83)90350-0</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Cell Aggregation - drug effects Cell differentiation, maturation, development, hematopoiesis Cell physiology central nervous system Chick Embryo chick embryos fibronectin Fibronectins - pharmacology Fundamental and applied biological sciences. Psychology Ganglia, Spinal - cytology Ganglia, Sympathetic - cytology Glycoproteins - pharmacology Laminin Mice Molecular and cellular biology neurites neurons Neurons - cytology Neurons - drug effects peripheral nervous system Rabbits Retinal Ganglion Cells - cytology Spinal Cord - cytology |
title | Neurite extension by peripheral and central nervous system neurons in response to substratum-bound fibronectin and laminin |
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