Changes in the distribution of GAP-43 during the development of neuronal polarity
GAP-43, a neuron specific growth-associated protein, is selectively distributed to the axonal domain in developing neurons; it is absent from dendrites and their growth cones. Using immunofluorescence microscopy, we have further examined the distribution of GAP-43 during the development of hippocamp...
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Veröffentlicht in: | The Journal of neuroscience 1990-02, Vol.10 (2), p.588-602 |
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description | GAP-43, a neuron specific growth-associated protein, is selectively distributed to the axonal domain in developing neurons; it is absent from dendrites and their growth cones. Using immunofluorescence microscopy, we have further examined the distribution of GAP-43 during the development of hippocampal neurons in culture, in order to determine when this polarized distribution arises. Cultured hippocampal neurons initially extend several short processes which have the potential to become either axons or dendrites. At this stage, before the morphological expression of polarity, GAP-43 is concentrated in the growth cones of these processes but is distributed more or less equally among them. Polarity becomes established when one of these processes elongates to become the axon. At the earliest stage when the emerging axon can be identified, GAP-43 is preferentially concentrated in its growth cone. During the next few days, as the remaining processes take on dendritic properties, they lose their residual GAP-43 immunoreactivity. Throughout development, GAP-43 remains highly concentrated in the axonal growth cone, but the concentration of GAP-43 in the axon shaft increases, beginning near the growth cone and progressing proximally until GAP-43 is uniformly distributed along the entire axon. At all stages of development, GAP-43 is also concentrated in the region of the Golgi apparatus. These results suggest that the selective sorting of at least one membrane protein into the axon coincides with the morphological expression of polarity. These results also raise the possibility that GAP-43 may play an important role in the early phases of axonal outgrowth, by which the functional polarity of neurons is established. |
doi_str_mv | 10.1523/jneurosci.10-02-00588.1990 |
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Using immunofluorescence microscopy, we have further examined the distribution of GAP-43 during the development of hippocampal neurons in culture, in order to determine when this polarized distribution arises. Cultured hippocampal neurons initially extend several short processes which have the potential to become either axons or dendrites. At this stage, before the morphological expression of polarity, GAP-43 is concentrated in the growth cones of these processes but is distributed more or less equally among them. Polarity becomes established when one of these processes elongates to become the axon. At the earliest stage when the emerging axon can be identified, GAP-43 is preferentially concentrated in its growth cone. During the next few days, as the remaining processes take on dendritic properties, they lose their residual GAP-43 immunoreactivity. Throughout development, GAP-43 remains highly concentrated in the axonal growth cone, but the concentration of GAP-43 in the axon shaft increases, beginning near the growth cone and progressing proximally until GAP-43 is uniformly distributed along the entire axon. At all stages of development, GAP-43 is also concentrated in the region of the Golgi apparatus. These results suggest that the selective sorting of at least one membrane protein into the axon coincides with the morphological expression of polarity. These results also raise the possibility that GAP-43 may play an important role in the early phases of axonal outgrowth, by which the functional polarity of neurons is established.</description><identifier>ISSN: 0270-6474</identifier><identifier>EISSN: 1529-2401</identifier><identifier>DOI: 10.1523/jneurosci.10-02-00588.1990</identifier><identifier>PMID: 2137532</identifier><identifier>CODEN: JNRSDS</identifier><language>eng</language><publisher>Washington, DC: Soc Neuroscience</publisher><subject>Animals ; Axons - metabolism ; Axons - physiology ; Biological and medical sciences ; Cell Survival ; Embryology: invertebrates and vertebrates. Teratology ; Fluorescent Antibody Technique ; Fundamental and applied biological sciences. Psychology ; GAP-43 Protein ; Golgi Apparatus - metabolism ; Growth Substances - metabolism ; Hippocampus - cytology ; Membrane Proteins - metabolism ; Microscopy, Fluorescence ; Molecular embryology ; Nerve Tissue Proteins - metabolism ; Neurons - metabolism ; Neurons - physiology ; Neurons - ultrastructure ; Synapsins ; Tissue Distribution</subject><ispartof>The Journal of neuroscience, 1990-02, Vol.10 (2), p.588-602</ispartof><rights>1991 INIST-CNRS</rights><rights>1990 by Society for Neuroscience 1990</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c635t-2498736443d4dfad9141797a595d37fe39306c5a353be152865ed2e2fc3aa2b73</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6570154/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6570154/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19386381$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2137532$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Goslin, K</creatorcontrib><creatorcontrib>Schreyer, DJ</creatorcontrib><creatorcontrib>Skene, JH</creatorcontrib><creatorcontrib>Banker, G</creatorcontrib><title>Changes in the distribution of GAP-43 during the development of neuronal polarity</title><title>The Journal of neuroscience</title><addtitle>J Neurosci</addtitle><description>GAP-43, a neuron specific growth-associated protein, is selectively distributed to the axonal domain in developing neurons; it is absent from dendrites and their growth cones. Using immunofluorescence microscopy, we have further examined the distribution of GAP-43 during the development of hippocampal neurons in culture, in order to determine when this polarized distribution arises. Cultured hippocampal neurons initially extend several short processes which have the potential to become either axons or dendrites. At this stage, before the morphological expression of polarity, GAP-43 is concentrated in the growth cones of these processes but is distributed more or less equally among them. Polarity becomes established when one of these processes elongates to become the axon. At the earliest stage when the emerging axon can be identified, GAP-43 is preferentially concentrated in its growth cone. During the next few days, as the remaining processes take on dendritic properties, they lose their residual GAP-43 immunoreactivity. Throughout development, GAP-43 remains highly concentrated in the axonal growth cone, but the concentration of GAP-43 in the axon shaft increases, beginning near the growth cone and progressing proximally until GAP-43 is uniformly distributed along the entire axon. At all stages of development, GAP-43 is also concentrated in the region of the Golgi apparatus. These results suggest that the selective sorting of at least one membrane protein into the axon coincides with the morphological expression of polarity. These results also raise the possibility that GAP-43 may play an important role in the early phases of axonal outgrowth, by which the functional polarity of neurons is established.</description><subject>Animals</subject><subject>Axons - metabolism</subject><subject>Axons - physiology</subject><subject>Biological and medical sciences</subject><subject>Cell Survival</subject><subject>Embryology: invertebrates and vertebrates. Teratology</subject><subject>Fluorescent Antibody Technique</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>GAP-43 Protein</subject><subject>Golgi Apparatus - metabolism</subject><subject>Growth Substances - metabolism</subject><subject>Hippocampus - cytology</subject><subject>Membrane Proteins - metabolism</subject><subject>Microscopy, Fluorescence</subject><subject>Molecular embryology</subject><subject>Nerve Tissue Proteins - metabolism</subject><subject>Neurons - metabolism</subject><subject>Neurons - physiology</subject><subject>Neurons - ultrastructure</subject><subject>Synapsins</subject><subject>Tissue Distribution</subject><issn>0270-6474</issn><issn>1529-2401</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkVtv1DAQhS0EKkvhJyBFSPCWxXfHPCBVq9IWVZRbny2v42xcOfZiJ13139fprlp44smS55szZ-YA8A7BJWKYfLwJdkoxG7dEsIa4hpA1zRJJCZ-BRSFkjSlEz8ECYgFrTgV9CV7lfAMhFBCJI3CEERGM4AX4sep12NhcuVCNva1al8fk1tPoYqhiV52dfK8pqdopubDZE_bW-rgdbBhn4MFK0L7aRq-TG-9egxed9tm-ObzH4PrL6e_VeX15dXaxOrmsDSdsLA5lIwinlLS07XQrEUVCCs0ka4noLJEEcsM0YWRty04NZ7bFFneGaI3XghyDz3vd7bQebGuKn6S92iY36HSnonbq30pwvdrEW8VZOQKjReDDQSDFP5PNoxpcNtZ7HWycshKSYw45_i-IGJOE4hn8tAdNSScn2z26QVDNyamv306vf179Wl3MPxCrh-TUnFxpfvv3Po-th6hK_f2hrrPRvks6GJefJkjScNKgJ653m37nklV50N4XVaR2u12Zi1UZSu4BOiixDw</recordid><startdate>19900201</startdate><enddate>19900201</enddate><creator>Goslin, K</creator><creator>Schreyer, DJ</creator><creator>Skene, JH</creator><creator>Banker, G</creator><general>Soc Neuroscience</general><general>Society for Neuroscience</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>19900201</creationdate><title>Changes in the distribution of GAP-43 during the development of neuronal polarity</title><author>Goslin, K ; Schreyer, DJ ; Skene, JH ; Banker, G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c635t-2498736443d4dfad9141797a595d37fe39306c5a353be152865ed2e2fc3aa2b73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>Animals</topic><topic>Axons - metabolism</topic><topic>Axons - physiology</topic><topic>Biological and medical sciences</topic><topic>Cell Survival</topic><topic>Embryology: invertebrates and vertebrates. Teratology</topic><topic>Fluorescent Antibody Technique</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>GAP-43 Protein</topic><topic>Golgi Apparatus - metabolism</topic><topic>Growth Substances - metabolism</topic><topic>Hippocampus - cytology</topic><topic>Membrane Proteins - metabolism</topic><topic>Microscopy, Fluorescence</topic><topic>Molecular embryology</topic><topic>Nerve Tissue Proteins - metabolism</topic><topic>Neurons - metabolism</topic><topic>Neurons - physiology</topic><topic>Neurons - ultrastructure</topic><topic>Synapsins</topic><topic>Tissue Distribution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Goslin, K</creatorcontrib><creatorcontrib>Schreyer, DJ</creatorcontrib><creatorcontrib>Skene, JH</creatorcontrib><creatorcontrib>Banker, G</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Goslin, K</au><au>Schreyer, DJ</au><au>Skene, JH</au><au>Banker, G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Changes in the distribution of GAP-43 during the development of neuronal polarity</atitle><jtitle>The Journal of neuroscience</jtitle><addtitle>J Neurosci</addtitle><date>1990-02-01</date><risdate>1990</risdate><volume>10</volume><issue>2</issue><spage>588</spage><epage>602</epage><pages>588-602</pages><issn>0270-6474</issn><eissn>1529-2401</eissn><coden>JNRSDS</coden><abstract>GAP-43, a neuron specific growth-associated protein, is selectively distributed to the axonal domain in developing neurons; it is absent from dendrites and their growth cones. Using immunofluorescence microscopy, we have further examined the distribution of GAP-43 during the development of hippocampal neurons in culture, in order to determine when this polarized distribution arises. Cultured hippocampal neurons initially extend several short processes which have the potential to become either axons or dendrites. At this stage, before the morphological expression of polarity, GAP-43 is concentrated in the growth cones of these processes but is distributed more or less equally among them. Polarity becomes established when one of these processes elongates to become the axon. At the earliest stage when the emerging axon can be identified, GAP-43 is preferentially concentrated in its growth cone. During the next few days, as the remaining processes take on dendritic properties, they lose their residual GAP-43 immunoreactivity. Throughout development, GAP-43 remains highly concentrated in the axonal growth cone, but the concentration of GAP-43 in the axon shaft increases, beginning near the growth cone and progressing proximally until GAP-43 is uniformly distributed along the entire axon. At all stages of development, GAP-43 is also concentrated in the region of the Golgi apparatus. These results suggest that the selective sorting of at least one membrane protein into the axon coincides with the morphological expression of polarity. These results also raise the possibility that GAP-43 may play an important role in the early phases of axonal outgrowth, by which the functional polarity of neurons is established.</abstract><cop>Washington, DC</cop><pub>Soc Neuroscience</pub><pmid>2137532</pmid><doi>10.1523/jneurosci.10-02-00588.1990</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Axons - metabolism Axons - physiology Biological and medical sciences Cell Survival Embryology: invertebrates and vertebrates. Teratology Fluorescent Antibody Technique Fundamental and applied biological sciences. Psychology GAP-43 Protein Golgi Apparatus - metabolism Growth Substances - metabolism Hippocampus - cytology Membrane Proteins - metabolism Microscopy, Fluorescence Molecular embryology Nerve Tissue Proteins - metabolism Neurons - metabolism Neurons - physiology Neurons - ultrastructure Synapsins Tissue Distribution |
title | Changes in the distribution of GAP-43 during the development of neuronal polarity |
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