A role for the cytoskeleton-associated protein palladin in neurite outgrowth
The outgrowth of neurites is a critical step in neuronal maturation, and it is well established that the actin cytoskeleton is involved in this process. Investigators from our laboratory recently described a novel protein named palladin, which has been shown to play an essential role in organizing t...
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Veröffentlicht in: | Molecular biology of the cell 2001-09, Vol.12 (9), p.2721-2729 |
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creator | Boukhelifa, M Parast, M M Valtschanoff, J G LaMantia, A S Meeker, R B Otey, C A |
description | The outgrowth of neurites is a critical step in neuronal maturation, and it is well established that the actin cytoskeleton is involved in this process. Investigators from our laboratory recently described a novel protein named palladin, which has been shown to play an essential role in organizing the actin cytoskeleton in cultured fibroblasts. We investigated the expression of palladin in the developing rat brain by Western blot and found that the E18 brain contained a unique variant of palladin that is significantly smaller (approximately 85 kDa) than the common form found in other developing tissues (90-92 kDa). Because the expression of a tissue-specific isoform suggests the possibility of a cell type-specific function, we investigated the localization and function of palladin in cultured cortical neurons. Palladin was found preferentially targeted to the developing axon but not the dendrites and was strongly localized to the axonal growth cone. When palladin expression was attenuated by transfection with antisense constructs in both the B35 neuroblastoma cell line and in primary cortical neurons, a reduction in the expression of palladin resulted in a failure of neurite outgrowth. These results implicate palladin as a critical component of the developing nervous system, with an important role in axonal extension. |
doi_str_mv | 10.1091/mbc.12.9.2721 |
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Investigators from our laboratory recently described a novel protein named palladin, which has been shown to play an essential role in organizing the actin cytoskeleton in cultured fibroblasts. We investigated the expression of palladin in the developing rat brain by Western blot and found that the E18 brain contained a unique variant of palladin that is significantly smaller (approximately 85 kDa) than the common form found in other developing tissues (90-92 kDa). Because the expression of a tissue-specific isoform suggests the possibility of a cell type-specific function, we investigated the localization and function of palladin in cultured cortical neurons. Palladin was found preferentially targeted to the developing axon but not the dendrites and was strongly localized to the axonal growth cone. When palladin expression was attenuated by transfection with antisense constructs in both the B35 neuroblastoma cell line and in primary cortical neurons, a reduction in the expression of palladin resulted in a failure of neurite outgrowth. These results implicate palladin as a critical component of the developing nervous system, with an important role in axonal extension.</description><identifier>ISSN: 1059-1524</identifier><identifier>EISSN: 1939-4586</identifier><identifier>DOI: 10.1091/mbc.12.9.2721</identifier><identifier>PMID: 11553711</identifier><language>eng</language><publisher>United States: The American Society for Cell Biology</publisher><subject>Actins - metabolism ; Animals ; Brain - cytology ; Brain - embryology ; Cell Differentiation ; Cell Size ; Cells, Cultured ; Cytoskeletal Proteins - antagonists & inhibitors ; Cytoskeletal Proteins - metabolism ; Cytoskeleton - metabolism ; Microscopy, Fluorescence ; Neurites - metabolism ; Phosphoproteins - antagonists & inhibitors ; Phosphoproteins - metabolism ; Rats ; Tumor Cells, Cultured</subject><ispartof>Molecular biology of the cell, 2001-09, Vol.12 (9), p.2721-2729</ispartof><rights>Copyright © 2001, The American Society for Cell Biology 2001</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c478t-7c3c9e47c0f6d827ecdcc7a902d77123318e90f3dbaa18603c828f876af8841c3</citedby><cites>FETCH-LOGICAL-c478t-7c3c9e47c0f6d827ecdcc7a902d77123318e90f3dbaa18603c828f876af8841c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC59707/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC59707/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11553711$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Drubin, David</contributor><creatorcontrib>Boukhelifa, M</creatorcontrib><creatorcontrib>Parast, M M</creatorcontrib><creatorcontrib>Valtschanoff, J G</creatorcontrib><creatorcontrib>LaMantia, A S</creatorcontrib><creatorcontrib>Meeker, R B</creatorcontrib><creatorcontrib>Otey, C A</creatorcontrib><title>A role for the cytoskeleton-associated protein palladin in neurite outgrowth</title><title>Molecular biology of the cell</title><addtitle>Mol Biol Cell</addtitle><description>The outgrowth of neurites is a critical step in neuronal maturation, and it is well established that the actin cytoskeleton is involved in this process. Investigators from our laboratory recently described a novel protein named palladin, which has been shown to play an essential role in organizing the actin cytoskeleton in cultured fibroblasts. We investigated the expression of palladin in the developing rat brain by Western blot and found that the E18 brain contained a unique variant of palladin that is significantly smaller (approximately 85 kDa) than the common form found in other developing tissues (90-92 kDa). Because the expression of a tissue-specific isoform suggests the possibility of a cell type-specific function, we investigated the localization and function of palladin in cultured cortical neurons. Palladin was found preferentially targeted to the developing axon but not the dendrites and was strongly localized to the axonal growth cone. When palladin expression was attenuated by transfection with antisense constructs in both the B35 neuroblastoma cell line and in primary cortical neurons, a reduction in the expression of palladin resulted in a failure of neurite outgrowth. These results implicate palladin as a critical component of the developing nervous system, with an important role in axonal extension.</description><subject>Actins - metabolism</subject><subject>Animals</subject><subject>Brain - cytology</subject><subject>Brain - embryology</subject><subject>Cell Differentiation</subject><subject>Cell Size</subject><subject>Cells, Cultured</subject><subject>Cytoskeletal Proteins - antagonists & inhibitors</subject><subject>Cytoskeletal Proteins - metabolism</subject><subject>Cytoskeleton - metabolism</subject><subject>Microscopy, Fluorescence</subject><subject>Neurites - metabolism</subject><subject>Phosphoproteins - antagonists & inhibitors</subject><subject>Phosphoproteins - metabolism</subject><subject>Rats</subject><subject>Tumor Cells, Cultured</subject><issn>1059-1524</issn><issn>1939-4586</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkMtLAzEQxoMoWqtHr7Inb1szye4mAS9SfEHBi55Dmp1tV7ebmmSV_vemtPiAgRmY75vHj5ALoBOgCq5XczsBNlETJhgckBEorvKilNVhqmmpcihZcUJOQ3ijFIqiEsfkBKAsuQAYkdlt5l2HWeN8FpeY2U104R07jK7PTQjOtiZina29i9j22dp0nalTkaLHwbcRMzfEhXdfcXlGjhrTBTzf5zF5vb97mT7ms-eHp-ntLLeFkDEXlluFhbC0qWrJBNraWmEUZbUQwDgHiYo2vJ4bA7Ki3EomGykq00hZgOVjcrObux7mK6wt9tGbTq99uzJ-o51p9f9O3y71wn3qUgkqkv1qb_fuY8AQ9aoNFtNjPboh6ARGgCghCfOd0HoXgsfmZwVQvaWvE30NTCu9pZ_0l3_v-lXvcfNvwkiC8A</recordid><startdate>20010901</startdate><enddate>20010901</enddate><creator>Boukhelifa, M</creator><creator>Parast, M M</creator><creator>Valtschanoff, J G</creator><creator>LaMantia, A S</creator><creator>Meeker, R B</creator><creator>Otey, C A</creator><general>The American Society for Cell Biology</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>20010901</creationdate><title>A role for the cytoskeleton-associated protein palladin in neurite outgrowth</title><author>Boukhelifa, M ; Parast, M M ; Valtschanoff, J G ; LaMantia, A S ; Meeker, R B ; Otey, C A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c478t-7c3c9e47c0f6d827ecdcc7a902d77123318e90f3dbaa18603c828f876af8841c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Actins - metabolism</topic><topic>Animals</topic><topic>Brain - cytology</topic><topic>Brain - embryology</topic><topic>Cell Differentiation</topic><topic>Cell Size</topic><topic>Cells, Cultured</topic><topic>Cytoskeletal Proteins - antagonists & inhibitors</topic><topic>Cytoskeletal Proteins - metabolism</topic><topic>Cytoskeleton - metabolism</topic><topic>Microscopy, Fluorescence</topic><topic>Neurites - metabolism</topic><topic>Phosphoproteins - antagonists & inhibitors</topic><topic>Phosphoproteins - metabolism</topic><topic>Rats</topic><topic>Tumor Cells, Cultured</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Boukhelifa, M</creatorcontrib><creatorcontrib>Parast, M M</creatorcontrib><creatorcontrib>Valtschanoff, J G</creatorcontrib><creatorcontrib>LaMantia, A S</creatorcontrib><creatorcontrib>Meeker, R B</creatorcontrib><creatorcontrib>Otey, C A</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>Molecular biology of the cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Boukhelifa, M</au><au>Parast, M M</au><au>Valtschanoff, J G</au><au>LaMantia, A S</au><au>Meeker, R B</au><au>Otey, C A</au><au>Drubin, David</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A role for the cytoskeleton-associated protein palladin in neurite outgrowth</atitle><jtitle>Molecular biology of the cell</jtitle><addtitle>Mol Biol Cell</addtitle><date>2001-09-01</date><risdate>2001</risdate><volume>12</volume><issue>9</issue><spage>2721</spage><epage>2729</epage><pages>2721-2729</pages><issn>1059-1524</issn><eissn>1939-4586</eissn><abstract>The outgrowth of neurites is a critical step in neuronal maturation, and it is well established that the actin cytoskeleton is involved in this process. Investigators from our laboratory recently described a novel protein named palladin, which has been shown to play an essential role in organizing the actin cytoskeleton in cultured fibroblasts. We investigated the expression of palladin in the developing rat brain by Western blot and found that the E18 brain contained a unique variant of palladin that is significantly smaller (approximately 85 kDa) than the common form found in other developing tissues (90-92 kDa). Because the expression of a tissue-specific isoform suggests the possibility of a cell type-specific function, we investigated the localization and function of palladin in cultured cortical neurons. Palladin was found preferentially targeted to the developing axon but not the dendrites and was strongly localized to the axonal growth cone. 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subjects | Actins - metabolism Animals Brain - cytology Brain - embryology Cell Differentiation Cell Size Cells, Cultured Cytoskeletal Proteins - antagonists & inhibitors Cytoskeletal Proteins - metabolism Cytoskeleton - metabolism Microscopy, Fluorescence Neurites - metabolism Phosphoproteins - antagonists & inhibitors Phosphoproteins - metabolism Rats Tumor Cells, Cultured |
title | A role for the cytoskeleton-associated protein palladin in neurite outgrowth |
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