Identification of CSF-1 as a brain macrophage migratory activity produced by astrocytes
Intraparenchymal migration of macrophages occurs in the CNS during development or as a consequence of tissue injuries. In the present study, we have shown, by using an in vitro chemotaxis assay, that cultured rat astrocytes obtained from the developing cerebral cortex and striatum produce soluble fa...
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Veröffentlicht in: | Glia 1998-10, Vol.24 (2), p.180-186 |
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description | Intraparenchymal migration of macrophages occurs in the CNS during development or as a consequence of tissue injuries. In the present study, we have shown, by using an in vitro chemotaxis assay, that cultured rat astrocytes obtained from the developing cerebral cortex and striatum produce soluble factors, which attract purified brain macrophages. The effect of astrocyte‐derived factors on macrophages was strongly reduced in the presence of antibodies neutralizing colony‐stimulating factor 1 (CSF‐1, also called M‐CSF), and recombinant CSF‐1 was found to act as a chemotactic agent on brain macrophages. Synthesis of CSF‐1 by cultured astrocytes was confirmed by northern detection of CSF‐1 transcripts. In contrast, the CSF‐1 gene was not expressed by cultured neurons from the cerebral cortex and striatum or by the brain macrophage population responsive to CSF‐1 gradient. ELISA detection of CSF‐1 in tissue extracts revealed the occurrence of this cytokine in the rat cerebral cortex during postnatal development and in adults. Altogether, our results demonstrate that astrocytes, through CSF‐1 secretion, can trigger the polarized migration of brain macrophages and suggest a new mechanism which could regulate the locomotion of these cells in the cerebral cortex during ontogenesis or following lesions. GLIA 24:180–186, 1998. © 1998 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/(SICI)1098-1136(199810)24:2<180::AID-GLIA3>3.0.CO;2-8 |
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In the present study, we have shown, by using an in vitro chemotaxis assay, that cultured rat astrocytes obtained from the developing cerebral cortex and striatum produce soluble factors, which attract purified brain macrophages. The effect of astrocyte‐derived factors on macrophages was strongly reduced in the presence of antibodies neutralizing colony‐stimulating factor 1 (CSF‐1, also called M‐CSF), and recombinant CSF‐1 was found to act as a chemotactic agent on brain macrophages. Synthesis of CSF‐1 by cultured astrocytes was confirmed by northern detection of CSF‐1 transcripts. In contrast, the CSF‐1 gene was not expressed by cultured neurons from the cerebral cortex and striatum or by the brain macrophage population responsive to CSF‐1 gradient. ELISA detection of CSF‐1 in tissue extracts revealed the occurrence of this cytokine in the rat cerebral cortex during postnatal development and in adults. Altogether, our results demonstrate that astrocytes, through CSF‐1 secretion, can trigger the polarized migration of brain macrophages and suggest a new mechanism which could regulate the locomotion of these cells in the cerebral cortex during ontogenesis or following lesions. 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Neuroglia ; Macrophage Colony-Stimulating Factor - biosynthesis ; Macrophage Colony-Stimulating Factor - physiology ; Macrophages - metabolism ; microglia ; Neurons - metabolism ; Rats ; Vertebrates: nervous system and sense organs</subject><ispartof>Glia, 1998-10, Vol.24 (2), p.180-186</ispartof><rights>Copyright © 1998 Wiley‐Liss, Inc.</rights><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4613-6fab55c1f29991c83b87d3f2a269a6d447c251f7e1daa5aaa8467757eb3794753</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%28199810%2924%3A2%3C180%3A%3AAID-GLIA3%3E3.0.CO%3B2-8$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2F%28SICI%291098-1136%28199810%2924%3A2%3C180%3A%3AAID-GLIA3%3E3.0.CO%3B2-8$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2403456$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9728764$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Calvo, Charles-Félix</creatorcontrib><creatorcontrib>Dobbertin, Alexandre</creatorcontrib><creatorcontrib>Gelman, Michèle</creatorcontrib><creatorcontrib>Glowinski, Jacques</creatorcontrib><creatorcontrib>Mallat, Michel</creatorcontrib><title>Identification of CSF-1 as a brain macrophage migratory activity produced by astrocytes</title><title>Glia</title><addtitle>Glia</addtitle><description>Intraparenchymal migration of macrophages occurs in the CNS during development or as a consequence of tissue injuries. In the present study, we have shown, by using an in vitro chemotaxis assay, that cultured rat astrocytes obtained from the developing cerebral cortex and striatum produce soluble factors, which attract purified brain macrophages. The effect of astrocyte‐derived factors on macrophages was strongly reduced in the presence of antibodies neutralizing colony‐stimulating factor 1 (CSF‐1, also called M‐CSF), and recombinant CSF‐1 was found to act as a chemotactic agent on brain macrophages. Synthesis of CSF‐1 by cultured astrocytes was confirmed by northern detection of CSF‐1 transcripts. In contrast, the CSF‐1 gene was not expressed by cultured neurons from the cerebral cortex and striatum or by the brain macrophage population responsive to CSF‐1 gradient. ELISA detection of CSF‐1 in tissue extracts revealed the occurrence of this cytokine in the rat cerebral cortex during postnatal development and in adults. Altogether, our results demonstrate that astrocytes, through CSF‐1 secretion, can trigger the polarized migration of brain macrophages and suggest a new mechanism which could regulate the locomotion of these cells in the cerebral cortex during ontogenesis or following lesions. GLIA 24:180–186, 1998. © 1998 Wiley‐Liss, Inc.</description><subject>Animals</subject><subject>Astrocytes - metabolism</subject><subject>Biological and medical sciences</subject><subject>Blotting, Northern</subject><subject>Brain - cytology</subject><subject>Brain Chemistry - physiology</subject><subject>Cell Division - physiology</subject><subject>Cell Movement - physiology</subject><subject>Cell Survival - physiology</subject><subject>Cells, Cultured</subject><subject>chemoattraction</subject><subject>Chemotaxis, Leukocyte - physiology</subject><subject>cytokine</subject><subject>Cytokines - biosynthesis</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Isolated neuron and nerve. Neuroglia</subject><subject>Macrophage Colony-Stimulating Factor - biosynthesis</subject><subject>Macrophage Colony-Stimulating Factor - physiology</subject><subject>Macrophages - metabolism</subject><subject>microglia</subject><subject>Neurons - metabolism</subject><subject>Rats</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0894-1491</issn><issn>1098-1136</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUuP0zAUhSMEGoaBn4CUBUIzixS_EtvlIbUpU4Iquhigy6sbxxk8tE2xU6D_HpdW3YA0K8vnHh8d3y9J3lIyoISwV5c3VVldUaJVRikvLqnWipIrJobsDVVkOBxVk2w6q0b8HR-QQTl_zTL1IDk_vXiYnBOlRUaFpo-TJyHcEULjRZ4lZ1oyJQtxniyqxq571zqDvevWadem5c11RlMMKaa1R7dOV2h8t_mGtzZduVuPfed3KZre_XT9Lt34rtka26R1FEPvO7PrbXiaPGpxGeyz43mRfLl-_7n8kM3m06oczTIjCsqzosU6zw1tmdaaGsVrJRveMmSFxqIRQhqW01Za2iDmiKhEIWUubc2lFjLnF8nLQ26s8WNrQw8rF4xdLnFtu20AyZUuCNf3GqlkUueE8lPT-OkQvG1h490K_Q4ogT0ZgD0Z2O8Z9nuGAxlgAhhEMgCRDPwlAxwIlPOoq5j7_FhgW69sc0o9oojzF8c5BoPL1uPauHCyMUG4yIto-3qw_XJLu_un2z3V_tfsIMTg7BDsQm9_n4LRf4dCcpnD4tMUyGI8nk7GH2HC_wBaxsPM</recordid><startdate>199810</startdate><enddate>199810</enddate><creator>Calvo, Charles-Félix</creator><creator>Dobbertin, Alexandre</creator><creator>Gelman, Michèle</creator><creator>Glowinski, Jacques</creator><creator>Mallat, Michel</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>199810</creationdate><title>Identification of CSF-1 as a brain macrophage migratory activity produced by astrocytes</title><author>Calvo, Charles-Félix ; Dobbertin, Alexandre ; Gelman, Michèle ; Glowinski, Jacques ; Mallat, Michel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4613-6fab55c1f29991c83b87d3f2a269a6d447c251f7e1daa5aaa8467757eb3794753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>Astrocytes - metabolism</topic><topic>Biological and medical sciences</topic><topic>Blotting, Northern</topic><topic>Brain - cytology</topic><topic>Brain Chemistry - physiology</topic><topic>Cell Division - physiology</topic><topic>Cell Movement - physiology</topic><topic>Cell Survival - physiology</topic><topic>Cells, Cultured</topic><topic>chemoattraction</topic><topic>Chemotaxis, Leukocyte - physiology</topic><topic>cytokine</topic><topic>Cytokines - biosynthesis</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Isolated neuron and nerve. Neuroglia</topic><topic>Macrophage Colony-Stimulating Factor - biosynthesis</topic><topic>Macrophage Colony-Stimulating Factor - physiology</topic><topic>Macrophages - metabolism</topic><topic>microglia</topic><topic>Neurons - metabolism</topic><topic>Rats</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Calvo, Charles-Félix</creatorcontrib><creatorcontrib>Dobbertin, Alexandre</creatorcontrib><creatorcontrib>Gelman, Michèle</creatorcontrib><creatorcontrib>Glowinski, Jacques</creatorcontrib><creatorcontrib>Mallat, Michel</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>Calvo, Charles-Félix</au><au>Dobbertin, Alexandre</au><au>Gelman, Michèle</au><au>Glowinski, Jacques</au><au>Mallat, Michel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of CSF-1 as a brain macrophage migratory activity produced by astrocytes</atitle><jtitle>Glia</jtitle><addtitle>Glia</addtitle><date>1998-10</date><risdate>1998</risdate><volume>24</volume><issue>2</issue><spage>180</spage><epage>186</epage><pages>180-186</pages><issn>0894-1491</issn><eissn>1098-1136</eissn><coden>GLIAEJ</coden><abstract>Intraparenchymal migration of macrophages occurs in the CNS during development or as a consequence of tissue injuries. In the present study, we have shown, by using an in vitro chemotaxis assay, that cultured rat astrocytes obtained from the developing cerebral cortex and striatum produce soluble factors, which attract purified brain macrophages. The effect of astrocyte‐derived factors on macrophages was strongly reduced in the presence of antibodies neutralizing colony‐stimulating factor 1 (CSF‐1, also called M‐CSF), and recombinant CSF‐1 was found to act as a chemotactic agent on brain macrophages. Synthesis of CSF‐1 by cultured astrocytes was confirmed by northern detection of CSF‐1 transcripts. In contrast, the CSF‐1 gene was not expressed by cultured neurons from the cerebral cortex and striatum or by the brain macrophage population responsive to CSF‐1 gradient. ELISA detection of CSF‐1 in tissue extracts revealed the occurrence of this cytokine in the rat cerebral cortex during postnatal development and in adults. Altogether, our results demonstrate that astrocytes, through CSF‐1 secretion, can trigger the polarized migration of brain macrophages and suggest a new mechanism which could regulate the locomotion of these cells in the cerebral cortex during ontogenesis or following lesions. GLIA 24:180–186, 1998. © 1998 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><pmid>9728764</pmid><doi>10.1002/(SICI)1098-1136(199810)24:2<180::AID-GLIA3>3.0.CO;2-8</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Astrocytes - metabolism Biological and medical sciences Blotting, Northern Brain - cytology Brain Chemistry - physiology Cell Division - physiology Cell Movement - physiology Cell Survival - physiology Cells, Cultured chemoattraction Chemotaxis, Leukocyte - physiology cytokine Cytokines - biosynthesis Enzyme-Linked Immunosorbent Assay Fundamental and applied biological sciences. Psychology Humans Isolated neuron and nerve. Neuroglia Macrophage Colony-Stimulating Factor - biosynthesis Macrophage Colony-Stimulating Factor - physiology Macrophages - metabolism microglia Neurons - metabolism Rats Vertebrates: nervous system and sense organs |
title | Identification of CSF-1 as a brain macrophage migratory activity produced by astrocytes |
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