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Rat choroid plexuses contain myeloid progenitors capable of differentiation toward macrophage or dendritic cell phenotypes
The interface between the blood and the cerebrospinal fluid (CSF) is formed by the choroid plexuses (CPs), which are specialized structures located within the brain ventricles. They are composed of a vascularized stroma surrounded by a tight epithelium that controls molecular and cellular traffic be...
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Published in: | Glia 2006-08, Vol.54 (3), p.160-171 |
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description | The interface between the blood and the cerebrospinal fluid (CSF) is formed by the choroid plexuses (CPs), which are specialized structures located within the brain ventricles. They are composed of a vascularized stroma surrounded by a tight epithelium that controls molecular and cellular traffic between the blood and the CSF. Cells expressing myeloid markers are present within the choroidal stroma. However, the exact identity, maturation state, and functions of these CP‐associated myeloid cells are not fully clarified. We show here that this cell population contains immature myeloid progenitors displaying a high proliferative potential. Thus, in neonate rats and, to a lesser extent, in adult rats, cultured CP stroma cells form large colonies of macrophages, in response to M‐CSF or GM‐CSF, while, under the same conditions, peripheral blood monocytes do not. In addition, under GM‐CSF treatment, free‐floating colonies of CD11c+ monocytic cells are generated which, when restimulated with GM‐CSF and IL‐4, differentiate into OX62+/MHC class II+ dendritic cells. Interestingly, in CP stroma cultures, myeloid cells are found in close association with fibroblastic‐like cells expressing the neural stem‐cell marker nestin. Similarly, in the developing brain, macrophages and nestin+ fibroblastic cells accumulate in vivo within the choroidal stroma. Taken together, these results suggest that the CP stroma represents a niche for myeloid progenitors and may serve as a reservoir for brain macrophages. © 2006 Wiley‐Liss, Inc. |
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They are composed of a vascularized stroma surrounded by a tight epithelium that controls molecular and cellular traffic between the blood and the CSF. Cells expressing myeloid markers are present within the choroidal stroma. However, the exact identity, maturation state, and functions of these CP‐associated myeloid cells are not fully clarified. We show here that this cell population contains immature myeloid progenitors displaying a high proliferative potential. Thus, in neonate rats and, to a lesser extent, in adult rats, cultured CP stroma cells form large colonies of macrophages, in response to M‐CSF or GM‐CSF, while, under the same conditions, peripheral blood monocytes do not. In addition, under GM‐CSF treatment, free‐floating colonies of CD11c+ monocytic cells are generated which, when restimulated with GM‐CSF and IL‐4, differentiate into OX62+/MHC class II+ dendritic cells. Interestingly, in CP stroma cultures, myeloid cells are found in close association with fibroblastic‐like cells expressing the neural stem‐cell marker nestin. Similarly, in the developing brain, macrophages and nestin+ fibroblastic cells accumulate in vivo within the choroidal stroma. Taken together, these results suggest that the CP stroma represents a niche for myeloid progenitors and may serve as a reservoir for brain macrophages. © 2006 Wiley‐Liss, Inc.</description><identifier>ISSN: 0894-1491</identifier><identifier>EISSN: 1098-1136</identifier><identifier>DOI: 10.1002/glia.20373</identifier><identifier>PMID: 16817190</identifier><identifier>CODEN: GLIAEJ</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animals ; Animals, Newborn ; Biological and medical sciences ; blood-brain barriers ; Bone Marrow Cells ; Bone Marrow Cells - cytology ; Cell Culture Techniques ; Cell Differentiation ; Cell Differentiation - drug effects ; Cell Division ; Cell Division - drug effects ; Cellular Biology ; Cerebral circulation. Blood-brain barrier. Choroid plexus. Cerebrospinal fluid. Circumventricular organ. Meninges ; Choroid Plexus ; Choroid Plexus - cytology ; Dendritic Cells ; Dendritic Cells - cytology ; Flow Cytometry ; Fundamental and applied biological sciences. Psychology ; Granulocyte-Macrophage Colony-Stimulating Factor ; Granulocyte-Macrophage Colony-Stimulating Factor - pharmacology ; Histocompatibility Antigens Class II ; Histocompatibility Antigens Class II - physiology ; Humans ; inflammation ; Interleukin-4 ; Interleukin-4 - pharmacology ; Isolated neuron and nerve. Neuroglia ; Life Sciences ; Macrophages ; Macrophages - cytology ; Macrophages - drug effects ; Mice ; neuroimmunology ; Rats ; Stem Cells ; Stem Cells - cytology ; Stem Cells - drug effects ; Stromal Cells ; Stromal Cells - cytology ; Vertebrates: nervous system and sense organs</subject><ispartof>Glia, 2006-08, Vol.54 (3), p.160-171</ispartof><rights>Copyright © 2006 Wiley‐Liss, Inc.</rights><rights>2006 INIST-CNRS</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5263-37edf706316f2027913fc0dadede174701bdf98dc1bd8bf55acf79151e3186423</citedby><cites>FETCH-LOGICAL-c5263-37edf706316f2027913fc0dadede174701bdf98dc1bd8bf55acf79151e3186423</cites><orcidid>0000-0002-9579-4805</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,777,781,882,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17972409$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16817190$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-00192872$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Nataf, Serge</creatorcontrib><creatorcontrib>Strazielle, Nathalie</creatorcontrib><creatorcontrib>Hatterer, Eric</creatorcontrib><creatorcontrib>Mouchiroud, Guy</creatorcontrib><creatorcontrib>Belin, Marie-Françoise</creatorcontrib><creatorcontrib>Ghersi-Egea, Jean-François</creatorcontrib><title>Rat choroid plexuses contain myeloid progenitors capable of differentiation toward macrophage or dendritic cell phenotypes</title><title>Glia</title><addtitle>Glia</addtitle><description>The interface between the blood and the cerebrospinal fluid (CSF) is formed by the choroid plexuses (CPs), which are specialized structures located within the brain ventricles. They are composed of a vascularized stroma surrounded by a tight epithelium that controls molecular and cellular traffic between the blood and the CSF. Cells expressing myeloid markers are present within the choroidal stroma. However, the exact identity, maturation state, and functions of these CP‐associated myeloid cells are not fully clarified. We show here that this cell population contains immature myeloid progenitors displaying a high proliferative potential. Thus, in neonate rats and, to a lesser extent, in adult rats, cultured CP stroma cells form large colonies of macrophages, in response to M‐CSF or GM‐CSF, while, under the same conditions, peripheral blood monocytes do not. In addition, under GM‐CSF treatment, free‐floating colonies of CD11c+ monocytic cells are generated which, when restimulated with GM‐CSF and IL‐4, differentiate into OX62+/MHC class II+ dendritic cells. Interestingly, in CP stroma cultures, myeloid cells are found in close association with fibroblastic‐like cells expressing the neural stem‐cell marker nestin. Similarly, in the developing brain, macrophages and nestin+ fibroblastic cells accumulate in vivo within the choroidal stroma. Taken together, these results suggest that the CP stroma represents a niche for myeloid progenitors and may serve as a reservoir for brain macrophages. © 2006 Wiley‐Liss, Inc.</description><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Biological and medical sciences</subject><subject>blood-brain barriers</subject><subject>Bone Marrow Cells</subject><subject>Bone Marrow Cells - cytology</subject><subject>Cell Culture Techniques</subject><subject>Cell Differentiation</subject><subject>Cell Differentiation - drug effects</subject><subject>Cell Division</subject><subject>Cell Division - drug effects</subject><subject>Cellular Biology</subject><subject>Cerebral circulation. Blood-brain barrier. Choroid plexus. Cerebrospinal fluid. Circumventricular organ. Meninges</subject><subject>Choroid Plexus</subject><subject>Choroid Plexus - cytology</subject><subject>Dendritic Cells</subject><subject>Dendritic Cells - cytology</subject><subject>Flow Cytometry</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Granulocyte-Macrophage Colony-Stimulating Factor</subject><subject>Granulocyte-Macrophage Colony-Stimulating Factor - pharmacology</subject><subject>Histocompatibility Antigens Class II</subject><subject>Histocompatibility Antigens Class II - physiology</subject><subject>Humans</subject><subject>inflammation</subject><subject>Interleukin-4</subject><subject>Interleukin-4 - pharmacology</subject><subject>Isolated neuron and nerve. Neuroglia</subject><subject>Life Sciences</subject><subject>Macrophages</subject><subject>Macrophages - cytology</subject><subject>Macrophages - drug effects</subject><subject>Mice</subject><subject>neuroimmunology</subject><subject>Rats</subject><subject>Stem Cells</subject><subject>Stem Cells - cytology</subject><subject>Stem Cells - drug effects</subject><subject>Stromal Cells</subject><subject>Stromal Cells - cytology</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0894-1491</issn><issn>1098-1136</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNqF0UGPEyEUB_CJ0bh19eIHMFw00WRWHszAzLFutF3TrIlZ45FQeLTodJiFqbv100u3dfemJwL84D34F8VLoGdAKXu_6rw-Y5RL_qiYAG2bEoCLx8WENm1VQtXCSfEspR-UQp7Ip8UJiAYktHRS_P6qR2LWIQZvydDh7TZhIib0o_Y92eywu9uIYYW9H0PMe3rQyw5JcMR65zBiP3o9-tCTMdzoaMlGmxiGtV5lFInF3kY_ekMMdh0Z1tiHcTdgel48cbpL-OI4nhbfPn28Op-Xiy-zi_PpojQ1E7zkEq2TVHAQjlEmW-DOUKstWgRZSQpL69rGmjw2S1fX2riMakAOjagYPy3eHu5d604N0W903KmgvZpPF2q_lv-lZY1kvyDbNwebX3y9xTSqjU_7vnWPYZuUaKQQUlT_hdByAQ2rM3x3gPlPUoro7lsAqvbxqX186i6-jF8db90uN2gf6DGvDF4fgU5Gdy7q3vj04GQrWUXb7ODgbnyHu3-UVLPFxfRv8fJwxqcRb-_P6PhTCcllrb5fzhT9PKvnH9iluuJ_ANQswrk</recordid><startdate>20060815</startdate><enddate>20060815</enddate><creator>Nataf, Serge</creator><creator>Strazielle, Nathalie</creator><creator>Hatterer, Eric</creator><creator>Mouchiroud, Guy</creator><creator>Belin, Marie-Françoise</creator><creator>Ghersi-Egea, Jean-François</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><general>Wiley</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><scope>1XC</scope><orcidid>https://orcid.org/0000-0002-9579-4805</orcidid></search><sort><creationdate>20060815</creationdate><title>Rat choroid plexuses contain myeloid progenitors capable of differentiation toward macrophage or dendritic cell phenotypes</title><author>Nataf, Serge ; Strazielle, Nathalie ; Hatterer, Eric ; Mouchiroud, Guy ; Belin, Marie-Françoise ; Ghersi-Egea, Jean-François</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5263-37edf706316f2027913fc0dadede174701bdf98dc1bd8bf55acf79151e3186423</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Biological and medical sciences</topic><topic>blood-brain barriers</topic><topic>Bone Marrow Cells</topic><topic>Bone Marrow Cells - cytology</topic><topic>Cell Culture Techniques</topic><topic>Cell Differentiation</topic><topic>Cell Differentiation - drug effects</topic><topic>Cell Division</topic><topic>Cell Division - drug effects</topic><topic>Cellular Biology</topic><topic>Cerebral circulation. Blood-brain barrier. Choroid plexus. Cerebrospinal fluid. Circumventricular organ. Meninges</topic><topic>Choroid Plexus</topic><topic>Choroid Plexus - cytology</topic><topic>Dendritic Cells</topic><topic>Dendritic Cells - cytology</topic><topic>Flow Cytometry</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Granulocyte-Macrophage Colony-Stimulating Factor</topic><topic>Granulocyte-Macrophage Colony-Stimulating Factor - pharmacology</topic><topic>Histocompatibility Antigens Class II</topic><topic>Histocompatibility Antigens Class II - physiology</topic><topic>Humans</topic><topic>inflammation</topic><topic>Interleukin-4</topic><topic>Interleukin-4 - pharmacology</topic><topic>Isolated neuron and nerve. Neuroglia</topic><topic>Life Sciences</topic><topic>Macrophages</topic><topic>Macrophages - cytology</topic><topic>Macrophages - drug effects</topic><topic>Mice</topic><topic>neuroimmunology</topic><topic>Rats</topic><topic>Stem Cells</topic><topic>Stem Cells - cytology</topic><topic>Stem Cells - drug effects</topic><topic>Stromal Cells</topic><topic>Stromal Cells - cytology</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nataf, Serge</creatorcontrib><creatorcontrib>Strazielle, Nathalie</creatorcontrib><creatorcontrib>Hatterer, Eric</creatorcontrib><creatorcontrib>Mouchiroud, Guy</creatorcontrib><creatorcontrib>Belin, Marie-Françoise</creatorcontrib><creatorcontrib>Ghersi-Egea, Jean-François</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><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Glia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nataf, Serge</au><au>Strazielle, Nathalie</au><au>Hatterer, Eric</au><au>Mouchiroud, Guy</au><au>Belin, Marie-Françoise</au><au>Ghersi-Egea, Jean-François</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rat choroid plexuses contain myeloid progenitors capable of differentiation toward macrophage or dendritic cell phenotypes</atitle><jtitle>Glia</jtitle><addtitle>Glia</addtitle><date>2006-08-15</date><risdate>2006</risdate><volume>54</volume><issue>3</issue><spage>160</spage><epage>171</epage><pages>160-171</pages><issn>0894-1491</issn><eissn>1098-1136</eissn><coden>GLIAEJ</coden><abstract>The interface between the blood and the cerebrospinal fluid (CSF) is formed by the choroid plexuses (CPs), which are specialized structures located within the brain ventricles. They are composed of a vascularized stroma surrounded by a tight epithelium that controls molecular and cellular traffic between the blood and the CSF. Cells expressing myeloid markers are present within the choroidal stroma. However, the exact identity, maturation state, and functions of these CP‐associated myeloid cells are not fully clarified. We show here that this cell population contains immature myeloid progenitors displaying a high proliferative potential. Thus, in neonate rats and, to a lesser extent, in adult rats, cultured CP stroma cells form large colonies of macrophages, in response to M‐CSF or GM‐CSF, while, under the same conditions, peripheral blood monocytes do not. In addition, under GM‐CSF treatment, free‐floating colonies of CD11c+ monocytic cells are generated which, when restimulated with GM‐CSF and IL‐4, differentiate into OX62+/MHC class II+ dendritic cells. Interestingly, in CP stroma cultures, myeloid cells are found in close association with fibroblastic‐like cells expressing the neural stem‐cell marker nestin. Similarly, in the developing brain, macrophages and nestin+ fibroblastic cells accumulate in vivo within the choroidal stroma. Taken together, these results suggest that the CP stroma represents a niche for myeloid progenitors and may serve as a reservoir for brain macrophages. © 2006 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>16817190</pmid><doi>10.1002/glia.20373</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-9579-4805</orcidid></addata></record> |
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subjects | Animals Animals, Newborn Biological and medical sciences blood-brain barriers Bone Marrow Cells Bone Marrow Cells - cytology Cell Culture Techniques Cell Differentiation Cell Differentiation - drug effects Cell Division Cell Division - drug effects Cellular Biology Cerebral circulation. Blood-brain barrier. Choroid plexus. Cerebrospinal fluid. Circumventricular organ. Meninges Choroid Plexus Choroid Plexus - cytology Dendritic Cells Dendritic Cells - cytology Flow Cytometry Fundamental and applied biological sciences. Psychology Granulocyte-Macrophage Colony-Stimulating Factor Granulocyte-Macrophage Colony-Stimulating Factor - pharmacology Histocompatibility Antigens Class II Histocompatibility Antigens Class II - physiology Humans inflammation Interleukin-4 Interleukin-4 - pharmacology Isolated neuron and nerve. Neuroglia Life Sciences Macrophages Macrophages - cytology Macrophages - drug effects Mice neuroimmunology Rats Stem Cells Stem Cells - cytology Stem Cells - drug effects Stromal Cells Stromal Cells - cytology Vertebrates: nervous system and sense organs |
title | Rat choroid plexuses contain myeloid progenitors capable of differentiation toward macrophage or dendritic cell phenotypes |
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