Microglia in the human fetal spinal cord—patterns of distribution, morphology and phenotype
Microglia, the intrinsic macrophages of the nervous system, colonise the cerebrum around the second trimester in man. In order to determine the extent of microglial influx into the nervous system, we have examined their distribution within the human fetal spinal cord in relation to astrocytic and va...
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Veröffentlicht in: | Brain research. Developmental brain research 1999-06, Vol.115 (1), p.71-81 |
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description | Microglia, the intrinsic macrophages of the nervous system, colonise the cerebrum around the second trimester in man. In order to determine the extent of microglial influx into the nervous system, we have examined their distribution within the human fetal spinal cord in relation to astrocytic and vascular development between 9 and 16 weeks of gestation, using conventional immunohistochemistry [CD11b; CD45; CD64; CD68; ICAM-1; ICAM-2; VCAM-1; PECAM; GFAP; vimentin] and lectin histochemistry [RCA-1]. Microglia are identifiable by 9 weeks, within the ventricular/sub-ventricular zones. Human fetal microglia display heterogeneity in phenotype and are more readily identified by CD68 in the spinal cord. There is a marked influx of cells dorsal and ventral to the neural cavity, from the marginal layer [meninges/connective tissue] with advancing gestational age, with greatest cell densities towards the end of the time period in this study. This inward migration is associated with progressive vascularisation, ICAM-2 expression and co-localises with GFAP and vimentin positive radial glia. The patterns of microglial migration in human fetal cord differ from that within the cerebrum, but generally conform to a route following white to gray matter. |
doi_str_mv | 10.1016/S0165-3806(99)00043-7 |
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In order to determine the extent of microglial influx into the nervous system, we have examined their distribution within the human fetal spinal cord in relation to astrocytic and vascular development between 9 and 16 weeks of gestation, using conventional immunohistochemistry [CD11b; CD45; CD64; CD68; ICAM-1; ICAM-2; VCAM-1; PECAM; GFAP; vimentin] and lectin histochemistry [RCA-1]. Microglia are identifiable by 9 weeks, within the ventricular/sub-ventricular zones. Human fetal microglia display heterogeneity in phenotype and are more readily identified by CD68 in the spinal cord. There is a marked influx of cells dorsal and ventral to the neural cavity, from the marginal layer [meninges/connective tissue] with advancing gestational age, with greatest cell densities towards the end of the time period in this study. This inward migration is associated with progressive vascularisation, ICAM-2 expression and co-localises with GFAP and vimentin positive radial glia. The patterns of microglial migration in human fetal cord differ from that within the cerebrum, but generally conform to a route following white to gray matter.</description><identifier>ISSN: 0165-3806</identifier><identifier>DOI: 10.1016/S0165-3806(99)00043-7</identifier><identifier>PMID: 10366704</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Blood vessel ; CD68 ; Colonisation ; Fetus - ultrastructure ; Gestational Age ; Human fetal ; Humans ; ICAM-2 ; Immunohistochemistry ; Microglia ; Microglia - ultrastructure ; PECAM ; Phenotype ; Spinal cord ; Spinal Cord - cytology ; Spinal Cord - embryology</subject><ispartof>Brain research. Developmental brain research, 1999-06, Vol.115 (1), p.71-81</ispartof><rights>1999 Elsevier Science B.V.</rights><rights>Copyright 1999 Elsevier Science B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c444t-a62d3e1a6ede01f08d5be44ca51d4bdedf1157a77f523e24572ba45fc0e669a23</citedby><cites>FETCH-LOGICAL-c444t-a62d3e1a6ede01f08d5be44ca51d4bdedf1157a77f523e24572ba45fc0e669a23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10366704$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rezaie, P</creatorcontrib><creatorcontrib>Patel, K</creatorcontrib><creatorcontrib>Male, D.K</creatorcontrib><title>Microglia in the human fetal spinal cord—patterns of distribution, morphology and phenotype</title><title>Brain research. Developmental brain research</title><addtitle>Brain Res Dev Brain Res</addtitle><description>Microglia, the intrinsic macrophages of the nervous system, colonise the cerebrum around the second trimester in man. In order to determine the extent of microglial influx into the nervous system, we have examined their distribution within the human fetal spinal cord in relation to astrocytic and vascular development between 9 and 16 weeks of gestation, using conventional immunohistochemistry [CD11b; CD45; CD64; CD68; ICAM-1; ICAM-2; VCAM-1; PECAM; GFAP; vimentin] and lectin histochemistry [RCA-1]. Microglia are identifiable by 9 weeks, within the ventricular/sub-ventricular zones. Human fetal microglia display heterogeneity in phenotype and are more readily identified by CD68 in the spinal cord. There is a marked influx of cells dorsal and ventral to the neural cavity, from the marginal layer [meninges/connective tissue] with advancing gestational age, with greatest cell densities towards the end of the time period in this study. This inward migration is associated with progressive vascularisation, ICAM-2 expression and co-localises with GFAP and vimentin positive radial glia. The patterns of microglial migration in human fetal cord differ from that within the cerebrum, but generally conform to a route following white to gray matter.</description><subject>Blood vessel</subject><subject>CD68</subject><subject>Colonisation</subject><subject>Fetus - ultrastructure</subject><subject>Gestational Age</subject><subject>Human fetal</subject><subject>Humans</subject><subject>ICAM-2</subject><subject>Immunohistochemistry</subject><subject>Microglia</subject><subject>Microglia - ultrastructure</subject><subject>PECAM</subject><subject>Phenotype</subject><subject>Spinal cord</subject><subject>Spinal Cord - cytology</subject><subject>Spinal Cord - embryology</subject><issn>0165-3806</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM1K7TAUhTPwol71EZSMRMFq0qZJOxI5-AeKA3UoIU12PZE26U1S4cx8CJ_QJ7HHIxdnTvaCvdfaCz6Edik5poTyk_tplFlREX5Q14eEEFZkYg1t_l9voL8xvkwHWlR0HW1QUnAuCNtET7dWB__cWYWtw2kOeD72yuEWkupwHKybRPtgPt7eB5USBBexb7GxMQXbjMl6d4R7H4a57_zzAitn8DAH59NigG30p1VdhJ1v3UKPF-cPs6vs5u7yenZ2k2nGWMoUz00BVHEwQGhLKlM2wJhWJTWsMWBaSkuhhGjLvICclSJvFCtbTYDzWuXFFtpf_R2C_zdCTLK3UUPXKQd-jJLXFeVFXv1qpCKvapEvP5Yr40QnxgCtHILtVVhISuQSuvyCLpd0ZV3LL-hSTLm974Kx6cH8SK2IT4bTlQEmHq8WgozagtNgbACdpPH2l4pPdyGV4w</recordid><startdate>19990608</startdate><enddate>19990608</enddate><creator>Rezaie, P</creator><creator>Patel, K</creator><creator>Male, D.K</creator><general>Elsevier B.V</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>7TK</scope><scope>7X8</scope></search><sort><creationdate>19990608</creationdate><title>Microglia in the human fetal spinal cord—patterns of distribution, morphology and phenotype</title><author>Rezaie, P ; Patel, K ; Male, D.K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c444t-a62d3e1a6ede01f08d5be44ca51d4bdedf1157a77f523e24572ba45fc0e669a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Blood vessel</topic><topic>CD68</topic><topic>Colonisation</topic><topic>Fetus - ultrastructure</topic><topic>Gestational Age</topic><topic>Human fetal</topic><topic>Humans</topic><topic>ICAM-2</topic><topic>Immunohistochemistry</topic><topic>Microglia</topic><topic>Microglia - ultrastructure</topic><topic>PECAM</topic><topic>Phenotype</topic><topic>Spinal cord</topic><topic>Spinal Cord - cytology</topic><topic>Spinal Cord - embryology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rezaie, P</creatorcontrib><creatorcontrib>Patel, K</creatorcontrib><creatorcontrib>Male, D.K</creatorcontrib><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>Brain research. Developmental brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rezaie, P</au><au>Patel, K</au><au>Male, D.K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Microglia in the human fetal spinal cord—patterns of distribution, morphology and phenotype</atitle><jtitle>Brain research. Developmental brain research</jtitle><addtitle>Brain Res Dev Brain Res</addtitle><date>1999-06-08</date><risdate>1999</risdate><volume>115</volume><issue>1</issue><spage>71</spage><epage>81</epage><pages>71-81</pages><issn>0165-3806</issn><abstract>Microglia, the intrinsic macrophages of the nervous system, colonise the cerebrum around the second trimester in man. In order to determine the extent of microglial influx into the nervous system, we have examined their distribution within the human fetal spinal cord in relation to astrocytic and vascular development between 9 and 16 weeks of gestation, using conventional immunohistochemistry [CD11b; CD45; CD64; CD68; ICAM-1; ICAM-2; VCAM-1; PECAM; GFAP; vimentin] and lectin histochemistry [RCA-1]. Microglia are identifiable by 9 weeks, within the ventricular/sub-ventricular zones. Human fetal microglia display heterogeneity in phenotype and are more readily identified by CD68 in the spinal cord. There is a marked influx of cells dorsal and ventral to the neural cavity, from the marginal layer [meninges/connective tissue] with advancing gestational age, with greatest cell densities towards the end of the time period in this study. This inward migration is associated with progressive vascularisation, ICAM-2 expression and co-localises with GFAP and vimentin positive radial glia. The patterns of microglial migration in human fetal cord differ from that within the cerebrum, but generally conform to a route following white to gray matter.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>10366704</pmid><doi>10.1016/S0165-3806(99)00043-7</doi><tpages>11</tpages></addata></record> |
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subjects | Blood vessel CD68 Colonisation Fetus - ultrastructure Gestational Age Human fetal Humans ICAM-2 Immunohistochemistry Microglia Microglia - ultrastructure PECAM Phenotype Spinal cord Spinal Cord - cytology Spinal Cord - embryology |
title | Microglia in the human fetal spinal cord—patterns of distribution, morphology and phenotype |
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