Hematopoietic Cells Differentiate into Both Microglia and Macroglia in the Brains of Adult Mice
Glial cells are thought to derive embryologically from either myeloid cells of the hematopoietic system (microglia) or neuroepithelial progenitor cells (astroglia and oligodendrocytes). However, it is unclear whether the glia in adult brains free of disease or injury originate solely from cells pres...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 1997-04, Vol.94 (8), p.4080-4085 |
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description | Glial cells are thought to derive embryologically from either myeloid cells of the hematopoietic system (microglia) or neuroepithelial progenitor cells (astroglia and oligodendrocytes). However, it is unclear whether the glia in adult brains free of disease or injury originate solely from cells present in the brain since the fetal stage of development, or if there is further input into such adult brains from cells originating outside the central nervous system. To test the ability of hematopoietic cells to contribute to the central nervous system, we have transplanted adult female mice with donor bone marrow cells genetically marked either with a retroviral tag or by using male donor cells. Using in situ hybridization histochemistry, a continuing influx of hematopoietic cells into the brain was detected. Marrow-derived cells were already detected in the brains of mice 3 days after transplant, and their numbers increased over the next several weeks, exceeding 14,000 cells per brain in several animals. Marrow-derived cells were widely distributed throughout the brain, including the cortex, hippocampus, thalamus, brain stem, and cerebellum. When in situ hybridization histochemistry was combined with immunohistochemical staining using lineage-specific markers, some bone marrow-derived cells were positive for the microglial antigenic marker F4/80. Other marrow-derived cells surprisingly expressed the astroglial marker glial fibrillary acidic protein. These results indicate that some microglia and astroglia arise from a precursor that is a normal constituent of adult bone marrow. |
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However, it is unclear whether the glia in adult brains free of disease or injury originate solely from cells present in the brain since the fetal stage of development, or if there is further input into such adult brains from cells originating outside the central nervous system. To test the ability of hematopoietic cells to contribute to the central nervous system, we have transplanted adult female mice with donor bone marrow cells genetically marked either with a retroviral tag or by using male donor cells. Using in situ hybridization histochemistry, a continuing influx of hematopoietic cells into the brain was detected. Marrow-derived cells were already detected in the brains of mice 3 days after transplant, and their numbers increased over the next several weeks, exceeding 14,000 cells per brain in several animals. Marrow-derived cells were widely distributed throughout the brain, including the cortex, hippocampus, thalamus, brain stem, and cerebellum. When in situ hybridization histochemistry was combined with immunohistochemical staining using lineage-specific markers, some bone marrow-derived cells were positive for the microglial antigenic marker F4/80. Other marrow-derived cells surprisingly expressed the astroglial marker glial fibrillary acidic protein. These results indicate that some microglia and astroglia arise from a precursor that is a normal constituent of adult bone marrow.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.94.8.4080</identifier><identifier>PMID: 9108108</identifier><language>eng</language><publisher>United States: National Academy of Sciences of the United States of America</publisher><subject>Animals ; Biological Sciences ; Bone marrow ; Bone marrow cells ; Bone marrow transplantation ; Brain ; Cell Differentiation ; Cell lines ; Cell transplantation ; Cellular biology ; Central nervous system ; Female ; Gene Transfer Techniques ; Genetic Markers ; Genetics ; Hematopoietic Stem Cell Transplantation ; Hematopoietic Stem Cells - cytology ; In Situ Hybridization ; Male ; Mice ; Mice, Inbred C57BL ; Microglia ; Microglia - cytology ; Myeloid cells ; Nervous system ; Neural stem cells ; Neuroglia ; Neuroglia - cytology ; Neurons ; Rodents ; Transplants & implants</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1997-04, Vol.94 (8), p.4080-4085</ispartof><rights>Copyright 1997 National Academy of Sciences</rights><rights>Copyright National Academy of Sciences Apr 15, 1997</rights><rights>1997</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c513t-6bb7eba174fad98d51fb90bb8fe9c7d23ad1ea4bd6884d2d7111fae0df6a6ae73</citedby><cites>FETCH-LOGICAL-c513t-6bb7eba174fad98d51fb90bb8fe9c7d23ad1ea4bd6884d2d7111fae0df6a6ae73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/94/8.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/41959$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/41959$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,803,885,27922,27923,53789,53791,58015,58248</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9108108$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Eglitis, Martin A.</creatorcontrib><creatorcontrib>Mezey, Eva</creatorcontrib><title>Hematopoietic Cells Differentiate into Both Microglia and Macroglia in the Brains of Adult Mice</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Glial cells are thought to derive embryologically from either myeloid cells of the hematopoietic system (microglia) or neuroepithelial progenitor cells (astroglia and oligodendrocytes). However, it is unclear whether the glia in adult brains free of disease or injury originate solely from cells present in the brain since the fetal stage of development, or if there is further input into such adult brains from cells originating outside the central nervous system. To test the ability of hematopoietic cells to contribute to the central nervous system, we have transplanted adult female mice with donor bone marrow cells genetically marked either with a retroviral tag or by using male donor cells. Using in situ hybridization histochemistry, a continuing influx of hematopoietic cells into the brain was detected. Marrow-derived cells were already detected in the brains of mice 3 days after transplant, and their numbers increased over the next several weeks, exceeding 14,000 cells per brain in several animals. Marrow-derived cells were widely distributed throughout the brain, including the cortex, hippocampus, thalamus, brain stem, and cerebellum. When in situ hybridization histochemistry was combined with immunohistochemical staining using lineage-specific markers, some bone marrow-derived cells were positive for the microglial antigenic marker F4/80. Other marrow-derived cells surprisingly expressed the astroglial marker glial fibrillary acidic protein. These results indicate that some microglia and astroglia arise from a precursor that is a normal constituent of adult bone marrow.</description><subject>Animals</subject><subject>Biological Sciences</subject><subject>Bone marrow</subject><subject>Bone marrow cells</subject><subject>Bone marrow transplantation</subject><subject>Brain</subject><subject>Cell Differentiation</subject><subject>Cell lines</subject><subject>Cell transplantation</subject><subject>Cellular biology</subject><subject>Central nervous system</subject><subject>Female</subject><subject>Gene Transfer Techniques</subject><subject>Genetic Markers</subject><subject>Genetics</subject><subject>Hematopoietic Stem Cell Transplantation</subject><subject>Hematopoietic Stem Cells - cytology</subject><subject>In Situ Hybridization</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Microglia</subject><subject>Microglia - cytology</subject><subject>Myeloid cells</subject><subject>Nervous system</subject><subject>Neural stem cells</subject><subject>Neuroglia</subject><subject>Neuroglia - cytology</subject><subject>Neurons</subject><subject>Rodents</subject><subject>Transplants & implants</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1r3DAQxUVpSbdprz0UCqKH3uxobNmSoJdk-5FCQi7tWciWlNXitbaSHJr_PjK7WTahUBAI8X5vZjQPofdASiCsPtuOKpaClrykhJMXaAFEQNFSQV6iBSEVKzit6Gv0JsY1IUQ0nJygEwGE57NA8tJsVPJb70xyPV6aYYj4q7PWBDMmp5LBbkweX_i0wteuD_52cAqrUeNr9fhyI04rgy-CcmPE3uJzPQ1pxs1b9MqqIZp3-_sU_f7-7dfysri6-fFzeX5V9A3UqWi7jplOAaNWacF1A7YTpOu4NaJnuqqVBqNop1vOqa40AwCrDNG2Va0yrD5FX3Z1t1O3MbrPwwc1yG1wGxXupVdOPlVGt5K3_k5WpGGQ7Z_39uD_TCYmuXGxz8tQo_FTlIwLmnuS_4LQAqFVyzP46Rm49lMY8w5yS6A1g6rNULmD8iZjDMYeBgYi53jlHK8UVHI5x5sNH4-_ecD3eR6NN_sO6qNf2mkYkvmbjgr9E8z6h52-jsmHA0BBNKJ-APkDw1I</recordid><startdate>19970415</startdate><enddate>19970415</enddate><creator>Eglitis, Martin A.</creator><creator>Mezey, Eva</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</general><general>National Academy of Sciences</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>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19970415</creationdate><title>Hematopoietic Cells Differentiate into Both Microglia and Macroglia in the Brains of Adult Mice</title><author>Eglitis, Martin A. ; Mezey, Eva</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c513t-6bb7eba174fad98d51fb90bb8fe9c7d23ad1ea4bd6884d2d7111fae0df6a6ae73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Animals</topic><topic>Biological Sciences</topic><topic>Bone marrow</topic><topic>Bone marrow cells</topic><topic>Bone marrow transplantation</topic><topic>Brain</topic><topic>Cell Differentiation</topic><topic>Cell lines</topic><topic>Cell transplantation</topic><topic>Cellular biology</topic><topic>Central nervous system</topic><topic>Female</topic><topic>Gene Transfer Techniques</topic><topic>Genetic Markers</topic><topic>Genetics</topic><topic>Hematopoietic Stem Cell Transplantation</topic><topic>Hematopoietic Stem Cells - cytology</topic><topic>In Situ Hybridization</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Microglia</topic><topic>Microglia - cytology</topic><topic>Myeloid cells</topic><topic>Nervous system</topic><topic>Neural stem cells</topic><topic>Neuroglia</topic><topic>Neuroglia - cytology</topic><topic>Neurons</topic><topic>Rodents</topic><topic>Transplants & implants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Eglitis, Martin A.</creatorcontrib><creatorcontrib>Mezey, Eva</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Eglitis, Martin A.</au><au>Mezey, Eva</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hematopoietic Cells Differentiate into Both Microglia and Macroglia in the Brains of Adult Mice</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1997-04-15</date><risdate>1997</risdate><volume>94</volume><issue>8</issue><spage>4080</spage><epage>4085</epage><pages>4080-4085</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>Glial cells are thought to derive embryologically from either myeloid cells of the hematopoietic system (microglia) or neuroepithelial progenitor cells (astroglia and oligodendrocytes). However, it is unclear whether the glia in adult brains free of disease or injury originate solely from cells present in the brain since the fetal stage of development, or if there is further input into such adult brains from cells originating outside the central nervous system. To test the ability of hematopoietic cells to contribute to the central nervous system, we have transplanted adult female mice with donor bone marrow cells genetically marked either with a retroviral tag or by using male donor cells. Using in situ hybridization histochemistry, a continuing influx of hematopoietic cells into the brain was detected. Marrow-derived cells were already detected in the brains of mice 3 days after transplant, and their numbers increased over the next several weeks, exceeding 14,000 cells per brain in several animals. Marrow-derived cells were widely distributed throughout the brain, including the cortex, hippocampus, thalamus, brain stem, and cerebellum. When in situ hybridization histochemistry was combined with immunohistochemical staining using lineage-specific markers, some bone marrow-derived cells were positive for the microglial antigenic marker F4/80. Other marrow-derived cells surprisingly expressed the astroglial marker glial fibrillary acidic protein. These results indicate that some microglia and astroglia arise from a precursor that is a normal constituent of adult bone marrow.</abstract><cop>United States</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>9108108</pmid><doi>10.1073/pnas.94.8.4080</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biological Sciences Bone marrow Bone marrow cells Bone marrow transplantation Brain Cell Differentiation Cell lines Cell transplantation Cellular biology Central nervous system Female Gene Transfer Techniques Genetic Markers Genetics Hematopoietic Stem Cell Transplantation Hematopoietic Stem Cells - cytology In Situ Hybridization Male Mice Mice, Inbred C57BL Microglia Microglia - cytology Myeloid cells Nervous system Neural stem cells Neuroglia Neuroglia - cytology Neurons Rodents Transplants & implants |
title | Hematopoietic Cells Differentiate into Both Microglia and Macroglia in the Brains of Adult Mice |
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