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QUANTITATIVE ANALYSIS OF MICROGLIAL CELLS IN THE DEGENERATING CEREBELLUM OF THE STAGGERER (RORAsg/sg) MUTANT MOUSE
Elevated levels of pro-inflammatory cytokines, such as IL-1β and IL-6, have been detected in the cerebellum of Rorasg/sg mice during the first postnatal month of neurodegenerative process. This suggests the existence of a microglial reaction in the context of an inflammatory process that would be tr...
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Published in: | Journal of Neurogenetics 2005-07, Vol.19 (3-4), p.143-154 |
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description | Elevated levels of pro-inflammatory cytokines, such as IL-1β and IL-6, have been detected in the cerebellum of Rorasg/sg mice during the first postnatal month of neurodegenerative process. This suggests the existence of a microglial reaction in the context of an inflammatory process that would be triggered by the massive neuronal loss. To test this hypothesis, we qualitatively and quantitatively studied the microglial cell population using lectin and nucleosidic diphosphatase labeling of the cerebellum of 30-day-old mice. The massive neuronal loss induces a 11.7-fold smaller size of the Rorasg/sg cerebellum compared to wild-types. We showed that the Rorasg/sg microglia population is exclusively composed of cells displaying the characteristic morphology of activated cells, with enlarged, heavily stained cell bodies and few thick processes, in contrast to microglial cells in the wild-type. The density of microglia is 2.7-fold higher in Rorasg/sg than wild-type mice (22444±5011 cells/mm3 versus 8158±1584 cells/mm3), although the absolute number is 4-fold smaller. These results show that neurodegeneration in the Rorasg/sg cerebellum leads to persistance of microglial activation while in wild-type it disappears around P10. |
doi_str_mv | 10.1080/01677060600569762 |
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This suggests the existence of a microglial reaction in the context of an inflammatory process that would be triggered by the massive neuronal loss. To test this hypothesis, we qualitatively and quantitatively studied the microglial cell population using lectin and nucleosidic diphosphatase labeling of the cerebellum of 30-day-old mice. The massive neuronal loss induces a 11.7-fold smaller size of the Rorasg/sg cerebellum compared to wild-types. We showed that the Rorasg/sg microglia population is exclusively composed of cells displaying the characteristic morphology of activated cells, with enlarged, heavily stained cell bodies and few thick processes, in contrast to microglial cells in the wild-type. The density of microglia is 2.7-fold higher in Rorasg/sg than wild-type mice (22444±5011 cells/mm3 versus 8158±1584 cells/mm3), although the absolute number is 4-fold smaller. These results show that neurodegeneration in the Rorasg/sg cerebellum leads to persistance of microglial activation while in wild-type it disappears around P10.</description><identifier>ISSN: 0167-7063</identifier><identifier>EISSN: 1563-5260</identifier><identifier>EISSN: 1364-6753</identifier><identifier>DOI: 10.1080/01677060600569762</identifier><identifier>PMID: 16540405</identifier><language>eng</language><publisher>England: Informa UK Ltd</publisher><subject>Acid Anhydride Hydrolases - metabolism ; Animals ; Atrophy ; Cell Count ; Cerebellum - pathology ; CNS ; Cognitive Sciences ; Heredodegenerative Disorders, Nervous System - genetics ; Heredodegenerative Disorders, Nervous System - pathology ; Inflammation ; Inflammation - genetics ; Inflammation - pathology ; Life Sciences ; Mice ; Mice, Inbred C57BL ; Mice, Neurologic Mutants ; Microglia - pathology ; Neurodegeneration ; Neurons and Cognition ; Rora</subject><ispartof>Journal of Neurogenetics, 2005-07, Vol.19 (3-4), p.143-154</ispartof><rights>2005 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2005</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c512t-f7590e7a4de2d056e1a88bf1b623abc83f7b9b2c64bed7ab83ccd63b8ce63fd03</citedby><cites>FETCH-LOGICAL-c512t-f7590e7a4de2d056e1a88bf1b623abc83f7b9b2c64bed7ab83ccd63b8ce63fd03</cites><orcidid>0000-0002-0313-1490 ; 0000-0002-2701-1581</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16540405$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-00078454$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Journiac, Nathalie</creatorcontrib><creatorcontrib>Doulazmi, Mohamed</creatorcontrib><creatorcontrib>Pajak, Fabrice</creatorcontrib><creatorcontrib>Mariani, Jean</creatorcontrib><creatorcontrib>Garabedian, Beatrice Vernet-der</creatorcontrib><title>QUANTITATIVE ANALYSIS OF MICROGLIAL CELLS IN THE DEGENERATING CEREBELLUM OF THE STAGGERER (RORAsg/sg) MUTANT MOUSE</title><title>Journal of Neurogenetics</title><addtitle>J Neurogenet</addtitle><description>Elevated levels of pro-inflammatory cytokines, such as IL-1β and IL-6, have been detected in the cerebellum of Rorasg/sg mice during the first postnatal month of neurodegenerative process. 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These results show that neurodegeneration in the Rorasg/sg cerebellum leads to persistance of microglial activation while in wild-type it disappears around P10.</description><subject>Acid Anhydride Hydrolases - metabolism</subject><subject>Animals</subject><subject>Atrophy</subject><subject>Cell Count</subject><subject>Cerebellum - pathology</subject><subject>CNS</subject><subject>Cognitive Sciences</subject><subject>Heredodegenerative Disorders, Nervous System - genetics</subject><subject>Heredodegenerative Disorders, Nervous System - pathology</subject><subject>Inflammation</subject><subject>Inflammation - genetics</subject><subject>Inflammation - pathology</subject><subject>Life Sciences</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Neurologic Mutants</subject><subject>Microglia - pathology</subject><subject>Neurodegeneration</subject><subject>Neurons and Cognition</subject><subject>Rora</subject><issn>0167-7063</issn><issn>1563-5260</issn><issn>1364-6753</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqFkV9v0zAUxS3ExMrgA_CC_ITYQ5gdJ3YieMlKlkZKE5E_SDxZjuOsmdJms1vQvj2OWg0hpCE_WLrnd-699gHgHUafMArQFcKUMUTtQT4NGXVfgAX2KXF8l6KXYDHrjgXIOXhtzB1CmFCXvgLnmPoe8pC_APpbE-V1Wkd1-j2GUR5lP6q0gsUNXKfLskiyNMrgMs6yCqY5rFcx_BoncR6X1pAnVinja6s269kyy1UdJYmtlvBjWZSRub0yt5dw3dR2DFwXTRW_AWe9GI16e7ovQHMT18uVkxVJuowyR_rY3Ts980OkmPA65Xb2fQqLIGh73FKXiFYGpGdt2LqSeq3qmGgDImVHSRtIRUnfIXIBLo99N2Lk93rYCv3IJzHwVZTxuYYQYoHnez-xZT8c2Xs9PRyU2fPtYKQaR7FT08FwZr8uRIz9F8Qhw16AXQviIyj1ZIxW_dMKGPE5Pf5Petbz_tT80G5V98dxissCX47AsOsnvRW_Jj12fC8ex0n3WuzkYDh5rv_nv-wbJcb9Rgqt-N100DubxjPb_QbMG7AU</recordid><startdate>20050701</startdate><enddate>20050701</enddate><creator>Journiac, Nathalie</creator><creator>Doulazmi, Mohamed</creator><creator>Pajak, Fabrice</creator><creator>Mariani, Jean</creator><creator>Garabedian, Beatrice Vernet-der</creator><general>Informa UK Ltd</general><general>Taylor & Francis</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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0002-0313-1490</orcidid><orcidid>https://orcid.org/0000-0002-2701-1581</orcidid></search><sort><creationdate>20050701</creationdate><title>QUANTITATIVE ANALYSIS OF MICROGLIAL CELLS IN THE DEGENERATING CEREBELLUM OF THE STAGGERER (RORAsg/sg) MUTANT MOUSE</title><author>Journiac, Nathalie ; Doulazmi, Mohamed ; Pajak, Fabrice ; Mariani, Jean ; Garabedian, Beatrice Vernet-der</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c512t-f7590e7a4de2d056e1a88bf1b623abc83f7b9b2c64bed7ab83ccd63b8ce63fd03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Acid Anhydride Hydrolases - metabolism</topic><topic>Animals</topic><topic>Atrophy</topic><topic>Cell Count</topic><topic>Cerebellum - pathology</topic><topic>CNS</topic><topic>Cognitive Sciences</topic><topic>Heredodegenerative Disorders, Nervous System - genetics</topic><topic>Heredodegenerative Disorders, Nervous System - pathology</topic><topic>Inflammation</topic><topic>Inflammation - genetics</topic><topic>Inflammation - pathology</topic><topic>Life Sciences</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Neurologic Mutants</topic><topic>Microglia - pathology</topic><topic>Neurodegeneration</topic><topic>Neurons and Cognition</topic><topic>Rora</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Journiac, Nathalie</creatorcontrib><creatorcontrib>Doulazmi, Mohamed</creatorcontrib><creatorcontrib>Pajak, Fabrice</creatorcontrib><creatorcontrib>Mariani, Jean</creatorcontrib><creatorcontrib>Garabedian, Beatrice Vernet-der</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>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Journal of Neurogenetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Journiac, Nathalie</au><au>Doulazmi, Mohamed</au><au>Pajak, Fabrice</au><au>Mariani, Jean</au><au>Garabedian, Beatrice Vernet-der</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>QUANTITATIVE ANALYSIS OF MICROGLIAL CELLS IN THE DEGENERATING CEREBELLUM OF THE STAGGERER (RORAsg/sg) MUTANT MOUSE</atitle><jtitle>Journal of Neurogenetics</jtitle><addtitle>J Neurogenet</addtitle><date>2005-07-01</date><risdate>2005</risdate><volume>19</volume><issue>3-4</issue><spage>143</spage><epage>154</epage><pages>143-154</pages><issn>0167-7063</issn><eissn>1563-5260</eissn><eissn>1364-6753</eissn><abstract>Elevated levels of pro-inflammatory cytokines, such as IL-1β and IL-6, have been detected in the cerebellum of Rorasg/sg mice during the first postnatal month of neurodegenerative process. This suggests the existence of a microglial reaction in the context of an inflammatory process that would be triggered by the massive neuronal loss. To test this hypothesis, we qualitatively and quantitatively studied the microglial cell population using lectin and nucleosidic diphosphatase labeling of the cerebellum of 30-day-old mice. The massive neuronal loss induces a 11.7-fold smaller size of the Rorasg/sg cerebellum compared to wild-types. We showed that the Rorasg/sg microglia population is exclusively composed of cells displaying the characteristic morphology of activated cells, with enlarged, heavily stained cell bodies and few thick processes, in contrast to microglial cells in the wild-type. The density of microglia is 2.7-fold higher in Rorasg/sg than wild-type mice (22444±5011 cells/mm3 versus 8158±1584 cells/mm3), although the absolute number is 4-fold smaller. These results show that neurodegeneration in the Rorasg/sg cerebellum leads to persistance of microglial activation while in wild-type it disappears around P10.</abstract><cop>England</cop><pub>Informa UK Ltd</pub><pmid>16540405</pmid><doi>10.1080/01677060600569762</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-0313-1490</orcidid><orcidid>https://orcid.org/0000-0002-2701-1581</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acid Anhydride Hydrolases - metabolism Animals Atrophy Cell Count Cerebellum - pathology CNS Cognitive Sciences Heredodegenerative Disorders, Nervous System - genetics Heredodegenerative Disorders, Nervous System - pathology Inflammation Inflammation - genetics Inflammation - pathology Life Sciences Mice Mice, Inbred C57BL Mice, Neurologic Mutants Microglia - pathology Neurodegeneration Neurons and Cognition Rora |
title | QUANTITATIVE ANALYSIS OF MICROGLIAL CELLS IN THE DEGENERATING CEREBELLUM OF THE STAGGERER (RORAsg/sg) MUTANT MOUSE |
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