Molecular biology of microglia cytokine and chemokine receptors and microglial activation
Activation of brain microglial cells can be subdivided into a number of stages. Early stages likely are proliferation and migration to sites of cell damage. These two stages have been studied exemplarily on the IL-3 receptor β-subunit and on the CC-chemokine receptor 5 using molecular biological met...
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Veröffentlicht in: | Life sciences (1973) 1998, Vol.62 (17), p.1707-1710 |
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creator | Spleiss, Olivia Appel, Kurt Boddeke, Hendrik W.G.M. Berger, Mathias Gebicke-Haerter, Peter J. |
description | Activation of brain microglial cells can be subdivided into a number of stages. Early stages likely are proliferation and migration to sites of cell damage. These two stages have been studied exemplarily on the IL-3 receptor β-subunit and on the CC-chemokine receptor 5 using molecular biological methods. First, IL-3 receptor β-subunit cDNA has been cloned in full length from rat microglia. Since cultured microglia are already activated to some extent, mRNA of this subunit has been detected in the isolated cells, but was absent in normal rat brain. Lipopolysaccharide (LPS) increased this mRNA in the cultured cells and LPS injected into the circulation of rats induced the mRNA specifically in brain microglia as revealed by in situ hybridizations. Next, we obtained partial cDNAs of receptor-coupled protein tyrosine kinases JAK 1 and JAK 2. These mRNAs were present both in cultured microglia and in rat brain, but were not influenced by LPS. Finally, a full-length cDNA of the rat chemokine receptor 5 has been obtained by PCR methodology. Its mRNA was increased by adminstration of LPS both in cultured microglia and in vivo. It is expected, that further investigations on these receptors could help to develop improved strategies to combat chronic inflammatory events in the brain. |
doi_str_mv | 10.1016/S0024-3205(98)00132-5 |
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Early stages likely are proliferation and migration to sites of cell damage. These two stages have been studied exemplarily on the IL-3 receptor β-subunit and on the CC-chemokine receptor 5 using molecular biological methods. First, IL-3 receptor β-subunit cDNA has been cloned in full length from rat microglia. Since cultured microglia are already activated to some extent, mRNA of this subunit has been detected in the isolated cells, but was absent in normal rat brain. Lipopolysaccharide (LPS) increased this mRNA in the cultured cells and LPS injected into the circulation of rats induced the mRNA specifically in brain microglia as revealed by in situ hybridizations. Next, we obtained partial cDNAs of receptor-coupled protein tyrosine kinases JAK 1 and JAK 2. These mRNAs were present both in cultured microglia and in rat brain, but were not influenced by LPS. Finally, a full-length cDNA of the rat chemokine receptor 5 has been obtained by PCR methodology. Its mRNA was increased by adminstration of LPS both in cultured microglia and in vivo. It is expected, that further investigations on these receptors could help to develop improved strategies to combat chronic inflammatory events in the brain.</description><subject>Animals</subject><subject>Base Sequence</subject><subject>chemokine receptor 5</subject><subject>DNA, Complementary - genetics</subject><subject>DNA, Complementary - metabolism</subject><subject>fever induction</subject><subject>Humans</subject><subject>IL-3 receptor</subject><subject>Janus kinases</subject><subject>MCAO stroke model</subject><subject>Microglia - physiology</subject><subject>Microglia - ultrastructure</subject><subject>microglia cytokine</subject><subject>Molecular Sequence Data</subject><subject>mRNA expression</subject><subject>Receptors, Chemokine - genetics</subject><subject>Receptors, Chemokine - physiology</subject><subject>Receptors, Cytokine - genetics</subject><subject>Receptors, Cytokine - physiology</subject><subject>RNA, Messenger - metabolism</subject><issn>0024-3205</issn><issn>1879-0631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1PwzAMhiMEGmPwEyb1hOBQSJqlSU4ITXxJIA7AgVOUJu4ItM1I2kn793TrtCsny_Zrv_aD0JTgK4JJfv2GcTZLaYbZhRSXGBOapewAjYngMsU5JYdovJcco5MYvzHGjHE6QiPJBCM5GaPPF1-B6SodksL5yi_WiS-T2pngF5XTiVm3_sc1kOjGJuYL6iELYGDZ-hC39b28SrRp3Uq3zjen6KjUVYSzXZygj_u79_lj-vz68DS_fU4NzXGblrwgPJdghZbWMqq5KQC0LIgsrO6fEhbPsMg44zkDSTPNJTczwyTVxoiCTtD5sHcZ_G8HsVW1iwaqSjfgu6i4FDljGe2FbBD2x8YYoFTL4God1opgtUGqtkjVhpeSQm2RKtbPTXcGXVGD3U_tGPb9m6EP_ZcrB0FF46AxYF2PqVXWu38c_gCQ1Idn</recordid><startdate>1998</startdate><enddate>1998</enddate><creator>Spleiss, Olivia</creator><creator>Appel, Kurt</creator><creator>Boddeke, Hendrik W.G.M.</creator><creator>Berger, Mathias</creator><creator>Gebicke-Haerter, Peter J.</creator><general>Elsevier Inc</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>7X8</scope></search><sort><creationdate>1998</creationdate><title>Molecular biology of microglia cytokine and chemokine receptors and microglial activation</title><author>Spleiss, Olivia ; Appel, Kurt ; Boddeke, Hendrik W.G.M. ; Berger, Mathias ; Gebicke-Haerter, Peter J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c360t-f7b1769ed8a9dd53a7cbeea9b19bda1328d0408275765e932a797c4c593acc8b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>Base Sequence</topic><topic>chemokine receptor 5</topic><topic>DNA, Complementary - genetics</topic><topic>DNA, Complementary - metabolism</topic><topic>fever induction</topic><topic>Humans</topic><topic>IL-3 receptor</topic><topic>Janus kinases</topic><topic>MCAO stroke model</topic><topic>Microglia - physiology</topic><topic>Microglia - ultrastructure</topic><topic>microglia cytokine</topic><topic>Molecular Sequence Data</topic><topic>mRNA expression</topic><topic>Receptors, Chemokine - genetics</topic><topic>Receptors, Chemokine - physiology</topic><topic>Receptors, Cytokine - genetics</topic><topic>Receptors, Cytokine - physiology</topic><topic>RNA, Messenger - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Spleiss, Olivia</creatorcontrib><creatorcontrib>Appel, Kurt</creatorcontrib><creatorcontrib>Boddeke, Hendrik W.G.M.</creatorcontrib><creatorcontrib>Berger, Mathias</creatorcontrib><creatorcontrib>Gebicke-Haerter, Peter J.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Life sciences (1973)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Spleiss, Olivia</au><au>Appel, Kurt</au><au>Boddeke, Hendrik W.G.M.</au><au>Berger, Mathias</au><au>Gebicke-Haerter, Peter J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular biology of microglia cytokine and chemokine receptors and microglial activation</atitle><jtitle>Life sciences (1973)</jtitle><addtitle>Life Sci</addtitle><date>1998</date><risdate>1998</risdate><volume>62</volume><issue>17</issue><spage>1707</spage><epage>1710</epage><pages>1707-1710</pages><issn>0024-3205</issn><eissn>1879-0631</eissn><abstract>Activation of brain microglial cells can be subdivided into a number of stages. 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subjects | Animals Base Sequence chemokine receptor 5 DNA, Complementary - genetics DNA, Complementary - metabolism fever induction Humans IL-3 receptor Janus kinases MCAO stroke model Microglia - physiology Microglia - ultrastructure microglia cytokine Molecular Sequence Data mRNA expression Receptors, Chemokine - genetics Receptors, Chemokine - physiology Receptors, Cytokine - genetics Receptors, Cytokine - physiology RNA, Messenger - metabolism |
title | Molecular biology of microglia cytokine and chemokine receptors and microglial activation |
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