Translocator Protein 18 kDa Negatively Regulates Inflammation in Microglia
Translocator protein 18 kDa (TSPO) is a mitochondrial outer membrane protein. Although TSPO expression is up-regulated during neuroinflammation, the role of TSPO and its signaling mechanisms in regulation of neuroinflammation remains to be elucidated at the molecular level. Here we demonstrate that...
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Veröffentlicht in: | Journal of neuroimmune pharmacology 2014-06, Vol.9 (3), p.424-437 |
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creator | Bae, Keun-Ryung Shim, Hyun-Jung Balu, Deebika Kim, Sang Ryong Yu, Seong-Woon |
description | Translocator protein 18 kDa (TSPO) is a mitochondrial outer membrane protein. Although TSPO expression is up-regulated during neuroinflammation, the role of TSPO and its signaling mechanisms in regulation of neuroinflammation remains to be elucidated at the molecular level. Here we demonstrate that TSPO is a negative regulator of neuroinflammation in microglia. Over-expression of TSPO decreased production of pro-inflammatory cytokines upon lipopolysaccharide treatment while TSPO knock-down had the opposite effect. Anti-inflammatory activity of TSPO is also supported by increased expression of alternatively activated M2 stage-related genes. These data suggest that up-regulation of TSPO level during neuroinflammation may be an adaptive response mechanism. We also provide the evidence that the repressive activity of TSPO is at least partially mediated by the attenuation of NF-κB activation. Neurodegenerative diseases are characterized by loss of specific subsets of neurons at the particular anatomical regions of the central nervous system. Cause of neuronal death is still largely unknown, but it is becoming clear that neuroinflammation plays a significant role in the pathophysiology of neurodegenerative diseases. Understanding the mechanisms underlying the inhibitory effects of TSPO on neuroinflammation can contribute to the therapeutic design for neurodegenerative diseases. |
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Although TSPO expression is up-regulated during neuroinflammation, the role of TSPO and its signaling mechanisms in regulation of neuroinflammation remains to be elucidated at the molecular level. Here we demonstrate that TSPO is a negative regulator of neuroinflammation in microglia. Over-expression of TSPO decreased production of pro-inflammatory cytokines upon lipopolysaccharide treatment while TSPO knock-down had the opposite effect. Anti-inflammatory activity of TSPO is also supported by increased expression of alternatively activated M2 stage-related genes. These data suggest that up-regulation of TSPO level during neuroinflammation may be an adaptive response mechanism. We also provide the evidence that the repressive activity of TSPO is at least partially mediated by the attenuation of NF-κB activation. Neurodegenerative diseases are characterized by loss of specific subsets of neurons at the particular anatomical regions of the central nervous system. Cause of neuronal death is still largely unknown, but it is becoming clear that neuroinflammation plays a significant role in the pathophysiology of neurodegenerative diseases. Understanding the mechanisms underlying the inhibitory effects of TSPO on neuroinflammation can contribute to the therapeutic design for neurodegenerative diseases.</description><identifier>ISSN: 1557-1890</identifier><identifier>EISSN: 1557-1904</identifier><identifier>DOI: 10.1007/s11481-014-9540-6</identifier><identifier>PMID: 24687172</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Animals ; Biomedical and Life Sciences ; Biomedicine ; Cell Biology ; Cell Line ; Immunology ; Inflammation - immunology ; Inflammation - metabolism ; Inflammation - prevention & control ; Inflammation Mediators - metabolism ; Male ; Mice ; Mice, Inbred C57BL ; Microglia - immunology ; Microglia - metabolism ; Microglia - pathology ; Neurosciences ; Original Article ; Pharmacology/Toxicology ; Proteins ; Receptors, GABA - physiology ; Virology</subject><ispartof>Journal of neuroimmune pharmacology, 2014-06, Vol.9 (3), p.424-437</ispartof><rights>Springer Science+Business Media New York 2014</rights><rights>Journal of Neuroimmune Pharmacology is a copyright of Springer, 2014.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c471t-b5bda4c63a8a7c64453b93620f89ebac4cc0d82a44b2ebef73baff78e6379ef53</citedby><cites>FETCH-LOGICAL-c471t-b5bda4c63a8a7c64453b93620f89ebac4cc0d82a44b2ebef73baff78e6379ef53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11481-014-9540-6$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11481-014-9540-6$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,778,782,27907,27908,41471,42540,51302</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24687172$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bae, Keun-Ryung</creatorcontrib><creatorcontrib>Shim, Hyun-Jung</creatorcontrib><creatorcontrib>Balu, Deebika</creatorcontrib><creatorcontrib>Kim, Sang Ryong</creatorcontrib><creatorcontrib>Yu, Seong-Woon</creatorcontrib><title>Translocator Protein 18 kDa Negatively Regulates Inflammation in Microglia</title><title>Journal of neuroimmune pharmacology</title><addtitle>J Neuroimmune Pharmacol</addtitle><addtitle>J Neuroimmune Pharmacol</addtitle><description>Translocator protein 18 kDa (TSPO) is a mitochondrial outer membrane protein. Although TSPO expression is up-regulated during neuroinflammation, the role of TSPO and its signaling mechanisms in regulation of neuroinflammation remains to be elucidated at the molecular level. Here we demonstrate that TSPO is a negative regulator of neuroinflammation in microglia. Over-expression of TSPO decreased production of pro-inflammatory cytokines upon lipopolysaccharide treatment while TSPO knock-down had the opposite effect. Anti-inflammatory activity of TSPO is also supported by increased expression of alternatively activated M2 stage-related genes. These data suggest that up-regulation of TSPO level during neuroinflammation may be an adaptive response mechanism. We also provide the evidence that the repressive activity of TSPO is at least partially mediated by the attenuation of NF-κB activation. Neurodegenerative diseases are characterized by loss of specific subsets of neurons at the particular anatomical regions of the central nervous system. Cause of neuronal death is still largely unknown, but it is becoming clear that neuroinflammation plays a significant role in the pathophysiology of neurodegenerative diseases. Understanding the mechanisms underlying the inhibitory effects of TSPO on neuroinflammation can contribute to the therapeutic design for neurodegenerative diseases.</description><subject>Animals</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cell Biology</subject><subject>Cell Line</subject><subject>Immunology</subject><subject>Inflammation - immunology</subject><subject>Inflammation - metabolism</subject><subject>Inflammation - prevention & control</subject><subject>Inflammation Mediators - metabolism</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Microglia - immunology</subject><subject>Microglia - metabolism</subject><subject>Microglia - pathology</subject><subject>Neurosciences</subject><subject>Original Article</subject><subject>Pharmacology/Toxicology</subject><subject>Proteins</subject><subject>Receptors, GABA - physiology</subject><subject>Virology</subject><issn>1557-1890</issn><issn>1557-1904</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqNkctKxTAQhoMo3h_AjRTcuKlm0kmTLsXrEW-IrkOaMz1Ue9GkFXx7o0dFBMHVDMw3_zB8jG0B3wPO1X4AQA0pB0wLiTzNF9gqSKlSKDgufvW64CtsLYQHzhGR82W2IjDXCpRYZed33nah6Z0dep_c-H6guktAJ49HNrmimR3qF2pek1uajY0dKCSTrmps28ZB3yWRvayd72dNbTfYUmWbQJufdZ3dnxzfHZ6lF9enk8ODi9ShgiEtZTm16PLMaqtcjiizsshywStdUGkdOsenWljEUlBJlcpKW1VKU56pgiqZrbPdee6T759HCoNp6-CoaWxH_RgMyAw1gtLiH6hAyKUQPKI7v9CHfvRdfMRAIbkSUn5QMKfizyF4qsyTr1vrXw1w8-7EzJ2Y6MS8OzF53Nn-TB7LlqbfG18SIiDmQIijbkb-x-k_U98AA6yVzw</recordid><startdate>20140601</startdate><enddate>20140601</enddate><creator>Bae, Keun-Ryung</creator><creator>Shim, Hyun-Jung</creator><creator>Balu, Deebika</creator><creator>Kim, Sang Ryong</creator><creator>Yu, Seong-Woon</creator><general>Springer US</general><general>Springer Nature 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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>7T5</scope><scope>7TK</scope><scope>H94</scope></search><sort><creationdate>20140601</creationdate><title>Translocator Protein 18 kDa Negatively Regulates Inflammation in Microglia</title><author>Bae, Keun-Ryung ; Shim, Hyun-Jung ; Balu, Deebika ; Kim, Sang Ryong ; Yu, Seong-Woon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c471t-b5bda4c63a8a7c64453b93620f89ebac4cc0d82a44b2ebef73baff78e6379ef53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cell Biology</topic><topic>Cell Line</topic><topic>Immunology</topic><topic>Inflammation - immunology</topic><topic>Inflammation - metabolism</topic><topic>Inflammation - prevention & control</topic><topic>Inflammation Mediators - metabolism</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Microglia - immunology</topic><topic>Microglia - metabolism</topic><topic>Microglia - pathology</topic><topic>Neurosciences</topic><topic>Original Article</topic><topic>Pharmacology/Toxicology</topic><topic>Proteins</topic><topic>Receptors, GABA - physiology</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bae, Keun-Ryung</creatorcontrib><creatorcontrib>Shim, Hyun-Jung</creatorcontrib><creatorcontrib>Balu, Deebika</creatorcontrib><creatorcontrib>Kim, Sang Ryong</creatorcontrib><creatorcontrib>Yu, Seong-Woon</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Journal of neuroimmune pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bae, Keun-Ryung</au><au>Shim, Hyun-Jung</au><au>Balu, Deebika</au><au>Kim, Sang Ryong</au><au>Yu, Seong-Woon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Translocator Protein 18 kDa Negatively Regulates Inflammation in Microglia</atitle><jtitle>Journal of neuroimmune pharmacology</jtitle><stitle>J Neuroimmune Pharmacol</stitle><addtitle>J Neuroimmune Pharmacol</addtitle><date>2014-06-01</date><risdate>2014</risdate><volume>9</volume><issue>3</issue><spage>424</spage><epage>437</epage><pages>424-437</pages><issn>1557-1890</issn><eissn>1557-1904</eissn><abstract>Translocator protein 18 kDa (TSPO) is a mitochondrial outer membrane protein. Although TSPO expression is up-regulated during neuroinflammation, the role of TSPO and its signaling mechanisms in regulation of neuroinflammation remains to be elucidated at the molecular level. Here we demonstrate that TSPO is a negative regulator of neuroinflammation in microglia. Over-expression of TSPO decreased production of pro-inflammatory cytokines upon lipopolysaccharide treatment while TSPO knock-down had the opposite effect. Anti-inflammatory activity of TSPO is also supported by increased expression of alternatively activated M2 stage-related genes. These data suggest that up-regulation of TSPO level during neuroinflammation may be an adaptive response mechanism. We also provide the evidence that the repressive activity of TSPO is at least partially mediated by the attenuation of NF-κB activation. Neurodegenerative diseases are characterized by loss of specific subsets of neurons at the particular anatomical regions of the central nervous system. 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subjects | Animals Biomedical and Life Sciences Biomedicine Cell Biology Cell Line Immunology Inflammation - immunology Inflammation - metabolism Inflammation - prevention & control Inflammation Mediators - metabolism Male Mice Mice, Inbred C57BL Microglia - immunology Microglia - metabolism Microglia - pathology Neurosciences Original Article Pharmacology/Toxicology Proteins Receptors, GABA - physiology Virology |
title | Translocator Protein 18 kDa Negatively Regulates Inflammation in Microglia |
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