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Glucocorticoids Induce Proteasome C3 Subunit Expression in L6 Muscle Cells by Opposing the Suppression of Its Transcription by NF-κB
Muscle wasting in catabolic conditions results from activation of the ubiquitin-proteasome proteolytic pathway by a process that requires glucocorticoids and is generally associated with increased levels of mRNAs encoding components of this proteolytic system. In L6 muscle cells, dexamethasone stimu...
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Published in: | The Journal of biological chemistry 2000-06, Vol.275 (26), p.19661-19666 |
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container_end_page | 19666 |
container_issue | 26 |
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container_title | The Journal of biological chemistry |
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creator | Du, Jie Mitch, William E. Wang, Xiaonan Price, S.Russ |
description | Muscle wasting in catabolic conditions results from activation of the ubiquitin-proteasome proteolytic pathway by a process that requires glucocorticoids and is generally associated with increased levels of mRNAs encoding components of this proteolytic system. In L6 muscle cells, dexamethasone stimulates proteolysis and increases the amount of the proteasome C3 subunit protein by augmenting its transcription. Transfection studies with human C3 promoter-luciferase reporter genes and electrophoretic mobility shift assays revealed that a NF-κB·protein complex containing Rel A is abundant in L6 muscle cell nuclei. Glucocorticoids stimulate C3 subunit expression by antagonizing the interaction of this NF-κB protein with an NF-κB response element in the C3 subunit promoter region. Dexamethasone also increased the cytosolic amounts of the NF-κB p65 subunit and the IκBα inhibitor proteins in L6 cells. Incubation of L6 cells with a cytokine mixture not only increased the amount of activated NF-κB but also decreased C3 promoter activity and lowered endogenous C3 subunit mRNA. Thus, NF-κB is a repressor of C3 proteasome subunit transcription in muscle cells, and glucocorticoids stimulate C3 subunit expression by opposing this suppressor action. |
doi_str_mv | 10.1074/jbc.M907258199 |
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In L6 muscle cells, dexamethasone stimulates proteolysis and increases the amount of the proteasome C3 subunit protein by augmenting its transcription. Transfection studies with human C3 promoter-luciferase reporter genes and electrophoretic mobility shift assays revealed that a NF-κB·protein complex containing Rel A is abundant in L6 muscle cell nuclei. Glucocorticoids stimulate C3 subunit expression by antagonizing the interaction of this NF-κB protein with an NF-κB response element in the C3 subunit promoter region. Dexamethasone also increased the cytosolic amounts of the NF-κB p65 subunit and the IκBα inhibitor proteins in L6 cells. Incubation of L6 cells with a cytokine mixture not only increased the amount of activated NF-κB but also decreased C3 promoter activity and lowered endogenous C3 subunit mRNA. Thus, NF-κB is a repressor of C3 proteasome subunit transcription in muscle cells, and glucocorticoids stimulate C3 subunit expression by opposing this suppressor action.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M907258199</identifier><identifier>PMID: 10867022</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Base Sequence ; Binding Sites ; Blotting, Northern ; Blotting, Western ; Cells, Cultured ; Cysteine Endopeptidases - biosynthesis ; Cysteine Endopeptidases - genetics ; Cytokines - metabolism ; Cytosol - metabolism ; dexamethasone ; Dexamethasone - pharmacology ; Dose-Response Relationship, Drug ; Electrophoresis, Polyacrylamide Gel ; Glucocorticoids - metabolism ; Humans ; Molecular Sequence Data ; Multienzyme Complexes - biosynthesis ; Multienzyme Complexes - genetics ; Muscles - metabolism ; NF-kappa B - antagonists & inhibitors ; NF-kappa B - metabolism ; Promoter Regions, Genetic ; Proteasome Endopeptidase Complex ; proteasomes ; Rats ; Time Factors ; Transcription Factor RelA ; Transcription, Genetic ; Transfection ; Ubiquitins - metabolism</subject><ispartof>The Journal of biological chemistry, 2000-06, Vol.275 (26), p.19661-19666</ispartof><rights>2000 © 2000 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c411t-9ab6b92f3ba7ab96ca5b616444ac9f86ca6746445120941a79eb90ccc6cf87433</citedby><cites>FETCH-LOGICAL-c411t-9ab6b92f3ba7ab96ca5b616444ac9f86ca6746445120941a79eb90ccc6cf87433</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0021925819800339$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3536,27901,27902,45756</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10867022$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Du, Jie</creatorcontrib><creatorcontrib>Mitch, William E.</creatorcontrib><creatorcontrib>Wang, Xiaonan</creatorcontrib><creatorcontrib>Price, S.Russ</creatorcontrib><title>Glucocorticoids Induce Proteasome C3 Subunit Expression in L6 Muscle Cells by Opposing the Suppression of Its Transcription by NF-κB</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>Muscle wasting in catabolic conditions results from activation of the ubiquitin-proteasome proteolytic pathway by a process that requires glucocorticoids and is generally associated with increased levels of mRNAs encoding components of this proteolytic system. In L6 muscle cells, dexamethasone stimulates proteolysis and increases the amount of the proteasome C3 subunit protein by augmenting its transcription. Transfection studies with human C3 promoter-luciferase reporter genes and electrophoretic mobility shift assays revealed that a NF-κB·protein complex containing Rel A is abundant in L6 muscle cell nuclei. Glucocorticoids stimulate C3 subunit expression by antagonizing the interaction of this NF-κB protein with an NF-κB response element in the C3 subunit promoter region. Dexamethasone also increased the cytosolic amounts of the NF-κB p65 subunit and the IκBα inhibitor proteins in L6 cells. Incubation of L6 cells with a cytokine mixture not only increased the amount of activated NF-κB but also decreased C3 promoter activity and lowered endogenous C3 subunit mRNA. Thus, NF-κB is a repressor of C3 proteasome subunit transcription in muscle cells, and glucocorticoids stimulate C3 subunit expression by opposing this suppressor action.</description><subject>Animals</subject><subject>Base Sequence</subject><subject>Binding Sites</subject><subject>Blotting, Northern</subject><subject>Blotting, Western</subject><subject>Cells, Cultured</subject><subject>Cysteine Endopeptidases - biosynthesis</subject><subject>Cysteine Endopeptidases - genetics</subject><subject>Cytokines - metabolism</subject><subject>Cytosol - metabolism</subject><subject>dexamethasone</subject><subject>Dexamethasone - pharmacology</subject><subject>Dose-Response Relationship, Drug</subject><subject>Electrophoresis, Polyacrylamide Gel</subject><subject>Glucocorticoids - metabolism</subject><subject>Humans</subject><subject>Molecular Sequence Data</subject><subject>Multienzyme Complexes - biosynthesis</subject><subject>Multienzyme Complexes - genetics</subject><subject>Muscles - metabolism</subject><subject>NF-kappa B - antagonists & inhibitors</subject><subject>NF-kappa B - metabolism</subject><subject>Promoter Regions, Genetic</subject><subject>Proteasome Endopeptidase Complex</subject><subject>proteasomes</subject><subject>Rats</subject><subject>Time Factors</subject><subject>Transcription Factor RelA</subject><subject>Transcription, Genetic</subject><subject>Transfection</subject><subject>Ubiquitins - metabolism</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNp1kMFu1DAURS0EokNhyxJ5xS6DnXiceAmjtow0pUgUiZ1lv7yAq0wc_BxEP4Cf4iP4JlxNBWzwxnr2uVf2Yey5FGspWvXqxsP60oi23nTSmAdsJUXXVM1GfnrIVkLUsjLl6oQ9IboRZSkjH7OTAulW1PWK_bgYF4gQUw4QQ098N_ULIH-fYkZH8YB82_APi1-mkPnZ9zkhUYgTDxPfa365EIwFwXEk7m_51TxHCtNnnr9gSc1_8DjwXSZ-ndxEkMKc7w5L4N159evnm6fs0eBGwmf3-yn7eH52vX1b7a8udtvX-wqUlLkyzmtv6qHxrnXeaHAbr6VWSjkwQ1dm3aoybmQtjJKuNeiNAAANQ9eqpjllL4-9c4pfF6RsD4GgPN5NGBeystWqaNUFXB9BSJEo4WDnFA4u3Vop7J14W8Tbv-JL4MV98-IP2P-DH00XoDsCWP73LWCyBAEnwD4khGz7GP7X_RtZdZNw</recordid><startdate>20000630</startdate><enddate>20000630</enddate><creator>Du, Jie</creator><creator>Mitch, William E.</creator><creator>Wang, Xiaonan</creator><creator>Price, S.Russ</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><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>7TM</scope></search><sort><creationdate>20000630</creationdate><title>Glucocorticoids Induce Proteasome C3 Subunit Expression in L6 Muscle Cells by Opposing the Suppression of Its Transcription by NF-κB</title><author>Du, Jie ; Mitch, William E. ; Wang, Xiaonan ; Price, S.Russ</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c411t-9ab6b92f3ba7ab96ca5b616444ac9f86ca6746445120941a79eb90ccc6cf87433</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Animals</topic><topic>Base Sequence</topic><topic>Binding Sites</topic><topic>Blotting, Northern</topic><topic>Blotting, Western</topic><topic>Cells, Cultured</topic><topic>Cysteine Endopeptidases - biosynthesis</topic><topic>Cysteine Endopeptidases - genetics</topic><topic>Cytokines - metabolism</topic><topic>Cytosol - metabolism</topic><topic>dexamethasone</topic><topic>Dexamethasone - pharmacology</topic><topic>Dose-Response Relationship, Drug</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>Glucocorticoids - metabolism</topic><topic>Humans</topic><topic>Molecular Sequence Data</topic><topic>Multienzyme Complexes - biosynthesis</topic><topic>Multienzyme Complexes - genetics</topic><topic>Muscles - metabolism</topic><topic>NF-kappa B - antagonists & inhibitors</topic><topic>NF-kappa B - metabolism</topic><topic>Promoter Regions, Genetic</topic><topic>Proteasome Endopeptidase Complex</topic><topic>proteasomes</topic><topic>Rats</topic><topic>Time Factors</topic><topic>Transcription Factor RelA</topic><topic>Transcription, Genetic</topic><topic>Transfection</topic><topic>Ubiquitins - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Du, Jie</creatorcontrib><creatorcontrib>Mitch, William E.</creatorcontrib><creatorcontrib>Wang, Xiaonan</creatorcontrib><creatorcontrib>Price, S.Russ</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Du, Jie</au><au>Mitch, William E.</au><au>Wang, Xiaonan</au><au>Price, S.Russ</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Glucocorticoids Induce Proteasome C3 Subunit Expression in L6 Muscle Cells by Opposing the Suppression of Its Transcription by NF-κB</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2000-06-30</date><risdate>2000</risdate><volume>275</volume><issue>26</issue><spage>19661</spage><epage>19666</epage><pages>19661-19666</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>Muscle wasting in catabolic conditions results from activation of the ubiquitin-proteasome proteolytic pathway by a process that requires glucocorticoids and is generally associated with increased levels of mRNAs encoding components of this proteolytic system. In L6 muscle cells, dexamethasone stimulates proteolysis and increases the amount of the proteasome C3 subunit protein by augmenting its transcription. Transfection studies with human C3 promoter-luciferase reporter genes and electrophoretic mobility shift assays revealed that a NF-κB·protein complex containing Rel A is abundant in L6 muscle cell nuclei. Glucocorticoids stimulate C3 subunit expression by antagonizing the interaction of this NF-κB protein with an NF-κB response element in the C3 subunit promoter region. Dexamethasone also increased the cytosolic amounts of the NF-κB p65 subunit and the IκBα inhibitor proteins in L6 cells. Incubation of L6 cells with a cytokine mixture not only increased the amount of activated NF-κB but also decreased C3 promoter activity and lowered endogenous C3 subunit mRNA. Thus, NF-κB is a repressor of C3 proteasome subunit transcription in muscle cells, and glucocorticoids stimulate C3 subunit expression by opposing this suppressor action.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>10867022</pmid><doi>10.1074/jbc.M907258199</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Base Sequence Binding Sites Blotting, Northern Blotting, Western Cells, Cultured Cysteine Endopeptidases - biosynthesis Cysteine Endopeptidases - genetics Cytokines - metabolism Cytosol - metabolism dexamethasone Dexamethasone - pharmacology Dose-Response Relationship, Drug Electrophoresis, Polyacrylamide Gel Glucocorticoids - metabolism Humans Molecular Sequence Data Multienzyme Complexes - biosynthesis Multienzyme Complexes - genetics Muscles - metabolism NF-kappa B - antagonists & inhibitors NF-kappa B - metabolism Promoter Regions, Genetic Proteasome Endopeptidase Complex proteasomes Rats Time Factors Transcription Factor RelA Transcription, Genetic Transfection Ubiquitins - metabolism |
title | Glucocorticoids Induce Proteasome C3 Subunit Expression in L6 Muscle Cells by Opposing the Suppression of Its Transcription by NF-κB |
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