Regulation of the expression of inducible nitric oxide synthase
Nitric oxide (NO) generated by the inducible isoform of nitric oxide synthase (iNOS) is involved in complex immunomodulatory and antitumoral mechanisms and has been described to have multiple beneficial microbicidal, antiviral and antiparasital effects. However, dysfunctional induction of iNOS expre...
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Veröffentlicht in: | Nitric oxide 2010-09, Vol.23 (2), p.75-93 |
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description | Nitric oxide (NO) generated by the inducible isoform of nitric oxide synthase (iNOS) is involved in complex immunomodulatory and antitumoral mechanisms and has been described to have multiple beneficial microbicidal, antiviral and antiparasital effects. However, dysfunctional induction of iNOS expression seems to be involved in the pathophysiology of several human diseases. Therefore iNOS has to be regulated very tightly.
Modulation of expression, on both the transcriptional and post-transcriptional level, is the major regulation mechanism for iNOS. Pathways resulting in the induction of iNOS expression vary in different cells or species. Activation of the transcription factors NF-κB and STAT-1α and thereby activation of the iNOS promoter seems to be an essential step for the iNOS induction in most human cells. However, at least in the human system, also post-transcriptional mechanisms involving a complex network of RNA-binding proteins build up by AUF1, HuR, KSRP, PTB and TTP is critically involved in the regulation of iNOS expression. Recent data also implicate regulation of iNOS expression by non-coding RNAs (ncRNAs). |
doi_str_mv | 10.1016/j.niox.2010.04.007 |
format | Article |
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Modulation of expression, on both the transcriptional and post-transcriptional level, is the major regulation mechanism for iNOS. Pathways resulting in the induction of iNOS expression vary in different cells or species. Activation of the transcription factors NF-κB and STAT-1α and thereby activation of the iNOS promoter seems to be an essential step for the iNOS induction in most human cells. However, at least in the human system, also post-transcriptional mechanisms involving a complex network of RNA-binding proteins build up by AUF1, HuR, KSRP, PTB and TTP is critically involved in the regulation of iNOS expression. Recent data also implicate regulation of iNOS expression by non-coding RNAs (ncRNAs).</description><identifier>ISSN: 1089-8603</identifier><identifier>EISSN: 1089-8611</identifier><identifier>DOI: 10.1016/j.niox.2010.04.007</identifier><identifier>PMID: 20438856</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Expression ; Gene Expression Regulation, Enzymologic ; Humans ; iNOS ; mRNA stability ; Nitric Oxide Synthase Type II - biosynthesis ; Nitric Oxide Synthase Type II - genetics ; Promoter ; Promoter Regions, Genetic - genetics ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; RNA-binding proteins ; RNA-Binding Proteins - metabolism ; Transcription factors ; Transcription Factors - metabolism</subject><ispartof>Nitric oxide, 2010-09, Vol.23 (2), p.75-93</ispartof><rights>2010 Elsevier Inc.</rights><rights>Copyright 2010 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-ffdbb88e9929bf7e3710de62706d63284a7d8a366ed512551e2a5ceb277492f73</citedby><cites>FETCH-LOGICAL-c421t-ffdbb88e9929bf7e3710de62706d63284a7d8a366ed512551e2a5ceb277492f73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1089860310000583$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20438856$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pautz, Andrea</creatorcontrib><creatorcontrib>Art, Julia</creatorcontrib><creatorcontrib>Hahn, Susanne</creatorcontrib><creatorcontrib>Nowag, Sebastian</creatorcontrib><creatorcontrib>Voss, Cornelia</creatorcontrib><creatorcontrib>Kleinert, Hartmut</creatorcontrib><title>Regulation of the expression of inducible nitric oxide synthase</title><title>Nitric oxide</title><addtitle>Nitric Oxide</addtitle><description>Nitric oxide (NO) generated by the inducible isoform of nitric oxide synthase (iNOS) is involved in complex immunomodulatory and antitumoral mechanisms and has been described to have multiple beneficial microbicidal, antiviral and antiparasital effects. However, dysfunctional induction of iNOS expression seems to be involved in the pathophysiology of several human diseases. Therefore iNOS has to be regulated very tightly.
Modulation of expression, on both the transcriptional and post-transcriptional level, is the major regulation mechanism for iNOS. Pathways resulting in the induction of iNOS expression vary in different cells or species. Activation of the transcription factors NF-κB and STAT-1α and thereby activation of the iNOS promoter seems to be an essential step for the iNOS induction in most human cells. However, at least in the human system, also post-transcriptional mechanisms involving a complex network of RNA-binding proteins build up by AUF1, HuR, KSRP, PTB and TTP is critically involved in the regulation of iNOS expression. Recent data also implicate regulation of iNOS expression by non-coding RNAs (ncRNAs).</description><subject>Expression</subject><subject>Gene Expression Regulation, Enzymologic</subject><subject>Humans</subject><subject>iNOS</subject><subject>mRNA stability</subject><subject>Nitric Oxide Synthase Type II - biosynthesis</subject><subject>Nitric Oxide Synthase Type II - genetics</subject><subject>Promoter</subject><subject>Promoter Regions, Genetic - genetics</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>RNA-binding proteins</subject><subject>RNA-Binding Proteins - metabolism</subject><subject>Transcription factors</subject><subject>Transcription Factors - metabolism</subject><issn>1089-8603</issn><issn>1089-8611</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kF1LwzAYhYMoTqd_wAvpnVet-WiTFASR4RcMBNHrkCZvXUbXzKSV7d_bsrlLr97DyzkHzoPQFcEZwYTfLrPW-U1G8fDAeYaxOEJnBMsylZyQ44PGbILOY1xijHMm-Sma0FHIgp-h-3f46hvdOd8mvk66BSSwWQeIcf9xre2NqxpIWtcFZxK_cRaSuG27hY5wgU5q3US43N8p-nx6_Ji9pPO359fZwzw1OSVdWte2qqSEsqRlVQtggmALnArMLWdU5lpYqRnnYAtCi4IA1YWBigqRl7QWbIpudr3r4L97iJ1auWigaXQLvo9KMFaUxbB7cNKd0wQfY4BarYNb6bBVBKuRm1qqkZsauSmcq4HbELre1_fVCuwh8gdqMNztDDCM_HEQVDQOWgPWBTCdst791_8LpQ1-qg</recordid><startdate>20100915</startdate><enddate>20100915</enddate><creator>Pautz, Andrea</creator><creator>Art, Julia</creator><creator>Hahn, Susanne</creator><creator>Nowag, Sebastian</creator><creator>Voss, Cornelia</creator><creator>Kleinert, Hartmut</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>20100915</creationdate><title>Regulation of the expression of inducible nitric oxide synthase</title><author>Pautz, Andrea ; Art, Julia ; Hahn, Susanne ; Nowag, Sebastian ; Voss, Cornelia ; Kleinert, Hartmut</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-ffdbb88e9929bf7e3710de62706d63284a7d8a366ed512551e2a5ceb277492f73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Expression</topic><topic>Gene Expression Regulation, Enzymologic</topic><topic>Humans</topic><topic>iNOS</topic><topic>mRNA stability</topic><topic>Nitric Oxide Synthase Type II - biosynthesis</topic><topic>Nitric Oxide Synthase Type II - genetics</topic><topic>Promoter</topic><topic>Promoter Regions, Genetic - genetics</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>RNA-binding proteins</topic><topic>RNA-Binding Proteins - metabolism</topic><topic>Transcription factors</topic><topic>Transcription Factors - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pautz, Andrea</creatorcontrib><creatorcontrib>Art, Julia</creatorcontrib><creatorcontrib>Hahn, Susanne</creatorcontrib><creatorcontrib>Nowag, Sebastian</creatorcontrib><creatorcontrib>Voss, Cornelia</creatorcontrib><creatorcontrib>Kleinert, Hartmut</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>Nitric oxide</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pautz, Andrea</au><au>Art, Julia</au><au>Hahn, Susanne</au><au>Nowag, Sebastian</au><au>Voss, Cornelia</au><au>Kleinert, Hartmut</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regulation of the expression of inducible nitric oxide synthase</atitle><jtitle>Nitric oxide</jtitle><addtitle>Nitric Oxide</addtitle><date>2010-09-15</date><risdate>2010</risdate><volume>23</volume><issue>2</issue><spage>75</spage><epage>93</epage><pages>75-93</pages><issn>1089-8603</issn><eissn>1089-8611</eissn><abstract>Nitric oxide (NO) generated by the inducible isoform of nitric oxide synthase (iNOS) is involved in complex immunomodulatory and antitumoral mechanisms and has been described to have multiple beneficial microbicidal, antiviral and antiparasital effects. However, dysfunctional induction of iNOS expression seems to be involved in the pathophysiology of several human diseases. Therefore iNOS has to be regulated very tightly.
Modulation of expression, on both the transcriptional and post-transcriptional level, is the major regulation mechanism for iNOS. Pathways resulting in the induction of iNOS expression vary in different cells or species. Activation of the transcription factors NF-κB and STAT-1α and thereby activation of the iNOS promoter seems to be an essential step for the iNOS induction in most human cells. However, at least in the human system, also post-transcriptional mechanisms involving a complex network of RNA-binding proteins build up by AUF1, HuR, KSRP, PTB and TTP is critically involved in the regulation of iNOS expression. Recent data also implicate regulation of iNOS expression by non-coding RNAs (ncRNAs).</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>20438856</pmid><doi>10.1016/j.niox.2010.04.007</doi><tpages>19</tpages></addata></record> |
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subjects | Expression Gene Expression Regulation, Enzymologic Humans iNOS mRNA stability Nitric Oxide Synthase Type II - biosynthesis Nitric Oxide Synthase Type II - genetics Promoter Promoter Regions, Genetic - genetics RNA, Messenger - genetics RNA, Messenger - metabolism RNA-binding proteins RNA-Binding Proteins - metabolism Transcription factors Transcription Factors - metabolism |
title | Regulation of the expression of inducible nitric oxide synthase |
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