Ca^sup 2+^/calmodulin-dependent protein kinase kinase [Beta] phosphorylation of Sirtuin 1 in endothelium is atheroprotective

Atheroprotective flow exerts antioxidative and anti-inflammatory effects on vascular endothelial cells (ECs), in part through the induction of Sirtuin 1 (SIRT1), a class III histone deacetylase. The role of .../calmodulin-dependent protein kinase kinase (CaMKK)β in flow induction of SIRT1 both in vi...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 2013-06, Vol.110 (26), p.E2420
Hauptverfasser: Wen, Liang, Chen, Zhen, Zhang, Fan, Cui, Xiaopei, Sun, Wei, Geary, Greg G, Wang, Yinsheng, Johnson, David A, Zhu, Yi, Chien, Shu, Shyy, John Y-J
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue 26
container_start_page E2420
container_title Proceedings of the National Academy of Sciences - PNAS
container_volume 110
creator Wen, Liang
Chen, Zhen
Zhang, Fan
Cui, Xiaopei
Sun, Wei
Geary, Greg G
Wang, Yinsheng
Johnson, David A
Zhu, Yi
Chien, Shu
Shyy, John Y-J
description Atheroprotective flow exerts antioxidative and anti-inflammatory effects on vascular endothelial cells (ECs), in part through the induction of Sirtuin 1 (SIRT1), a class III histone deacetylase. The role of .../calmodulin-dependent protein kinase kinase (CaMKK)β in flow induction of SIRT1 both in vitro and in vivo was investigated. Pulsatile shear stress mimicking atheroprotective flow increased the level of SIRT1 in cultured ECs by enhancing its stability, and this effect was abolished by inhibition or knockdown of CaMKKβ. Flow-enhanced SIRT1 stability was primarily mediated by CaMKKβ phosphorylation of SIRT1 at Ser-27 and Ser-47, as evidenced by in vitro kinase assay, mass spectrometry, and experiments using loss- or gain-of-function SIRT1 mutants. Flow-induced CaMKKβ phosphorylation of SIRT1 Ser-27 and Ser-47 increased antioxidative and anti-inflammatory capacities. Ablation of CaMKKβ or SIRT1 in mice with an apolipoprotein E-null background showed increased atherosclerosis both in athero-prone and in athero-protective areas. The results suggest that the CaMKKβ-SIRT1 axis in ECs is mechanosensitive, antioxidative, and anti-inflammatory. (ProQuest: ... denotes formulae/symbols omitted.)
format Article
fullrecord <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_journals_1372466568</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3008405571</sourcerecordid><originalsourceid>FETCH-proquest_journals_13724665683</originalsourceid><addsrcrecordid>eNqNjMkKwjAURYMoWId_eOBSimntuFUU97oTlWCfmJomNYMg-PEG0b2LO8A93A4JIlpGYZaUtEsCSuM8LJI46ZOBMTWltEwLGpDXkh2NayGeHmdnJhpVOcFlWGGLskJpodXKIpdw45IZ_MV-gZYdoL0q46WfglmuJKgLbLm2zvMRePMfyl5RcNcAN8B81-rzeLb8gSPSuzBhcPzNIZmsV7vlJvTI3aGxp1o5Lf10iuZ5nGRZmhXz_6g3PmhROw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1372466568</pqid></control><display><type>article</type><title>Ca^sup 2+^/calmodulin-dependent protein kinase kinase [Beta] phosphorylation of Sirtuin 1 in endothelium is atheroprotective</title><source>Jstor Complete Legacy</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><source>Free Full-Text Journals in Chemistry</source><creator>Wen, Liang ; Chen, Zhen ; Zhang, Fan ; Cui, Xiaopei ; Sun, Wei ; Geary, Greg G ; Wang, Yinsheng ; Johnson, David A ; Zhu, Yi ; Chien, Shu ; Shyy, John Y-J</creator><creatorcontrib>Wen, Liang ; Chen, Zhen ; Zhang, Fan ; Cui, Xiaopei ; Sun, Wei ; Geary, Greg G ; Wang, Yinsheng ; Johnson, David A ; Zhu, Yi ; Chien, Shu ; Shyy, John Y-J</creatorcontrib><description>Atheroprotective flow exerts antioxidative and anti-inflammatory effects on vascular endothelial cells (ECs), in part through the induction of Sirtuin 1 (SIRT1), a class III histone deacetylase. The role of .../calmodulin-dependent protein kinase kinase (CaMKK)β in flow induction of SIRT1 both in vitro and in vivo was investigated. Pulsatile shear stress mimicking atheroprotective flow increased the level of SIRT1 in cultured ECs by enhancing its stability, and this effect was abolished by inhibition or knockdown of CaMKKβ. Flow-enhanced SIRT1 stability was primarily mediated by CaMKKβ phosphorylation of SIRT1 at Ser-27 and Ser-47, as evidenced by in vitro kinase assay, mass spectrometry, and experiments using loss- or gain-of-function SIRT1 mutants. Flow-induced CaMKKβ phosphorylation of SIRT1 Ser-27 and Ser-47 increased antioxidative and anti-inflammatory capacities. Ablation of CaMKKβ or SIRT1 in mice with an apolipoprotein E-null background showed increased atherosclerosis both in athero-prone and in athero-protective areas. The results suggest that the CaMKKβ-SIRT1 axis in ECs is mechanosensitive, antioxidative, and anti-inflammatory. (ProQuest: ... denotes formulae/symbols omitted.)</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><language>eng</language><publisher>Washington: National Academy of Sciences</publisher><subject>Cells ; Kinases ; Mutation ; Phosphorylation ; Rodents</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2013-06, Vol.110 (26), p.E2420</ispartof><rights>Copyright National Academy of Sciences Jun 25, 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids></links><search><creatorcontrib>Wen, Liang</creatorcontrib><creatorcontrib>Chen, Zhen</creatorcontrib><creatorcontrib>Zhang, Fan</creatorcontrib><creatorcontrib>Cui, Xiaopei</creatorcontrib><creatorcontrib>Sun, Wei</creatorcontrib><creatorcontrib>Geary, Greg G</creatorcontrib><creatorcontrib>Wang, Yinsheng</creatorcontrib><creatorcontrib>Johnson, David A</creatorcontrib><creatorcontrib>Zhu, Yi</creatorcontrib><creatorcontrib>Chien, Shu</creatorcontrib><creatorcontrib>Shyy, John Y-J</creatorcontrib><title>Ca^sup 2+^/calmodulin-dependent protein kinase kinase [Beta] phosphorylation of Sirtuin 1 in endothelium is atheroprotective</title><title>Proceedings of the National Academy of Sciences - PNAS</title><description>Atheroprotective flow exerts antioxidative and anti-inflammatory effects on vascular endothelial cells (ECs), in part through the induction of Sirtuin 1 (SIRT1), a class III histone deacetylase. The role of .../calmodulin-dependent protein kinase kinase (CaMKK)β in flow induction of SIRT1 both in vitro and in vivo was investigated. Pulsatile shear stress mimicking atheroprotective flow increased the level of SIRT1 in cultured ECs by enhancing its stability, and this effect was abolished by inhibition or knockdown of CaMKKβ. Flow-enhanced SIRT1 stability was primarily mediated by CaMKKβ phosphorylation of SIRT1 at Ser-27 and Ser-47, as evidenced by in vitro kinase assay, mass spectrometry, and experiments using loss- or gain-of-function SIRT1 mutants. Flow-induced CaMKKβ phosphorylation of SIRT1 Ser-27 and Ser-47 increased antioxidative and anti-inflammatory capacities. Ablation of CaMKKβ or SIRT1 in mice with an apolipoprotein E-null background showed increased atherosclerosis both in athero-prone and in athero-protective areas. The results suggest that the CaMKKβ-SIRT1 axis in ECs is mechanosensitive, antioxidative, and anti-inflammatory. (ProQuest: ... denotes formulae/symbols omitted.)</description><subject>Cells</subject><subject>Kinases</subject><subject>Mutation</subject><subject>Phosphorylation</subject><subject>Rodents</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqNjMkKwjAURYMoWId_eOBSimntuFUU97oTlWCfmJomNYMg-PEG0b2LO8A93A4JIlpGYZaUtEsCSuM8LJI46ZOBMTWltEwLGpDXkh2NayGeHmdnJhpVOcFlWGGLskJpodXKIpdw45IZ_MV-gZYdoL0q46WfglmuJKgLbLm2zvMRePMfyl5RcNcAN8B81-rzeLb8gSPSuzBhcPzNIZmsV7vlJvTI3aGxp1o5Lf10iuZ5nGRZmhXz_6g3PmhROw</recordid><startdate>20130625</startdate><enddate>20130625</enddate><creator>Wen, Liang</creator><creator>Chen, Zhen</creator><creator>Zhang, Fan</creator><creator>Cui, Xiaopei</creator><creator>Sun, Wei</creator><creator>Geary, Greg G</creator><creator>Wang, Yinsheng</creator><creator>Johnson, David A</creator><creator>Zhu, Yi</creator><creator>Chien, Shu</creator><creator>Shyy, John Y-J</creator><general>National Academy of Sciences</general><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20130625</creationdate><title>Ca^sup 2+^/calmodulin-dependent protein kinase kinase [Beta] phosphorylation of Sirtuin 1 in endothelium is atheroprotective</title><author>Wen, Liang ; Chen, Zhen ; Zhang, Fan ; Cui, Xiaopei ; Sun, Wei ; Geary, Greg G ; Wang, Yinsheng ; Johnson, David A ; Zhu, Yi ; Chien, Shu ; Shyy, John Y-J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_13724665683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Cells</topic><topic>Kinases</topic><topic>Mutation</topic><topic>Phosphorylation</topic><topic>Rodents</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wen, Liang</creatorcontrib><creatorcontrib>Chen, Zhen</creatorcontrib><creatorcontrib>Zhang, Fan</creatorcontrib><creatorcontrib>Cui, Xiaopei</creatorcontrib><creatorcontrib>Sun, Wei</creatorcontrib><creatorcontrib>Geary, Greg G</creatorcontrib><creatorcontrib>Wang, Yinsheng</creatorcontrib><creatorcontrib>Johnson, David A</creatorcontrib><creatorcontrib>Zhu, Yi</creatorcontrib><creatorcontrib>Chien, Shu</creatorcontrib><creatorcontrib>Shyy, John Y-J</creatorcontrib><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wen, Liang</au><au>Chen, Zhen</au><au>Zhang, Fan</au><au>Cui, Xiaopei</au><au>Sun, Wei</au><au>Geary, Greg G</au><au>Wang, Yinsheng</au><au>Johnson, David A</au><au>Zhu, Yi</au><au>Chien, Shu</au><au>Shyy, John Y-J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ca^sup 2+^/calmodulin-dependent protein kinase kinase [Beta] phosphorylation of Sirtuin 1 in endothelium is atheroprotective</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><date>2013-06-25</date><risdate>2013</risdate><volume>110</volume><issue>26</issue><spage>E2420</spage><pages>E2420-</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>Atheroprotective flow exerts antioxidative and anti-inflammatory effects on vascular endothelial cells (ECs), in part through the induction of Sirtuin 1 (SIRT1), a class III histone deacetylase. The role of .../calmodulin-dependent protein kinase kinase (CaMKK)β in flow induction of SIRT1 both in vitro and in vivo was investigated. Pulsatile shear stress mimicking atheroprotective flow increased the level of SIRT1 in cultured ECs by enhancing its stability, and this effect was abolished by inhibition or knockdown of CaMKKβ. Flow-enhanced SIRT1 stability was primarily mediated by CaMKKβ phosphorylation of SIRT1 at Ser-27 and Ser-47, as evidenced by in vitro kinase assay, mass spectrometry, and experiments using loss- or gain-of-function SIRT1 mutants. Flow-induced CaMKKβ phosphorylation of SIRT1 Ser-27 and Ser-47 increased antioxidative and anti-inflammatory capacities. Ablation of CaMKKβ or SIRT1 in mice with an apolipoprotein E-null background showed increased atherosclerosis both in athero-prone and in athero-protective areas. The results suggest that the CaMKKβ-SIRT1 axis in ECs is mechanosensitive, antioxidative, and anti-inflammatory. (ProQuest: ... denotes formulae/symbols omitted.)</abstract><cop>Washington</cop><pub>National Academy of Sciences</pub></addata></record>
fulltext fulltext
identifier ISSN: 0027-8424
ispartof Proceedings of the National Academy of Sciences - PNAS, 2013-06, Vol.110 (26), p.E2420
issn 0027-8424
1091-6490
language eng
recordid cdi_proquest_journals_1372466568
source Jstor Complete Legacy; PubMed Central; Alma/SFX Local Collection; Free Full-Text Journals in Chemistry
subjects Cells
Kinases
Mutation
Phosphorylation
Rodents
title Ca^sup 2+^/calmodulin-dependent protein kinase kinase [Beta] phosphorylation of Sirtuin 1 in endothelium is atheroprotective
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-21T09%3A54%3A06IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Ca%5Esup%202+%5E/calmodulin-dependent%20protein%20kinase%20kinase%20%5BBeta%5D%20phosphorylation%20of%20Sirtuin%201%20in%20endothelium%20is%20atheroprotective&rft.jtitle=Proceedings%20of%20the%20National%20Academy%20of%20Sciences%20-%20PNAS&rft.au=Wen,%20Liang&rft.date=2013-06-25&rft.volume=110&rft.issue=26&rft.spage=E2420&rft.pages=E2420-&rft.issn=0027-8424&rft.eissn=1091-6490&rft_id=info:doi/&rft_dat=%3Cproquest%3E3008405571%3C/proquest%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1372466568&rft_id=info:pmid/&rfr_iscdi=true