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...
Gespeichert in:
Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 2013-06, Vol.110 (26), p.E2420 |
---|---|
Hauptverfasser: | , , , , , , , , , , |
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 & 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 |