| pubmed-article:20850011 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:20850011 | lifeskim:mentions | umls-concept:C0596901 | lld:lifeskim |
| pubmed-article:20850011 | lifeskim:mentions | umls-concept:C0033684 | lld:lifeskim |
| pubmed-article:20850011 | lifeskim:mentions | umls-concept:C1414119 | lld:lifeskim |
| pubmed-article:20850011 | lifeskim:mentions | umls-concept:C1421412 | lld:lifeskim |
| pubmed-article:20850011 | lifeskim:mentions | umls-concept:C0205263 | lld:lifeskim |
| pubmed-article:20850011 | pubmed:issue | 6 | lld:pubmed |
| pubmed-article:20850011 | pubmed:dateCreated | 2010-9-20 | lld:pubmed |
| pubmed-article:20850011 | pubmed:abstractText | In response to many apoptotic stimuli, oligomerization of Bax is essential for mitochondrial outer membrane permeabilization and the ensuing release of cytochrome c. These events are accompanied by mitochondrial fission that appears to require Drp1, a large GTPase of the dynamin superfamily. Loss of Drp1 leads to decreased cytochrome c release by a mechanism that is poorly understood. Here we show that Drp1 stimulates tBid-induced Bax oligomerization and cytochrome c release by promoting tethering and hemifusion of membranes in vitro. This function of Drp1 is independent of its GTPase activity and relies on arginine 247 and the presence of cardiolipin in membranes. In cells, overexpression of Drp1 R247A/E delays Bax oligomerization and cell death. Our findings uncover a function of Drp1 and provide insight into the mechanism of Bax oligomerization. | lld:pubmed |
| pubmed-article:20850011 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20850011 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20850011 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20850011 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20850011 | pubmed:language | eng | lld:pubmed |
| pubmed-article:20850011 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20850011 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:20850011 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20850011 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20850011 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20850011 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20850011 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20850011 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20850011 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20850011 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20850011 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:20850011 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:20850011 | pubmed:issn | 1097-4172 | lld:pubmed |
| pubmed-article:20850011 | pubmed:author | pubmed-author:MartinouJean-... | lld:pubmed |
| pubmed-article:20850011 | pubmed:author | pubmed-author:MansteinDietm... | lld:pubmed |
| pubmed-article:20850011 | pubmed:author | pubmed-author:MedaPaoloP | lld:pubmed |
| pubmed-article:20850011 | pubmed:author | pubmed-author:Bossy-WetzelE... | lld:pubmed |
| pubmed-article:20850011 | pubmed:author | pubmed-author:MontessuitSyl... | lld:pubmed |
| pubmed-article:20850011 | pubmed:author | pubmed-author:BasañezGorkaG | lld:pubmed |
| pubmed-article:20850011 | pubmed:author | pubmed-author:Schwarzenbach... | lld:pubmed |
| pubmed-article:20850011 | pubmed:author | pubmed-author:TerronesOihan... | lld:pubmed |
| pubmed-article:20850011 | pubmed:author | pubmed-author:Lucken-Ardjom... | lld:pubmed |
| pubmed-article:20850011 | pubmed:author | pubmed-author:HerzigSébasti... | lld:pubmed |
| pubmed-article:20850011 | pubmed:author | pubmed-author:SomasekharanS... | lld:pubmed |
| pubmed-article:20850011 | pubmed:copyrightInfo | Copyright © 2010 Elsevier Inc. All rights reserved. | lld:pubmed |
| pubmed-article:20850011 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:20850011 | pubmed:day | 17 | lld:pubmed |
| pubmed-article:20850011 | pubmed:volume | 142 | lld:pubmed |
| pubmed-article:20850011 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:20850011 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:20850011 | pubmed:pagination | 889-901 | lld:pubmed |
| pubmed-article:20850011 | pubmed:dateRevised | 2010-12-17 | lld:pubmed |
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| pubmed-article:20850011 | pubmed:meshHeading | pubmed-meshheading:20850011... | lld:pubmed |
| pubmed-article:20850011 | pubmed:meshHeading | pubmed-meshheading:20850011... | lld:pubmed |
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| pubmed-article:20850011 | pubmed:meshHeading | pubmed-meshheading:20850011... | lld:pubmed |
| pubmed-article:20850011 | pubmed:year | 2010 | lld:pubmed |
| pubmed-article:20850011 | pubmed:articleTitle | Membrane remodeling induced by the dynamin-related protein Drp1 stimulates Bax oligomerization. | lld:pubmed |
| pubmed-article:20850011 | pubmed:affiliation | Department of Cell Biology, University of Geneva, Sciences III, 30 quai Ernest Ansermet, 1211 Geneva 4, Switzerland. | lld:pubmed |
| pubmed-article:20850011 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:20850011 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:20850011 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:20850011 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:20850011 | lld:entrezgene |
