Source:http://linkedlifedata.com/resource/pubmed/id/17226776
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
|
pubmed:dateCreated |
2007-7-31
|
pubmed:abstractText |
Phospholipid scramblase 3 (PLS3) is a member of the phospholipid scramblase family present in mitochondria. PLS3 plays an important role in regulation of mitochondrial morphology, respiratory function, and apoptotic responses. PLS3 is phosphorylated by PKC-delta at Thr21 and is the mitochondrial target of PKC-delta-induced apoptosis. Cells with overexpression of PLS3, but not the phosphoinhibitory mutant PLS3(T21A), are more susceptible to apoptosis induced by AD198, an extranuclear targeted anthracycline that activates PKC-delta. Here we report that the phosphomimetic mutant of PLS3(T21D) by itself can induce apoptosis in HeLa cells. Using proteoliposomes with addition of pyrene-labeled phosphatidylcholine (PC) at the outer leaflet, we measured the lipid flip-flop activity of PLS3 and its phosphorylation mutant. PLS3(T21D) is more potent than wild-type PLS3 or PLS3(T21A) to transfer pyrene-PC from the outer leaflet to the inner leaflet of liposomes. Based on our previous finding that PLS3 enhances tBid-induced mitochondrial damages, we tested the hypothesis that PLS3 enhances cardiolipin translocation to mitochondrial surface and facilitates tBid targeting. Fluorescein-labeled tBid(G94E) was used as a probe to quantify cardiolipin on the surface of mitochondria. Mitochondria from cells treated with AD198 or cells expressing PLS3(T21D) had a higher level of tBid-binding capacity than control cells or cells expressing wild-type PLS3. These findings indicate that phosphorylation of PLS3 by PKC-delta induces PLS3 activation to facilitate mitochondrial targeting of tBid and apoptosis.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/BH3 Interacting Domain Death...,
http://linkedlifedata.com/resource/pubmed/chemical/Doxorubicin,
http://linkedlifedata.com/resource/pubmed/chemical/Mutant Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/N-benzyladriamycin-14-valerate,
http://linkedlifedata.com/resource/pubmed/chemical/PLSCR3 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Phospholipid Transfer Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinase C-delta
|
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
0730-2312
|
pubmed:author | |
pubmed:copyrightInfo |
(c) 2007 Wiley-Liss, Inc.
|
pubmed:issnType |
Print
|
pubmed:day |
1
|
pubmed:volume |
101
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1210-21
|
pubmed:dateRevised |
2009-11-19
|
pubmed:meshHeading |
pubmed-meshheading:17226776-Apoptosis,
pubmed-meshheading:17226776-BH3 Interacting Domain Death Agonist Protein,
pubmed-meshheading:17226776-Down-Regulation,
pubmed-meshheading:17226776-Doxorubicin,
pubmed-meshheading:17226776-Enzyme Activation,
pubmed-meshheading:17226776-HeLa Cells,
pubmed-meshheading:17226776-Humans,
pubmed-meshheading:17226776-Mitochondria,
pubmed-meshheading:17226776-Mutant Proteins,
pubmed-meshheading:17226776-Phospholipid Transfer Proteins,
pubmed-meshheading:17226776-Phosphorylation,
pubmed-meshheading:17226776-Protein Binding,
pubmed-meshheading:17226776-Protein Kinase C-delta,
pubmed-meshheading:17226776-Protein Transport,
pubmed-meshheading:17226776-Transgenes
|
pubmed:year |
2007
|
pubmed:articleTitle |
Phosphorylation of mitochondrial phospholipid scramblase 3 by protein kinase C-delta induces its activation and facilitates mitochondrial targeting of tBid.
|
pubmed:affiliation |
Kunming Medical College, Kunming, Yunnan, P.R. China.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
|