Ceramide kinase uses ceramide provided by ceramide transport protein: localization to organelles of eicosanoid synthesis

被引:96
作者
Lamour, Nadia F.
Stahelin, Robert V.
Wijesinghe, Dayanjan S.
Maceyka, Michael
Wang, Elaine
Allegood, Jeremy C.
Merrill, Alfred H., Jr.
Cho, Wonhwa
Chalfant, Charles E. [1 ]
机构
[1] Virginia Commonwealth Univ, Med Coll Virginia, Dept Biochem, Richmond, VA 23298 USA
[2] Indiana Univ, Sch Med, Dept Biochem & Mol Biol, South Bend, IN 46617 USA
[3] Georgia Inst Technol, Dept Biol, Atlanta, GA 30332 USA
[4] Univ Illinois, Dept Chem, Chicago, IL 60607 USA
[5] Hunter Holmes McGuire Vet Adm Med Ctr, Res & Dev, Richmond, VA 23249 USA
关键词
ceramide-1-phosphate; prostaglandins; phospholipase A(2); inflammation; arachidonic acid;
D O I
10.1194/jlr.M700083-JLR200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ceramide kinase (CERK) is a critical mediator of eicosanoid synthesis, and its product, ceramide-1-phosphate (C1P), is required for the production of prostaglandins in response to several inflammatory agonists. In this study, mass spectrometry analysis disclosed that the main forms of C1P in cells were C-16:0 C1P and C-18:0 C1P, suggesting that CERK uses ceramide transported to the trans-Golgi apparatus by ceramide transport protein (CERT). To this end, downregulation of CERT by RNA interference technology dramatically reduced the levels of newly synthesized C1P (kinase-derived) as well as significantly reduced the total mass levels of C1P in cells. Confocal microscopy, subcellular fractionation, and surface plasmon resonance analysis were used to further localize CERK to the trans-Golgi network, placing the generation of C1P in the proper intracellular location for the recruitment of cytosolic phospholipase A2 alpha. In conclusion, these results demonstrate that CERK localizes to areas of eicosanoid synthesis and uses a ceramide "pool" transported in an active manner via CERT.
引用
收藏
页码:1293 / 1304
页数:12
相关论文
共 42 条
[1]  
Bajjalieh S, 2000, METHOD ENZYMOL, V311, P207
[2]  
BAJJALIEH SM, 1989, J BIOL CHEM, V264, P14354
[3]   Roles of ionic residues of the C1 domain in protein kinase C-α activation and the origin of phosphatidylserine specificity [J].
Bittova, L ;
Stahelin, RV ;
Cho, W .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (06) :4218-4226
[4]  
BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
[5]   Ceramide kinase targeting and activity determined by its N-terminal pleckstrin homology domain [J].
Carré, A ;
Graf, C ;
Stora, S ;
Mechtcheriakova, D ;
Csonga, R ;
Urtz, N ;
Billich, A ;
Baumruker, T ;
Bornancin, F .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 324 (04) :1215-1219
[6]  
DRESSLER KA, 1990, J BIOL CHEM, V265, P14917
[7]   Cobalt-catalyzed allylation of aldimines by allylic acetates [J].
Gomes, P ;
Gosmini, C ;
Périchon, J .
LETTERS IN ORGANIC CHEMISTRY, 2004, 1 (02) :105-108
[8]  
GOMEZMUNOZ A, 1995, MOL PHARMACOL, V47, P883
[9]   Association of cPLA2-α and COX-1 with the Golgi apparatus of A549 human lung epithelial cells [J].
Grewal, S ;
Ponnambalam, S ;
Walker, JH .
JOURNAL OF CELL SCIENCE, 2003, 116 (11) :2303-2310
[10]   Molecular machinery for non-vesicular trafficking of ceramide [J].
Hanada, K ;
Kumagai, K ;
Yasuda, S ;
Miura, Y ;
Kawano, M ;
Fukasawa, M ;
Nishijima, M .
NATURE, 2003, 426 (6968) :803-809