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Journal of Pharmacology And Experimental Therapeutics Fast Forward
First published on February 10, 2005; DOI: 10.1124/jpet.104.081992


0022-3565/05/3133-1017-1026$20.00
JPET 313:1017-1026, 2005
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CARDIOVASCULAR

Intact Actin Filaments Are Required for Cytosolic Phospholipase A2 Translocation but Not for Its Activation by Norepinephrine in Vascular Smooth Muscle Cells{boxs}

Soghra Fatima, Fariborz A. Yaghini, Zoran Pavicevic, Shailaja Kalyankrishna, Nauzanene Jafari, Elizabeth Luong, Anne Estes, and Kafait U. Malik

Department of Pharmacology, College of Medicine, University of Tennessee Health Science Center, Memphis, Tennessee

Cytosolic phospholipase A2 (cPLA2) is activated and translocated to the nuclear envelope by various vasoactive agents, including norepinephrine (NE), and releases arachidonic acid (AA) from tissue phospholipids. We previously demonstrated that NE-induced cPLA2 translocation to the nuclear envelope is mediated via its phosphorylation by calcium/calmodulin-dependent kinase-II in rabbit vascular smooth muscle cells (VSMCs). Cytoskeletal structures actin and microtubule filaments have been implicated in the trafficking of proteins to various cellular sites. This study was conducted to investigate the contribution of actin and microtubule filaments to cPLA2 translocation to the nuclear envelope and its activation by NE in rabbit VSMCs. NE (10 µM) caused cPLA2 translocation to the nuclear envelope as determined by immunofluorescence. Cytochalasin D (CD; 0.5 µM) and latrunculin A (LA; 0.5 µM) that disrupted actin filaments, blocked cPLA2 translocation elicited by NE. On the other hand, disruption of microtubule filaments by 10 µM colchicine did not block NE-induced cPLA2 translocation to the nuclear envelope. CD and LA did not inhibit NE-induced increase in cytosolic calcium and cPLA2 activity, determined from the hydrolysis of L-1-[14C]arachidonyl phosphatidylcholine and release of AA. Coimmunoprecipitation studies showed an association of actin with cPLA2, which was not altered by CD or LA. Far-Western analysis showed that cPLA2 interacts directly with actin. Our data suggest that NE-induced cPLA2 translocation to the nuclear envelope requires an intact actin but not microtubule filaments and that cPLA2 phosphorylation and activation and AA release are independent of its translocation to the nuclear envelope in rabbit VSMCs.


Received December 9, 2004; accepted February 8, 2005.

Address correspondence to: Dr. Kafait U. Malik, Department of Pharmacology, College of Medicine, 874 Union Ave., University of Tennessee Health Science Center, Memphis, TN 38163. E-mail: kmalik{at}utmem.edu




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[Abstract] [Full Text] [PDF]




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