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Vol. 42, No. 6, 2005
Issue release date: November–December 2005
Section title: Research Paper
J Vasc Res 2005;42:483–491

Serine 68 Phospholemman Phosphorylation during Forskolin-Induced Swine Carotid Artery Relaxation

Rembold C.M.a-c · Ripley M.L.a · Meeks M.K.a · Geddis L.M.c · Kutchai H.C.c · Marassi F.M.d · Cheung J.Y.e · Moorman J.R.a, b
aCardiovascular Division, Department of Internal Medicine, bCardiovascular Research Center, cDepartment of Molecular Physiology and Biological Physics, University of Virginia Health System, Charlottesville, Va., dThe Burnham Institute, La Jolla, Calif., and eDepartment of Cellular and Molecular Physiology, Pennsylvania State University College of Medicine, Hershey, Pa., USA
email Corresponding Author

Christopher M. Rembold, MD

Cardiovascular Division, Box 801395

University of Virginia Health System

Charlottesville, VA 22908-1395 (USA)

Tel. +1 434 924 2825, Fax +1 434 982 3162, E-Mail

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Background: Phospholemman (PLM) is an abundant phosphoprotein in the plasma membrane of cardiac, skeletal and smooth muscle. It is a member of the FXYD family of proteins that bind to and regulate the Na,K-ATPase. Protein kinase A (PKA) is known to phosphorylate PLM on serine 68 (S68), although the functional effect of S68 PLM phosphorylation is unclear. We therefore evaluated S68 PLM phosphorylation in swine carotid arteries. Methods: Two anti-PLM antibodies, one to S68 phosphorylated PLM and one to unphosphorylated PLM, were made to PLM peptides in rabbits and tested with purified PLM and PKA-treated PLM. Swine carotid arteries were mounted isometrically, contracted, relaxed with forskolin and then homogenized. Proteins were separated on SDS gels and the intensity of immunoreactivity to the two PLM antibodies determined on immunoblots. Results: The antipeptide antibody ‘C2’ primarily reacted with unphosphorylated PLM, and the antipeptide antibody ‘CP68’ detected S68 PLM phosphorylation. Histamine stimulation of intact swine carotid artery induced a contraction, increased the CP68 PLM antibody signal and reduced the C2 PLM antibody signal. High extracellular [K+] depolarization induced a contraction without altering the C2 or CP68 PLM signal. Forskolin-induced relaxation of histamine or extracellular [K+] contracted arteries correlated with an increased CP68 signal. Nitroglycerin-induced relaxation was not associated with changes in the C2 or CP68 PLM signal. Conclusions: These data suggest that a contractile agonist increased S68 PLM phosphorylation. Agents that increase [cAMP], but not agents that increase [cGMP], increased S68 PLM phosphorylation. S68 PLM phosphorylation may be involved in cAMP-dependent regulation of smooth muscle force.

© 2005 S. Karger AG, Basel

Article / Publication Details

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Abstract of Research Paper

Received: 1/5/2005
Accepted: 6/26/2005
Published online: 10/20/2005

Number of Print Pages: 9
Number of Figures: 6
Number of Tables: 0

ISSN: 1018-1172 (Print)
eISSN: 1423-0135 (Online)

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