Plasma membrane Ca2+-ATPase associates with CLP36, α-actinin and actin in human platelets

Larry D. Bozulic; Mohammad T. Malik; David W. Powell; Adrian Nanez; Andrew J. Link; Kenneth S. Ramos; William L. Dean

doi:10.1160/TH06-08-0438

Thrombosis and Haemostasis, Table of Contents

Thromb Haemost 2007; 97(04): 587-597
DOI: 10.1160/TH06-08-0438

Platelets and Blood Cells

Schattauer GmbH

Plasma membrane Ca²⁺-ATPase associates with CLP36, α-actinin and actin in human platelets

Larry D. Bozulic

¹Department of Biochemistry and Molecular Biology

,

Mohammad T. Malik

¹Department of Biochemistry and Molecular Biology

,

David W. Powell

¹Department of Biochemistry and Molecular Biology

²Department of Medicine, University of Louisville, School of Medicine, Louisville, Kentucky, USA

,

Adrian Nanez

¹Department of Biochemistry and Molecular Biology

,

Andrew J. Link

³Department of Microbiology and Immunology, Vanderbilt University School of Medicine, Nashville, Tennessee, USA

,

Kenneth S. Ramos

¹Department of Biochemistry and Molecular Biology

,

William L. Dean

¹Department of Biochemistry and Molecular Biology

› Author Affiliations

Abstract

Summary

The plasma membrane Ca²⁺-ATPase (PMCA) plays an essentialrole in maintaining low cytosolic Ca²⁺ in resting platelets. Earlier studies demonstrated that the 4b isoform of PMCA interacts viaits C-terminal end with the PDZ domains of membrane-associated guanylate kinase proteins. Activation of saponin-permeabilized platelets in the presence of a peptide composed of the lastten residues of the PMCA4b C-terminus leads to a significant decrease of PMCA associated with the cytoskeleton, suggesting that PDZ domain interactions play a role in tethering the pumpto the cytoskeleton. Here we present experiments conducted to evaluate the mechanism of this association. Co-immunoprecipitationassays coupled with liquid chromatography/tandemmass spectrometry analysis and immunoblotting were used to identify proteins that interact with PMCA in the resting platelet. Our results indicate that the only PDZ domain-containing proteinassociated with PMCA is the LIM family protein, CLP36. Glutathione-S-transferase pull-down from a platelet extractusing a fusion protein containing the C-terminal PDZ domainbinding motif of PMCA confirmed binding of CLP36 to PMCA. Gel filtration chromatography of detergent-solubilized plateletsdemonstrated the existence of a 1,000-kDa complex containingPMCA and CLP36, and in addition, α -actinin and actin. Immunoflourescencemicroscopy confirmed the co-localization ofPMCA with CLP36 in resting and activated platelets. Taken togetherthese results suggest that PMCA is localized in non-filamentousactin complexes in resting platelets by means of PDZdomain interactions and then associates with the actin cytoskeletonduring cytoskeletal rearrangement upon platelet activation. Thus, in addition to the reversible serine/threonine andtyrosine phosphorylation events previously described in humanplatelets, PMCA function may be regulated by interactions withanchoring and cytoskeletal proteins.

Keywords

Platelets - plasma membrane Ca²⁺-ATPase - calcium signaling - filopodia

Full Text

References

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