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Calpain-mediated Regulation of Platelet Signaling Pathways

Overview
Specialty Hematology
Date 2007 Apr 7
PMID 17414215
Citations 25
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Abstract

Purpose Of Review: There is considerable interest in understanding the function and mechanism of calpains in platelet aggregation, spreading, and granular secretion pathways. Recent insights from the calpain-1 knockout platelets suggest a pivotal role of these cysteine proteases in the regulation of outside-in signaling, aggregation, and clot retraction.

Recent Findings: The calpain-1 knockout mouse provided direct evidence for the role of calpain-1 in platelet aggregation and clot retraction. Reduced tyrosine phosphorylation of platelet proteins correlated with reduced platelet aggregation and clot retraction. Future investigations of the mechanism of platelet defects in calpain-1 null mice may unveil the physiological functions of this important and elusive protease in mammalian cells.

Summary: This review focuses on the role of calpains in platelets with a particular emphasis on recent findings in calpain-1 null platelets. Previous studies used synthetic inhibitors to study the role of calpains in platelet function yielding useful information about the identification of calpain substrates. The development of calpain-1 null mice demonstrated that calpain-1 plays an important function in the regulation of platelet aggregation and clot retraction. Since the combined deletion of calpain-1 and calpain-2 genes results in embryonic lethality, the calpain-1 null mouse remains the only experimental model available to study the physiological role of calpains in mammalian cells.

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References
1.
Mazharian A, Roger S, Berrou E, Adam F, Kauskot A, Nurden P . Protease-activating receptor-4 induces full platelet spreading on a fibrinogen matrix: involvement of ERK2 and p38 and Ca2+ mobilization. J Biol Chem. 2007; 282(8):5478-87. DOI: 10.1074/jbc.M609881200. View

2.
Ren Q, Barber H, Crawford G, Karim Z, Zhao C, Choi W . Endobrevin/VAMP-8 is the primary v-SNARE for the platelet release reaction. Mol Biol Cell. 2006; 18(1):24-33. PMC: 1751319. DOI: 10.1091/mbc.e06-09-0785. View

3.
Harper A, Sage S . A role for the intracellular protease calpain in the activation of store-operated calcium entry in human platelets. Cell Calcium. 2006; 41(2):169-78. DOI: 10.1016/j.ceca.2006.05.008. View

4.
Pula G, Schuh K, Nakayama K, Nakayama K, Walter U, Poole A . PKCdelta regulates collagen-induced platelet aggregation through inhibition of VASP-mediated filopodia formation. Blood. 2006; 108(13):4035-44. DOI: 10.1182/blood-2006-05-023739. View

5.
Xi X, Flevaris P, Stojanovic A, Chishti A, Phillips D, Lam S . Tyrosine phosphorylation of the integrin beta 3 subunit regulates beta 3 cleavage by calpain. J Biol Chem. 2006; 281(40):29426-30. DOI: 10.1074/jbc.C600039200. View