The overall hypothesis of this proposal is that platelet actin reorganization plays a critical role in arterial hemostasis and thrombosis. The reorganization of filamentous actin is one of the earliest events of platelet activation. Our recent data has focused on two critical aspects of platelet actin dynamics, phospholipid signaling and post-translational actin modifications. Phosphatidylinositol bisphosphate (PIP2) is critical for the regulation of the platelet cytoskeleton and is required for several steps of actin assembly. This includes serving as a substrate for phosphoinositide second messenger formation, as well as directly binding to and thereby regulating actin-binding proteins. Platelets have both the (3 and y isoforms of phosphatidylinositol phosphate 5-kinase I (PIP5KI) that are each capable of converting PI4P to PI4.5P2 (PIP2), so it is unclear why platelets require more than one isoform to perform this single biochemical reaction. To test the hypothesis that these isoforms have non-overlapping functions, we have generated mice containing null mutations in either the PIP5KI3 or the PIPSKIy genes, which encode for the dominant PIP5KI isoforms in platelets. Our preliminary studies of platelets from these mice suggest that production of PIP2 by PIP5KI3 is required to generate second messengers, while synthesis of PIP2 by PIP5Kly is required to maintain the integrity of the membrane skeleton. We have also recently reported that at the leading edge of migrating fibroblasts, actin must have an arginine post-translationally added onto its N-terminus. Absence of this modification impairs fibroblast adhesion and migration, demonstrating the essential role of this modification in actin assembly. Our preliminary studies indicate that in response to agonist stimulation, platelet actin is also arginylated. We hypothesize that this recently discovered post-translational modification is critical for platelet actin dynamics. The goal of this application is to understand on a molecular basis the in vivo platelet actin changes, and to determine whether actin reorganization is vital for stable platelet adhesion.
In Aim 1, we will define the biologic roles of PIP5KI in platelets using our recently developed murine models.
In Aim 2, we will determine how integrins regulate PIP2 production by a combination of biochemistry, murine genetics, and platelet adhesion models.
In Aim 3, we will address the contribution of actin arginylation on platelet adhesion using biochemistry and mice genetically altered to lack the ability to arginylate platelet actin.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL040387-24
Application #
8249416
Study Section
Heart, Lung, and Blood Initial Review Group (HLBP)
Project Start
Project End
Budget Start
2011-04-01
Budget End
2012-03-31
Support Year
24
Fiscal Year
2011
Total Cost
$433,511
Indirect Cost
Name
University of Pennsylvania
Department
Type
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
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