World-wide, spurious thrombosis accounts for 1 in 4 non-communicable disease deaths. Normally platelets respond to vascular damage and secrete granule cargo that are essential for recruiting more platelets, their adhesion, and thrombosis. This releasate promotes normal sequelae but can also contribute to disease. Do platelets actively control what they release? How much releasate is enough? These are key questions to understand how platelets affect their vascular microenvironments. Membrane proteins (v- and t-SNAREs) fuse granule and plasma membranes to allow cargo release. In platelets, VAMPs, SNAP-23, and Syntaxin-11 form a membrane-spanning complex that mediates fusion. Formation of this complex requires post-translational modifications and a host of SNARE-regulators. This controls the complexity of the platelet release reaction: its rate, extent, and content. We hypothesize that by manipulating the platelet secretory machinery, we can modulate thrombosis with only modest effects on hemostasis. We propose three Aims: 1) Determine how alterations in platelet exocytosis affect thrombosis and hemostasis. Using our unique collection of transgenic mice, we will genetically titrate platelet secretory machinery to determine how much secretion is needed for thrombosis and hemostasis. 2) Determine if platelet exocytosis can be controlled by targeting post-translational modifications of t-SNAREs. We will examine two post-translational modifications: SNAP-23 phosphorylation, by I?B kinase, and t-SNARE acylation. We will test inhibitors to determine if they can be repurposed as anti-thrombotics. t- SNARE acylation is highly dynamic in platelets. We will alter its cycling with acyl transferase and thioesterase inhibitors to define its importance to secretion and whether acylation can be targeted to affect platelet exocytosis. 3) Determine the roles of new elements of the platelet exocytosis machinery. We will probe the roles of two novel secretory elements: ?-synuclein and RalA/B. Our proposal expands our knowledge of the molecular requirements and the sequence of protein-protein interactions controlling platelet exocytosis. Our work is significant because it provides the needed mechanistic insights to identify potential targets for therapeutic intervention and to evaluate the relevance of the increasing volume of gene/risk associations.

Public Health Relevance

Relevance of the Project to Public Health: Worldwide, thrombotic events, e.g., strokes and heart attacks, account for 1 of 4 deaths, not caused by communicable diseases. Platelet secretion is essential for clot formation and thus is a target for controlling thrombosis; however, we need to know more about the process before we can manipulate it. This proposal will yield the knowledge necessary to understand the process of platelet secretion and will identify strategies to control it.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL056652-20
Application #
9672517
Study Section
Hemostasis and Thrombosis Study Section (HT)
Program Officer
Sarkar, Rita
Project Start
1996-07-01
Project End
2020-03-31
Budget Start
2019-04-01
Budget End
2020-03-31
Support Year
20
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Kentucky
Department
Biochemistry
Type
Schools of Medicine
DUNS #
939017877
City
Lexington
State
KY
Country
United States
Zip Code
40526
Zhang, Jinchao; Huang, Yunjie; Chen, Jing et al. (2018) Dynamic cycling of t-SNARE acylation regulates platelet exocytosis. J Biol Chem 293:3593-3606
Joshi, Smita; Banerjee, Meenakshi; Zhang, Jinchao et al. (2018) Alterations in platelet secretion differentially affect thrombosis and hemostasis. Blood Adv 2:2187-2198
Pokrovskaya, Irina D; Joshi, Smita; Tobin, Michael et al. (2018) SNARE-dependent membrane fusion initiates ?-granule matrix decondensation in mouse platelets. Blood Adv 2:2947-2958
Whiteheart, Sidney W (2017) Fueling Platelets: Where Does the Glucose Come From? Arterioscler Thromb Vasc Biol 37:1592-1594
Joshi, Smita; Whiteheart, Sidney W (2017) The nuts and bolts of the platelet release reaction. Platelets 28:129-137
Banerjee, Meenakshi; Whiteheart, Sidney W (2017) The ins and outs of endocytic trafficking in platelet functions. Curr Opin Hematol 24:467-474
Banerjee, Meenakshi; Joshi, Smita; Zhang, Jinchao et al. (2017) Cellubrevin/vesicle-associated membrane protein-3-mediated endocytosis and trafficking regulate platelet functions. Blood 130:2872-2883
Banerjee, Meenakshi; Whiteheart, Sidney W (2016) How Does Protein Disulfide Isomerase Get Into a Thrombus? Arterioscler Thromb Vasc Biol 36:1056-7
Jones, Mark B; Oswald, Douglas M; Joshi, Smita et al. (2016) B-cell-independent sialylation of IgG. Proc Natl Acad Sci U S A 113:7207-12
Huang, Yunjie; Joshi, Smita; Xiang, Binggang et al. (2016) Arf6 controls platelet spreading and clot retraction via integrin ?IIb?3 trafficking. Blood 127:1459-67

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