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Active NON-SBIR/STTR RPGS NIH (US)

TLT-1 intracellular function

$4.35M USD

Funder NATIONAL HEART, LUNG, AND BLOOD INSTITUTE
Recipient Organization Oakland University
Country United States
Start Date Sep 01, 2024
End Date Aug 31, 2027
Duration 1,094 days
Number of Grantees 1
Roles Principal Investigator
Data Source NIH (US)
Grant ID 10974515
Grant Description

Project Summary/Abstract TREM Like transcript (TLT-1), is a highly abundant platelet protein that mediates the earliest states of platelet activation. Inhibition of TLT-1 function is associated with bleeding in the inflammatory arena; however vascular hemostasis does not seem to be adversely affected. Our

studies have shown that TLT-1 presents itself as a potential target to control thrombosis without the introduction of bleeding. However, to pursue the therapeutic aspects of TLT-1, we must first understand the mechanisms of TLT-1 function. This project is focused on identifying the critical signaling motifs of TLT-1 function. To accomplish this goal, we have outlined two specific AIMs:

Aim 1: Characterize TLT-1 phosphorylation sites, Aim 2: Decipher the intracellular cues that regulate TLT-1 trafficking in platelets At the completion of these aims we will have a clear understanding of the importance of the platelet to regulation of edema and how we can manipulate platelet interactions to improve disease outcomes.

All Grantees

Oakland University

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