HPK1-Mediated Lymphocyte Signal Transduction Mechanisms. The JNK kinase cascade plays a pivotal role in T-cell activation, differentiation and apoptosis. Hematopoietic progenitor kinase 1 (HPK1), a STE20-1ike kinase, is a hematopoietic-specific activator of the JNK signaling pathway. Our working hypothesis about the HPK1 signaling pathway is as follows: Receptors -> adaptors, kinases -> HPK1 (also called MAP4K1) -> MAP3Ks (MEKK1, TAK1, MLK3) -> MAP2Ks (MKK4, MKKT) !->JNK -> cell activation or apoptosis. This application plans to study the function of HPK1 in T-cell activation and T-cell mediated immune responses. In this application, we will test the hypothesis that HPK1 negatively regulates T-cell activation by inhibiting ERK and/or activating JNK. The approach will be: (i) to understand the underlying signal transduction mechanisms of the HPK1 pathway in the negative regulation of T-cell activation, and (ii) to study the in vivo functions of HPK1 in Th1/Th2 differentiation, immune responses, autoimmunity, and professional antigen-presenting cell (APC) function. Ultimately, we plan to dissect various HPK1-mediated signaling pathways in immune responses, leukemia/lymphoma, and immunological diseases. Our future understanding of host factors involved in the HPK1-mediated lymphocyte signaling pathways will provide information fundamental to the discovery, design, and evaluation of effective intracellular therapeutic agents for leukemia/lymphoma and immunological disorders such as autoimmunity.
The specific aims are:
AIM 1. Study the roles of HPK1 in T-cell activation and differentiation using HPK1 knockout mice.
AIM 2. Study in vivo functions of HPK1 in T-cell mediated immune responses, autoimmunity, and antigen-presenting cell (APC) function using HPK1 knockout mice.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
High Priority, Short Term Project Award (R56)
Project #
2R56AI042532-06A1
Application #
7023516
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Mallia, Conrad M
Project Start
1998-09-01
Project End
2007-02-28
Budget Start
2005-03-15
Budget End
2007-02-28
Support Year
6
Fiscal Year
2005
Total Cost
$300,000
Indirect Cost
Name
Baylor College of Medicine
Department
Pathology
Type
Schools of Medicine
DUNS #
051113330
City
Houston
State
TX
Country
United States
Zip Code
77030
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