The experiments proposes to analyze the signal transduction pathway induced in T cells by the binding of HIV to CD4 receptors. In preliminary studies the investigator has shown that HIV or gp120 binding induced the association and activation of lck and raf-1 kinases. Binding did not induce ras activation or ras association with raf-1, thereby disassociating HIV pathways from one of the classical activation pathways. This proposal addresses the hypothesis that activation of this pathway is an important component of early gene activation which enhances HIV replication. The proposed studies will investigate this novel activation scheme through: (1) analysis of the lck/raf-1 pathway in CD4 cells of rapid and LTNP; (2) investigation of the impact of suppression of the lck/raf-1 pathway on nuclear transcription, using dominant negative and ribozyme approaches within raf-1 and ras; and (3) definition of the raf-1 binding domain that interacts with lck, and the importance of lck/raf-1 association in HIV replication.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
1R01AI040838-01
Application #
2005392
Study Section
AIDS and Related Research Study Section 1 (ARRA)
Project Start
1996-12-15
Project End
1999-11-30
Budget Start
1996-12-15
Budget End
1997-11-30
Support Year
1
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218