The objective of this proposal is the define the signal transduction pathways that mediate Interleukin 9 (IL-8) receptor regulation of cell function, specifically chemotaxis. The recruitment and activation of neurophilis by IL-8 has been implicated in the tissue damage and destruction of a variety of pulmonary diseases. Additionally, the recruitment of neurophils and/or other cell types by IL-8 may have a significant role in the control of malignant cell growth. Defining the signal transduction pathways and cellular functions stimulated by Il-8 will aid in an understanding of the role Il-8 has in lung disease and the control of malignant cell growth. To address this objective, the following specific aims will be carried out: 1a) determine the effect in human neutrophils of peptides which activate or inhibit the p85/p110 phosphatidylinositol-3-kinase (P13K); 1b) determine whether p38 is activated in response to Il-8 receptor activation; 2a) define and reconstitute, if necessary, the signal transduction pathways (phospholipase C, Ras/Raf/MAPK, P13K and p38-MARK) activated in neutrophils by Il-8 in Il- 8RB positive HEK-293 cells; 2b) define the signal transduction pathways required for coupling the Il-8 receptor to chemotaxis in HEK-293 cells using inhibitory and constitutive active mutants of p110-P13K, P13K-gamma, cdc42Hs, Rac,Ras and p38-MAPK.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32HL009640-02
Application #
2519245
Study Section
Pharmacology A Study Section (PHRA)
Project Start
1997-02-18
Project End
Budget Start
1997-09-01
Budget End
1998-08-31
Support Year
2
Fiscal Year
1997
Total Cost
Indirect Cost
Name
National Jewish Health
Department
Type
DUNS #
City
Denver
State
CO
Country
United States
Zip Code
80206
Sandilos, Joanna K; Chiu, Yu-Hsin; Chekeni, Faraaz B et al. (2012) Pannexin 1, an ATP release channel, is activated by caspase cleavage of its pore-associated C-terminal autoinhibitory region. J Biol Chem 287:11303-11