Smooth muscle cell proliferation initiates intimal hyperplasia, a response to vessel wall injury. After wall injury, platelets accumulate on the injured surface and release lysophosphatidic acid (LPA) which inhibits PKA thereby regulating CREB/CREM/ICER. Understanding the regulation of CREB/CREM/ICER is important as it affects smooth muscle cell proliferation. In this proposal, I plan to investigate the regulation of CREB/CREM/ICER by LPA as it pertains to AP-1 transcription and smooth muscle cell proliferation. Ultimately, this information will be used in the development of therapeutic intervention to address the clinically relevant problem of vessel restenosis caused by intimal hyperplasia.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32HL072564-01A1
Application #
6695398
Study Section
Special Emphasis Panel (ZRG1-F05 (20))
Program Officer
Schucker, Beth
Project Start
2003-07-03
Project End
2004-07-02
Budget Start
2003-07-03
Budget End
2004-07-02
Support Year
1
Fiscal Year
2003
Total Cost
$48,148
Indirect Cost
Name
University of Rochester
Department
Surgery
Type
Schools of Dentistry
DUNS #
041294109
City
Rochester
State
NY
Country
United States
Zip Code
14627