SMOOTH MUSCLE APOPTOSIS

平滑肌细胞凋亡

• 批准号: 6620945
• 负责人: DANIEL F BOWEN-POPE
• 金额: $ 30.32万
• 依托单位: UNIVERSITY OF WASHINGTON
• 依托单位国家: 美国
• 财政年份: 2001
• 资助国家: 美国
• 起止时间: 2001-12-01 至 2005-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6620945
• 关键词: CD95 molecule; apoptosis; atherosclerotic plaque; biological signal transduction; carotid artery; cysteine endopeptidases; enzyme linked immunosorbent assay; gene expression; genetic regulation; human genetic material tag; inflammation; interleukin 1; laboratory rat; macrophage; membrane proteins; microarray technology; monocyte chemoattractant protein 1; polymerase chain reaction; receptor expression; thrombosis; tissue /cell culture; vascular endothelium; vascular smooth muscle

DESCRIPTION (provided by applicant): Unlike necrosis, apoptosis is classically considered to be "silent," i.e., self-contained and non-inflammatory. We have developed a system for regulating apoptosis of smooth muscle cells (SMCs) in the rat carotid artery in vivo, and have used this system to determine that SMC apoptosis initiated by FADD over expression, or by Fas ligation, includes a specific program of expression of pro-inflammatory genes that results in recruitment of macrophages. In this application, we propose to further define this program of gene expression, determine the mechanism through which it is regulated, and further investigate the consequences of smooth muscle cell apoptosis in vivo. To do this, we propose the following specific aims: SPECIFIC AIM 1: Use tet-regulated expression of FADD in the rat carotid artery to determine the long-term consequences of SMC apoptosis in the neointima, including the clinically important processes of vascular remodeling, thrombosis, and plaque rupture. SPECIFIC AIM 2. Determine whether the program of gene expression activated by Fas in human SMCs includes additional genes, whether it is cell-type specific, and how activation of expression of component genes reflect activation of specific signal transduction pathways. SPECIFIC AIM 3. Determine the signal transduction pathway(s) through which Fas activation leads to transcript up regulation in human SMCs. SPECIFiC AIM 4. Determine the mechanisms that regulate SMC resistance to Fas-induced apoptosis and that may promote SMC proliferation under some circumstances.

描述（由申请人提供）：与坏死不同，细胞凋亡是典型的