Angiogenesis depends upon proper collagen biosynthesis and crosslinking, moreover, type I collagen is an ideal scaffold for angiogenesis in vitro. Despite this, mechanisms of type I collagen-mediated angiogenesis remain poorly understood. We propose to define the features of the type / collagen fibril, endothelial cell surface, and intracellutar signaling pathways that act together to mediate type I collagen- induced angiogenesis. We have developed a unique model for studying endothelial tube morphogenesis in vitro. Our oreliminary data using our system sUPport the hypothe_i_ that engagement between the c_2B1 integrin receotor and integrin-binding sequences of _pe I collagen result in D38MAPK activation, and inactivation of Focal Adhesion Kinase during endothelial tube morphogenesis. We will test this hypothesis in the following aims:l) Define the roles of endothelial cell surface a1_1, a2111, and c_V_3 integrin receptors, sulfated proteoglycans, and fibronectin by testing the activities of integrin or fibronectin function-blocking antibodies and inhibitors of GAG function on angiogenesis; 2) Synthesize triple helical, type I collagen mimetic peptides (THPs) including putative integrin-binding sites, and study their capacities to inhibit cell- collagen attachment, bind integrin receptors, and influence angiogenesis; 3) Study the consequences of integrin function-blocking antibodies, integrin-binding THPs, and chemical and dominant-negative construct inhibitors of signaling pathway function on p38MAPK and FAK activation and angiogenesis; and 4) Examine the role of c_2_1 integrin ligation of discrete collagen sequences, and the p38MAPK and FAK pathways, a) in vivo in the chick CAM, and b) in angiogenesis induction by other polymers including heterotypic collagen fibrils and fibrin. Our work will define the type I collagen structural features critical for its morphogenic activity, probe the functional link between o_2_1 integrin-collagen ligation, p38 MAPK and FAK activation, and langiogenesis, and contribute to the understanding and treatment of human diseases involving vascular insufficiencies, such as ischemia, or abnormal angiogenesis, as in tumor growth.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
3R01HL053590-08S1
Application #
7385399
Study Section
Pathology A Study Section (PTHA)
Program Officer
Goldman, Stephen
Project Start
1997-04-01
Project End
2008-09-28
Budget Start
2006-04-01
Budget End
2008-09-28
Support Year
8
Fiscal Year
2007
Total Cost
$45,407
Indirect Cost
Name
Thomas Jefferson University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
053284659
City
Philadelphia
State
PA
Country
United States
Zip Code
19107
San Antonio, James D; Zoeller, Jason J; Habursky, Kari et al. (2009) A key role for the integrin alpha2beta1 in experimental and developmental angiogenesis. Am J Pathol 175:1338-47
Sweeney, Shawn M; Orgel, Joseph P; Fertala, Andrzej et al. (2008) Candidate cell and matrix interaction domains on the collagen fibril, the predominant protein of vertebrates. J Biol Chem 283:21187-97