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标题：Defining the domains of type I collagen involved in heparin- binding and endothelial tube formation
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作者：Shawn M. Sweeney ; Cynthia A. Guy ; Gregg B. Fields 等
期刊名称：Proceedings of the National Academy of Sciences
印刷版ISSN：0027-8424
电子版ISSN：1091-6490
出版年度：1998
卷号：95
期号：13
页码：7275-7280
DOI：10.1073/pnas.95.13.7275
语种：English
出版社：The National Academy of Sciences of the United States of America
摘要：Cell surface heparan sulfate proteoglycan (HSPG) interactions with type I collagen may be a ubiquitous cell adhesion mechanism. However, the HSPG binding sites on type I collagen are unknown. Previously we mapped heparin binding to the vicinity of the type I collagen N terminus by electron microscopy. The present study has identified type I collagen sequences used for heparin binding and endothelial cell-collagen interactions. Using affinity coelectrophoresis, we found heparin to bind as follows: to type I collagen with high affinity (Kd {approx} 150 nM); triple-helical peptides (THPs) including the basic N-terminal sequence 1(I)87-92, KGHRGF, with intermediate affinities (Kd {approx} 2 {micro}M); and THPs including other collagenous sequences, or single-stranded sequences, negligibly (Kd >> 10 {micro}M). Thus, heparin-type I collagen binding likely relies on an N-terminal basic triple-helical domain represented once within each monomer, and at multiple sites within fibrils. We next defined the features of type I collagen necessary for angiogenesis in a system in which type I collagen and heparin rapidly induce endothelial tube formation in vitro. When peptides, denatured or monomeric type I collagen, or type V collagen was substituted for type I collagen, no tubes formed. However, when peptides and type I collagen were tested together, only the most heparin-avid THPs inhibited tube formation, likely by influencing cell interactions with collagen-heparin complexes. Thus, induction of endothelial tube morphogenesis by type I collagen may depend upon its triple-helical and fibrillar conformations and on the N-terminal heparin-binding site identified here.