Adhesions between fibroblastic cells and extracellular matrix have been stu
died extensively in vitro, but tittle is known about their in vivo counterp
arts. Here, we characterized the composition and function of adhesions in t
hree-dimensional (3D) matrices derived from tissues or cell culture. "3D-ma
trix adhesions" differ from focal and fibrillar adhesions characterized on
2D substrates in their content of alpha (5)beta (1) and alpha (v)beta (3) i
ntegrins, paxillin, other cytoskeletal components, and tyrosine phosphoryla
tion of focal adhesion kinase (FAK). Relative to 2D substrates, 3D-matrix i
nteractions also display enhanced cell biological activities and narrowed i
ntegrin usage. These distinctive in vivo 3D-matrix adhesions differ in stru
cture, localization, and function from classically described in vitro adhes
ions, and as such they may be more biologically relevant to living organism
s.