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Evidence for sequential utilization of fibronectin, vitronectin, and collagen during fibroblast‐mediated collagen contraction
Author(s) -
Sethi Kamaljit K.,
Yannas Ioannis V.,
Mudera Vivek,
Eastwood Mark,
McFarland Clive,
Brown Robert A.
Publication year - 2002
Publication title -
wound repair and regeneration
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.847
H-Index - 109
eISSN - 1524-475X
pISSN - 1067-1927
DOI - 10.1046/j.1524-475x.2002.10609.x
Subject(s) - vitronectin , fibronectin , integrin , extracellular matrix , chemistry , microbiology and biotechnology , fibroblast , wound healing , focal adhesion , collagen receptor , receptor , biochemistry , immunology , biology , cell , in vitro
Contraction plays a major role in wound healing and is inevitably mediated through the mechanical interaction of fibroblast cytoskeleton and integrins with their extracellular matrix ligands. Cell–matrix attachment is critical for such events. In human dermal fibroblasts most such interactions are mediated by the β1‐type integrins. This study investigated the role played by key components in this system, notably fibronectin, vitronectin, and integrin subcomponents α2 and α5, which recognize collagen and fibronectin. Inhibition of adhesion through these ligands was studied either by antibody blocking or with fibronectin and/or vitronectin depletion. Functional effects of inhibition were monitored as force generation in collagen‐glycosaminoglycan (Integra TM ) sponges, over 20 hours using a culture force monitor. Dose and time‐course inhibition studies indicated that initial attachment and force generation (approx. 0–5 hours postseeding) was through fibronectin receptors and this was followed by vitronectin ligand and receptor utilization (4 hours onward). Utilization of the collagen integrin subcomponent α2 appeared to be increasingly important between 6 and 16 hours and dominant thereafter. Additionally, there was evidence for functional interdependence between the three ligand systems fibronectin, vitronectin, and collagen. We propose that there is a short cascade of sequential integrin–ligand interactions as cells attach to, extend through, and eventually contract their matrix. (WOUND REP REG 2002;10:–408)