Human peritoneal mesothelial cells lie on a basement membrane-like mat
erial consisting of fibronectin (FN), type I collagen (CI), type III c
ollagen (CIII) and laminin (LA). To understand how these extracellular
matrix (ECM) proteins affect mesothelial cell behavior, we investigat
ed their effect on the adhesion and proliferation of mesothelial cells
. A modified methyltetrazolium dye method was used to assess cell numb
er. The results showed that FN, CI, CIII and LA, all increased adhesio
n of mesothelial cells. The adhesive effect was blocked dose-dependent
ly by a synthetic Arg-Gly-Asp-containing (RGD) peptide. When coated as
a substratum (immobilized form), FN, CI, CIII and LA, all enhanced se
rum-stimulated and epidermal-growth-factor-stimulated cellular prolife
ration as compared with bovine-serum-albumin-blocked plastic surfaces.
When added in a soluble form, all matrix proteins except FN inhibited
serum-stimulated and epidermal-growth-factor-stimulated cellular prol
iferation at high concentrations (CI and CIII: 1-10 mu g/ml, LA: 3-10
mu g/ml). We conclude that peritoneal mesothelial cells possess an RGD
-sensitive receptor and that the ECM can modulate adhesion and prolife
ration of peritoneal mesothelial cells. The growth-modulating effect d
epends on the form and concentration of the ECM proteins.