Decreased wound healing and increased infection are major problems in
patients with diabetes mellitus. Fibronectin plays a fundamental role
in wound healing and acts as an opsonin for the phagocytosis of foreig
n antigens. The aim of this study was to ascertain the functional acti
vity of plasma fibronectin from patients with diabetes mellitus. Initi
ally, a modified Boyden chamber technique was used to measure cell mig
ration on fibronectin purified from patient's plasma and an enzyme-lin
ked immunosorbent assay was used to measure the binding of gelatin. A
sandwich assay was developed that enabled the capture of fibronectin d
irectly from patient's plasma without prior purification. With the use
of a 96-well format, the binding of two different monoclonal antibodi
es could be compared simultaneously with the binding of gelatin and ce
ll adhesion. In this way, differences in the function of particular do
mains of fibronectin from diabetic patients and control subjects could
be measured. Results showed no difference between fibronectin from di
abetic patients and control subjects with respect to the monoclonal an
tibodies binding in 1) the cell adhesion domain and 2) the heparin-bin
ding domain. Furthermore, no detectable differences were noted with re
spect to cell adhesion, cell migration, or gelatin binding. These resu
lts suggest that diabetic patients receiving insulin treatment show no
modulation of plasma fibronectin function, despite raised levels of c
irculating glucose.