
Fig. 2. Expression of surface tTG induces the binding of 42 kDa Fn fragment and Fn
to cells. (A) Analysis of binding of [125I]42 kDa fragment to
vector, tTG[2] and tTGC277S[2] transfectants in suspension. (B)
Anti-tTG antibody suppresses the binding of [125I]42 kDa fragment
to tTG[2] transfectants in suspension. (C) Binding of [125I]Fn to
vector and tTG[2] transfectants in suspension. (D) The lack of binding of
[125I]42 kDa fragment to monolayers of vector, tTG[2] and
tTGC277S[2] transfectants. Adherent cells plated for 2 or 72 hours
were analyzed for binding [125I]42 kDa fragment. (B,C) Where
indicated, 20 µg/ml anti-tTG antibody, blocking anti-
5ß1
integrin mAb BMA5, control nonimmune IgG or 5 µM unlabeled 42 kDa fragment
was used during incubation of cells with 125I-labeled proteins.
Nonspecific binding in the presence of excess unlabeled 42 kDa fragment was
subtracted. The results are representative of three independent experiments
(mean±s.e.m.).