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. 1999 Mar 22;144(6):1285–1294. doi: 10.1083/jcb.144.6.1285

Figure 5.

Figure 5

Caveolin is required for uPAR/β1 integrin complexes and uPAR-dependent adhesion to vitronectin. (A) The bottom panel shows uPAR/293 cells expressing varying levels of antisense caveolin (clones m1–m5) tested for adhesion to vitronectin as described in Materials and Methods. The corresponding decrease in caveolin levels for each of the clones, as judged by densitometry of immunoblots, was as follows: m1, 0% decrease; m2, 83%; m3, 89%; m4, 96%; and m5, 73%. The top panel shows β1 integrins of uPAR/293 cells cotransfected with antisense caveolin (clones m1–m5) immunoprecipitated and immunoblotted for relative amounts of uPAR as quantified by densitometry. (B) Immunoprecipitates of β1 integrins sequentially immunoblotted for caveolin, Src, and cortactin as in Fig. 4. (C) uPAR-expressing or uPAR and caveolin–coexpressing 293 cells were detached and allowed to adhere on vitronectin (Vn) fibronectin (Fn)-coated 96-well plates. After washing, the percentage of adherent cells was quantitated by spectrophotometric absorbance of stained cells. Adhesion assays were performed three times with identical results.