Fig. 3.
Fig. 3. Translocation of p47phox and p67phox to plasma membrane in intact cells activated with PMA and in the cell-free oxidase reconstitution assay stimulated with SDS. (A) The indicated cells undergone granulocytic differentiation for 5 days were stimulated with (+) or without (−) PMA (500 ng/mL) for 10 minutes at 37°C, and the plasma membranes were prepared on discontinuous sucrose gradients and analyzed for translocation of p47phox and p67phox by immunoblot analysis using p47phox and p67phox antibodies (left panel). After stripping, the blots were reprobed with gp91phox and p22phox monoclonal antibodies to show an equal loading (right panel). Each lane was loaded with 5 μg of proteins. (B) Membranes separated from the indicated cells were mixed with 3-fold of neutrophil cytosol in the cell-free oxidase reconstitution assay. After 10 minutes of incubation at 25°C in the presence (+) or absence (−) of 100 μmol/L SDS, the membranes were reisolated by ultracentrifugation and detected for the translocation of p47phox and p67phox (left panel) by immunoblot analysis as described in (A). Each lane was loaded with 5 μg of proteins.

Translocation of p47phox and p67phox to plasma membrane in intact cells activated with PMA and in the cell-free oxidase reconstitution assay stimulated with SDS. (A) The indicated cells undergone granulocytic differentiation for 5 days were stimulated with (+) or without (−) PMA (500 ng/mL) for 10 minutes at 37°C, and the plasma membranes were prepared on discontinuous sucrose gradients and analyzed for translocation of p47phox and p67phox by immunoblot analysis using p47phox and p67phox antibodies (left panel). After stripping, the blots were reprobed with gp91phox and p22phox monoclonal antibodies to show an equal loading (right panel). Each lane was loaded with 5 μg of proteins. (B) Membranes separated from the indicated cells were mixed with 3-fold of neutrophil cytosol in the cell-free oxidase reconstitution assay. After 10 minutes of incubation at 25°C in the presence (+) or absence (−) of 100 μmol/L SDS, the membranes were reisolated by ultracentrifugation and detected for the translocation of p47phox and p67phox (left panel) by immunoblot analysis as described in (A). Each lane was loaded with 5 μg of proteins.

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