Protein kinase B/akt and Rab5 mediate Ras activation of endocytosis
Article
Barbieri, MA, Kohn, AD, Roth, RA et al. (1998). Protein kinase B/akt and Rab5 mediate Ras activation of endocytosis
. JOURNAL OF BIOLOGICAL CHEMISTRY, 273(31), 19367-19370. 10.1074/jbc.273.31.19367
Barbieri, MA, Kohn, AD, Roth, RA et al. (1998). Protein kinase B/akt and Rab5 mediate Ras activation of endocytosis
. JOURNAL OF BIOLOGICAL CHEMISTRY, 273(31), 19367-19370. 10.1074/jbc.273.31.19367
Transient expression of oncogenic Ha-Ras (Ras:V12) stimulates endocytosis. Using NIH3T3 cells expressing constitutively active protein kinase B/akt (PKB/akt) or kinase-dead PKB/akt, we show that PKB/akt mediates the stimulatory effect of Ras on endocytosis. Fluid phase endocytosis of horseradish peroxidase in cells expressing the constitutively active form of PKB/akt was elevated and insensitive to phosphatidylinositol 3-kinase inhibitors. However, expression of dominant negative Rab5:N34 blocked endocytosis in cells expressing the constitutively active form of PKB/akt. Transient expression of either Rab5:wt or Rab5:L79, a GTPase deficient mutant of Rab5, in cells expressing constitutively activated PKB/akt further increased endocytic rate. However, in cells expressing kinase-dead PKB/akt, endocytic rate was not affected by transient expression of Rab5:wt. Rab5:L79, on the other hand, increased endocytosis in cells expressing kinase-dead PKB/akt. Similar results were obtained using an in vitro endosome fusion reconstitution assay with cytosol prepared from cells expressing the activated PKB/akt or kinase-dead PKB/akt. Both Rab5:wt and Rab5:L79 stimulated endosome fusion when assayed in cytosol containing the activated PKB/akt, whereas only Rab5:L79 activated fusion when the assay utilized cytosol from kinase-dead expressing cells. We conclude that Ras activation of endocytosis requires both PKB/akt and Rab5 and that active kinase is required for activation Rab5.
