Skip to main content
. 2000 Apr 17;149(2):307–316. doi: 10.1083/jcb.149.2.307

Figure 3.

OSM induces hnRNP A1 phosphorylation. Metabolically 32P-labeled NIH-3T3 cells were either left untreated or were exposed to OSM (DME + 400 mM sorbitol (A) or DME + 600 mM sorbitol (B)) for the indicated times. Total protein was isolated, endogenous hnRNP A1 was immunoprecipitated with the monoclonal antibody 4B10, and its phosphorylation level was determined by autoradiography following SDS-PAGE. Western blotting analysis using the 4B10 antibody showed comparable amounts of hnRNP A1 protein present in all lanes (lower panel in A and B). Exposure of NIH-3T3 cells to 600 mM sorbitol resulted in cytoplasmic accumulation of hnRNP A1 in ∼100% of the cells after 2 h, and hnRNP A1 cytoplasmic localization was not reversible after 5 h.

graphic file with name JCB9908117.f3a.jpg

graphic file with name JCB9908117.f3b.jpg