Figure 5.
Figure 5. Coculture with adipocyte-differentiated MSCs stimulates the phosphorylation of STAT3 and MAPK. NB4 cells (A), ZnSO4 pretreated PR9 cells (200 μM, 24 hours) (B), and untreated PR9 cells (C) were cultured alone (control) or cocultured with undifferentiated MSCs or adipocyte-differentiated MSCs at the indicated conditions (with or without chimeric blocking OB-R or MAPK inhibitor) for 24 hours. Clarified lysates were probed with antibodies to phospho-MAPK, ERK2, STAT3, Tyr-705 phospho-Ab, STAT3, and β-actin by Western blotting. Results shown are representative of 3 experiments.

Coculture with adipocyte-differentiated MSCs stimulates the phosphorylation of STAT3 and MAPK. NB4 cells (A), ZnSO4 pretreated PR9 cells (200 μM, 24 hours) (B), and untreated PR9 cells (C) were cultured alone (control) or cocultured with undifferentiated MSCs or adipocyte-differentiated MSCs at the indicated conditions (with or without chimeric blocking OB-R or MAPK inhibitor) for 24 hours. Clarified lysates were probed with antibodies to phospho-MAPK, ERK2, STAT3, Tyr-705 phospho-Ab, STAT3, and β-actin by Western blotting. Results shown are representative of 3 experiments.

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