Fig. 7.
Fig. 7. Contact between normal human B-cell precursors and stromal cells increases tyrosine phosphorylation of multiple stromal cell but not B-cell precursor proteins. Stromal cells and normal human CD10+ CD19+ surface IgM− B-cell precursors were incubated at 37°C, collected, lysed, electrophoresed, and immunoblotted as detailed in the Materials and Methods. (A) Stromal cells in medium for 5 minutes (−) or in contact with B-cell precursors for the times indicated (in minutes). (B) B-cell precursors in medium alone (−) or in contact with stromal cells for the times indicated (in minutes). (Upper panel) Antiphosphotyrosine immunostaining. (Middle panel) Anti-vav immunostaining. (Lower panel) Anti–β-tubulin immunostaining. Asterisks indicate the major stromal cell protein species demonstrating consistent increases in tyrosine phosphorylation. Results are representative of two individual experiments.

Contact between normal human B-cell precursors and stromal cells increases tyrosine phosphorylation of multiple stromal cell but not B-cell precursor proteins. Stromal cells and normal human CD10+ CD19+ surface IgM B-cell precursors were incubated at 37°C, collected, lysed, electrophoresed, and immunoblotted as detailed in the Materials and Methods. (A) Stromal cells in medium for 5 minutes (−) or in contact with B-cell precursors for the times indicated (in minutes). (B) B-cell precursors in medium alone (−) or in contact with stromal cells for the times indicated (in minutes). (Upper panel) Antiphosphotyrosine immunostaining. (Middle panel) Anti-vav immunostaining. (Lower panel) Anti–β-tubulin immunostaining. Asterisks indicate the major stromal cell protein species demonstrating consistent increases in tyrosine phosphorylation. Results are representative of two individual experiments.

Close Modal

or Create an Account

Close Modal
Close Modal