Fig. 5.
Fig. 5. Presence of p210BCR/ABL in normal CD34+ cells prevents adhesion-mediated proliferation inhibition. / Cord blood CD34+ cells (5 × 106) were transduced on 3 consecutive days with the control vector, eGFP, or with p210-eGFP and were plated in fibronectin or poly-L-lysine–coated dishes for 12 hours in the presence of the β1-integrin activating antibody, 8A2. Nonadherent and adherent cells were collected separately, cells were fixed and incubated with propidium iodide, and the cell cycle status of CD34+/eGFP+ cells was analyzed by FACS using Modfit-LT software. A representative example of fibronectin-nonadherent and fibronectin-adherent p210-eGFP–transduced cells is shown.

Presence of p210BCR/ABL in normal CD34+ cells prevents adhesion-mediated proliferation inhibition.

Cord blood CD34+ cells (5 × 106) were transduced on 3 consecutive days with the control vector, eGFP, or with p210-eGFP and were plated in fibronectin or poly-L-lysine–coated dishes for 12 hours in the presence of the β1-integrin activating antibody, 8A2. Nonadherent and adherent cells were collected separately, cells were fixed and incubated with propidium iodide, and the cell cycle status of CD34+/eGFP+ cells was analyzed by FACS using Modfit-LT software. A representative example of fibronectin-nonadherent and fibronectin-adherent p210-eGFP–transduced cells is shown.

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