Figure 4
Figure 4. High levels of Id2 expression inhibit neutrophil differentiation in vitro and promote myeloid progenitor proliferation in vitro and in vivo. (A) 5FU-BMCs were transduced with MSCV or MSCV-Id2 retrovirus and cultured in mGM-CSF to induce neutrophil differentiation. Myeloid cells in the culture were analyzed for c-kit, Sca-1, Gr-1, and Mac-1 surface markers. (B) Total cell numbers of Gr-1+Mac-1+ cells and c-kit+ cells from MSCV- or MSCV-Id2–transduced 5FU-BMC culture. *P < .05 in 2-sided t test. (C) Cell-cycle analysis of MSCV- or MSCV-Id2–transduced 5FU-BMCs was analyzed by propidium iodide staining. (D) Myeloid development in recipient bone marrow and spleen was examined 5 months after transplantation by FACS analysis with the use of Gr-1, and Mac-1 antibodies. Total cell number of Gr-1+Mac-1+ cells was shown. *P < .05 in 2-sided t test. Four recipient mice were used in each group. Three independent experiments were performed.

High levels of Id2 expression inhibit neutrophil differentiation in vitro and promote myeloid progenitor proliferation in vitro and in vivo. (A) 5FU-BMCs were transduced with MSCV or MSCV-Id2 retrovirus and cultured in mGM-CSF to induce neutrophil differentiation. Myeloid cells in the culture were analyzed for c-kit, Sca-1, Gr-1, and Mac-1 surface markers. (B) Total cell numbers of Gr-1+Mac-1+ cells and c-kit+ cells from MSCV- or MSCV-Id2–transduced 5FU-BMC culture. *P < .05 in 2-sided t test. (C) Cell-cycle analysis of MSCV- or MSCV-Id2–transduced 5FU-BMCs was analyzed by propidium iodide staining. (D) Myeloid development in recipient bone marrow and spleen was examined 5 months after transplantation by FACS analysis with the use of Gr-1, and Mac-1 antibodies. Total cell number of Gr-1+Mac-1+ cells was shown. *P < .05 in 2-sided t test. Four recipient mice were used in each group. Three independent experiments were performed.

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