Figure 4.
Figure 4. gp130flox/flox/TCre bone marrow retains progenitor cells. (A) Quantification of the indicated myeloerythroid colonies that developed from bone marrow or spleen cells suspended in methylcellulose. Data represent the mean ± SD of triplicate determinations and are representative of 3 independent experiments. *P < .001 compared with gp130+/+/TCre. (B) To determine the relative proportions of hematopoietic stem/progenitor cells, Lin- bone marrow cells were stained with PE–anti-Sca-1 and APC–anti-c-kit and then were analyzed by flow cytometry. The c-kitHiSca-1+, c-kitHiSca-1-, and c-kitLoSca-1-/Lo populations are gated with open boxes. The percentage of cells in each population is shown. (C) Quantification of the indicated myeloerythroid colonies that developed from 200 sorted Lin-c-kitHiSca-1+ cells suspended in methylcellulose. Data represent the mean ± SD of triplicate determinations from cells pooled from 5 mice per genotype and are representative of 2 independent experiments.

gp130flox/flox/TCre bone marrow retains progenitor cells. (A) Quantification of the indicated myeloerythroid colonies that developed from bone marrow or spleen cells suspended in methylcellulose. Data represent the mean ± SD of triplicate determinations and are representative of 3 independent experiments. *P < .001 compared with gp130+/+/TCre. (B) To determine the relative proportions of hematopoietic stem/progenitor cells, Lin- bone marrow cells were stained with PE–anti-Sca-1 and APC–anti-c-kit and then were analyzed by flow cytometry. The c-kitHiSca-1+, c-kitHiSca-1-, and c-kitLoSca-1-/Lo populations are gated with open boxes. The percentage of cells in each population is shown. (C) Quantification of the indicated myeloerythroid colonies that developed from 200 sorted Lin-c-kitHiSca-1+ cells suspended in methylcellulose. Data represent the mean ± SD of triplicate determinations from cells pooled from 5 mice per genotype and are representative of 2 independent experiments.

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