Figure 1.
Microbiota increase MPPs and regulate their differentiation toward the myeloid lineage. (A) Numbers of LSK cells and further separation of HSPCs into HSC, ST-HSC, HPC-2, and MPP cells in the BM of SPF, GF, and CoH-GF mice (n = 10-14). Each circle represents an individual mouse. (B) Relative expression of genes related to each lineage differentiation in the MPP population. Data are presented as log2 fold changes in mRNA levels measured by reverse-transcription quantitative polymerase chain reaction (GF/SPF and CoH-GF/SPF) with cells pooled from 6 to 8 mice per group. Data are pooled from 2 independent experiments (A) and are representative of 2 independent experiment with similar results (B). Data are mean ± standard error of the mean. *P < .05, **P < .01, ***P < .001, 1-way ANOVA with Bonferroni multiple comparison. E/MegE, erythroid/megakaryocytic-erythroid; Lympho, lymphoid; Myelo, myeloid.

Microbiota increase MPPs and regulate their differentiation toward the myeloid lineage. (A) Numbers of LSK cells and further separation of HSPCs into HSC, ST-HSC, HPC-2, and MPP cells in the BM of SPF, GF, and CoH-GF mice (n = 10-14). Each circle represents an individual mouse. (B) Relative expression of genes related to each lineage differentiation in the MPP population. Data are presented as log2 fold changes in mRNA levels measured by reverse-transcription quantitative polymerase chain reaction (GF/SPF and CoH-GF/SPF) with cells pooled from 6 to 8 mice per group. Data are pooled from 2 independent experiments (A) and are representative of 2 independent experiment with similar results (B). Data are mean ± standard error of the mean. *P < .05, **P < .01, ***P < .001, 1-way ANOVA with Bonferroni multiple comparison. E/MegE, erythroid/megakaryocytic-erythroid; Lympho, lymphoid; Myelo, myeloid.

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