Figure 4
Figure 4. Loss of β-catenin prevents rapid exhaustion of Apc-deficient HSCs in vivo. (A) Flow cytometric analysis of the frequency of stem cell-enriched population (Lin-c-Kit+Sca+ [LSK]) and HSCs (LSK CD150+CD48−) in BM from representative ApcΔ/Δ and ApcΔ/Δβ-cateninΔ/Δ mice 10-14 days after induction. (B-D) The histograms depict the total number of HSCs in BM (B) from ApcΔ/Δ and ApcΔ/Δβ-cateninΔ/Δ mice 10-14 days after induction (mean ± standard deviation [SD], n = 5-8), (C) from ApcΔ/Δβ-cateninΔ/Δ, β-cateninΔ/Δ, and β-cateninfl/fl mice 5 weeks after induction (mean ± SD, n = 3), and (D) from ApcΔ/Δβ-cateninΔ/Δ (6 months after induction) and Mx1-Cre Apcfl/flβ-cateninfl/fl (mean ± SD, n = 2-4). *P < .05; ***P < .001.

Loss of β-catenin prevents rapid exhaustion of Apc-deficient HSCs in vivo. (A) Flow cytometric analysis of the frequency of stem cell-enriched population (Lin-c-Kit+Sca+ [LSK]) and HSCs (LSK CD150+CD48) in BM from representative ApcΔ/Δ and ApcΔ/Δβ-cateninΔ/Δ mice 10-14 days after induction. (B-D) The histograms depict the total number of HSCs in BM (B) from ApcΔ/Δand ApcΔ/Δβ-cateninΔ/Δ mice 10-14 days after induction (mean ± standard deviation [SD], n = 5-8), (C) from ApcΔ/Δβ-cateninΔ/Δ, β-cateninΔ/Δ, and β-cateninfl/fl mice 5 weeks after induction (mean ± SD, n = 3), and (D) from ApcΔ/Δβ-cateninΔ/Δ (6 months after induction) and Mx1-Cre Apcfl/flβ-cateninfl/fl (mean ± SD, n = 2-4). *P < .05; ***P < .001.

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