Figure 7
Figure 7. Antioxidant restoration of E47-deficient MPPs. (A) Quantitative PCR analysis of redox-associated genes in purified HSCs (flk2−CD150+CD48− LSKs) or MPPs (flk2+ LSKs) from E47 KO mice compared with E47 WT mice. Data are mean ± SD of triplicate wells, representative of 2 or 3 independent sorts. *P < .05. (B) Mice treated with 1 mg/mL N-acetyl cysteine in the drinking water were killed after 14 days, and lymphoid organs stained to detect bone marrow multipotent progenitors (flk2− and flk2+ LSKs), common lymphoid progenitors (CLPs: lin−IL7R+AA4.1+Sca-llo), and early thymic progenitors precursors (ETPs: lin−CD44+CD25+c-kit+IL-7R−). (C) Quantitation of hematopoietic subsets in B (n = 5 mice/group). *P < .05. ns indicates not significant.

Antioxidant restoration of E47-deficient MPPs. (A) Quantitative PCR analysis of redox-associated genes in purified HSCs (flk2CD150+CD48 LSKs) or MPPs (flk2+ LSKs) from E47 KO mice compared with E47 WT mice. Data are mean ± SD of triplicate wells, representative of 2 or 3 independent sorts. *P < .05. (B) Mice treated with 1 mg/mL N-acetyl cysteine in the drinking water were killed after 14 days, and lymphoid organs stained to detect bone marrow multipotent progenitors (flk2 and flk2+ LSKs), common lymphoid progenitors (CLPs: linIL7R+AA4.1+Sca-llo), and early thymic progenitors precursors (ETPs: linCD44+CD25+c-kit+IL-7R). (C) Quantitation of hematopoietic subsets in B (n = 5 mice/group). *P < .05. ns indicates not significant.

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