Figure 5.
Figure 5. SP analysis of subsets defined by CD34 expression intensity. Analysis of a representative (8-12 weeks) murine marrow Hoechst stained and labeled for Lin, SCA-1, CD117, and CD34. Linneg/SCA-1+/CD117+ cells (KLS) were divided into subsets of CD34 high, low, and negative intensity (A). Provided for comparison is a CD117/CD34 plot of the SP fraction from the same experiment with the same CD34 high, low, and negative gates. Dotted lines on both plots indicate the level of matched-isotype control. Most SP cells were CD34low or CD34neg in mice 8 to 12 weeks of age (B, upper row). In contrast, significant numbers of KLS+/CD34high were only seen in the older (> 15 weeks) mice. Most interestingly, in all 3 older mice analyzed, the KLS+/CD34neg subset was associated with the cells which most efficiently effluxed the Hoechst dye (B, lower panel).

SP analysis of subsets defined by CD34 expression intensity. Analysis of a representative (8-12 weeks) murine marrow Hoechst stained and labeled for Lin, SCA-1, CD117, and CD34. Linneg/SCA-1+/CD117+ cells (KLS) were divided into subsets of CD34 high, low, and negative intensity (A). Provided for comparison is a CD117/CD34 plot of the SP fraction from the same experiment with the same CD34 high, low, and negative gates. Dotted lines on both plots indicate the level of matched-isotype control. Most SP cells were CD34low or CD34neg in mice 8 to 12 weeks of age (B, upper row). In contrast, significant numbers of KLS+/CD34high were only seen in the older (> 15 weeks) mice. Most interestingly, in all 3 older mice analyzed, the KLS+/CD34neg subset was associated with the cells which most efficiently effluxed the Hoechst dye (B, lower panel).

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