FIGURE 2. Long-term multi-lineage reconstitution by HSCs and multipotent progenitors from p16Ink4a-/-p19Arf-/-Trp53-/- mice.

From the following article:

Long-term haematopoietic reconstitution by Trp53-/-p16Ink4a-/-p19Arf-/- multipotent progenitors

Omobolaji O. Akala, In-Kyung Park, Dalong Qian, Michael Pihalja, Michael W. Becker & Michael F. Clarke

Nature 453, 228-232(8 May 2008)

doi:10.1038/nature06869

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a, Long-term reconstitution by double-sorted HSCs (CD150+Sca-1+c-kit+CD48-Lin-) from wild-type mice. b, Transplantation of HSCs from p16Ink4a-/-p19Arf-/-Trp53-/- mice results in long-term multi-lineage reconstitution of recipient mice when analysed 14–20 weeks after transplantation (four of four mice). c, Double-sorted multipotent progenitors (Sca-1+c-kit+CD150-CD48-Lin-) from wild-type mice are only capable of contributing to long-lived lymphocyte B220+ and CD3+ populations and not to short-lived myeloid Mac-1+ and Gr-1+ populations. d, Transplanted double-sorted multipotent progenitors from triple mutant mice also resulted in long-term multi-lineage reconstitution of recipient mice when analysed 14–20 weeks after transplantation (four of four mice). e, Double-sorted c-kit+Sca-1-Lin- myeloid progenitors do not contribute to short-lived myeloid Mac-1+ and Gr-1+ populations.

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