| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2135238 | Experimental Hematology | 2006 | 10 Pages |
ObjectiveImproved understanding of hematopoietic stem cell (HSC) differentiation, proliferation, and self-renewal is sought to develop improved stem cell–based therapies as well as to define novel therapies for stem cell–based diseases such as leukemia. Shp-2 is a widely expressed nonreceptor protein tyrosine phosphatase that participates early in hematopoietic development. The following study was performed to examine the role of Shp-2 in HSC function.MethodsBone marrow low-density mononuclear cells were isolated from WT and Shp-2+/− littermate controls and utilized in competitive repopulation studies, homing analysis, cell-cycle analysis, and serial transplantation studies.ResultsHaploinsufficiency of Shp-2 causes a threefold reduction in HSC repopulating units following transplantation into lethally irradiated recipients. Homing of Shp-2+/− and WT cells to the bone marrow and spleen compartments was equal. Cell-cycle analysis studies revealed that the Shp-2+/− lin−Sca-1+c-kit+ cells are less quiescent than WT cells, providing a potential etiology for the observed reduced engraftment of the Shp-2+/− cells. Consistently, in serial transplantation studies, we observed a significant reduction of Shp-2+/− self-renewal compared to that of WT cells.ConclusionThese data demonstrate that Shp-2 is required for the physiologic homeostasis of the HSC compartment and potentially provide insight into how oncogenic Shp-2 may contribute to the pathogenesis of myeloproliferative disorders and leukemias.
