Figure 6
Figure 6. Impaired HSC retention of primitive HSCs in GPC3−/− BM resulting in a higher proportion of circulating HSPCs. (A) Flow cytometric analysis to assess the proportion of primitive HSCs and hematopoietic progenitors in WT (top panel) and GPC3−/− (bottom panel) mice BM. Lin−c-kit+ cells (hematopoietic progenitors) were gated and analyzed for Sca-1+CD150+ cells (primitive HSCs). (B) The proportion of hematopoietic progenitors and primitive HSCs in WT and GPC3−/− BM was compared. (C) Cell-cycle analysis of gated Lin− (left) and KLS (right) cells from BM of WT and GPC3−/− cells. (D) Comparison of the number of KLS cells in peripheral blood of WT, GPC1−/−, and GPC3−/− mice by flow cytometry. (E) Comparison of the circulating hematopoietic progenitors in WT, GPC1−/−, and GPC3−/− mice by CFC assay. n = 8-12; *P < .05.

Impaired HSC retention of primitive HSCs in GPC3−/− BM resulting in a higher proportion of circulating HSPCs. (A) Flow cytometric analysis to assess the proportion of primitive HSCs and hematopoietic progenitors in WT (top panel) and GPC3−/− (bottom panel) mice BM. Linc-kit+ cells (hematopoietic progenitors) were gated and analyzed for Sca-1+CD150+ cells (primitive HSCs). (B) The proportion of hematopoietic progenitors and primitive HSCs in WT and GPC3−/− BM was compared. (C) Cell-cycle analysis of gated Lin (left) and KLS (right) cells from BM of WT and GPC3−/− cells. (D) Comparison of the number of KLS cells in peripheral blood of WT, GPC1−/−, and GPC3−/− mice by flow cytometry. (E) Comparison of the circulating hematopoietic progenitors in WT, GPC1−/−, and GPC3−/− mice by CFC assay. n = 8-12; *P < .05.

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