The effect of a hematopoietic-promoting factor (HPF) extracted from porcine kidney on the proliferation of human hematopoietic progenitor cells.
Takahashi Ta, K Shibata, Ikuo Kashiwakura, Yukitoshi Hayase, Yoshinari Takagi, S Sekiguchi
Abstract
Takahashi Ta, K Shibata, Ikuo Kashiwakura, Yukitoshi Hayase, Yoshinari Takagi, S Sekiguchi
Abstract
Hematopoietic-promoting factor (HPF), which was found in porcine kidney, has been demonstrated to act synergistically with colony-stimulating factor and erythropoietin on murine myeloid colony formation. We investigated the effect of HPF on the proliferation of human hematopoietic progenitor cells prepared from cord blood cells (CB) and peripheral blood cells (PB). HPF enhanced granulocyte colony-stimulating factor plus interleukin-3 and erythropoietin-induced colony formation, where the number of colonies were increased by 7.9-fold in CB and by 1.8-fold in PB, respectively. When we compared the effect of HPF with stem cell factor (SCF) on the colony formation derived from PB in serum-free cultures, HPF enhanced the number of erythroid burst-forming units (BFU-E) to the same extent as SCF. But the effect of HPF on promoting the growth of granulocyte-macrophage colony-forming units (CFU-GM) was less than SCF. When the enriched CD34+ cells from CB and PB were incubated in liquid culture with HPF and IL-3 for 7 days, CFU-GM was increased by 48-fold in CB, and by 25-fold in PB, respectively. The data demonstrate that HPF can potentiate expansion of hematopoietic stem cells to the same extent as SCF, and that the effects of HPF on hematopoitic stem cells differ from that of SCF.
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Hematopoietic-promoting factor (HPF), which was found in porcine kidney, has been demonstrated to act synergistically with colony-stimulating factor and erythropoietin on murine myeloid colony formation. We investigated the effect of HPF on the proliferation of human hematopoietic progenitor cells prepared from cord blood cells (CB) and peripheral blood cells (PB). HPF enhanced granulocyte colony-stimulating factor plus interleukin-3 and erythropoietin-induced colony formation, where the number of colonies were increased by 7.9-fold in CB and by 1.8-fold in PB, respectively. When we compared the effect of HPF with stem cell factor (SCF) on the colony formation derived from PB in serum-free cultures, HPF enhanced the number of erythroid burst-forming units (BFU-E) to the same extent as SCF. But the effect of HPF on promoting the growth of granulocyte-macrophage colony-forming units (CFU-GM) was less than SCF. When the enriched CD34+ cells from CB and PB were incubated in liquid culture with HPF and IL-3 for 7 days, CFU-GM was increased by 48-fold in CB, and by 25-fold in PB, respectively. The data demonstrate that HPF can potentiate expansion of hematopoietic stem cells to the same extent as SCF, and that the effects of HPF on hematopoitic stem cells differ from that of SCF.
Key concepts: Haematopoiesis, Stem cell factor, Erythropoietin, CD34, Progenitor cell, CFU-GM, Cord blood, Stem cell