Pegylated granulocyte colony-stimulating factor mobilizes CD34+ cells with different stem and progenitor subsets and distinct functional properties in comparison with unconjugated granulocyte colony-stimulating factor
Abstract:BackgroundPegylated granulocyte colony-stimulating factor (G-CSF) has recently been introduced as a new compound for mobilization of CD34 + hematopoietic stem and progenitor cells. In this study, we compared the molecular and functional characteristics of CD34 + cells mobilized by pegylated G-CSF with those mobilized by unconjugated G-CSF.
“…Our results are in complete agreement with published data indicating stimulation of hemopoietic precursors release into peripheral blood under the effect of G-CSF, in parallel with the increase in functional activity of CFU-GM [1,2,8,13].…”
The effects of granulocytic CSF immobilized on polyethylenoxide by nanotechnology on the bone marrow and circulating pools of mesenchymal and hemopoietic precursors were studied. Immobilized granulocytic CSF caused the release of progenitor cells of different classes into the blood. The effect of injected immobilized granulocytic CSF was superior to that of nonconjugated granulocytic CSF. Specific activity of oral immobilized granulocytic CSF after oral administration was demonstrated.
“…Our results are in complete agreement with published data indicating stimulation of hemopoietic precursors release into peripheral blood under the effect of G-CSF, in parallel with the increase in functional activity of CFU-GM [1,2,8,13].…”
The effects of granulocytic CSF immobilized on polyethylenoxide by nanotechnology on the bone marrow and circulating pools of mesenchymal and hemopoietic precursors were studied. Immobilized granulocytic CSF caused the release of progenitor cells of different classes into the blood. The effect of injected immobilized granulocytic CSF was superior to that of nonconjugated granulocytic CSF. Specific activity of oral immobilized granulocytic CSF after oral administration was demonstrated.
“…6 RNA was purified as described 6 and samples were stored at -80°C. For detection and quantification of mRNA levels of RPS14 and GAPDH the LightCycler 1.2 technology (Roche, Mannheim, Germany) was used.…”
Section: Sample Preparation and Quantitative Rt-pcrmentioning
“…It is important to realize that G-CSF, PEG-G-CSF and CXCR-4 antagonists recruit different cell populations according to global gene and mRNA expression levels. [34][35][36] Finally, it is possible that biosimilars of G-CSF and EPO will also be applied in healthy donors although recent statements from the European Group for Blood and Marrow Transplantation (EBMT) and WMDA do not recommend it outside of the context of well set up safety studies. This emphasizes the need to include all current mobilizing agents as well as any new agents that will be introduced into clinical practice in the future in a prospective follow-up.…”
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