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IL‐12 indirectly enhances proliferation of 5‐FU‐treated human hematopoietic peripheral blood CD34 + cells
Author(s) -
Grafte Stéphanie,
Lévêque Catherine,
Paysant Jérôme,
Vasse Marc,
Soria Claudine,
Vannier JeanPierre
Publication year - 1998
Publication title -
american journal of hematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.456
H-Index - 105
eISSN - 1096-8652
pISSN - 0361-8609
DOI - 10.1002/(sici)1096-8652(199807)58:3<183::aid-ajh4>3.0.co;2-n
Subject(s) - haematopoiesis , cd34 , stem cell factor , cytokine , stem cell , interleukin 3 , biology , immunology , microbiology and biotechnology , interleukin 12 , chemistry , cancer research , interleukin 21 , immune system , t cell , in vitro , cytotoxic t cell , biochemistry
Interleukin‐12 (IL‐12) or natural killer cell stimulatory factor (NKSF), has multiple effects on T lymphocytes and natural killer cells. In this study, the effect of IL‐12 on human hematopoiesis was studied by analyzing the growth of CD34 + peripheral blood stem cells (PBSC), in steady state. In the presence of Epo, IL‐12 alone or in combination with IL‐3 or SCF had no effect on the formation of colonies from CD34 + cells. In culture with Epo, G‐CSF, and IL‐3, the effect of Flt3‐ligand (FL) on CD34 + PBSC was investigated in the presence or absence of IL‐12. No additional effect of IL‐12 was observed when combined with FL. We evaluated 5‐FU‐treated human CD34 + PBSC proliferation in cultures with Epo, G‐CSF, and IL‐3, in the presence or absence of IL‐12. No cytokine combination enhanced colony formation from 5‐FU‐treated CD34 + cells. However, in cultures of 5‐FU‐treated human CD34 + cells, the most efficient combination was IL‐3 + Epo + G‐CSF + Accessory cells (CD34 − ). Furthermore, IL‐12 enhanced this colony formation significantly. To investigate whether immature CD34 + cells were responsible for FL or SCF, 5‐FU‐treated human CD34 + cells were cultured with or without IL‐12. Whereas no synergistic effect was observed in combination with IL‐12, SCF alone significantly enhanced colony formation. However, the colony number was found to be smaller than with the potent combination of accessory cells in the presence of IL‐12. These results indicate that accessory cells, lost in CD34 + cell purification, could be partly responsible for an IL‐12 effect on immature human PBSC proliferation. J. Hematol. 58:183–188, 1998. © 1998 Wiley‐Liss, Inc.