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In Vitro Effect of Interleukin-11 (IL-11) on Megakaryopoiesis from Umbilical Cord Blood Cells  

Lee, Kuk-Kyung (Department of Internal Medicine, SoonChunHyang University College of Medicine)
Kim, Chan-Kyu (Department of Internal Medicine, SoonChunHyang University College of Medicine)
Lee, Nam-Su (Department of Internal Medicine, SoonChunHyang University College of Medicine)
Kim, Sook-Ja (Institute for Clinical Biology Research, SoonChunHyang University College of Medicine)
Cheong, Hee-Jeong (Institute for Clinical Biology Research, SoonChunHyang University College of Medicine)
Lee, Kyu-Tack (Department of Internal Medicine, SoonChunHyang University College of Medicine)
Park, Sung-Kyu (Department of Internal Medicine, SoonChunHyang University College of Medicine)
Baick, Seung-Ho (Department of Internal Medicine, SoonChunHyang University College of Medicine)
Won, Jong-Ho (Department of Internal Medicine, SoonChunHyang University College of Medicine)
Hong, Dae-Sik (Department of Internal Medicine, SoonChunHyang University College of Medicine)
Park, Hee-Sook (Department of Internal Medicine, SoonChunHyang University College of Medicine)
Publication Information
IMMUNE NETWORK / v.3, no.1, 2003 , pp. 47-52 More about this Journal
Abstract
Background: The megakaryopoiesis and platelet production is regulated by several hematopoietc factors such as thrombopoietin (TPO), interleukin-11 (IL-11) and interleukin- 3 (IL-3). IL-11 is a potent stimulator of megakaryopoiesis in vivo, and acts primarily as a megakaryocyte maturation factor in vitro and it can act synergistically with IL-3 and TPO. We performed this study to investigate the effects of recombinant human IL-11 (rhIL-11) with other hematopoietic factors on megakaryocyte colony formation in vitro. Methods: CD34+ cells were separated from umbilical cord blood and megakaryocyte colonies using MegaCult Assay Kit were cultured with rhIL-11, recombinant human IL-3 (rhIL-3), and recombinant human TPO (rhTPO) for 7 and 14 days. The number and percentage of CD34+ and CD41a+ cells were determined by flowcytometry. Results: The number of CD41a+ cells were $0.54{\pm}0.05{\times}10^4$ (rhIL-11 100 ng/ml), $5.32{\pm}0.23{\times}10^4$ (rhIL-3 100 ng/ml), and $8.76{\pm}0.15{\times}10^4$ (rhTPO 50 ng/ml) of total expanded cells during the culture of the purified CD34+ cells in liquid phase for 7 days. The number of CD41a+ cells were increased to $7.47{\pm}0.69{\times}10^4$ (rhIL-3+ rhIL-11), $11.92{\pm}0.19{\times}10^4$ (rhTPO+rhIL-11) of total expanded cells, respectively, during the culture of the purified CD34+ cells in liquid phase for 7 days in the presence of rhIL-11 (100 ng/ml). When the purified CD34+ cells were cultured in semisolid mediaincluding various concentration of rhIL-11, the megakaryocyte colonies were not formed. When the purified CD34+ cells were cultured with rhIL-11 and rhTPO or with rhIL-11 and rhIL-3, the number of megakaryocyte colonies were increased compared with rhTPO or rhIL-3 alone. Conclusion: These results indicate that IL-11 exerts a potent proliferative activity to colony forming unit-megakaryocyte from human umbilical cord blood, and it acts with other hematopoietic factors synergistically.
Keywords
Megakaryopoiesis; thrombopoietin; interleukin-11; interleukin-3;
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