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2014 | 19 | 4 |

Tytuł artykułu

Promoted megakaryocytic differentiation of K562 cells through oxidative stress caused by near ultraviolet irradiation

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Reactive oxygen species (ROS) have been proven to be important activators for various cellular activities, including cell differentiation. Several reports showed the necessity of ROS during cell differentiation of the megakaryocytic (MK) lineage. In this study, we employed near ultraviolet (near-UV) irradiation to generate endogenous oxidative stress in an MK differentiation process of K562 cells with phorbol 12-myristate 13-acetate (PMA) induction. A significant increase in the intracellular ROS level was detected on day 1 after near-UV irradiation. In the initial stage of differentiation, a shifted fraction of G1 and G2 phase cells was obtained using near-UV irradiation, giving an increased percentage of G2 phase cells (up from 31.1 to 68.7%). The near-UV irradiation-induced upregulation of the p21 gene, which is a cell cycle inhibitor, suggested that the G2 phase cells were prevented from undergoing cell division. It was found that the percentage of high ploidy (8N and 16N) cells was enhanced significantly at the later stage of the K562 cell culture with near-UV irradiation. Moreover, time-lapse analysis showed that near-UV irradiation encouraged the expression of CD41, a specific surface marker of megakaryocytes. This is the first report that the elevated oxidative stress through the near-UV irradiation promoted the MK differentiation of PMA-induced K562 cells.

Wydawca

-

Rocznik

Tom

19

Numer

4

Opis fizyczny

p.590-600,fig.,ref.

Twórcy

  • Division of Chemical Engineering, Department of Materials Engineering Science, Graduate School of Engineering Science, Osaka University, 1-3 Machikaneyama-cho, Toyonaka, Osaka, 560-8531, Japan
autor
  • Division of Chemical Engineering, Department of Materials Engineering Science, Graduate School of Engineering Science, Osaka University, 1-3 Machikaneyama-cho, Toyonaka, Osaka, 560-8531, Japan
autor
  • Division of Chemical Engineering, Department of Materials Engineering Science, Graduate School of Engineering Science, Osaka University, 1-3 Machikaneyama-cho, Toyonaka, Osaka, 560-8531, Japan
autor
  • Division of Chemical Engineering, Department of Materials Engineering Science, Graduate School of Engineering Science, Osaka University, 1-3 Machikaneyama-cho, Toyonaka, Osaka, 560-8531, Japan

Bibliografia

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  • 4. Sardina J.L., Lopez-Ruano, G., Sanchez-Abarca, L.I., Perez-Simon, J.A., Gaztelumendi, A., Trigueros, C., Llanillo, M., Sanchez-Yague, J. and Hernandez-Hernandez, A. p22phox-dependent NADPH oxidase activity is required for megakaryocytic differentiation. Cell Death Differ. 17 (2010) 1842–1854.
  • 5. Mostafa, S.S., Miller, W.M. and Papoutsakis, E.T. Oxygen tension influences the differentiation, maturation and apoptosis of human megakaryocytes. Br. J. Haematol. 111 (2000) 879–889.
  • 6. Hirose, K., Monzen, S., Sato, H., Sato, M., Aoki, M., Hatayama, Y., Kawaguchi, H., Narita, Y., Takai, Y. and Kashiwakura, I. Megakaryocytic differentiation in human chronic myelogenous leukemia K562 cells induced by ionizing radiation in combination with phorbol 12-myristate 13-acetate. J. Radiat. Res. 54 (2013) 438–446.
  • 7. Ojima, Y., Duncan, M.T., Nurhayati, R.W., Taya, M. and Miller W.M. Synergistic effect of hydrogen peroxide on polyploidization during the megakaryocytic differentiation of K562 leukemia cells by PMA. Exp. Cell Res. 319 (2013) 2205–2215.
  • 8. Butler, T.M., Ziemiecki, A. and Friis, R.R. Megakaryocytic differentiation of K562 cells is associated with changes in the cytoskeletal organization and the pattern of chromatographically distinct forms of phosphotyrosyl-specific protein phosphatases. Cancer Res. 50 (1990) 6323–6329.
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  • 10. Tetteroo, P.A., Massaro, F., Mulder, A., Schreuder van Gelder, R. and von dem Borne, A.E.G. Megakaryoblastic differentiation of proerythroblastic K562 cell-line cells. Leukem. Res. 8 (1984) 197–206.
  • 11. Fukuda, M. Tumor-promoting phorbol diester-induced specific changes in cell surface glycoprotein profile of K562 human leukemic cells. Cancer Res. 41 (1981) 4621–4628.
  • 12. Giammona, L.M., Fuhrken, P.G., Papoutsakis, E.T. and Miller, W.M. Nicotinamide (vitamin B3) increases the polyploidization and proplatelet formation of cultured primary human megakaryocytes. Br. J. Haematol. 135 (2006) 554–566.
  • 13. Shelly, C., Petruzzelli, L. and Herrera, R. K562 cells resistant to phorbol 12-myristate 13-acetate-induced growth arrest: dissociation of mitogenactivated protein kinase activation and Egr-1 expression from megakaryocyte differentiation. Cell Death Differ. 11 (2000) 501–506.
  • 14. Kulkarni, A.P., Mittal, S.P.K., Devasagayam, T.P.A. and Pal, J.K. Oxidative stress perturbs cell proliferation in human K562 cells by modulating protein synthesis and cell cycle. Free Rad. Res. 43 (2009) 1090–1100.
  • 15. Nagata, Y., Muro, Y. and Todokoro, K. Thrombopoietin-induced polyploidization of bone marrow megakaryocytes is due to a unique regulatory mechanism in late mitosis. J. Cell Biol. 139 (1997) 449–456.
  • 16. Baccini, V., Roy, L., Vitrat, N., Chagraoui, H., Sabri, S., Couedic, J.P., Debili, N., Wendling, F. and Vainchenker, W. Role of p21Cip1/Waf1 in cellcycle exit of endomitotic megakaryocytes. Blood 98 (2001) 3274–3282.
  • 17. Wuerzerberger-Davis, S.M., Chang, P.Y., Berchtold, C. and Miyamoto, S. Enhanced G2-M arrest by nuclear factor-κ-B-dependent p21waf1/cip1 induction. Mol. Cancer Res. 3 (2005) 345–352.
  • 18. Kang, C.D., Han, C.S., Kim, K.W., Do, I.R., Kim, C.M., Kim, S.H., Lee, E.Y. and Chung, B.S. Activation of NF-κB mediates the PMA-induced differentiation of K562 cells. Cancer Lett. 132 (1998) 99–106.
  • 19. Mitjavila-Garcia, M.T., Cailleret, M., Godin, I., Nogueira, M.M., CohenSolal, K., Schiavon, V., Lecluse, Y., Pesteur, F., Lagrue, A.H. and Vainchenker, W. Expression of CD41 on hematopoietic progenitors derived from embryonic hematopoietic cells. Development 129 (2002) 2003–2013.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

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