Effect of Genistein on Apoptosis of T Iymphocyte and Phagocytosis of Peritoneal Macrophage

Genistein이 T lymphocyte의 Apoptosis 및 복강 Macrophage의 탐식능에 미치는 영향

  • Published : 2002.02.01

Abstract

The effects of genistein on murine thymocytes for inducing apoptotic cell death and phagocytic activity of peritoneal macrophage were studied in vitro. Addition of genistein (10 and 50$\mu$M) to cultured thymocytes from BALB/c mice definitely promoted DNA fragmentation. Also, cytofluorometric analysis of these cells demonstrated a reduction in mitochondrial transmembrane potential ($\Delta$Ψm). But, repeated administration of genistein (1 mg/mouse/day) to mice for 7 days did not cause any detectable DNA fragmentation. Genistein decreased lucigenin chemiluminescence and engulfment of fluorescein-conjugated E. coli particles in peritoneal macrophage. These results suggest that genistein induce an apoptosis of thymocyte via reduction in $\Delta$Ψm and decrease phagocytic activity of peritoneal macrophage in vitro.

Keywords

References

  1. J. Cin. Lab. Invest. v.50 no.3 Western diet and western disease; Some hormonal and biochemical mechanism and associations. Scand Adlercreurz, H.
  2. Environ.Health Perspect v.103 no.Supple7 Phytoestrogens; epidermiology and a possible role in cancer protection Adlercreurz, H.
  3. JNCI v.83 The role of soy products in reducing risk of cancer Messina, M.;Barnes, S. https://doi.org/10.1093/jnci/83.8.541
  4. Nutz Cancer v.21 Soy intake and cancer risk;a review of in vitro and in vivo data Messina, M.;barnes, S.
  5. Prog. Clin. Biol. Res. v.347 Soybeans inhibit mammary tumors in models of breast cancer Barnes, S.;Grubbs, C.;Setchell, KDR.;Carlson, J.
  6. Nutrition and Cancer v.30 no.3 Effect of soy-derived isoflavonoids on the induced growth of MCF-7 cells by estrogenic enviromental chemicals Verna, S. P.;Goldin, B. R. https://doi.org/10.1080/01635589809514669
  7. Nutrition and Cancer v.30 no.1 Effect of isoflavones genistein and daidzein in the inhibition of lung metastasis in mice induced by B16F-10 melanoma cells Meno, L. G.;Muttan, R.;Nair, M. G.;Chang, Y. G.;Kutten, G. https://doi.org/10.1080/01635589809514644
  8. Cancer Research v.58 Inhibition of Murine bladder tumorigenesis by soy isoflavones via alterations in the cell cycle, apoptosis and angiogenesis Zhou, J. R.;Mukherjee, P.;Gugger, E. T.;Tanaka, T.;Blackburn, L.;Clinton, S. K.
  9. Jpn. J. Clin. Oncol. v.28 no.6 Effects of soybean isoflavones on cell growth and apoptosis of the human prostatic cancer cell line LNCaP Onozawa, M.;Fukuda, K.;Ohtani, M.;Akaza, H.;Sugimura, T.;Wakabayashi, K. https://doi.org/10.1093/jjco/28.6.360
  10. Am. J. Clin. Nutr. v.40 Nonsteroidal estrogens of dietary origin; Possible roles in hormone-dependent disease Setchell, K. D. R.;Borriello, S. P.;Hulme, P. ;Kirk, D. N.;Axelson, M. https://doi.org/10.1093/ajcn/40.3.569
  11. J. Biol. Chem. v.262 Genistein, a specific inhibitor of tyrosine-specific protein kinase Akiyama, T.;Ishia, J.;Nakagawa, S.;Ogawara, H.;Watanabe, S. I.
  12. Methods Enzymol v.201 Use and specificity of genistein as inhibitor of protein-tyrosine kinases Akiyama, T.;Ogawara, H. https://doi.org/10.1016/0076-6879(91)01032-W
  13. Semin. Oncol. Nurs. v.8 The role of the immune system in the pathogenesis of cancer Appelbaum, J. W. https://doi.org/10.1016/0749-2081(92)90008-Q
  14. Endocr. Rev. v.5 Regulation of the immune system by sex steroids Grossman, C. J. https://doi.org/10.1210/edrv-5-3-435
  15. Science v.227 Interactions between the gonadal steroids and the immune system Grossman, C. J. https://doi.org/10.1126/science.3871252
  16. Ann. Med. v.26 Hormonal regulation of immune responses Paavonen, T. https://doi.org/10.3109/07853899409147900
  17. Nutr. Cancer v.29 Enhancement of immune function in mice fed high doses of daidzein Zhang, R.;Li. Y.;Wang, W. https://doi.org/10.1080/01635589709514597
  18. Cell Immuno v.152 no.1 Induction of mouse thymocyte apoptosis by inhibitors of tyrosine kinases is associated with dephosphorylation of nuclear proteins Azuma, Y.;Onishi, Y.;Sato Y.;Kizaki, H. https://doi.org/10.1006/cimm.1993.1287
  19. Yakhak Oheji v.44 no.2 Effect of daidzein and genistein on immune function in mice Eun, J. S.;Cho, S. K.;Kwon, J.;Suh, E. S.;Jeon, H.;Yum, J. Y.
  20. Proc. Nat1. Acad. Sci. USA v.75 Planning for lymphocytes: A method for cell selection Wysocki, L. J.;Sato, V. L. https://doi.org/10.1073/pnas.75.6.2844
  21. J. Immuno. v.120 Characterization of lymphocyte-activating factor(LAF) produced by the macrophage cell line P388D1 Mizel, S. B.;Openheim, J. J.;Rosensteich, D. L.
  22. J. Immunol. methods v.655 Rapid colorimetric assay for celluar growth and survival: application to proliferation and cytotoxic assays Mosmann, T.
  23. J. Immuno. methods v.129 A simple and rapid method to determine hematopoietic growth factor activity Kotnic, V.;Fleischmann, W. R. Jr. https://doi.org/10.1016/0022-1759(90)90416-S
  24. J. Immuno. methods v.139 Rapid and Simple method for mesuring thymocyte apoptosis by propidium iodide staining and flow cytometry Nicoletti, I.;Migliorati, G.;Pagliacci, M. C.;Grignani, F.;Riccardi, C. A. https://doi.org/10.1016/0022-1759(91)90198-O
  25. J. Immunology. v.147 Evidence of synergy between Thy-1 and CD3/TCR complex in signal deluvery to murine thymocytes for cell death Nakashima, I.;Zhang, Y. H.;Rahman, S. M. J.;Yoshida, T.;Isobe, K.;Ding, L.;Iwamoto, T.;Hamaguchi, M.;Ikezawa, H.;Taguchi, R.
  26. J. Exp. Med. v.181 Reduction in mitochondrial potential constitues an early irreversible stp of programmed lymphocyte death in vivo Zamzini, N.;Petit, P. X.;kroemer, G. https://doi.org/10.1084/jem.181.5.1661
  27. J. Immunol. Methods v.174 Chemiluminenscence and nitrite determinations by the MALU macrophage cell line Boudard, F.;Vallot, N.;Cabaner, C.;Bastide, M. https://doi.org/10.1016/0022-1759(94)90030-2
  28. J. Immunol. Methods v.112 Measurement of phagocyte chemiluminenscence in a microtiter plate format Blair, A. L.;Cree, I. A.;Beck, J. S.;Hating, M. J. G.
  29. J. Immunol. Methods v.162 A rapid and simple microfluotometric phagocytosis assay Chok, P. W.;Choon, S. P.;Benjamin, H. S.;Hating, M. J. G. https://doi.org/10.1016/0022-1759(93)90400-2
  30. Nutr. Cancer. v.29 no.1 Individual and combinaory effects of soy isoflavones on the in vitro potentiation of lymphocyte activation Wang, W.;Higuchi, C. M.;Zhang, R. https://doi.org/10.1080/01635589709514598
  31. Biochem. Biophys. Res. Commun. v.194 no.2 genistein induces apoptosis in immature human thymocytes by inhiniting topoisorr..erase-II McCabe, M. J. Jr.;Orrenius, S. https://doi.org/10.1006/bbrc.1993.1912
  32. Infect. Immun v.45 Intra- and extracellular evevts in lumino-dependent chemilulinescence of polymorphonuclear leukocytes Breiheim, G.;Stendahl, O.;Dahlgren, C.