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C형 간염바이러스의 core 단백질에 의해 암화된 쥐의 섬유아세포에서 phospholipase D 효소활성의 증가

Phospholipase D Activity is Elevated in Hepatitis C Virus Core Protein-Transformed NIH 3T3 Mouse Fibroblast Cells

  • Kim, Joonmo (Department of Physiology, College of Medicine, The Catholic University of Korea) ;
  • Jung, Eun-Young (Department of Microbiology, College of Natural Sciences, Pusan National University) ;
  • Jang, Kyung-Lib (Department of Microbiology, College of Natural Sciences, Pusan National University) ;
  • Min, Do-Sik (Department of Physiology, College of Medicine, The Catholic University of Korea)
  • 발행 : 2003.10.01

초록

C형 간염바이러스는 간암을 야기하는 심각한 바이러스이다. C형 간염바이러스의 core 단백질의 과발현은 섬유아세포를 암화시키는 것으로 알려져 있다. Phospholipase D (PLD)의 효소활성이 세포증식 신호전달에 의해 활성화되어 있으며, 사람의 암조직에서 과발현 및 활성이 증가되어 있는 것으로 알려져 있다. 본 연구의 목적은, core 단백질에 의해 암화된 세포에서 PLD가 어떻게 조절되는지를 이해하고자 하는 것이다. 자극이 없는 상태에서뿐만 아니라 PMA에 의해 유도되는 PLD효소활성은, 암화된 세포에서 더 증가하였으며, control 세포와 core 단백질에 의해 암화된 세포에서 PLD와 PKC 단백질의 발현은 서로 유사하였다. PKC 특이적인 억제제와 PKC의 세포막으로의 이동에 관한 실험을 통해서, PKC-d가 암화된 세포에서 PMA에 의해 유도되는 PLD활성의 증가에 중요하게 관여하고 있음을 밝혔다. 이러한 결과는, PLD가 core 단백질에 의해 유도되는 세포의 암화과정에 관여하고 있을 것으로 추정된다.

Hepatitis C Virus (HCV) is associated with a severe liver disease and increased frequency in the development of hepatocellular carcinoma. Overexpression of HCV core protein is known to transform fibroblast cells. Phospholipase D (PLD) activity is commonly elevated in response to mitogenic signals, and PLD has been also reported to be overexpressed and hyperactivated in some human cancer. The aim of this study was to understand how PLD can be regulated in HCV core protein-transformed NIH3T3 mouse fibroblast cells. We observed that in unstimulated state, basal PLD activity was higher in NIH3T3 cells overexpressing HCV core protein than in vector-transfected cells. Although expression of PLD and protein kinase C (PKC) in core protein-transformed cells was similar with that of control cells, phorbol 12-myristate 13-acetate (PMA), which is known to activate PKC, stimulated significantly PLD activity in core protein-transformed cells, compared with that of the control cells. PLD activity assay using PKC isozyme-specific inhibitor, and PKC translocation experiment showed that PKC-$\delta$ was mainly involved in the PMA-induced PLD activation in the core-transformed cells. Taken together, these results suggest that PLD might be implicated in core protein-induced transformation.

키워드

참고문헌

  1. Mo.1-Cell. Biol. v.23 Transmodulation beween phospholipase-D and c-Src enhances cell proliferation Ahn,B.H;S.Y.Kim;E.H.Kim;K.S.Choi;T.K.Kwon;Y.H.Lee;J.S.Chang;M.S.Kim;Y.H.Jo;D.S.Min https://doi.org/10.1128/MCB.23.9.3103-3115.2003
  2. J. Biol. Chem. v.272 Nuclear ADP-ribosylation factor (ARF)- and oleate-dependent phospholipase D (PLD) in rat liver cells.Inceases of ARF-dependent PLD activity in regenerating liver cells Banno,Y.K;Trmiya-Koizumi;H.Oshima;A.Morikawa;S.Yoshida;Y.Nozawa https://doi.org/10.1074/jbc.272.8.5208
  3. Curr. Biol. v.7 Phospholipase D2, a distinct phospholipase D isoform with novel regulatory properties that provokes cytoskeletal reorganization Colley,W.C.;T.C.Sung;R.Roll;J.Jenco;S.M.Hammond;Y.Altshuller;D. Bar-Sagi;A.J.Morris;M.A.Frohman https://doi.org/10.1016/S0960-9822(97)70090-3
  4. Int. J. cancer v.85 Changes of phospholipase D isoform activity and expression in multidrug-resistant human cancer cells Fiucci,G.;M.Y.Czarny;Y.Lavie;D.Zhao;B.Berse;J.K.Blusztajn;M.Liscovitch https://doi.org/10.1002/(SICI)1097-0215(20000315)85:6<882::AID-IJC24>3.0.CO;2-E
  5. Biochem. Biophys. Res. Commun. v.255 Ral and Rho-dependent activation of phospholipase D in v-Raf-transformed cells Frankel.P.;M.Ramos;J.Flom;S.Bychenok;T.Joseph;E.Kerkhof;U.R.Rapp;L.A.Feig;D.A.Foster https://doi.org/10.1006/bbrc.1999.0234
  6. J. Biol.Chem. v.272 Characterization of two alternately spliced forms of phospholipase D1. Activation of the purified enzymes by phosphatidylinositol 4,5-bisphosphate,ADP-ribosylation factor,and Rho family monomeric GTP-binding proteins and protein kinase C-a Hammond,S.M.;J.M.Jenco;S.Nakashima;K.Cawallader;Q.Gu;S.Cook;Y.Nozawa;G.D.Prestwich;M.A.Frohman;A.J.Morris https://doi.org/10.1074/jbc.272.6.3860
  7. FEBS Lett v.518 Coopeative repression of cyclin-dependent kinase inhibitor p21 gene expression by hepatitis B virus X protein and hepatitis C virus core protein Han,H.J;E.Y.Jung;W.J.Lee;K.L.Jang https://doi.org/10.1016/S0014-5793(02)02694-7
  8. Bio-chem. Biophys. Res. Commun v.203 Phosphatidylcholine-specific phospholipase D activity is elevated in v-Fps-transformed cells Jiang,Y.W.;J.Song;Q.Zhang;D.A.Foster https://doi.org/10.1006/bbrc.1994.2309
  9. Virus Res. v.94 Cooperatove transformation of murine fibroblast NIH3T3 cells by hepatitis C virus core protein and hepatitis B virus X protein Jung,E.Y;H.K.Kang;J.Chang;D.Y.Yu;K.L.Jang https://doi.org/10.1016/S0168-1702(03)00135-7
  10. Virus Res. v.79 The repressive activity of hepatitis C virus core protein on the transcription of p21 (waf1) is regulated by protein kinase A-mediated phosphorylation Jung,E.Y.;M.N.Lee;H.Y.Yang;D.Yu;K.L.Jang https://doi.org/10.1016/S0168-1702(01)00335-5
  11. Oncology v.62 no.Suppl 1 Molecular mechanism of viral hepatocarcinogenesis Koike,K.;K.Tsutsumi;H.Fujie;Y.Shintani;M.Kyoji https://doi.org/10.1159/000048273
  12. Virology v.294 Conformational changes accompanying self-assembly of the hepatitis C virus core protein Kunkel,M.;S.J.Watowich https://doi.org/10.1006/viro.2001.1325
  13. Brain Res. v.864 Immunohistochemical localization of phosphlipase D1 in rat central nervous system Lee,M.Y.;Y.J.Jo;M.H.Chun;J.W.Chung;M.S.Kim;D.S.Min https://doi.org/10.1016/S0006-8993(00)02134-X
  14. Biochem. J. v.345 Phospholipase D: molecular and cell biology of a novel gene family Liscovitch,M.;M.Czarny;G.Fiucci;X.Tang https://doi.org/10.1042/0264-6021:3450401
  15. J. Virol. v.73 Hepatitis C virus core protein inhibits Fas- and tumor necrosis factor alpha-mediated apoptosis via NF-kappaB activation Marusawa,H.;M.Hijikata;T.Chiba;K.Shimotohno
  16. Carcinogenesis v.22 Neoplastic transformation and tumorigenesis associated with overexpression of phospholipase D isozymes in cultured murine fibroblasts Min,D.S.;T.K.Kwon;W.S.Park;J.S.Chang;S.K.Park;B.H.Ahn;Z.Y.Ryoo;Y.H.Lee;Y.S.Lee;D.J.Rhie;S.H.Yoon;S.J.Hahn;M.S.Kim;Y.H.Jo https://doi.org/10.1093/carcin/22.10.1641
  17. Nat. Med. v.4 The core protein of hepatitis C virus induces hepatocellular carcinoma in transgenic mice Moriya,K.;H.Fujie;Y.Shintani;H.Yotsuyangi;T.Tsutsumi;K.Ishibashi;Y.Matsuura;S.Kimura;T.Miyamura;K.Koike https://doi.org/10.1038/2053
  18. FEMS Microbiol. Lett. v.202 Hepatitis C virus core protein: intriguing properites and functional relevance Ray,R.B;R.Ray https://doi.org/10.1111/j.1574-6968.2001.tb10796.x
  19. J. Biol. Chem. v.272 Transcriptional repression of p53 promoter by hepatitis C virus core protein Ray,R.B.;R.Steele;K.Meyer;R.Ray https://doi.org/10.1074/jbc.272.17.10983
  20. Proc. Natl. Acad. Sci. v.87 Hepatitis C virus infection is associated with the development of hepatocellular carcinoma Saito,T.;A.Miyamura;H.Ohbayashi;T.Harada;T.Katayama;S.Kikuchi;Y.Watanabe;S.Koi;M.Onji;Q.L.Choo;M.Houghton;G.Kuo https://doi.org/10.1073/pnas.87.17.6547
  21. J. Virol. v.72 Ectopic expression of hepatitis C virus core protein diferentially regulates muclear transcription factors Shiravastava,A.;S.K.Manna;R.Ray
  22. Curr. Pharmaceu. Biotech. v.2 Intracellular signaling by phospholipase D as therapeutic target Steed,P.M.;A.H;M.Chow https://doi.org/10.2174/1389201013378644
  23. Intervirology v.37 Pathology of hepatitis C Uchida,T.
  24. Anticancer Res. v.19 Phospholipase D activity in human gastric carcinoma Uchida,N.;S.Okamura;H.Kuwano
  25. J. Cancer Res. Clin. Oncol. v.13 Increased phospholipase D activity in human breast cancer Uchida,N.;S.Okamura;lY.Nagamachi
  26. Biochem. Biophys. Res. Commun v.278 Increased activity and in tracellular expression of phospholipase D in humanrenal cancer Zhao,Y;H.Ehara;Y.Akao;lM.Shamato;Y.Nakagawa;Y.banno;lT.Deguchi;N.Ohishi;K.Yaki;Y.Nozawa https://doi.org/10.1006/bbrc.2000.3719