The Change of c-jun Promoter Activity in TPA-Induced U937 Cells Infected with Human Cytomegalovirus (HCMV)

TPA로 분화된 U937 세포에서 사람 세포거대바이러스에 의한 c-jun Promoter 활성도의 변화

  • Park, Chung-Gyu (Department of Microbiology, College of Medicine and Institute of Endemic Diseases, Medical Research Center, Seoul National University) ;
  • Kim, Dae-Joong (Department of Microbiology, College of Medicine and Institute of Endemic Diseases, Medical Research Center, Seoul National University) ;
  • Kim, Jin-Hee (Department of Microbiology, College of Medicine and Institute of Endemic Diseases, Medical Research Center, Seoul National University) ;
  • Han, Tae-Hee (Department of Microbiology and Immunology, Sung Kyun Kwan University College of Medicine) ;
  • Hwan, Eung-Soo (Department of Microbiology, College of Medicine and Institute of Endemic Diseases, Medical Research Center, Seoul National University) ;
  • Choi, Myong-Sik (Department of Microbiology, College of Medicine and Institute of Endemic Diseases, Medical Research Center, Seoul National University) ;
  • Kook, Yoon-Hoh (Department of Microbiology, College of Medicine and Institute of Endemic Diseases, Medical Research Center, Seoul National University) ;
  • Choi, Sung-Bae (Department of Microbiology, College of Medicine and Institute of Endemic Diseases, Medical Research Center, Seoul National University) ;
  • Cha, Chang-Yong (Department of Microbiology, College of Medicine and Institute of Endemic Diseases, Medical Research Center, Seoul National University)
  • 박정규 (서울대학교 의과대학 미생물학교실 및 의학연구원 감염병연구소) ;
  • 김대중 (서울대학교 의과대학 미생물학교실 및 의학연구원 감염병연구소) ;
  • 김진희 (서울대학교 의과대학 미생물학교실 및 의학연구원 감염병연구소) ;
  • 한태희 (성균관대학교 의과대학 미생물학 및 면역학교실) ;
  • 황응수 (서울대학교 의과대학 미생물학교실 및 의학연구원 감염병연구소) ;
  • 최명식 (서울대학교 의과대학 미생물학교실 및 의학연구원 감염병연구소) ;
  • 국윤호 (서울대학교 의과대학 미생물학교실 및 의학연구원 감염병연구소) ;
  • 최성배 (서울대학교 의과대학 미생물학교실 및 의학연구원 감염병연구소) ;
  • 차창룡 (서울대학교 의과대학 미생물학교실 및 의학연구원 감염병연구소)
  • Published : 1999.06.30

Abstract

Transient transfection assay has been done to evaluate whether the c-jun activation would be prerequisite to the induction of permissiveness against human cytomegalovirus using in vitro cell model in which U937 has been induced to express CD11b and CD14 to become potential monocyte/macrophage cells by TPA treatment. U937 cells were treated with $10\;{\mu}M$, $50\;{\mu}M$ or $100\;{\mu}M$ of TPA. The cell morphology change was observed and the expression of the CD11b and CD14 was confirmed by FACS. Differentiated cells were transfected with pJLuc reporter vector which contained the wild type murine c-jun promoter spanning the SP1, CTF, ATF/CREB and MEF-2 binding sites upstream of the firefly luciferase gene. After 48 hrs of transfection, the cells were infected with HCMV Towne strain and the luciferase activity was assessed at 1 hand 4 h pi. The transfection assay showed no activation of the c-jun promoter at 1 h pi, instead, it showed 2 times increase of the its activity at 4 h pi. There was no difference of the c-jun promoter activation between TPA treated and untreated U937 cells, implying that c-jun activation might not be prerequisite for allowing cells to be premissive to HCMV, although HCMV infection itself could activate c-jun promoter.

Keywords