Establishment of 8-Azaguanine Resistant Human Plasmacytoma Cell Line

8-Azaguanine 내성 인형 형질세포종 세포주의 확립

  • Cha, Chang-Yong (Department of Microbiology, College of Medicine, Seoul National University) ;
  • Hwang, Eung-Soo (Department of Microbiology, College of Medicine, Seoul National University) ;
  • Kook, Yoon-Ho (Department of Microbiology, College of Medicine, Seoul National University) ;
  • Lim, Dong-Kyun (Department of Microbiology, College of Medicine, Seoul National University) ;
  • Cho, Han-Ik (Cancer Research Institutes, College of Medicine, Seoul National University) ;
  • Park, Myung-Hee (Cancer Research Institutes, College of Medicine, Seoul National University) ;
  • Kim, Noe-Kyung (Cancer Research Institutes, College of Medicine, Seoul National University) ;
  • Chang, Woo-Hyun (Department of Microbiology, College of Medicine, Seoul National University) ;
  • Lee, Mun-Ho (Cancer Research Institutes, College of Medicine, Seoul National University)
  • 차창룡 (서울대학교 의과대학 미생물학 교실) ;
  • 황응수 (서울대학교 의과대학 미생물학 교실) ;
  • 국윤호 (서울대학교 의과대학 미생물학 교실) ;
  • 임동균 (서울대학교 의과대학 미생물학 교실) ;
  • 조한익 (서울대학교 의과대학 암연구소) ;
  • 박명희 (서울대학교 의과대학 암연구소) ;
  • 김노경 (서울대학교 의과대학 암연구소) ;
  • 장우현 (서울대학교 의과대학 미생물학 교실) ;
  • 이문호 (서울대학교 의과대학 암연구소)
  • Published : 1986.09.30

Abstract

This study was performed to establish human plasmacytoma cell line as the partner cells for producing human hybridoma. Bone marrow cells from a multiple myeloma patient from Seoul National University Hospital, Korea were cultured and established as the cell line, named as HMC-BM4. HMC-BM4 cells were cultivated in RPMI 1640 media containing 8-azaguanine(8-AG; gradually increasing concentration from $1\;{\mu}g/ml$ to $20\;{\mu}g/ml$). 8-AG resistant cells were collected and cloned by limiting dilution. Each clone was divided and tested to die in hypoxanthine, aminopterine and thymidine (HAT) selection media. Finally one clone was selected and named as HMC-AR, which was sensitive to HAT selection media. HMC-AR cells showed typical morphology of plamacytoma in Wright staining. No cell formed the rosette with sheep erythrocytes. Surface membrane $\mu$ heavy chain was detected in 20% of HMC-AR cells and cytoplasmic $\mu$ heavy chain in 90% of them by direct immunofluorescent staining. Ia-like antigen was found in 90% of HMC-AR cells by indirect immunofluorescent staining using anti-Ia-like antigen monoclonal antibody, 1BD9-2. And about $1.0\;{\mu}g/ml$ of human $\mu$ heavy chain was detected in the 3-day culture supernatant of HMC-AR cells. 88% of cells contained 46 chromosomes. Mycoplasma was not detected in HMC-AR cells by Hoechst 33258 staining. This cell line would be used for making hybridomas secreting human monoclonal antibody.

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