방사선조사 후 유표피암종세포내 칼슘농도의 변화와 apoptosis 발현에 관한 연구

A study of the [$Ca^{2+}$] and the Apoptosis of the KB Cell Lines after 10Gy Irradiation

  • 문제운 (서울대학교 치과대학 구강악안면방사선학교실 및 치학연구소) ;
  • 이삼선 (서울대학교 치과대학 구강악안면방사선학교실 및 치학연구소) ;
  • 허민석 (서울대학교 치과대학 구강악안면방사선학교실 및 치학연구소) ;
  • 최순철 (서울대학교 치과대학 구강악안면방사선학교실 및 치학연구소) ;
  • 박태원 (서울대학교 치과대학 구강악안면방사선학교실 및 치학연구소) ;
  • 유동수 (서울대학교 치과대학 구강악안면방사선학교실 및 치학연구소)
  • Moon Je-Woon (Department of Oral and Maxillofacial Radiology & Dental Research Institute, College of Dentistry, Seoul National University) ;
  • Lee Sam-Sun (Department of Oral and Maxillofacial Radiology & Dental Research Institute, College of Dentistry, Seoul National University) ;
  • Heo Min-Suk (Department of Oral and Maxillofacial Radiology & Dental Research Institute, College of Dentistry, Seoul National University) ;
  • Choi Soon-Chul (Department of Oral and Maxillofacial Radiology & Dental Research Institute, College of Dentistry, Seoul National University) ;
  • Park Tae-Won (Department of Oral and Maxillofacial Radiology & Dental Research Institute, College of Dentistry, Seoul National University) ;
  • You Dong-Soo (Department of Oral and Maxillofacial Radiology & Dental Research Institute, College of Dentistry, Seoul National University)
  • 발행 : 1999.02.01

초록

Purpose: Ionizing radiations have been reported as an apoptosis initiating stimulus in various cells and it has established that sustained elevations in [Ca/sup 2+/] can lead to DNA fragmentation by Ca/sup 2+/-dependent endonucleases, ultimately resulting in apoptotic cell death. The previous experiments have been reported by using primarily thymocytes and lymphocytes and the change of [Ca/sup 2+/] was measured only by minutes or hours respectively. We need to evaluate [Ca/sup 2+/] in both several minutes and hours after irradiation of radiation of radiation therapy and verify the apoptotic cells. Materials and Methods: We have measured [Ca/sup 2+/] in human gingival epitheloid cancer cell with 10Gy irradiation, at minutely intervals and hourly intervals using digitized video-intensified fluorescence microscopy and the fluorescent Ca/sup 2+/ indicator dye, fura-2. In order to find out that the transient rise in [Ca/sup 2+/] could induced apoptosis, cells were incubated for 1 hour at 37℃ with TdT enzyme, rinsed and resuspended containing fluorescence and observed under a confocal fluorescence microscope. MTT assay was done to determine cell activity and LDH assay was done to determine the amount of necrotic cells. Results: After irradiation, the transient and temporal increasing of [Ca/sup 2+/] in the KB cells was founded. Though, there was no change in the intracellular [Ca/sup 2+/] at 30 minutes and 2 hours after irradiation. We could detect of DNA fragmented cells at 4 hours after 10Gy irradiated cells. There were no significant differences between 4 hour, 1 day, 3 day cells. There were no significant differences in MTT and LDH assay between the irradiated group and the control group after 4 hours and 1 day. Though after 3 days there were differences in MTT and LDH assay between the irradiated group was significantly decreased than the control group, in LDH assay the number of necrotic cell death of the irradiated was higher than the control group. Conclusion: In KB cells there were incipient and temporal increasing of the [Ca/sup 2+/] with 10Gy irradiation and the apoptosis was founded from 4 hours later which was earlier than seeing of the change of the amount of the cellular ability and necrosis.

키워드