TY - JOUR
T1 - Tumor cell detection method using complement-mediated cytolytic reaction and imaging sensor system
AU - Suzuki, Masayasu
AU - Watamabe, Nobuyuki
AU - Tamiya, Eiichi
AU - Kataoka, Tetsuro
AU - Tokunaga, Tohru
AU - Karube, Isao
PY - 1987/10
Y1 - 1987/10
N2 - A novel tumor-detection system consisting of complementmediated cytolytic reaction and an image processing system was developed for the simple and rapid determination of tumor cells. The present system consists of a CCD image sensor, image memory board, personal computer, and microscope. When monoclonal antibody 3C4, which is specific to the guinea pig hepatoma L-10, was added to cell suspension, only L-10 cytolysis occurred. Cytolysis caused a decrease in brightness of the cells observed by phase-contrast microscopy. The phase contrast image of the cells before cytolysis was converted to a digitalized signal and stored in computer memory. After cytolysis, a brightness threshold above that of lysed cells was subtracted from the digitalized signal and compared to the signal stored before reaction. L-10 cells in mixed cell suspension were determined specifically by the system. Measurement time was only 2 sec and overall time, including reaction time, was approximately 30 min. Since this method does not require a cell washing process, automation of the whole system is possible.
AB - A novel tumor-detection system consisting of complementmediated cytolytic reaction and an image processing system was developed for the simple and rapid determination of tumor cells. The present system consists of a CCD image sensor, image memory board, personal computer, and microscope. When monoclonal antibody 3C4, which is specific to the guinea pig hepatoma L-10, was added to cell suspension, only L-10 cytolysis occurred. Cytolysis caused a decrease in brightness of the cells observed by phase-contrast microscopy. The phase contrast image of the cells before cytolysis was converted to a digitalized signal and stored in computer memory. After cytolysis, a brightness threshold above that of lysed cells was subtracted from the digitalized signal and compared to the signal stored before reaction. L-10 cells in mixed cell suspension were determined specifically by the system. Measurement time was only 2 sec and overall time, including reaction time, was approximately 30 min. Since this method does not require a cell washing process, automation of the whole system is possible.
KW - Hepatocarcinoma cell
KW - complement
KW - cytolytic reaction
KW - imaging sensor system
KW - monoclonal antibody
KW - phase-contrast microscope
UR - http://www.scopus.com/inward/record.url?scp=0023611079&partnerID=8YFLogxK
U2 - 10.1007/BF02798448
DO - 10.1007/BF02798448
M3 - 学術論文
C2 - 3454129
AN - SCOPUS:0023611079
SN - 0273-2289
VL - 15
SP - 191
EP - 200
JO - Applied Biochemistry and Biotechnology
JF - Applied Biochemistry and Biotechnology
IS - 3
ER -