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Title   MTT ¹æ¹ýÀ» ÀÌ¿ëÇÑ ¸²ÇÁŲȰ¼º »ìÇؼ¼Æ÷ ( LAK cell ) È°¼ºµµ ÃøÁ¤¿¡ °üÇÑ ¿¬±¸ ( Testing of LAK Cell Activity Using a Tetrazolium-based Colorimetric ( MTT ) Assay )
Publicationinfo   1987 Jan; 019(02): 68-79.
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Abstract   Peripheral blood lymphocytes of normal individuals can be activated by culture with recombinant Interleukin-2 (donated by Genetic Engineering Center, KAIST, Seoul, Korea) leading to expression of cytotoxic activity toward on colorectal carcinoma cell line SNU-C5. After 4 days incubation, the LAK cells were removed by 4 times washing and the number of live target cells in the microtest plates were counted by the tetazolium-based colorimetric (MTT) assay and the survival rate of the target cells was calculated against the control in which the target cells were incubated without Interleukin-2 and effector cells. During 5 days culture, the recombinant KAIST Interleukin-2 induced the potent LAK cells at the concentration of 0.1 U/ml. After 4 days incubation, almost all target cells (SNU-C5) were killed by the LAK cells of 5 days culture when the Effector:Target ratio were 10 : 1 and 5 : l. SNU C5 represented high adhesiveness to the culture flask and microtest plate bottom, so it can be used for the tetazolium based colorimetric (MTT) assay. Tetrazolium-based colorimetric (MTT) assay shows good carrelation between spectrophotometric absorbance and cell number, and it is long-term assay over other cytotoxicity test methods, so semiautomated MTT assay offers a valid. rapid, and simple method to assess cytotoxicity of LAK cells.
Àú ÀÚ   ¹ÚÀç°©(Jae Gahb Park),±Ç¿ÀÁß(Oh Hoong Kwon),±è¼±È¸(Sun Whe Kim),±èÁøº¹(Jin Pok Kim),ÇÔ¼ö(Kyung Soo Hahm),Çѹ®Èñ(Moon H . Han)