CAJ | 학술논문

试验研究了北方地区黑白花奶牛乳腺上皮细胞的最佳冻存方法。采用内蒙古地区健康黑白花奶牛的新鲜乳腺组织,将组织进行Ⅱ型胶原酶消化后原代培养,培养的细胞经5代纯化后将密度调整为1×106个/mL。采用6种处理方法进行冻存,各设3个重复。液氮冻存1个月后,分别将6种不同方法冻存的细胞复苏后测定细胞活性,包括冻存死亡率、贴壁细胞占活细胞的比率、凋亡率等,同时进行形态学观察。结果显示,处理1组与2、3、5组间冻存死亡率存在极显著差异（P〈0.01）,处理1、4、6组间冻存死亡率无显著差异（P〉0.05）,处理2、6组间冻存死亡率存在极显著差异（P〈0.01）;处理4组的贴壁率高于处理2、5、6组,存在极显著差异（P〈0.01）。形态学观察结果发现,处理1、4组细胞较其他组生长状态良好。因此,处理4可作为黑白花奶牛乳腺上皮细胞的最佳冻存方法。
시험연구료북방지구흑백화내우유선상피세포적최가동존방법。채용내몽고지구건강흑백화내우적신선유선조직,장조직진행Ⅱ형효원매소화후원대배양,배양적세포경5대순화후장밀도조정위1×106개/mL。채용6충처리방법진행동존,각설3개중복。액담동존1개월후,분별장6충불동방법동존적세포복소후측정세포활성,포괄동존사망솔、첩벽세포점활세포적비솔、조망솔등,동시진행형태학관찰。결과현시,처리1조여2、3、5조간동존사망솔존재겁현저차이（P〈0.01）,처리1、4、6조간동존사망솔무현저차이（P〉0.05）,처리2、6조간동존사망솔존재겁현저차이（P〈0.01）;처리4조적첩벽솔고우처리2、5、6조,존재겁현저차이（P〈0.01）。형태학관찰결과발현,처리1、4조세포교기타조생장상태량호。인차,처리4가작위흑백화내우유선상피세포적최가동존방법。
The effects of different cryopreservation methods of Holstein cow mammary epithelial cells on its viability were studied. Primary bovine mammary epithelial cells were passing five generations and adjusting the cell density to 1×106 cells/mL,and then being cryopreserved by 6 different methods.The viability of cells including mortality,adhering dish rate,apoptosis rate was measured after being recovered.The results showed that the death rate of cell being cryopreserved by treatments 2,3,5 was significantly different from treatment 1（P0.01）.Whereas no significant difference was found among treatments 1,4 and 6（P 0.05）.There was significantly different for death rate of cryopreserved cell between treatment 2 and 6（P0.01）.Adhering rate of cryopreserved cell from treatment 4 was significantly higher than treatment 2,5 and 6（P0.01）.Cell growth state of treatment 1 and 4 were better than others. The results indicated that the treatment 4 was the best cryopreservation method in this study.