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鲤鱼(Cyprinus carpio)体细胞系的建立及其生物学特性分析(简报)
引用本文:孟凡华,尹洪滨,孙中武,陈维多.鲤鱼(Cyprinus carpio)体细胞系的建立及其生物学特性分析(简报)[J].实验生物学报,2005,38(1):80-84.
作者姓名:孟凡华  尹洪滨  孙中武  陈维多
作者单位:[1]中国水产科学研究院黑龙江水产研究所,哈尔滨150070//东北农业大学生命科学院,哈尔滨150030 [2]中国水产科学研究院黑龙江水产研究所,哈尔滨150070 [3]东北林业大学生命科学院,哈尔滨150000
摘    要:动物细胞的培养技术是1907年哈里逊在淋巴块中对蛙的神经板培养成功开始的,其后近一个世纪以来,陆续成功地培养了哺乳动物、昆虫等各种动物细胞,并广泛用于生物科学的各个分支。鱼类的细胞培养的系统研究和建系实践大约起始于60年代,被公认的真骨鱼类的第一个永久性的细胞系——虹鳟性腺细胞系(RTG-2)是由Wolf建立的。随后各种鱼类细胞系相继建立,涉及的组织来源有吻端、肾脏、卵巢、尾鳍、性腺、肝脏、胚胎、囊胚、原肠胚、鳍条等,同时也进行了细胞体外培养条件、

关 键 词:细胞系  淋巴  性腺  细胞体外培养  神经  肾脏  肝脏  鱼类  种鱼  虹鳟

Construction and characteristics analysis of somatic cell lines from common carp Cyprinus carpio]
Fan Hua Meng,Hong Bin Yin,Zhong Wu Sun,Wei Duo Chen.Construction and characteristics analysis of somatic cell lines from common carp Cyprinus carpio][J].Acta Biologiae Experimentalis Sinica,2005,38(1):80-84.
Authors:Fan Hua Meng  Hong Bin Yin  Zhong Wu Sun  Wei Duo Chen
Institution:Heilongjiang River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Harbin 150070.
Abstract:Epithelia of rostral side and fins from common carp were taken to culture in vitro. As a result, cells of tail fins were successfully passed from generation to generation, and constructed cell lines. During the culture procedure, the passage cells were observed and their biological characteristics were analyzed, which consist of morphologic analysis, drawing of growth curve, detection of producing rate for clones, insight of adaptation to temperatures, calculation of chromosomes and investigation for thaw of frozen cells. According to the observation results, we found that (1) there is an increase trend of fibroblast. epithelia of rostral side and tail fin from common carp are the best materials for culturing cells; (2) the optimum culturing temperature is 27 degrees C; (3) there isn't any change in cell chromosomes, which still are normal diploid. However, with, the generations increasing, the mode of chromosome has an inclination of decrease in normal ranges. We inferred the donor cells from 4-10 generations are the best choice for nuclear transplanted experiments in order to guarantee their genetic stabilities and survival rates after transplanting the nuclei. And, the cells will grow extremely well when cultured for 48-72h at 27 degrees C. We suggest the temperature should be descended little by little involving in preserving cells with DMSO. So far, the cells were passed 30th generations and part of them was preserved into liquid nitrogen.
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