Song Jimei, Hua Song, Song Kai, Zhang Yong
Institute of Bioengineering, Northwest A & F University, Yangling, Shanxi Province 712100, China.
In Vitro Cell Dev Biol Anim. 2007 Jul-Aug;43(7):203-9. doi: 10.1007/s11626-007-9043-3. Epub 2007 Sep 1.
Tiger (Panthera tigris Linnaeus, 1758) is a characteristic species of Asia, which is in severe danger. Siberian tiger (Panthera tigris altaica) is the largest one of the five existent tiger subspecies. It is extremely endangered. One new way for tiger protection and rescue is to study interspecies cloning. But there is few research data about Siberian tiger. In this study, we cultured Siberian tiger fibroblasts in vitro, analyzed their biological characteristics, chromosomes, and cell cycles, to provide not only nuclear donors with good morphology, normal biological characteristics, and chromosome quantity for tiger interspecies cloning, but also reliable data for further studying Siberian tiger. The results indicated that Siberian tiger ear fibroblasts can be successfully obtained by tissue culture either with or without overnight cold digestion, the cultured cells were typical fibroblasts with normal morphology, growth curve, and chromosome quantity; G0/G1 percentage increased and S percentage decreased with the confluence of cells. G0/G1 and S stage rate was significantly different between 40-50% and 80-90%, 95-100% confluence; there is no distinct difference between 80-90% and 95-100% confluence. The cells at the same density (80-90% confluence) were treated with or without 0.5% serum starving, GO/G1 rate of the former was higher than the latter, but the difference was not significant. GO/G1 proportion of 95-100% confluence was slightly higher than serum starving (80-90% confluence), but no significant difference. Therefore, the Siberian tiger fibroblasts we cultured in vitro can be used as donor cells, and the donor cells do not need to be treated with normal serum starvation during nuclear transfer; if we will just consider the rate of the G0/G1 stage cells, serum starvation can be replaced by confluence inhibition when cultured cells were more than 80-90% confluence.
虎(Panthera tigris Linnaeus,1758)是亚洲的代表性物种,处于极度濒危状态。东北虎(Panthera tigris altaica)是现存五个虎亚种中体型最大的一种,极度濒危。虎保护与拯救的一种新方法是研究种间克隆。但关于东北虎的研究数据很少。在本研究中,我们体外培养东北虎成纤维细胞,分析其生物学特性、染色体和细胞周期,不仅为虎种间克隆提供形态良好、生物学特性正常且染色体数量正常的核供体,也为进一步研究东北虎提供可靠数据。结果表明,采用过夜冷消化或不采用过夜冷消化的组织培养方法均可成功获得东北虎耳成纤维细胞,培养的细胞为典型的成纤维细胞,形态、生长曲线和染色体数量正常;随着细胞汇合度增加,G0/G1期百分比升高,S期百分比降低。40 - 50%汇合度与80 - 90%、95 - 100%汇合度之间的G0/G1期和S期比例差异显著;80 - 90%与95 - 100%汇合度之间无明显差异。对相同密度(80 - 90%汇合度)的细胞进行0.5%血清饥饿处理或不处理,前者的G0/G1期比例高于后者,但差异不显著。95 - 100%汇合度的G0/G1期比例略高于血清饥饿处理(80 - 90%汇合度),但无显著差异。因此,我们体外培养的东北虎成纤维细胞可作为供体细胞,核移植时供体细胞无需进行正常血清饥饿处理;若仅考虑G0/G1期细胞比例,当培养细胞汇合度超过80 - 90%时,汇合度抑制可替代血清饥饿处理。