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Establishment and characterization of rough-tailed gecko original tail cells

机译:粗尾壁虎原始尾细胞的建立与表征

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摘要

Some of lizard species have the ability to lose their tail in order to defend against predators and regenerate the new tail. Lizard's regenerated tail has attracted scientists' attention for unraveling the regeneration process, but less information is known about the cellular characterization and cell growth properties of original tail. This research aimed to report cell culture and banking process of rough-tailed gecko or Cyrtopodion scabrum's original tail cell sample from inner tissue without skin using tissue explant technique. For banking reports, it is essential to analyze this cells' potential to proliferate, to investigate biological aspects such as cell culture features, differentiation and chromosome number and to report its species identification and quality control. To achieve optimal growth conditions, three different temperatures for incubation including 18, 23 and 37 degrees C and two different media including DMEM and L-15 were applied. The expanded cells were studied for their potential to adipose and osteoblast differentiation. Results indicated that lizard's original tail cells could be successfully obtained by explant technique. The cells demonstrated fibroblast like morphology with population doubling times of approximately 24 +/- 0.5h. Karyotyping analysis showed a distribution of 2n=40 chromosome number for this cell line. The comparison of different incubation media and temperatures showed that cell growth is equally optimal in all mentioned conditions according to growth curves. Adipose and osteoblast differentiation was obviously observed in these cells which confirms the hint of stem-ness in the produced mixed cells. According to cell banking policies, produced cells were also checked for bacterial, fungal, yeast and mycoplasma contaminations and no contamination was observed. Multiplex PCR for identification of species confirmed the species of lizard with no cross-contamination with other cells in the cell bank. Establishment of authentic
机译:一些蜥蜴物种有能力失去尾巴,以抵御捕食者并再生新的尾巴。蜥蜴的再生尾巴引起了科学家的关注,因为它揭示了再生过程,但关于原始尾巴的细胞特征和细胞生长特性的信息却知之甚少。本研究旨在使用组织外植体技术报告粗尾壁虎或 Cyrtopodion scabrum 的原始尾细胞样本的细胞培养和储存过程,这些样本来自无皮肤的内部组织。对于银行报告,必须分析这种细胞的增殖潜力,研究细胞培养特征、分化和染色体数量等生物学方面,并报告其物种鉴定和质量控制。为了达到最佳生长条件,应用了三种不同的培养温度(包括18、23和37°C)和两种不同的培养基(包括DMEM和L-15)。研究了扩增细胞的脂肪和成骨细胞分化的潜力。结果表明,通过外植体技术可以成功获得蜥蜴的原始尾细胞。这些细胞表现出类似成纤维细胞的形态,群体倍增时间约为 24 +/- 0.5 小时。核型分析显示该细胞系的染色体数分布为 2n=40。不同孵育培养基和温度的比较表明,根据生长曲线,在所有上述条件下,细胞生长同样最佳。在这些细胞中明显观察到脂肪和成骨细胞分化,这证实了产生的混合细胞中干细胞的暗示。根据细胞库政策,还检查了产生的细胞是否受到细菌、真菌、酵母菌和支原体污染,没有观察到污染。用于物种鉴定的多重PCR证实了蜥蜴的种类,没有与细胞库中的其他细胞交叉污染。建立正宗

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