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在合成冰阻断剂存在的情况下,建立并冻存源自云南半细毛羊的皮肤成纤维细胞系

Establishment and cryopreservation of a skin fibroblast cell line derived from Yunnan semi-fine wool sheep in the presence of synthetic ice blocker.

作者信息

Wu Shuai Shuai, Li Dong Jiang, Lv Chun Rong, Yang Hong Yuan, Zhu Lan, Li Wei Juan, Quan Guo Bo, Hong Qiong Hua

机构信息

Yunnan Animal Science and Veterinary Institute, Qinglongshan, Jindian, Panlong County, Kunming 650224, Yunnan province, China.

出版信息

Cryo Letters. 2013 Sep-Oct;34(5):497-507.

Abstract

In this study, the fibroblasts cell line derived from ear marginal tissue of Yunnan semi-fine wool sheep was successfully established using the primary explants technique and cryopreservation technology. Additionally, the protective effect of synthetic ice blocker (SIB) including 1, 3-cyclohexanediol (1, 3-CHD) and 1, 4-cyclohexanediol (1, 4-CHD) on frozen fibroblast cells was also assessed and compared. Propidium iodide (PI) was used to stain the dead cells following cryopreservation and thawing. The results showed that compared with Medium 199 (M199) and Dulbecco's modified Eagle's medium : Nutrient Mixture F-12 (1 : 1) Mixture (DMEM/F12), Dulbecco's modified Eagle's medium (DMEM) may be more suitable for the primary culture of fibroblast cells of Yunnan semi-fine wool sheep. The growth curve of cells is a typical "S" type. After subculture for four days, the cells entered the plateau phase and began to degenerate. Biological analysis showed that the population doubling time (PDT) for subculturing fibroblast cells was approximately 26h. The Karyotyping data indicated that the percentage of fibroblast cells with normal chromosome number 2n = 54 was over 90% following subculture for 10 passages. Moreover, the tests for bacteria, fungi, viruses and mycoplasma were negative. After serial subculture for 5 generations, the fibroblast cells were cryopreserved in the presence or absence of 1, 3-CHD or 1, 4-CHD. The data indicated that with increase of the synthetic ice blocker concentrations, the viability of frozen-thawed fibroblast cells was firstly increased and then decreased. When the concentration of 1, 3-CHD or 1, 4-CHD was 50 mM, the viable percentage of frozen-thawed fibroblast cells was 91.93% +/- 2.24% and 94.13% +/- 0.55% respectively and significantly higher than that of the cells frozen in the absence of synthetic ice blockers (88.10% +/- 1.49%, P < 0.05). In conclusion, the skin fibroblast cell line of Yunnan semi-fine wool sheep was firstly established in this study. Additionally, the presence of synthetic ice blocker can increase the viability of frozen-thawed sheep fibroblast cell line.

摘要

在本研究中,采用原代外植体技术和冷冻保存技术成功建立了源自云南半细毛羊耳部边缘组织的成纤维细胞系。此外,还评估并比较了包含1,3 - 环己二醇(1,3 - CHD)和1,4 - 环己二醇(1,4 - CHD)的合成冰阻断剂(SIB)对冷冻成纤维细胞的保护作用。在冷冻保存和解冻后,使用碘化丙啶(PI)对死细胞进行染色。结果表明,与199培养基(M199)和杜氏改良 Eagle 培养基:营养混合物 F - 12(1:1)混合物(DMEM/F12)相比,杜氏改良 Eagle 培养基(DMEM)可能更适合云南半细毛羊成纤维细胞的原代培养。细胞生长曲线为典型的“S”型。传代培养四天后,细胞进入平台期并开始退化。生物学分析表明,成纤维细胞传代培养的群体倍增时间(PDT)约为26小时。核型分析数据表明,传代培养10代后,染色体数目正常(2n = 54)的成纤维细胞百分比超过90%。此外,细菌、真菌、病毒和支原体检测均为阴性。连续传代培养5代后,在有或无1,3 - CHD或1,4 - CHD存在的情况下对成纤维细胞进行冷冻保存。数据表明,随着合成冰阻断剂浓度的增加,冻融后成纤维细胞的活力先升高后降低。当1,3 - CHD或1,4 - CHD的浓度为50 mM时,冻融后成纤维细胞的存活百分比分别为91.93%±2.24%和94.13%±0.55%,显著高于未添加合成冰阻断剂冷冻的细胞(88.10%±1.49%,P < 0.05)。总之,本研究首次建立了云南半细毛羊皮肤成纤维细胞系。此外,合成冰阻断剂的存在可提高冻融后绵羊成纤维细胞系的活力。

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