Mollard Richard
Faculty of Veterinary and Agricultural Sciences, University of Melbourne, Parkville, 3052, Australia.
Cryobiology. 2018 Apr;81:201-205. doi: 10.1016/j.cryobiol.2018.03.004. Epub 2018 Mar 13.
This study describes the culture, cryobanking, thawing and passaging of karyotypically validated cells from two life history stages of the "least concern" Australian native amphibian species Litoria infrafrenata. Adult frog toe and tadpole macerates were generated from animals euthanized due to ill health following injury. Cultured cells proliferated and formed colonies after one to two weeks of culture. Cultures were cryopreserved in liquid nitrogen for a minimum of one month, thawed, passaged for expansion and karyotyped. Post-thaw karyotypes revealed the expected 2N = 24 diploid chromosome number in approximately 90% of all metaphase spreads. Further, metacentric, submetacentric and subtelocentric configurations were the same as previously described karyotype configurations obtained from living frogs of this same species. Using cryobanked and prospectively validated cell lines, conservation programs including assisted reproduction technologies and genomic, mitochondrial and proteomic mining initiatives may therefore be complemented with minimal or no disturbance to living and healthy animals.
本研究描述了来自“无危”澳大利亚本土两栖物种——棕树蛙(Litoria infrafrenata)两个生活史阶段的经核型验证的细胞的培养、冷冻保存、解冻及传代过程。成年蛙的脚趾和蝌蚪匀浆取自因受伤后健康状况不佳而实施安乐死的动物。培养的细胞在培养一至两周后开始增殖并形成集落。将培养物在液氮中冷冻保存至少一个月,然后解冻、传代扩增并进行核型分析。解冻后的核型显示,在所有中期分裂相中,约90%呈现预期的2N = 24条二倍体染色体数。此外,中着丝粒、亚中着丝粒和近端着丝粒构型与先前描述的从该物种活体青蛙获得的核型构型相同。因此,利用冷冻保存且经前瞻性验证的细胞系,包括辅助生殖技术以及基因组、线粒体和蛋白质组挖掘计划在内的保护项目,在对活体健康动物造成最小干扰或无干扰的情况下即可得到补充。