Wang Shengnan, Duan Yanchao, Chen Bingbing, Qiu Shuai, Huang Tianzhuang, Si Wei
State Key Laboratory of Primate Biomedical Research, Institute of Primate Translational Medicine, Kunming University of Science and Technology, Kunming 650500, China.
Yunnan Key Laboratory of Primate Biomedical Research, Kunming 650500, China.
Vet Sci. 2023 Feb 1;10(2):104. doi: 10.3390/vetsci10020104.
Nonhuman primates (NHPs) have been considered as the best models for biomedical research due to their high similarities in genomic, metabolomic, physiological and pathological features to humans. However, generation of genetically modified NHPs through traditional methods, such as microinjection into the pronuclei of one-cell embryos, is prohibitive due to the targeting efficiency and the number of NHPs needed as oocyte/zygote donors. Using spermatogonial stem cells (SSCs) as the target of gene editing, producing gene-edited sperm for fertilization, is proven to be an effective way to establish gene editing animal disease models. In this experiment, we used ultrasound to guide the echo dense injection needle into the rete testis space, allowing the EGFP lentivirus to be slowly injected at positive pressure from the rete testis into seminiferous tubules. We found Thy1 can be used as a surface marker of cynomolgus monkey SSCs, confirming that SSCs carry the GFP gene. Finally, we successfully obtained transgenic sperm, with a similar freezing and recovery rate to that of WT animals.
由于非人灵长类动物(NHPs)在基因组、代谢组、生理和病理特征方面与人类高度相似,它们一直被认为是生物医学研究的最佳模型。然而,通过传统方法,如显微注射到单细胞胚胎的原核中,来生成基因编辑的非人灵长类动物是受到限制的,这是由于靶向效率以及作为卵母细胞/合子供体所需的非人灵长类动物数量。使用精原干细胞(SSCs)作为基因编辑的靶点,生产用于受精的基因编辑精子,已被证明是建立基因编辑动物疾病模型的有效方法。在本实验中,我们使用超声引导回声密集注射针进入睾丸网间隙,使增强型绿色荧光蛋白(EGFP)慢病毒从睾丸网以正压缓慢注入生精小管。我们发现Thy1可用作食蟹猴精原干细胞的表面标志物,证实精原干细胞携带绿色荧光蛋白基因。最后,我们成功获得了转基因精子,其冷冻和复苏率与野生型动物相似。