Sharjah Equine Hospital, Sharjah, United Arab Emirates.
Sharjah Equine Hospital, Sharjah, United Arab Emirates.
J Equine Vet Sci. 2020 Oct;93:103194. doi: 10.1016/j.jevs.2020.103194. Epub 2020 Jul 17.
Vitrification of embryos >300 µm in diameter requires puncture of the glycoprotein capsule, although the size of the hole compatible with embryo survival is unknown. Forty-five day-7 or -8 embryos were punctured using a 30-µm glass biopsy pipette mounted on a micromanipulator (n = 20) or manually with either an acupuncture needle (∼100-µm diameter -hole; n = 10) or a microneedle with a <1 µm tip to produce a ∼30-µm diameter hole (n = 15) before transferring to recipient mares; further 12 embryos were punctured with either the acupuncture needle or microneedle before being cultured in vitro for 48 hrs (n = 3 per puncture group) or transferred to recipient mares and recovered 48 hrs later (n = 3 per puncture group). No pregnancies resulted from the 10 embryos punctured with the acupuncture needle, whereas 15 of 20 (75%) and 10 of 15 (67%) punctured on the micromanipulator or manually with the microneedle resulted pregnancies. Neither acupunctured nor microneedle-punctured embryos repaired their capsules in vitro. The acupunctured embryos also failed to repair their capsule after 48 hrs in vivo and subsequent uterine flushing yielded numerous capsular vesicles. The microneedle-punctured embryos did repair their capsule in vivo. Puncture with the microneedle opens the way for development of a manual method to vitrify equine embryos.
直径大于 300 µm 的胚胎进行玻璃化需要刺穿糖蛋白胶囊,尽管与胚胎存活兼容的孔的大小尚不清楚。使用安装在微操作器上的 30 µm 玻璃活检吸管(n = 20)或手动用针灸针(∼100-µm 直径孔;n = 10)或尖端直径小于 1 µm 的微针(产生∼30-µm 直径孔;n = 15)对 45 天 7 或 8 天的胚胎进行穿刺,然后转移到受体母马;进一步对 12 个胚胎进行穿刺,用针灸针或微针进行穿刺,然后在体外培养 48 小时(每组 3 个)或转移到受体母马并在 48 小时后回收(每组 3 个)。用针灸针穿刺的 10 个胚胎中没有怀孕,而用微操作器或手动用微针穿刺的 20 个胚胎中的 15 个(75%)和 15 个中的 10 个(67%)怀孕。无论是针刺还是微针穿刺的胚胎在体外均未修复其囊。在体内 48 小时后,针刺的胚胎也未能修复其囊,随后子宫冲洗产生了许多囊泡。微针穿刺的胚胎在体内确实修复了它们的囊。微针的穿刺为开发手动玻璃化马胚胎的方法开辟了道路。