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成功对植入前小鼠胚胎进行单细胞活检和冷冻保存。

Successful single-cell biopsy and cryopreservation of preimplantation mouse embryos.

作者信息

Wilton L J, Shaw J M, Trounson A O

机构信息

Centre for Early Human Development, Monash Medical Centre, Clayton, Victoria, Australia.

出版信息

Fertil Steril. 1989 Mar;51(3):513-7. doi: 10.1016/s0015-0282(16)60564-2.

Abstract

We have previously observed that preimplantation embryo biopsy in the mouse causes a reduction in implantation rate in utero. After minor modifications to the technique, we now find that sampling a single blastomere from the 4-cell mouse embryo does not compromise continued development in vitro or in vivo. When transferred to pseudopregnant foster mice, 60.3% and 64.3% of biopsied and control embryos, respectively, implanted into the uterine wall, and 52.6% and 52.4% of biopsied and control embryos, respectively, developed into fetuses. In a separate series of experiments, we have demonstrated that biopsied mouse embryos can be successfully cryopreserved by ultrarapid freezing even though they have a punctured zona pellucida. Biopsied (frozen-thawed), control (frozen-thawed), and nonfrozen embryos had an implantation rate of 81.1%, 74.3%, and 74.1%, respectively, and a fetal formation rate of 62.2%, 62.9%, and 66.7%, respectively.

摘要

我们之前观察到,对小鼠进行植入前胚胎活检会导致子宫内着床率降低。对该技术进行微小改进后,我们现在发现从4细胞期小鼠胚胎中取样单个卵裂球不会影响其在体外或体内的持续发育。将活检胚胎和对照胚胎移植到假孕代孕小鼠体内后,分别有60.3%和64.3%的胚胎着床于子宫壁,分别有52.6%和52.4%的胚胎发育成胎儿。在另一系列实验中,我们证明了即使活检小鼠胚胎的透明带已被穿刺,也可通过超速冷冻成功进行冷冻保存。活检(冻融)胚胎、对照(冻融)胚胎和未冷冻胚胎的着床率分别为81.1%、74.3%和74.1%,胎儿形成率分别为62.2%、62.9%和66.7%。

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