Carboxylated ε-poly-L-lysine, a cryoprotective agent, is an effective partner of ethylene glycol for the vitrification of embryos at various preimplantation stages

被引:3
作者
Kawasaki, Yuki [1 ]
Kohaya, Natsuki [1 ]
Shibao, Yurie [1 ]
Suyama, Ayumi [1 ]
Kageyama, Atsuko [2 ]
Fujiwara, Katsuyoshi [2 ]
Kamoshita, Maki [2 ]
Matsumura, Kazuaki [3 ]
Hyon, Suong-Hyu [4 ]
Ito, Junya [1 ,2 ]
Kashiwazaki, Naomi [1 ,2 ]
机构
[1] Azabu Univ, Sch Vet Med, Lab Anim Reprod, Sagamihara, Kanagawa 2525201, Japan
[2] Azabu Univ, Grad Sch Vet Sci, Sagamihara, Kanagawa 2525201, Japan
[3] Japan Adv Inst Sci & Technol, Sch Mat Sci, Nomi 9231291, Japan
[4] Kagoshima Univ, Joint Fac Vet Med, Kagoshima 8900065, Japan
关键词
Vitrification; Mouse; Germ cells; CRYOPRESERVATION; OOCYTES; POLYAMPHOLYTES;
D O I
10.1016/j.cryobiol.2020.10.004
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
It has been known that different protocols are used for embryo preservation at different stages due to different sensitivity to the physical and physiological stress caused by vitrification. In this study, we developed a common vitrification protocol using carboxlated epsilon-poly-L-lysine (COOH-PLL), a new cryoprotective agent for the vitrification of mouse embryos at different stages. The IVF-derived Crl:CD1(ICR) x B6D2F1/Crl pronuclear, 2-cell, 4cell, and 8-cell, morula and blastocyst stage embryos were vitrified with 15% (v/v) ethylene glycol (EG) and 10% (w/v) COOH-PLL (E15P15) or 15% (v/v) EG and 15% (v/v) dimethyl sulfoxide (E15D15) using the minimal volume cooling method. The survival of vitrified embryos from pronuclear to blastocyst stages was equivalent between E15P15 and E15D15 groups. However, the rate of development to blastocysts was significantly lower in E15P15 than E15D15. The rates of survival and development to blastocysts were dramatically improved by a slight modification of EG and COOH-PLL concentrations (E20P10). After transferring 17 (E20P10) and 15 (E15D15) vitrified/warmed blastocysts, 8 and 7 pups were obtained (47.1% and 46.7%, respectively). Taken together, these results indicate that our vitrification protocol is appropriate for the vitrification of mouse embryos at different stages.
引用
收藏
页码:245 / 249
页数:5
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