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A new method for the simple and temperature-permissive cryopreservation of mouse embryos.
https://repo.qst.go.jp/records/47303
https://repo.qst.go.jp/records/47303b6d2ec9b-1f39-406d-8b9f-269d4beb4297
Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2015-09-16 | |||||
タイトル | ||||||
タイトル | A new method for the simple and temperature-permissive cryopreservation of mouse embryos. | |||||
言語 | ||||||
言語 | eng | |||||
資源タイプ | ||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
資源タイプ | journal article | |||||
アクセス権 | ||||||
アクセス権 | metadata only access | |||||
アクセス権URI | http://purl.org/coar/access_right/c_14cb | |||||
著者 |
Mochida, Keiji
× Mochida, Keiji× Hasegawa, Ayumi× Li, Ming-Wen× D., Fray Martin× Kito, Seiji× M., Vallelunga Jadine× C., Kent Lloyd K.× Yoshiki, Atsushi× Obata, Yuichi× Ogura, Atsuo× 鬼頭 靖司 |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | Procedures for cryopreserving embryos vary considerably, each having its specific advantages and disadvantages in terms of technical feasibility, embryo survival yield, temperature permissibility and species- or strain-dependent applicability. Here we report a high osmolality vitrification (HOV) method that is advantageous in these respects. Cryopreservation by vitrification is generally very simple, but, unlike slow freezing, embryos should be kept at a supercooling temperature (below –130uC) to avoid cryodamage. We overcame this problem by using an HOV solution containing 42.5% (v/v) ethylene glycol, 17.3% (w/v) Ficoll and 1.0 M sucrose. This solution is more viscous than other cryopreservation solutions, but easy handling of embryos was assured by employing a less viscous equilibration solution before vitrification. Most (.80%) embryos cryopreserved in this solution survived at –80uC for at least 30 days. Normal mice were recovered even after intercontinental transportation in a conventional dry-ice package for 2–3 days, indicating that special containers such as dry shippers with liquid nitrogen vapor are unnecessary. The HOV solution could also be employed for long-term storage in liquid nitrogen, as with other conventional cryoprotectants. Finally, we confirmed that this new vitrification method could be applied successfully to embryos of all six strains of mice we have tested so far. Thus, our HOV method provides an efficient and reliable strategy for the routine cryopreservation of mouse embryos in animal facilities and biomedical laboratories, and for easy and cheap transportation. | |||||
書誌情報 |
PLoS ONE (Online only:URL:http://www.plosone.org) 巻 8, 号 1, p. 1-8, 発行日 2013-01 |
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ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 1932-6203 | |||||
DOI | ||||||
識別子タイプ | DOI | |||||
関連識別子 | 10.1371/journal.pone.0049316 | |||||
関連サイト | ||||||
識別子タイプ | URI | |||||
関連識別子 | http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0049316 | |||||
関連名称 | http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0049316 |