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Mouse and human spermatozoa can be freeze-dried without damaging their chromosomes

https://asahikawa-med.repo.nii.ac.jp/records/1338
https://asahikawa-med.repo.nii.ac.jp/records/1338
96079410-d94c-4932-af33-3afcd9f145e8
名前 / ファイル ライセンス アクション
1623.pdf 1623.pdf (391.6 kB)
Item type 学術雑誌論文 / Journal Article_02(1)
公開日 2009-03-11
タイトル
タイトル Mouse and human spermatozoa can be freeze-dried without damaging their chromosomes
言語 en
言語
言語 eng
資源タイプ
資源タイプ journal article
著者 日下部, 博一

× 日下部, 博一

日下部, 博一

ja-Kana クサカベ, ヒロカズ

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Yanagimachi, R

× Yanagimachi, R

Yanagimachi, R

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Kamiguchi, Y

× Kamiguchi, Y

Kamiguchi, Y

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著者 ローマ字
Kusakabe, Hirokazu
書誌情報 Human Reproduction

巻 23, 号 2, p. 233-239, 発行日 2008-02-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 0268-1161
DOI
識別子タイプ DOI
関連識別子 10.1093/humrep/dem252
リンクURL
内容記述タイプ Other
内容記述 http://dx.doi.org/10.1093/humrep/dem252 | http://dx.doi.org/10.1093/humrep/dem252
抄録
内容記述タイプ Abstract
内容記述 BACKGROUND: Although mouse spermatozoa can be freeze-dried without losing their reproductive capacity, the technique needs further improvements to reduce the incidence of chromosomal damages to spermatozoa. Effects of freeze-drying on human spermatozoa are unknown. METHODS: Mouse spermatozoa were suspended in a Tris-buffered EGTA solution briefly (about 10 min at 37℃) or for 1-7 days at 4℃ before freeze-drying. Freeze-dried spermatozoa were maintained for up to 1 year at 4℃ before injection. Sperm chromosomes were examined during the first mitosis (cleavage) of zygotes. Sperm’s ability to support embryo development was assessed by examining mid-gestation fetuses after transfer of 2-cell embryos to surrogate mothers. Chromosome integrity of freeze-dried human spermatozoa was examined by injecting individual spermatozoa into mouse oocytes which were previously enucleated. RESULTS: When mouse spermatozoa were freeze-dried immediately after suspension in Tris-buffered EGTA solution, only about 40% had normal chromosomes. When the spermatozoa were kept in the same solution for 3-7 days before freeze-drying, 85-95% had normal chromosomes and they were able to support embryo development better than those which were in the solution briefly. Freeze-dried human spermatozoa well maintained their chromosomes regardless of the duration of pre-freeze-drying incubation of spermatozoa in the Tris-buffered EGTA solution. CONCLUSIONS: Prior incubation of mouse spermatozoa in Tris-buffered EGTA solution for several days makes sperm chromosomes more resistant to freeze-drying. As the consequence, spermatozoa freeze-dried this way support embryo development better than those exposed to Tris-buffered EGTA solution only briefly. Freeze-dried human spermatozoa well maintained their chromosomes without pre-freeze-drying incubation in Tris-buffered EGTA solution.
注記
内容記述タイプ Other
注記 This is a pre-copy-editing, author-produced PDF of an article accepted for publication in Human Reproduction following peer review. The definitive publisher-authenticated version Kusakabe, H. ; Yanagimachi, R. ; Kamiguchi, Y., Mouse and human spermatozoa can be freeze-dried without damaging their chromosomes, Human Reproduction 23(2), FEB 2008, pp. 233-239, is available online at: http://humrep.oxfordjournals.org/cgi/content/abstract/23/2/233
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資源タイプ
内容記述タイプ Other
資源タイプ text
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内容記述タイプ Other
内容記述 application/pdf
ID(XooNIps)
18056060
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1385
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日下部, 博一, Yanagimachi, R, Kamiguchi, Y, n.d., Mouse and human spermatozoa can be freeze-dried without damaging their chromosomes: 233–239 p.

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