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冻干精子中的染色体完整性与DNA损伤

Chromosomal integrity and DNA damage in freeze-dried spermatozoa.

作者信息

Kusakabe Hirokazu

机构信息

Department of Biological Sciences Asahikawa Medical University 2-1-1-1 Midorigaoka-higashi 078-8510 Asahikawa Japan.

出版信息

Reprod Med Biol. 2011 Jun 1;10(4):199-210. doi: 10.1007/s12522-011-0092-7. eCollection 2011 Dec.

DOI:10.1007/s12522-011-0092-7
PMID:29699095
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5907138/
Abstract

Freeze-drying technology may one day be used to preserve mammalian spermatozoa indefinitely without cryopreservation. Freeze-dried mouse spermatozoa stored below 4°C for up to 1 year have maintained the ability to fertilize oocytes and support normal development. The maximum storage period for spermatozoa increases at lower storage temperatures. Freeze-drying, per se, may reduce the integrity of chromosomes in freeze-dried mouse spermatozoa, but induction of chromosomal damage is suppressed if spermatozoa are incubated with divalent cation chelating agents prior to freeze-drying. Nevertheless, chromosomal damage does accumulate in spermatozoa stored at temperatures above 4°C. Currently, no established methods or strategies can prevent or reduce damage accumulation, and damage accumulation during storage is a serious obstacle to advances in freeze-drying technology. Chromosomal integrity of freeze-dried human spermatozoa have roughly background levels of chromosomal damage after storage at 4°C for 1 month, but whether these spermatozoa can produce healthy newborns is unknown. The safety of using freeze-dried human spermatozoa must be evaluated based on the risks of heritable chromosome and DNA damage that accumulates during storage.

摘要

冷冻干燥技术或许有一天可用于无限期保存哺乳动物精子而无需冷冻保存。在4°C以下储存长达1年的冷冻干燥小鼠精子仍保持使卵母细胞受精并支持正常发育的能力。精子的最长储存期在较低储存温度下会延长。冷冻干燥本身可能会降低冷冻干燥小鼠精子中染色体的完整性,但如果精子在冷冻干燥前与二价阳离子螯合剂一起孵育,染色体损伤的诱导会受到抑制。然而,在4°C以上储存的精子中染色体损伤确实会累积。目前,尚无既定方法或策略能够预防或减少损伤累积,而储存期间的损伤累积是冷冻干燥技术进步的严重障碍。冷冻干燥的人类精子在4°C储存1个月后,其染色体完整性大致处于染色体损伤的背景水平,但这些精子能否产生健康的新生儿尚不清楚。必须基于储存期间累积的可遗传染色体和DNA损伤风险来评估使用冷冻干燥人类精子的安全性。

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本文引用的文献

1
Characterization of chromosomal damage accumulated in freeze-dried mouse spermatozoa preserved under ambient and heat stress conditions.在常温及热应激条件下保存的冻干小鼠精子中染色体损伤的特征。
Mutagenesis. 2011 May;26(3):447-53. doi: 10.1093/mutage/ger003. Epub 2011 Mar 2.
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An investigation of the potential effect of vacuoles in human sperm on DNA damage using a chromosome assay and the TUNEL assay.采用染色体分析和 TUNEL 分析检测人精子空泡对 DNA 损伤的潜在影响。
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Intracytoplasmic injection of morphologically selected spermatozoa (IMSI) improves outcome after assisted reproduction by deselecting physiologically poor quality spermatozoa.胞浆内形态选择精子注射(IMSI)通过选择生理质量差的精子来改善辅助生殖的结局。
J Assist Reprod Genet. 2011 Mar;28(3):253-62. doi: 10.1007/s10815-010-9505-5. Epub 2010 Nov 12.
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Advanced age increases chromosome structural abnormalities in human spermatozoa.高龄增加人类精子染色体结构异常。
Eur J Hum Genet. 2011 Feb;19(2):145-51. doi: 10.1038/ejhg.2010.166. Epub 2010 Nov 3.
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Comparison of day 2 embryo quality after conventional ICSI versus intracytoplasmic morphologically selected sperm injection (IMSI) using sibling oocytes.比较常规 ICSI 和胞浆内形态选择精子注射(IMSI)使用同卵妹妹卵子后第 2 天胚胎质量。
Eur J Obstet Gynecol Reprod Biol. 2010 May;150(1):42-6. doi: 10.1016/j.ejogrb.2010.01.004. Epub 2010 Feb 19.
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