Effect of supplementation of cryoprotectant solution with hydroxypropyl cellulose for vitrification of bovine oocytes.

IF 1 4区 生物学 Q3 BIOLOGY
Cryo letters Pub Date : 2023-01-01
M J Park, S E Lee, W Yoon, H J Park, S H Kim, S H Oh, D G Lee, D B Pyeon, E Y Kim, S P Park
{"title":"Effect of supplementation of cryoprotectant solution with hydroxypropyl cellulose for vitrification of bovine oocytes.","authors":"M J Park,&nbsp;S E Lee,&nbsp;W Yoon,&nbsp;H J Park,&nbsp;S H Kim,&nbsp;S H Oh,&nbsp;D G Lee,&nbsp;D B Pyeon,&nbsp;E Y Kim,&nbsp;S P Park","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Successful cryopreservation of bovine oocytes is very important for research and commercial applications. However, the survival and development rate of vitrified-thawed (VT) oocytes are lower than those of non-vitrified-thawed (non-VT) oocytes.</p><p><strong>Objective: </strong>To investigate the effect of adding hydroxypropyl cellulose (HPC) to the vitrification solution for bovine oocytes.</p><p><strong>Materials and methods: </strong>For vitrification, bovine metaphase II oocytes were pretreated with a solution containing 10% ethylene glycol supplemented with 0, 10, 50, or 100 ug/mL HPC for 5 min, exposed to a solution containing 30% ethylene glycol supplemented with 0, 10, 50, or 100 ug/mL HPC for 30 s, and then directly plunged into liquid nitrogen.</p><p><strong>Results: </strong>The survival rate of oocytes was significantly higher in the 50 HPC group than in the 0, 10, and 100 HPC groups. The reactive oxygen species level was lower in the non-VT and 50 HPC groups than in the other groups. The mRNA levels of proapoptotic genes (Bax) were lower in the non-VT, 0, and 50 HPC groups than in the other groups. The mRNA levels of antiapoptotic genes (BCl2) were higher in the non-VT than in the other groups. The development rates of embryos (day 8) obtained via parthenogenetic activation (PA) were determined in the non-VT, 0 HPC, and 50 HPC groups. The cleavage rate was significantly higher in the non-VT group.</p><p><strong>Conclusion: </strong>Supplementation of vitrification solution with HPC improves the survival of VT bovine oocytes and the development capacity of embryos derived from these oocytes via PA. doi.org/10.54680/fr23110110212.</p>","PeriodicalId":10937,"journal":{"name":"Cryo letters","volume":"44 1","pages":"37-46"},"PeriodicalIF":1.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cryo letters","FirstCategoryId":"99","ListUrlMain":"","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Successful cryopreservation of bovine oocytes is very important for research and commercial applications. However, the survival and development rate of vitrified-thawed (VT) oocytes are lower than those of non-vitrified-thawed (non-VT) oocytes.

Objective: To investigate the effect of adding hydroxypropyl cellulose (HPC) to the vitrification solution for bovine oocytes.

Materials and methods: For vitrification, bovine metaphase II oocytes were pretreated with a solution containing 10% ethylene glycol supplemented with 0, 10, 50, or 100 ug/mL HPC for 5 min, exposed to a solution containing 30% ethylene glycol supplemented with 0, 10, 50, or 100 ug/mL HPC for 30 s, and then directly plunged into liquid nitrogen.

Results: The survival rate of oocytes was significantly higher in the 50 HPC group than in the 0, 10, and 100 HPC groups. The reactive oxygen species level was lower in the non-VT and 50 HPC groups than in the other groups. The mRNA levels of proapoptotic genes (Bax) were lower in the non-VT, 0, and 50 HPC groups than in the other groups. The mRNA levels of antiapoptotic genes (BCl2) were higher in the non-VT than in the other groups. The development rates of embryos (day 8) obtained via parthenogenetic activation (PA) were determined in the non-VT, 0 HPC, and 50 HPC groups. The cleavage rate was significantly higher in the non-VT group.

Conclusion: Supplementation of vitrification solution with HPC improves the survival of VT bovine oocytes and the development capacity of embryos derived from these oocytes via PA. doi.org/10.54680/fr23110110212.

添加羟丙基纤维素冷冻保护剂溶液对牛卵母细胞玻璃化的影响。
背景:牛卵母细胞的成功低温保存对研究和商业应用具有重要意义。然而,玻璃化解冻(VT)卵母细胞的存活率和发育率低于非玻璃化解冻(non-VT)卵母细胞。目的:探讨在牛卵母细胞玻璃化液中加入羟丙基纤维素(HPC)的效果。材料和方法:为了玻璃化,将牛中期II卵母细胞用含有10%乙二醇和0、10、50或100 ug/mL HPC的溶液预处理5分钟,在含有30%乙二醇和0、10、50或100 ug/mL HPC的溶液中暴露30秒,然后直接投入液氮中。结果:50 HPC组卵母细胞存活率明显高于0、10、100 HPC组。非vt组和50 HPC组的活性氧水平低于其他各组。非vt、0、50 HPC组细胞凋亡前基因(Bax) mRNA表达水平低于其他各组。非vt组抗凋亡基因(BCl2) mRNA水平明显高于其他各组。测定非vt组、0 HPC组和50 HPC组通过孤雌生殖激活(PA)获得的胚胎(第8天)发育率。非vt组的卵裂率明显较高。结论:添加HPC的玻璃化液可提高VT牛卵母细胞的存活率,并可通过PA提高这些卵母细胞的胚胎发育能力。doi.org/10.54680/fr23110110212。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Cryo letters
Cryo letters 生物-生理学
CiteScore
1.80
自引率
10.00%
发文量
50
审稿时长
1 months
期刊介绍: A bimonthly international journal for low temperature sciences, including cryobiology, cryopreservation or vitrification of cells and tissues, chemical and physical aspects of freezing and drying, and studies involving ecology of cold environments, and cold adaptation The journal publishes original research reports, authoritative reviews, technical developments and commissioned book reviews of studies of the effects produced by low temperatures on a wide variety of scientific and technical processes, or those involving low temperature techniques in the investigation of physical, chemical, biological and ecological problems.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信