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玻璃化处理前后分离的牛前腔卵泡中连接蛋白 43 和跨带投射的保存。

Preservation of connexin 43 and transzonal projections in isolated bovine pre-antral follicles before and following vitrification.

机构信息

Faculty of Pharmaceutical, Biomedical and Veterinary Sciences, Laboratory of Veterinary Physiology and Biochemistry, Gamete Research Centre, University of Antwerp, Universiteitsplein 1, U building, 2610, Wilrijk, Belgium.

Department of Obstetrics, Gynecology and Reproductive Sciences, Yale University School of Medicine, 310 Cedar Street, New Haven, CT, 06510, USA.

出版信息

J Assist Reprod Genet. 2021 Feb;38(2):479-492. doi: 10.1007/s10815-020-01993-2. Epub 2020 Nov 6.

Abstract

PURPOSE

Gap junctions and transzonal projections play a crucial role in intercellular communication between different follicular components and are necessary for follicle development. We aimed to demonstrate gap junction protein connexin 43 (Cx43) and transzonal projections (TZPs) in viable, category 1, isolated bovine pre-antral follicles (PAFs) during short-term culture and after vitrification and warming.

METHODS

This study involved four experimental groups: fresh control, 2-day culture, 4-day culture, and vitrified secondary PAFs. Isolated PAFs were vitrified using a simple and efficient cryopreservation method by means of mini cell strainers.

RESULTS

Cx43 and TZPs were detected in pre-antral follicles of all stages, as well as in every experimental group. The group fresh follicles showed a higher percentage of follicles that were positive for Cx43 (91.7%) than the follicles that were vitrified (77.4%). All follicles that were cultured for 2 days were Cx43-positive (100%). Follicles cultured for 4 days (65.8%) (P = 0.002) showed the lowest percentage of follicles that were Cx43-positive. The percentages of the presence or (partial) absence of the TZP network were shown to be very heterogeneous between follicles in different treatment groups.

CONCLUSIONS

These results suggest the maintenance of communication between the oocyte and the somatic companion cells after vitrification and warming. The varying percentages of the expression of the TZP network within groups suggests that it will be of interest to investigate whether this is truly due to variability in TZP integrity and follicle quality or due to methodological limitations.

摘要

目的

缝隙连接和跨带投射在不同滤泡成分之间的细胞间通讯中起着至关重要的作用,是卵泡发育所必需的。我们旨在证明在短期培养以及玻璃化和复温后,有活力的、1 类的、分离的牛前腔卵泡(PAF)中连接蛋白 43(Cx43)和跨带投射(TZP)的存在。

方法

本研究包括四个实验组:新鲜对照组、2 天培养组、4 天培养组和玻璃化的次级 PAF 组。使用小型细胞滤器的简单高效的冷冻保存方法对分离的 PAF 进行玻璃化处理。

结果

在所有阶段的前腔卵泡以及每个实验组中都检测到了 Cx43 和 TZP。新鲜卵泡组中 Cx43 阳性的卵泡比例(91.7%)高于玻璃化的卵泡(77.4%)。培养 2 天的所有卵泡均为 Cx43 阳性(100%)。培养 4 天的卵泡(65.8%)(P=0.002)显示出 Cx43 阳性的卵泡比例最低。不同处理组卵泡中 TZP 网络的存在或(部分)缺失的百分比显示出非常不均匀。

结论

这些结果表明,玻璃化和复温后卵母细胞和体细胞伴细胞之间的通讯得以维持。在组内 TZP 网络表达的百分比变化表明,有必要研究这是否真的是由于 TZP 完整性和卵泡质量的可变性,还是由于方法学的局限性。

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