Mapping the follicle-specific regulation of extracellular vesicle-mediated microRNA transport in the southern white rhinoceros (Ceratotherium simum simum)†.

IF 3.1 2区 生物学 Q2 REPRODUCTIVE BIOLOGY Biology of Reproduction Pub Date : 2024-08-15 DOI:10.1093/biolre/ioae081
Ahmed Gad, Nico G Menjivar, Rachel Felton, Barbara Durrant, Dawit Tesfaye, Elena Ruggeri
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Abstract

Efforts to implement effective assisted reproductive technologies (ARTs) for the conservation of the northern white rhinoceros (NWR; Ceratotherium simum cottoni) to prevent its forthcoming extinction, could be supported by research conducted on the closely related southern white rhinoceros (SWR; Ceratotherium simum simum). Within the follicle, extracellular vesicles (EVs) play a fundamental role in the bidirectional communication facilitating the crucial transport of regulatory molecules such as microRNAs (miRNAs) that control follicular growth and oocyte development. This study aimed to elucidate the dynamics of EV-miRNAs in stage-dependent follicular fluid (FF) during SWR ovarian antral follicle development. Three distinct follicular stages were identified based on diameter: Growing (G; 11-17 mm), Dominant (D; 18-29 mm), and Pre-ovulatory (P; 30-34 mm). Isolated EVs from the aspirated FF of segmented follicle stages were used to identify EV-miRNAs previously known via subsequent annotation to all equine (Equus caballus; eca), bovine (Bos taurus; bta), and human (Homo sapiens; hsa) miRNAs. A total of 417 miRNAs were detected, with 231 being mutually expressed across all three stages, including eca-miR-148a and bta-miR-451 as the top highly expressed miRNAs. Distinct expression dynamics in miRNA abundance were observed across the three follicular stages, including 31 differentially expressed miRNAs that target various pathways related to follicular growth and development, with 13 miRNAs commonly appearing amidst two different comparisons. In conclusion, this pioneering study provides a comprehensive understanding of the stage-specific expression dynamics of FF EV-miRNAs in the SWR. These findings provide insights that may lead to novel approaches in enhancing ARTs to catalyze rhinoceros conservation efforts.

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绘制南方白犀牛(Ceratotherium simum simum)细胞外囊介导的微RNA运输的卵泡特异性调控图。
为保护北方白犀牛(NWR;Ceratotherium simum cottoni)而实施有效的辅助生殖技术(ARTs)以防止其即将灭绝的努力,可以从对密切相关的南方白犀牛(SWR;Ceratotherium simum simum)的研究中得到支持。在卵泡内,细胞外囊泡(EVs)在双向交流中发挥着重要作用,促进了控制卵泡生长和卵母细胞发育的微核糖核酸(miRNAs)等调控分子的重要运输。本研究旨在阐明在SWR卵巢前卵泡发育过程中,卵泡液(FF)中与阶段相关的EV-miRNA的动态变化。根据直径确定了三个不同的卵泡阶段:生长期(G;11-17 毫米)、优势期(D;18-29 毫米)和排卵前期(P;30-34 毫米)。从分段卵泡阶段抽吸的FF中分离出的EV被用来鉴定EV-miRNA,这些EV-miRNA是通过随后注释所有马(Equus caballus;eca)、牛(Bos taurus;bta)和人类(Homo sapiens;hsa)的miRNA而已知的。共检测到 417 个 miRNA,其中 231 个在所有三个阶段相互表达,包括 eca-miR-148a 和 bta-miR-451 是最高表达的 miRNA。在卵泡的三个阶段中,观察到了不同的 miRNA 丰度表达动态,包括 31 个靶向与卵泡生长发育相关的不同通路的差异表达 miRNA,其中 13 个 miRNA 常见于两种不同的比较中。总之,这项开创性的研究全面了解了西南红细胞中FF EV-miRNA的特异性表达动态。这些发现提供了深入的见解,可能会为加强ARTs以促进犀牛保护工作提供新的方法。
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来源期刊
Biology of Reproduction
Biology of Reproduction 生物-生殖生物学
CiteScore
6.30
自引率
5.60%
发文量
214
审稿时长
1 months
期刊介绍: Biology of Reproduction (BOR) is the official journal of the Society for the Study of Reproduction and publishes original research on a broad range of topics in the field of reproductive biology, as well as reviews on topics of current importance or controversy. BOR is consistently one of the most highly cited journals publishing original research in the field of reproductive biology.
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