Extracellular vesicles secreted by cumulus cells contain microRNAs that are potential regulatory factors of mouse oocyte developmental competence

Author:

Fiorentino Giulia1ORCID,Merico Valeria1,Zanoni Mario1,Comincini Sergio2,Sproviero Daisy3,Garofalo Maria4,Gagliardi Stella4,Cereda Cristina5,Lin Chih-Jen6,Innocenti Federica7,Taggi Marilena7,Vaiarelli Alberto7ORCID,Ubaldi Filippo Maria7,Rienzi Laura78,Cimadomo Danilo7ORCID,Garagna Silvia1,Zuccotti Maurizio1ORCID

Affiliation:

1. Laboratory of Biology and Biotechnology of Reproduction, Department of Biology and Biotechnology ‘Lazzaro Spallanzani’, University of Pavia , Pavia, Italy

2. Functional Genomics Laboratory, Department of Biology and Biotechnology ‘Lazzaro Spallanzani’, University of Pavia , Pavia, Italy

3. IFOM, IFOM—The FIRC Institute of Molecular Oncology , Milan, Italy

4. Molecular Biology and Transcriptomics Unit, IRCCS Mondino Foundation , Pavia, Italy

5. Department of Pediatrics, Center of Functional Genomics and Rare Diseases, Buzzi Children’s Hospital , Milan, Italy

6. Centre for Reproductive Health, Institute for Regeneration and Repair, University of Edinburgh , Edinburgh, UK

7. IVIRMA Global Research Alliance, GENERA, Clinica Valle Giulia , Rome, Italy

8. Department of Biomolecular Sciences, University of Urbino “Carlo Bo” , Urbino, Italy

Abstract

Abstract The role of cumulus cells (CCs) in the acquisition of oocyte developmental competence is not yet fully understood. In a previous study, we matured cumulus-denuded fully-grown mouse oocytes to metaphase II (MII) on a feeder layer of CCs (FL-CCs) isolated from developmentally competent (FL-SN-CCs) or incompetent (FL-NSN-CCs) SN (surrounded nucleolus) or NSN (not surrounding nucleolus) oocytes, respectively. We observed that oocytes cultured on the former could develop into blastocysts, while those matured on the latter arrested at the 2-cell stage. To investigate the CC factors contributing to oocyte developmental competence, here we focused on the CCs' release into the medium of extracellular vesicles (EVs) and on their miRNA content. We found that, during the 15-h transition to MII, both FL-SN-CCs and FL-NSN-CCs release EVs that can be detected, by confocal microscopy, inside the zona pellucida (ZP) or the ooplasm. The majority of EVs are <200 nm in size, which is compatible with their ability to cross the ZP. Next-generation sequencing of the miRNome of FL-SN-CC versus FL-NSN-CC EVs highlighted 74 differentially expressed miRNAs, with 43 up- and 31 down-regulated. Although most of these miRNAs do not have known roles in the ovary, in silico functional analysis showed that seven of these miRNAs regulate 71 target genes with specific roles in meiosis resumption (N = 24), follicle growth (N = 23), fertilization (N = 1), and the acquisition of oocyte developmental competence (N = 23). Overall, our results indicate CC EVs as emerging candidates of the CC-to-oocyte communication axis and uncover a group of miRNAs as potential regulatory factors.

Funder

University of Pavia with the Young Research Fund

Publisher

Oxford University Press (OUP)

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