Evidence map›Paper›PMID 42430017›Full record

ArticleMolecular biology reports2026

Vitrification altered αV and β3 integrin expression in mouse oocytes in a maturation stage-dependent manner.

Sahar Andi, Farzad Rajaei, Shahram Darabi

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Article in Molecular biology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

3 authors.

Sahar AndiCellular and Molecular Research Center, Research Institute for Prevention of Non-Communicable Diseases, Qazvin University of Medical Sciences, Qazvin, Iran.
Farzad RajaeiCellular and Molecular Research Center, Research Institute for Prevention of Non-Communicable Diseases, Qazvin University of Medical Sciences, Qazvin, Iran. frajaei@csu.edu.au.
Shahram DarabiCellular and Molecular Research Center, Research Institute for Prevention of Non-Communicable Diseases, Qazvin University of Medical Sciences, Qazvin, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveIntegrin αVβ3 has been implicated in oocyte membrane organization and sperm-oocyte interaction. This study investigated the effects of vitrification on post-warming survival and on the surface expression of integrin αV and β3 subunits in mouse oocytes at the germinal vesicle (GV) and metaphase II (MII) stages. MATERIALS AND

methodsA total of 400 oocytes were collected from NMRI mice and allocated into four equal groups: non-vitrified GV, vitrified GV, non-vitrified MII, and vitrified MII (n = 100 per group). Vitrification was performed using the Cryotop method, followed by one month of storage in liquid nitrogen at - 196 °C. Post-warming survival was assessed morphologically. Integrin αV and β3 expression was evaluated at the protein level by immunocytochemistry and at the transcript level by quantitative real-time reverse-transcription PCR (RT-qPCR).

resultsVitrification did not significantly affect post-warming survival rates in GV or MII oocytes compared with their non-vitrified counterparts (90% vs. 88%, P > 0.05). Immunocytochemical analysis demonstrated that both αV and β3 surface protein expression was significantly higher in MII oocytes than in GV oocytes, irrespective of vitrification status. Vitrification significantly reduced αV and β3 protein expression in MII oocytes compared with non-vitrified MII oocytes (P < 0.05 and P < 0.001, respectively), whereas reductions in GV oocytes were not statistically significant (P > 0.05). Quantitative RT-PCR broadly corroborated these findings: non-vitrified MII oocytes exhibited the highest transcript levels for both subunits, and β3 mRNA was significantly decreased in vitrified MII oocytes (P < 0.05). Although αV transcript levels showed a downward trend following vitrification, these reductions did not reach statistical significance in either stage (P > 0.05).

conclusionDespite preserving post-warming morphological survival, vitrification induced significant alterations in αV and β3 integrin expression in a maturation stage-dependent manner, with MII oocytes being disproportionately affected. These findings suggest that molecular analysis of membrane-associated proteins may provide information complementary to morphological criteria when assessing oocyte quality following cryopreservation.

Indexed as

Integrin alphaVIntegrin beta3OocytesVitrificationAnimalsCryopreservationFemaleMetaphaseMiceIntegrin alphaVIntegrin beta3CryotopIntegrin αVIntegrin β3Mouse oocyteSurvival rateVitrification

Identifiers

PMID42430017
PMCPMC13354663

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