The ultrastructural nature of human oocytes' cytoplasmic abnormalities and the role of cytoskeleton dysfunction.

Cytoskeleton dysmorphism electron microscopy human oocyte oocyte abnormalities

Journal

F&S science
ISSN: 2666-335X
Titre abrégé: F S Sci
Pays: United States
ID NLM: 101765857

Informations de publication

Date de publication:
Nov 2023
Historique:
received: 31 07 2023
revised: 13 09 2023
accepted: 14 09 2023
medline: 20 11 2023
pubmed: 21 9 2023
entrez: 20 9 2023
Statut: ppublish

Résumé

To investigate the structural bases of human oocytes' cytoplasmic abnormalities and the causative mechanism of their emergence. Knowledge of an abnormal oocyte's intracellular organization is vital to establishing reliable criteria for clinical evaluation of oocyte morphology. Laboratory-based study on experimental material provided by a private assisted reproduction clinic. University laboratory and imaging center. A total of 105 women undergoing hormonal stimulation for in vitro fertilization (IVF) donated their spare oocytes for this study. Transmission electron microscopy (TEM) was used to analyze the fine morphology of 22 dysmorphic IVF oocytes exhibiting different types of cytoplasmic irregularities, namely, refractile bodies; centrally located cytoplasmic granularity (CLCG); smooth endoplasmic reticulum (SER) disc; and vacuoles. A total of 133 immature oocytes were exposed to cytoskeleton-targeting compounds or matured in control conditions, and their morphology was examined using fluorescent and electron microscopy. The ultrastructural morphology of dysmorphic oocytes was analyzed. Drug-treated oocytes had their maturation efficiency, chromosome-microtubule configurations, and fine intracellular morphology examined. TEM revealed ultrastructural characteristics of common oocyte aberrations and indicated that excessive organelle clustering was the underlying cause of 2 of the studied morphotypes. Inhibition experiments showed that disruption of actin, not microtubules, allows for inordinate aggregation of subcellular structures, resembling the ultrastructural pattern seen in morphologically abnormal oocytes retrieved in IVF cycles. These results imply that actin serves as a regulator of organelle distribution during human oocyte maturation. The ultrastructural analogy between dysmorphic oocytes and oocytes, in which actin network integrity was perturbed, suggests that dysfunction of the actin cytoskeleton might be implicated in generating common cytoplasmic aberrations. Knowledge of human oocytes' inner workings and the origin of morphological abnormalities is a step forward to a more objective oocyte quality assessment in IVF practice.

Identifiants

pubmed: 37730013
pii: S2666-335X(23)00050-2
doi: 10.1016/j.xfss.2023.09.002
pii:
doi:

Substances chimiques

Actins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

267-278

Informations de copyright

Copyright © 2023 The Author(s). Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests M.T. has nothing to disclose. Z.T. has nothing to disclose. D.K. has nothing to disclose. P.O. has nothing to disclose. S.K. has nothing to disclose. Z.H. has nothing to disclose.

Auteurs

Martina Tatíčková (M)

Department of Histology and Embryology, Faculty of Medicine, Masaryk University, Brno, Czech Republic.

Zuzana Trebichalská (Z)

Department of Histology and Embryology, Faculty of Medicine, Masaryk University, Brno, Czech Republic.

Drahomíra Kyjovská (D)

Reprofit International, Clinic of Reproductive Medicine, Brno, Czech Republic.

Pavel Otevřel (P)

Reprofit International, Clinic of Reproductive Medicine, Brno, Czech Republic.

Soňa Kloudová (S)

Reprofit International, Clinic of Reproductive Medicine, Brno, Czech Republic.

Zuzana Holubcová (Z)

Department of Histology and Embryology, Faculty of Medicine, Masaryk University, Brno, Czech Republic; Reprofit International, Clinic of Reproductive Medicine, Brno, Czech Republic. Electronic address: zholub@med.muni.cz.

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Classifications MeSH