4.6 Article

Membrane-permeable trehalose improves the freezing ability and developmental competence of in-vitro matured feline oocytes

Journal

THERIOGENOLOGY
Volume 181, Issue -, Pages 16-23

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.theriogenology.2022.01.003

Keywords

Cat; Cryopreservation; Oocyte; Trehalose hexaacetate

Funding

  1. 90th Anniversary of Chulalongkorn University (Ratchadaphiseksomphot Endowment Fund)
  2. Thailand Research Fund [RSA6180053]
  3. MSCA Rise (EU H2020 Drynet) [GA 734434]
  4. 100th Anniversary Chulalongkorn University Fund for Doctoral Scholarship

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The addition of membrane-permeable trehalose improves the freezing ability and developmental potential of feline oocytes during cryopreservation.
Oocytes are highly sensitive to cryopreservation, which frequently results in an irreversible loss of developmental competence. We examined the effect of membrane-permeable trehalose on the freezing ability of feline oocytes matured in vitro. In Experiment 1, intracellular trehalose (trehalose hexaacetate; Tre-(OAc)(6)) was synthesized from trehalose precursor and subjected to spectroscopic characterization. The membrane permeability of the Tre-(OAc)(6) was investigated by incubating oocytes with different concentrations of Tre-(OAc)(6) (3, 15, and 30 mM). Optimum concentration and the toxicity of Tre-(OAc)(6) were assessed in Experiment 2. The effects of Tre-(OAc)(6) on freezing ability in terms of apoptotic gene expression and developmental competence of in-vitro matured oocytes were examined in Experiments 3 and 4, respectively. The Tre-(OAc)(6) permeated into the ooplasm of cat oocytes in a dose-and time dependent manner. The highest concentration of intracellular trehalose was detected when the oocytes were incubated for 24 h with 30 mM Tre-(OAc)(6). For the toxicity test, incubation of oocytes with 3 mM Tre-(OAc)(6) for 24 h did not affect maturation rate and embryo development. However, high doses of Tre-(OAc)(6) (15 and 30 mM) significantly reduced maturation and fertilization rates (p < 0.05). In addition, frozen-thawed oocytes treated with 3 mM Tre-(OAc)(6) significantly upregulated anti-apoptotic (BCL-2) gene expression compared with the control (0 mM) and other Tre-(OAc)(6) concentrations (15 and 30 mM). Oocyte maturation in the presence of 3 mM Tre-(OAc)(6) prior to cryopreservation significantly improved oocyte developmental competence in terms of cleavage and blastocyst rates when compared with the control group (p < 0.05). Our results lead us to infer that increasing the levels of intracellular trehalose by Tre-(OAc)6 during oocyte maturation improves the freezing ability of feline oocytes, albeit at specific concentrations.(c) 2022 Elsevier Inc. All rights reserved.

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