Zinc supplementation alleviates endoplasmic reticulum stress during porcine oocyte in vitro maturation by upregulating zinc transporters

Ridlo, Muhammad Rosyid and Kim, Geon A. and Taweechaipaisankul, Anukul and Kim, Eui Hyun and Lee, Byeong Chun (2021) Zinc supplementation alleviates endoplasmic reticulum stress during porcine oocyte in vitro maturation by upregulating zinc transporters. Journal of Cellular Physiology, 236 (4). 2869 – 2880. ISSN 00219541

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Abstract

Endoplasmic reticulum (ER) stress is a major contributor to embryonic development failure. Mammalian oocytes have a high risk of exposure to cellular stress during in vitro embryo production. We investigated the effects of zinc supplementation during in vitro maturation under ER stress. We evaluated cumulus expansion, embryonic development derived by parthenogenetic activation, reactive oxygen species, protein expression of X-box binding protein 1 (XBP1), and expression of genes related to ER stress. Supplementation with 1 μg/ml zinc significantly increased the nuclear maturation of oocytes, cleavage and blastocyst formation rates, and total blastocyst cell number (p <.05). Under ER stress, zinc significantly reduced protein expression of XBP1, and increased cleavage and blastocyst rates (p <.05). Concomitantly, zinc supplementation upregulated the expression of zinc transporters (SLC39A14 and SLC39A10), PTGS2, and downregulated ER stress-related genes (sXBP1, uXBP1, ATF4, and PTPN1/PTP1B), and caspase 3. These results suggest that zinc supplementation alleviates ER stress by providing essential metal-ion transporters for oocyte maturation and subsequent embryonic development. © 2020 Wiley Periodicals LLC

Item Type: Article
Additional Information: Cited by: 16
Uncontrolled Keywords: Activating Transcription Factor 4; Animals; Caspase 3; Cation Transport Proteins; Cells, Cultured; Cyclooxygenase 2; Embryonic Development; Endoplasmic Reticulum Stress; Female; Gene Expression Regulation, Developmental; In Vitro Oocyte Maturation Techniques; Oocytes; Parthenogenesis; Protein Tyrosine Phosphatase, Non-Receptor Type 1; Reactive Oxygen Species; Sus scrofa; Up-Regulation; X-Box Binding Protein 1; Zinc Sulfate; activating transcription factor 4; caspase 3; messenger RNA; protein tyrosine phosphatase 1B; ptgs2 protein; reactive oxygen metabolite; slc39a10 protein; slc39a14 protein; unclassified drug; X box binding protein 1; zinc; zinc transporter; activating transcription factor 4; caspase 3; cation transport protein; cyclooxygenase 2; protein tyrosine phosphatase 1B; reactive oxygen metabolite; X box binding protein 1; zinc sulfate; animal cell; Article; blastocyst; blastocyte; cell expansion; controlled study; cumulus cell; down regulation; embryo; embryo development; endoplasmic reticulum stress; female; gene expression; gene expression level; in vitro oocyte maturation; in vitro study; mRNA expression level; nonhuman; oocyte cleavage; pig; priority journal; protein expression; unfolded protein response; upregulation; animal; cell culture; drug effect; endoplasmic reticulum stress; gene expression regulation; genetics; metabolism; oocyte; parthenogenesis
Subjects: Veterinary Medicine
Divisions: Vocational School
Depositing User: Sri JUNANDI
Date Deposited: 05 Nov 2024 01:33
Last Modified: 05 Nov 2024 01:33
URI: https://ir.lib.ugm.ac.id/id/eprint/10607

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