The effects of cycloastragenol on bovine embryo development, implantation potential and telomerase activity

端粒酶 卵母细胞 胚泡 胚胎 男科 生物 端粒酶逆转录酶 体外成熟 胚胎发生 细胞生物学 化学 分子生物学 遗传学 医学 基因
作者
Abdul Majid Khan,Muhammad Idrees,Chalani Dilshani Perera,Zaheer Haider,Myeong‐Don Joo,Ji-Su Kang,S. L. Lee,Il‐Keun Kong
出处
期刊:Reproduction, Fertility and Development [CSIRO Publishing]
卷期号:35 (10): 527-538 被引量:5
标识
DOI:10.1071/rd22280
摘要

Telomerase reverse transcriptase is a key factor responsible for structural and cellular alterations in aged oocytes and changes in the structure of the zona pellucida and mitochondria. Telomerase expression is reduced in aged cumulus oocyte complexes, and its activation or enhanced expression would be beneficial for in vitro oocyte maturation and in vitro embryo development.This study aimed to investigate telomerase activation by cycloastragenol and its effect on bovine oocyte in vitro maturation, fertilisation, and early embryo development.We used qPCR, Western blot, immunofluorescence, reactive oxygen species (ROS) assay,TUNEL assay, JC-1 assay, and invasion assay to analyse the affect of cycloastragenol (CAG) on bovine oocyte maturation, embryo development, embryo quality and implantation potential.Cycloastragenol treatment of oocytes in in vitro maturation (IVM) media significantly (P <0.05) improved oocyte IVM (90.87%), embryo cleavage (90.78%), blastocyst hatching (27.04%), and embryo implantation potential. Telomerase also interacts with mitochondria, and JC-1 staining results showed significantly (P <0.05) higher mitochondrial membrane potential (ΔΨ m) in the CAG-treated group. Furthermore, the inner cell mass (OCT4 and SOX2) and trophoblasts (CDX2) of the control and CAG groups were examined. Moreover, CAG treatment to primary cultured bovine cumulus cells substantially enhanced telomerase activity.Telomerase activation via cycloastragenol is beneficial for bovine oocyte IVM and for the production of high-quality bovine embryos.Cycloastragenol is a natural telomerase activator, and could be useful as a permanent component of oocyte maturation media.
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