In Vitro Embryo Culture Impacts Heart Mitochondria in Male Adolescent Sheep.

IF 2.2 Q3 DEVELOPMENTAL BIOLOGY
Reza Amanollahi, Stacey L Holman, Ashley S Meakin, Monalisa Padhee, Kimberley J Botting-Lawford, Song Zhang, Severence M MacLaughlin, David O Kleemann, Simon K Walker, Jennifer M Kelly, Skye R Rudiger, I Caroline McMillen, Michael D Wiese, Mitchell C Lock, Janna L Morrison
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Abstract

Assisted reproductive technology (ART)such as in vitro embryo culture (IVC), is widely used in human infertility treatments; however, its long-term effects on the cardiac health of offspring remain unclear. This study aimed to determine whether the effects of IVC on cardiac metabolism and associated signaling pathways persist after birth into adolescence. Embryos were either transferred to an intermediate ewe (ET) or cultured in vitro in the absence (IVC) or presence of human serum (IVCHS) with methionine supplementation (IVCHS+M) for 6 days after mating. Naturally mated (NM) ewes were used as controls. Protein expression and hormone concentrations in the left ventricle (LV) were analyzed using Western blot and LC-MS/MS analyses, respectively. IVC was associated with sex-specific alterations in cardiac mitochondria, with males exhibiting reduced mitochondrial abundance. Cardiac protein expression of oxidative phosphorylation (OXPHOS) complexes 1 and 4 was reduced by IVC. Additionally, IVC reduced protein expression of PDK-4 and Mn-SOD in the IVCHS+M group, which may impact energy efficiency and defense against oxidative stress. These changes may predispose IVC offspring to cardiac oxidative stress and mitochondrial dysfunction, particularly in males. This study provides insights into the sex-dependent effects of IVC on cardiac health, emphasizing the importance of evaluating long-term cardiovascular risks associated with IVC protocols.

体外胚胎培养对雄性青春期绵羊心脏线粒体的影响。
辅助生殖技术(ART),如体外胚胎培养(IVC),广泛应用于人类不孕症的治疗;然而,其对后代心脏健康的长期影响尚不清楚。本研究旨在确定IVC对心脏代谢和相关信号通路的影响是否在出生后持续到青春期。交配后,将胚胎转移到中间母羊(ET)体内,或在没有人血清(IVC)或有人血清(IVCHS)的情况下体外培养(IVCHS+M) 6天。以自然交配母羊为对照。分别采用Western blot和LC-MS/MS分析左心室(LV)蛋白表达和激素浓度。IVC与心脏线粒体的性别特异性改变有关,男性表现出线粒体丰度降低。心脏氧化磷酸化(OXPHOS)复合物1和4的表达被IVC降低。此外,IVC降低了IVCHS+M组PDK-4和Mn-SOD的蛋白表达,这可能影响能量效率和对氧化应激的防御。这些变化可能使IVC后代易患心脏氧化应激和线粒体功能障碍,特别是在男性中。这项研究揭示了静脉血栓对心脏健康的性别依赖效应,强调了评估与静脉血栓方案相关的长期心血管风险的重要性。
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来源期刊
Journal of Developmental Biology
Journal of Developmental Biology Biochemistry, Genetics and Molecular Biology-Developmental Biology
CiteScore
4.10
自引率
18.50%
发文量
44
审稿时长
11 weeks
期刊介绍: The Journal of Developmental Biology (ISSN 2221-3759) is an international, peer-reviewed, quick-refereeing, open access journal, which publishes reviews, research papers and communications on the development of multicellular organisms at the molecule, cell, tissue, organ and whole organism levels. Our aim is to encourage researchers to effortlessly publish their new findings or concepts rapidly in an open access medium, overseen by their peers. There is no restriction on the length of the papers; the full experimental details must be provided so that the results can be reproduced. Electronic files regarding the full details of the experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material. Journal of Developmental Biology focuses on: -Development mechanisms and genetics -Cell differentiation -Embryonal development -Tissue/organism growth -Metamorphosis and regeneration of the organisms. It involves many biological fields, such as Molecular biology, Genetics, Physiology, Cell biology, Anatomy, Embryology, Cancer research, Neurobiology, Immunology, Ecology, Evolutionary biology.
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