Cytokine supplementation influences bovine embryo transcriptome during the preimplantation period.

IF 3.4 Q2 REPRODUCTIVE BIOLOGY
Katy S McDonald, Randall S Prather, M Sofia Ortega
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Abstract

Abstract: The central goal of the following studies was to understand how FGF2, LIF, and IGF1, a cocktail called "FLI," influence bovine embryo development by the degree of transcriptomic variation throughout preimplantation development. All embryos were produced in vitro with or without FLI supplementation at the beginning of culture. For each treatment, embryos were collected at the 4-6 cell, 9-16 cell, morula, or blastocyst stages and RNA was isolated and sequenced at a depth of 50 million reads per sample. In the FLI group, at the 9-16 cell stage, there were 7 upregulated and 6 downregulated differentially expressed genes (DEGs). At the morula stage, of the 1856 DEGs, 580 were upregulated in FLI. Gene ontology analysis showed increased MAPK signaling, TGF-beta signaling, and Hippo signaling, which all help regulate cell adhesion, lineage commitment, and growth regulation in the developing embryo. In FLI blastocyst stage embryo, 199 upregulated and 545 downregulated DEGs revealed an increase in processes associated with interferon-gamma production and cell differentiation. Overall, FLI modulates many of the regulatory pathways in the developing embryo to drive increased cell survival, cell integrity, and overall embryo development.

Lay summary: This study investigated whether adding three supportive proteins-FGF2, LIF, and IGF1 (together called FLI)-could improve the development of cow embryos grown in vitro. In cattle breeding, embryos are often produced outside the body to enhance fertility and support genetic selection. However, many embryos fail to develop properly under laboratory conditions. To address this, researchers tested whether FLI could create a more favorable environment for early embryo growth. Although embryos grown with and without FLI appeared similar under the microscope, gene expression analysis revealed important differences. Embryos exposed to FLI showed signs of improved cell survival, healthier growth, and reduced stress. These molecular changes suggest that FLI may help embryos become more resilient to key procedures such as freezing and transfer. The findings support the use of FLI as a culture supplement to improve the efficiency and success of in vitro embryo production systems used in livestock reproductive biotechnologies.

细胞因子补充对着床前牛胚胎转录组的影响。
摘要:以下研究的中心目标是了解FGF2、LIF和IGF1(一种称为FLI的混合物)如何通过在着床前发育过程中转录组变异的程度影响牛胚胎发育。所有胚胎均在体外培养开始时添加或不添加FLI。在每个处理中,收集4-6细胞、9-16细胞、桑葚胚或囊胚期的胚胎,分离RNA并对每个样本进行5000万reads的深度测序。FLI组在9-16细胞期有7个差异表达基因上调,6个差异表达基因下调。在桑葚期,1856个deg中有580个在FLI中上调。基因本体分析显示MAPK信号、tgf - β信号和Hippo信号的增加,这些信号都有助于调节胚胎发育过程中的细胞粘附、谱系承诺和生长调节。在FLI囊胚期胚胎中,199个上调的deg和545个下调的deg显示与干扰素γ产生和细胞分化相关的过程增加。总的来说,FLI调节了胚胎发育中的许多调控途径,以促进细胞存活、细胞完整性和胚胎的整体发育。摘要:本研究探讨了添加三种支持蛋白——fgf2、LIF和IGF1(合称为FLI)是否能促进体外生长的奶牛胚胎的发育。在牛的育种中,胚胎通常在体外产生,以提高生育力和支持遗传选择。然而,许多胚胎不能在实验室条件下正常发育。为了解决这个问题,研究人员测试了FLI是否可以为早期胚胎生长创造更有利的环境。虽然有FLI和没有FLI的胚胎在显微镜下看起来相似,但基因表达分析显示了重要的差异。暴露于FLI的胚胎显示出细胞存活率提高、生长更健康、压力减少的迹象。这些分子变化表明,FLI可能有助于胚胎在冷冻和移植等关键过程中变得更有弹性。该研究结果支持使用FLI作为培养补充物,以提高用于牲畜生殖生物技术的体外胚胎生产系统的效率和成功率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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