Cuello Cristina, Martinez Cristina A, Cambra Josep M, González-Plaza Alejandro, Parrilla Inmaculada, Rodriguez-Martinez Heriberto, Gil Maria A, Martinez Emilio A
Department of Medicine and Animal Surgery, Faculty of Veterinary Medicine, International Excellence Campus for Higher Education and Research "Campus Mare Nostrum," Institute for Biomedical Research of Murcia (IMIB-Arrixaca), University of Murcia, Murcia, Spain.
Department of Biomedical & Clinical Sciences (BKV), BKH/Obstetrics & Gynaecology, Faculty of Medicine and Health Sciences, Linköping University, Linköping, Sweden.
Front Vet Sci. 2021 Nov 12;8:771996. doi: 10.3389/fvets.2021.771996. eCollection 2021.
Despite the reported promising farrowing rates after non-surgical and surgical transfers of vitrified porcine morulae and blastocysts produced (range: 70-75%), the pregnancy loss is 5-15 fold higher with vitrified than with fresh embryos. The present study aimed to investigate whether vitrification affects the transcriptome of porcine morulae, using microarrays and RT-qPCR validation. Morulae were obtained surgically from weaned sows ( = 13) on day 6 (day 0 = estrus onset). A total of 60 morulae were vitrified (treatment group). After 1 week of storage, the vitrified morulae were warmed. Vitrified-warmed and non-vitrified fresh morulae (control; = 40) were cultured for 24 h to assess embryo survival by stereomicroscopy after. A total of 30 vitrified/warmed embryos that were deemed viable and 30 fresh control embryos (three pools of 10 for each experimental group) were selected for microarray analysis. Gene expression was assessed with a GeneChip® Porcine Genome Array (Affymetrix). An ANOVA analysis p-unadjusted <0.05 and a fold change cut-off of ±1.5 were set to identify differentially expressed genes (DEGs). Data analysis and biological interpretation were performed using the Partek Genomic Suite 7.0 software. The survival rate of morulae after vitrification and warming (92.0 ± 8.3%) was similar to that of the control (100%). A total of 233 DEGs were identified in vitrified morulae (38 upregulated and 195 downregulated), compared to the control group. Nine pathways were significantly modified. Go-enrichment analysis revealed that DEGs were mainly related to the Biological Process functional group. Up-regulated DEGs were involved in glycosaminoglycan degradation, metabolic pathways and tryptophan metabolism KEGG pathways. The pathways related to the down-regulated DEGs were glycolysis/gluconeogenesis, protein export and fatty acid elongation. The disruption of metabolic pathways in morulae could be related to impaired embryo quality and developmental potential, despite the relatively high survival rates after warming observed . In conclusion, vitrification altered the gene expression pattern of porcine morulae produced , generating alterations in the transcriptome that may interfere with subsequent embryo development and pregnancy after embryo transfer.
尽管有报道称,经玻璃化处理的猪桑椹胚和囊胚进行非手术和手术移植后产仔率很有前景(范围:70 - 75%),但与新鲜胚胎相比,玻璃化胚胎的妊娠损失要高5 - 15倍。本研究旨在使用微阵列和RT - qPCR验证来调查玻璃化是否会影响猪桑椹胚的转录组。在第6天(第0天 = 发情开始)从断奶母猪(n = 13)手术获取桑椹胚。总共60个桑椹胚进行玻璃化处理(处理组)。储存1周后,将玻璃化的桑椹胚复温。将玻璃化复温的桑椹胚和未玻璃化的新鲜桑椹胚(对照组;n = 40)培养24小时,之后通过体视显微镜评估胚胎存活率。总共选择30个被认为存活的玻璃化/复温胚胎和30个新鲜对照胚胎(每个实验组3个包含10个胚胎的样本池)进行微阵列分析。使用基因芯片®猪基因组阵列(Affymetrix)评估基因表达。设定方差分析p值未校正 < 0.05以及倍数变化阈值为±1.5来鉴定差异表达基因(DEG)。使用Partek Genomic Suite 7.0软件进行数据分析和生物学解释。玻璃化和复温后桑椹胚的存活率(92.0 ± 8.3%)与对照组(100%)相似。与对照组相比,在玻璃化桑椹胚中总共鉴定出233个差异表达基因(38个上调和195个下调)。九条通路有显著改变。基因本体富集分析表明,差异表达基因主要与生物过程功能组相关。上调的差异表达基因参与糖胺聚糖降解、代谢途径和色氨酸代谢KEGG途径。与下调的差异表达基因相关的通路是糖酵解/糖异生、蛋白质输出和脂肪酸延长。尽管观察到复温后存活率相对较高,但桑椹胚中代谢途径的破坏可能与胚胎质量受损和发育潜力有关。总之,玻璃化改变了所产生的猪桑椹胚的基因表达模式,在转录组中产生改变,这可能会干扰胚胎移植后的后续胚胎发育和妊娠。