Brinkhof Bas, van Tol Helena T A, Groot Koerkamp Marian J A, Riemers Frank M, IJzer Sascha G, Mashayekhi Kaveh, Haagsman Henk P, Roelen Bernard A J
Department of Farm Animal Health, Faculty of Veterinary Medicine, Utrecht University, Yalelaan 104, Utrecht, 3584 CM, The Netherlands.
University Medical Center Utrecht, Molecular Cancer Research, PO Box 85060, Utrecht, 3508 AB, The Netherlands.
BMC Genomics. 2015 Apr 10;16(1):277. doi: 10.1186/s12864-015-1448-x.
Genes and signalling pathways involved in pluripotency have been studied extensively in mouse and human pre-implantation embryos and embryonic stem (ES) cells. The unsuccessful attempts to generate ES cell lines from other species including cattle suggests that other genes and pathways are involved in maintaining pluripotency in these species. To investigate which genes are involved in bovine pluripotency, expression profiles were generated from morula, blastocyst, trophectoderm and inner cell mass (ICM) samples using microarray analysis. As MAPK inhibition can increase the NANOG/GATA6 ratio in the inner cell mass, additionally blastocysts were cultured in the presence of a MAPK inhibitor and changes in gene expression in the inner cell mass were analysed.
Between morula and blastocyst 3,774 genes were differentially expressed and the largest differences were found in blastocyst up-regulated genes. Gene ontology (GO) analysis shows lipid metabolic process as the term most enriched with genes expressed at higher levels in blastocysts. Genes with higher expression levels in morulae were enriched in the RNA processing GO term. Of the 497 differentially expressed genes comparing ICM and TE, the expression of NANOG, SOX2 and POU5F1 was increased in the ICM confirming their evolutionary preserved role in pluripotency. Several genes implicated to be involved in differentiation or fate determination were also expressed at higher levels in the ICM. Genes expressed at higher levels in the ICM were enriched in the RNA splicing and regulation of gene expression GO term. Although NANOG expression was elevated upon MAPK inhibition, SOX2 and POU5F1 expression showed little increase. Expression of other genes in the MAPK pathway including DUSP4 and SPRY4, or influenced by MAPK inhibition such as IFNT, was down-regulated.
The data obtained from the microarray studies provide further insight in gene expression during bovine embryonic development. They show an expression profile in pluripotent cells that indicates a pluripotent, epiblast-like state. The inability to culture ICM cells as stem cells in the presence of an inhibitor of MAPK activity together with the reported data indicates that MAPK inhibition alone is not sufficient to maintain a pluripotent character in bovine cells.
多能性相关基因和信号通路已在小鼠和人类植入前胚胎及胚胎干细胞(ES细胞)中得到广泛研究。从包括牛在内的其他物种中生成ES细胞系的尝试未成功,这表明其他基因和通路参与维持这些物种的多能性。为了研究哪些基因参与牛的多能性,使用微阵列分析从桑椹胚、囊胚、滋养外胚层和内细胞团(ICM)样本中生成了表达谱。由于丝裂原活化蛋白激酶(MAPK)抑制可增加内细胞团中NANOG/GATA6的比例,此外还在MAPK抑制剂存在的情况下培养囊胚,并分析了内细胞团中基因表达的变化。
在桑椹胚和囊胚之间,有3774个基因差异表达,最大差异存在于囊胚上调基因中。基因本体(GO)分析表明脂质代谢过程是囊胚中表达水平较高的基因最富集的术语。桑椹胚中表达水平较高的基因在RNA加工GO术语中富集。在比较ICM和TE的497个差异表达基因中,NANOG、SOX2和POU5F1在ICM中的表达增加,证实了它们在多能性方面进化保守的作用。一些与分化或命运决定有关的基因在ICM中也有较高水平的表达。ICM中表达水平较高的基因在RNA剪接和基因表达调控GO术语中富集。虽然MAPK抑制后NANOG表达升高,但SOX2和POU5F1表达几乎没有增加。MAPK通路中其他基因(包括DUSP4和SPRY4)的表达,或受MAPK抑制影响的基因(如IFNT)的表达下调。
从微阵列研究中获得的数据为牛胚胎发育过程中的基因表达提供了进一步的见解。它们显示了多能细胞中的一种表达谱,表明处于一种多能的、外胚层样状态。在存在MAPK活性抑制剂的情况下无法将ICM细胞培养为干细胞,以及已报道的数据表明,仅MAPK抑制不足以维持牛细胞中的多能特性。