van Montfoort Aafke P A, Geraedts Joep P M, Dumoulin John C M, Stassen Alphons P M, Evers Johannes L H, Ayoubi Torik A Y
Department of Obstetrics and Gynaecology, Research Institute Growth and Development (GROW), Academic Hospital Maastricht, Maastricht, The Netherlands.
Mol Hum Reprod. 2008 Mar;14(3):157-68. doi: 10.1093/molehr/gam088. Epub 2008 Jan 18.
Besides the established selection criteria based on embryo morphology and blastomere number, new parameters for embryo viability are needed to improve the clinical outcome of IVF and more particular of elective single-embryo transfer. Genome-wide gene expression in cumulus cells was studied, since these cells surround the oocyte inside the follicle and therefore possibly reflect oocyte developmental potential. Early cleavage (EC) was chosen as a parameter for embryo viability. Gene expression in cumulus cells from eight oocytes resulting in an EC embryo (EC-CC; n = 8) and from eight oocytes resulting in a non-EC (NEC) embryo (NEC-CC; n = 8) was analysed using microarrays (n = 16). A total of 611 genes were differentially expressed (P < 0.01), mainly involved in cell cycle, angiogenesis, apoptosis, epidermal growth factor, fibroblast growth factor and platelet-derived growth factor signalling, general vesicle transport and chemokine and cytokine signalling. Of the 25 selected differentially expressed genes analysed by quantitative real-time PCR 15 (60%) genes could be validated in the original samples. Of these 8 (53%) could also be validated in 24 (12-EC-CC and 12 NEC-CC) extra independent samples. The most differentially expressed genes among these were CCND2, CXCR4, GPX3, CTNND1 DHCR7, DVL3, HSPB1 and TRIM28, which probably point to hypoxic conditions or a delayed oocyte maturation in NEC-CC samples. This opens up perspectives for new molecular embryo or oocyte selection parameters which might also be useful in countries where the selection has to be made at the oocyte stage before fertilization instead of at the embryonic stage.
除了基于胚胎形态和卵裂球数量的既定选择标准外,还需要新的胚胎活力参数来改善体外受精的临床结局,尤其是选择性单胚胎移植的结局。对卵丘细胞中的全基因组基因表达进行了研究,因为这些细胞在卵泡内围绕卵母细胞,因此可能反映卵母细胞的发育潜力。选择早期卵裂(EC)作为胚胎活力的参数。使用微阵列分析了来自8个产生EC胚胎的卵母细胞(EC-CC;n = 8)和8个产生非EC(NEC)胚胎的卵母细胞(NEC-CC;n = 8)的卵丘细胞中的基因表达(n = 16)。共有611个基因差异表达(P < 0.01),主要涉及细胞周期、血管生成、细胞凋亡、表皮生长因子、成纤维细胞生长因子和血小板衍生生长因子信号传导、一般囊泡运输以及趋化因子和细胞因子信号传导。通过定量实时PCR分析的25个选定差异表达基因中,有15个(60%)基因可以在原始样本中得到验证。其中8个(53%)基因也可以在24个(12个EC-CC和12个NEC-CC)额外的独立样本中得到验证。其中差异表达最明显的基因是CCND2、CXCR4、GPX3、CTNND1、DHCR7、DVL3、HSPB1和TRIM28,这可能表明NEC-CC样本中存在缺氧状况或卵母细胞成熟延迟。这为新的分子胚胎或卵母细胞选择参数开辟了前景,这些参数在必须在受精前的卵母细胞阶段而非胚胎阶段进行选择的国家可能也有用。