Domínguez Francisco, Gadea Blanca, Esteban Francisco J, Horcajadas Jose Antonio, Pellicer Antonio, Simón Carlos
Fundacion IVI, Instituto Universitario IVI, Valencia University, C/Guadassuar 1 bajo, Valencia 46015, Spain.
Hum Reprod. 2008 Sep;23(9):1993-2000. doi: 10.1093/humrep/den205. Epub 2008 Jun 12.
New approaches for non-invasive embryo-quality assessment are among the major goals in Reproductive Medicine. We hypothesize that the detection of changes in the protein profile of the culture media in which blastocysts are cultured could be a potential indicator of the viability of the embryo and, thus, a useful tool for selecting the more appropriate blastocysts to be transferred.
Using protein-array technology, we analysed the protein profile corresponding to 24 h conditioned media of blastocysts that implanted versus those that did not implant. A statistical approach was followed to compare each of these media versus a medium in the absence of blastocysts (control medium). In addition, a gene ontology functional analysis-including those proteins showing a statistical difference among conditions-was performed, and a network with the predicted functional partners and corresponding relationships was obtained.
The soluble TNF receptor 1 and IL-10 increased significantly and MSP-alpha, SCF, CXCL13, TRAILR3 and MIP-1beta decreased significantly when the protein profile of the blastocyst culture medium was compared with the control medium. CXCL13 (BLC) and granulocyte-macrophage colony-stimulating factor was also decreased significantly in the implanted blastocyst media compared with that in media from the non-implanted counterparts with a similar morphology. None of the proteins included in the array was increased significantly in the implanted blastocyst-conditioned media.
The differences identified in the protein profile of the culture media in the presence of implanted versus non-implanted blastocysts can be considered a new non-invasive approach in the search for new tools to diagnose blastocyst viability.
非侵入性胚胎质量评估的新方法是生殖医学的主要目标之一。我们假设,检测培养囊胚的培养基中蛋白质谱的变化可能是胚胎活力的潜在指标,因此是选择更合适的囊胚进行移植的有用工具。
我们使用蛋白质阵列技术,分析了着床囊胚与未着床囊胚24小时条件培养基的蛋白质谱。采用统计学方法将每种培养基与不含囊胚的培养基(对照培养基)进行比较。此外,进行了基因本体功能分析,包括那些在不同条件下显示出统计学差异的蛋白质,并获得了具有预测功能伙伴和相应关系的网络。
与对照培养基相比,囊胚培养基的蛋白质谱中,可溶性肿瘤坏死因子受体1和白细胞介素-10显著增加,而MSP-α、干细胞因子、CXCL13、肿瘤坏死因子相关凋亡诱导配体受体3和巨噬细胞炎性蛋白-1β显著降低。与形态相似的未着床囊胚培养基相比,着床囊胚培养基中的CXCL13(BLC)和粒细胞-巨噬细胞集落刺激因子也显著降低。阵列中包含的蛋白质在着床囊胚条件培养基中均未显著增加。
着床与未着床囊胚存在时培养基蛋白质谱的差异可被视为一种新的非侵入性方法,用于寻找诊断囊胚活力的新工具。