Department of Obstetrics & Gynaecology, GROW School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, The Netherlands.
Department of Bioinformatics-BiGCaT, Maastricht University, Maastricht, The Netherlands.
Hum Reprod. 2015 Oct;30(10):2303-11. doi: 10.1093/humrep/dev179. Epub 2015 Jul 22.
Is gene expression in human preimplantation embryos affected by the medium used for embryo culture in vitro during an IVF treatment?
Six days of in vitro culture of human preimplantation embryos resulted in medium-dependent differences in expression level of genes involved in apoptosis, protein degradation, metabolism and cell-cycle regulation.
Several human studies have shown an effect of culture medium on embryo development, pregnancy outcome and birthweight. However, the underlying mechanisms in human embryos are still unknown. In animal models of human development, it has been demonstrated that culture of preimplantation embryos in vitro affects gene expression. In humans, it has been found that culture medium affects gene expression of cryopreserved embryos that, after thawing, were cultured in two different media for 2 more days.
STUDY DESIGN, SIZE, DURATION: In a multicenter trial, women were randomly assigned to two culture medium groups [G5 and human tubal fluid (HTF)]. Data on embryonic development were collected for all embryos. In one center, embryos originating from two pronuclei (2PN) zygotes that were not selected for transfer or cryopreservation on Day 2 or 3 because of lower morphological quality, were cultured until Day 6 and used in this study, if couples consented.
PARTICIPANTS/MATERIALS, SETTING, METHODS: Ten blastocysts each from the G5 and HTF study groups, matched for fertilization method, maternal age and blastocyst quality, were selected and their mRNA was isolated and amplified. Embryos were examined individually for genome-wide gene expression using Agilent microarrays and PathVisio was used to identify the pathways that showed a culture medium-dependent activity.
Expression of 951 genes differed significantly (P < 0.01) between the G5 and HTF groups. Eighteen pathways, involved in apoptosis, metabolism, protein processing and cell-cycle regulation, showed a significant overrepresentation of differentially expressed genes. The DNA replication, G1 to S cell-cycle control and oxidative phosphorylation pathways were up-regulated in the G5 group compared with the HTF group. This is in agreement with the morphological assessment of the 1527 embryos (originating from 2PN zygotes), which showed that embryos consisted of more cells on Day 2 (3.73 ± 1.30 versus 3.40 ± 1.35, P < 0.001) and Day 3 (7.00 ± 2.41 versus 5.84 ± 2.36, P < 0.001) in the G5 group when compared with the HTF group. Furthermore, the implantation rate was significantly higher in the G5 group compared with the HTF group (26.7% versus 14.7%, P = 0.002) after transfer on the second or the third day after fertilization.
LIMITATIONS, REASONS FOR CAUTION: Despite careful matching of the embryos, it cannot be excluded that the differences observed between the study groups are caused by factors that we did not investigate. Extrapolation of these results to embryos used for transfer demands caution as in the present study embryos that were not selected for either embryo transfer or cryopreservation have been used for the culture experiment until Day 6.
This study shows that gene expression in human preimplantation embryos is altered by the culture medium used during IVF treatment and provides insight into the biological pathways that are affected. Whether these changes in gene expression have any long-term effects on children born after IVF remains unknown. However, it is possible that early adaptations of the preimplantation embryo to its environment persist during fetal and post-natal development.
STUDY FUNDING/COMPETING INTERESTS: No funding and no competing interests declared.
Not applicable.
体外受精治疗过程中,胚胎培养的培养液是否会影响人类胚胎的基因表达?
人类胚胎体外培养 6 天会导致凋亡、蛋白降解、代谢和细胞周期调控相关基因的表达水平出现培养液依赖性差异。
几项人类研究表明,培养液会影响胚胎发育、妊娠结局和出生体重。但是,人类胚胎的潜在机制仍不清楚。在人类发育的动物模型中,已经证明体外培养的胚胎会影响基因表达。在人类中,已经发现培养液会影响经过冷冻保存的胚胎的基因表达,解冻后,这些胚胎在两种不同的培养液中再培养 2 天。
研究设计、规模、持续时间:在一项多中心试验中,女性被随机分配到两种培养液组[G5 和人输卵管液(HTF)]。收集了所有胚胎的胚胎发育数据。在一个中心,如果夫妇同意,将选择第 2 天或第 3 天由于形态质量较差而未选择用于转移或冷冻保存的 2 原核(2PN)受精卵培养至第 6 天,并用于本研究。
参与者/材料、设置、方法:从 G5 和 HTF 研究组中各选择 10 个囊胚,分别匹配受精方法、母亲年龄和囊胚质量,然后分离和扩增其 mRNA。使用 Agilent 微阵列对胚胎进行个体全基因组基因表达检测,并使用 PathVisio 识别显示培养液依赖性活性的途径。
G5 和 HTF 组之间有 951 个基因的表达差异显著(P < 0.01)。涉及凋亡、代谢、蛋白加工和细胞周期调控的 18 个途径表现出显著差异表达基因的过表达。与 HTF 组相比,G5 组的 DNA 复制、G1 到 S 细胞周期控制和氧化磷酸化途径上调。这与对 1527 个胚胎(来自 2PN 受精卵)的形态评估结果一致,这些胚胎在第 2 天(3.73 ± 1.30 比 3.40 ± 1.35,P < 0.001)和第 3 天(7.00 ± 2.41 比 5.84 ± 2.36,P < 0.001)时,G5 组中的胚胎包含更多的细胞。此外,与 HTF 组相比,G5 组的移植率显著更高(26.7%比 14.7%,P = 0.002),受精后第 2 天或第 3 天进行转移。
局限性、谨慎的原因:尽管对胚胎进行了仔细匹配,但不能排除我们未研究的因素导致了观察组之间的差异。由于在本研究中,未选择用于胚胎转移或冷冻保存的胚胎直到第 6 天才用于培养实验,因此将这些结果外推到用于转移的胚胎时需要谨慎。
本研究表明,人类胚胎在体外受精治疗过程中,培养液会改变其基因表达,并提供了有关受影响的生物学途径的见解。这些基因表达的变化是否对体外受精后出生的儿童有任何长期影响仍不清楚。然而,胚胎在早期对环境的适应可能会在胎儿和产后发育过程中持续存在。
研究资金/利益冲突:无资金和无利益冲突声明。
不适用。