Pfeifer N, Baston-Büst D M, Hirchenhain J, Friebe-Hoffmann U, Rein D T, Krüssel J S, Hess A P
Department of OB/GYN and REI (UniKiD), Medical Center University of Düsseldorf, Moorenstr. 5, 40225 Düsseldorf, Germany.
ScientificWorldJournal. 2012;2012:479315. doi: 10.1100/2012/479315. Epub 2012 Jul 31.
The aim of this paper was to determine the influence of different in vitro culture media on mRNA expression of Hedgehog genes, il-6, and important genes regarding reactive oxygen species in single mouse embryos.
Reverse transcription of single embryos either cultured in vitro from day 0.5 until 3.5 (COOK's Cleavage medium or Vitrolife's G-1 PLUS medium) or in vivo until day 3.5 post coitum. PCR was carried out for β-actin followed by nested-PCR for shh, ihh, il-6, nox, gpx4, gpx1, and prdx2.
The number of murine blastocysts cultured in COOK medium which expressed il-6, gpx4, gpx1, and prdx2 mRNA differed significantly compared to the in vivo group. Except for nox, the mRNA profile of the Vitrolife media group embryos varied significantly from the in vivo ones regarding the number of blastocysts expressing the mRNA of shh, ihh, il-6, gpx4, gpx1 and prdx2.
The present study shows that different in vitro culture media lead to different mRNA expression profiles during early development. Even the newly developed in vitro culture media are not able to mimic the female reproductive tract. The question of long-term consequences for children due to assisted reproduction techniques needs to be addressed in larger studies.
本文旨在确定不同的体外培养基对单个小鼠胚胎中刺猬基因、白细胞介素-6(IL-6)以及与活性氧相关的重要基因的mRNA表达的影响。
将单个胚胎从第0.5天体外培养至3.5天(使用库克公司的卵裂培养基或维特利夫公司的G-1 PLUS培养基),或体内培养至交配后3.5天,然后进行逆转录。先对β-肌动蛋白进行PCR,随后对音猬因子(shh)、印度刺猬因子(ihh)、IL-6、烟酰胺腺嘌呤二核苷酸磷酸氧化酶(nox)、谷胱甘肽过氧化物酶4(gpx4)、谷胱甘肽过氧化物酶1(gpx1)和过氧化物还原酶2(prdx2)进行巢式PCR。
与体内组相比,在库克培养基中培养的表达IL-6、gpx4、gpx1和prdx2 mRNA的小鼠囊胚数量有显著差异。除nox外,维特利夫培养基组胚胎在表达shh、ihh、IL-6、gpx4、gpx1和prdx2 mRNA的囊胚数量方面,其mRNA谱与体内组有显著差异。
本研究表明,不同的体外培养基在早期发育过程中会导致不同的mRNA表达谱。即使是新开发的体外培养基也无法模拟雌性生殖道。辅助生殖技术对儿童的长期影响问题需要在更大规模的研究中加以解决。