Soygur Bikem, Moore Harry
Department of Biomedical Science, Centre for Stem Cell Biology, University of Sheffield, Sheffield S10 2UH, UK Present address: Department of Histology and Embryology, Akdeniz University School of Medicine, Antalya, Turkey.
Department of Biomedical Science, Centre for Stem Cell Biology, University of Sheffield, Sheffield S10 2UH, UK
Hum Reprod. 2016 Jul;31(7):1455-61. doi: 10.1093/humrep/dew097. Epub 2016 May 12.
As Syncytin 1 (human endogenous retrovirus (HERV-W)) is crucial for human embryo placentation is it expressed during preimplantation embryo development?
Syncytin 1 was expressed mainly in trophoblast cells of the blastocyst particularly in cells underlying the inner cell mass (ICM).
Syncytin 1 (along with HERV-FRD or Syncytin 2) is expressed in first-trimester placenta and required for cell-cell fusion to enable formation of syncytiotrophoblast and effective placentation.
STUDY DESIGN, SIZE AND DURATION: Preimplantation human embryos donated for research were cultured in vitro and protein expression of Syncytin 1 at the blastocyst stage of development investigated. Comparisons were made with protein (Syncytin 1) and mRNA (Syncytin 1 and 2) expression in human embryonic stem cells (hESCs) undergoing differentiation to trophoblast-like cells in vitro. In total, 10 blastocysts (×3 or 4 replicates) were analysed and 4 hESC lines. The study was terminated after consistent observations of embryos were made.
PARTICIPANTS/MATERIALS, SETTING, METHODS: Donated embryos were thawed and cultured to blastocyst, fixed with 4% w/v paraformaldehyde. Syncytin 1 protein expression was determined by immunofluorescent localisation and confocal microscopy. Additionally, hESCs were differentiated to trophoblast-like cells in standard and conditioned culture medium with growth factors (bone morphogenetic protein 4 (BMP4) or fibroblast growth factor 4 (FGF4) and assessed for mRNA (Syncytin 1 and 2) by quantitative polymerase chain reaction (qPCR) and protein expression by immunolocalization and western blot.
Syncytin 1 was expressed in cytoplasm and on the cell surface of some trophoblast cells, and consistently the trophectoderm underlying the ICM of the blastocyst. There was weak but consistent expression of Syncytin 1 in cells on the periphery of the ICM also displaying pluripotency antibody marker (Tra-1-60). Three-dimensional reconstruction of confocal slice data provided good visualization of expression. The time course of expression of Syncytin 1 was replicated in hESCs differentiated in vitro confirming the embryo observations and providing statistically significant differences in protein and mRNA level (P= 0.002) and (P< 0.05), respectively.
LIMITATION, REASONS FOR CAUTION: Culture of a limited number of embryos to blastocyst in vitro may not replicate the range and quality of development in situ. Probes (antibodies, PCR) were tested for specificity, but might have non-specific reactions.
Syncytin expression is a prerequisite for embryo implantation and placentation. Understanding when expression first occurs during embryo development may be informative for understanding conditions of abnormal gestations such as pre-clampsia.
STUDY FUNDING/COMPETING INTERESTS: The study was supported partly by an ERASMUS training grant and grant G0801059 from the Medical Research Council, U.K. There were no competing interests.
由于合胞素1(人类内源性逆转录病毒(HERV-W))对人类胚胎着床至关重要,那么它在植入前胚胎发育过程中是否表达?
合胞素1主要在囊胚的滋养层细胞中表达,尤其是在内细胞团(ICM)下方的细胞中。
合胞素1(与HERV-FRD或合胞素2一起)在孕早期胎盘中表达,是细胞间融合所必需的,可促使合体滋养层形成和有效着床。
研究设计、规模与持续时间:将捐赠用于研究的植入前人类胚胎进行体外培养,并研究合胞素1在发育囊胚阶段的蛋白质表达。将其与体外分化为滋养层样细胞的人类胚胎干细胞(hESCs)中的蛋白质(合胞素1)和mRNA(合胞素1和2)表达进行比较。总共分析了10个囊胚(×3或4个重复样本)和4个人类胚胎干细胞系。在对胚胎进行了一致的观察后,研究终止。
参与者/材料、环境、方法:将捐赠的胚胎解冻并培养至囊胚期,用4% 重量/体积的多聚甲醛固定。通过免疫荧光定位和共聚焦显微镜确定合胞素1的蛋白质表达。此外,将人类胚胎干细胞在含有生长因子(骨形态发生蛋白4(BMP4)或成纤维细胞生长因子4(FGF4))的标准和条件培养基中分化为滋养层样细胞,并通过定量聚合酶链反应(qPCR)评估mRNA(合胞素1和2),通过免疫定位和蛋白质印迹评估蛋白质表达。
合胞素1在一些滋养层细胞的细胞质和细胞表面表达,并且始终在囊胚内细胞团下方的滋养外胚层中表达。在内细胞团周边也显示多能性抗体标记(Tra-1-60)的细胞中,合胞素1有微弱但持续的表达。共聚焦切片数据的三维重建很好地显示了表达情况。合胞素1的表达时间进程在体外分化的人类胚胎干细胞中得到了重复,证实了胚胎观察结果,并分别在蛋白质和mRNA水平上提供了具有统计学意义的差异(P = 0.002)和(P < 0.05)。
局限性、谨慎原因:在体外将有限数量的胚胎培养至囊胚期可能无法复制原位发育的范围和质量。探针(抗体、PCR)经过了特异性测试,但可能存在非特异性反应。
合胞素表达是胚胎着床和胎盘形成的先决条件。了解其在胚胎发育过程中何时首次表达可能有助于理解异常妊娠情况,如先兆子痫。
研究资金/利益冲突:该研究部分得到了伊拉斯谟培训资助以及英国医学研究理事会的G0801059资助。不存在利益冲突。