Honguntikar Sachin D, Salian Sujith Raj, D'Souza Fiona, Uppangala Shubhashree, Kalthur Guruprasad, Adiga Satish Kumar
Division of Clinical Embryology, Level 2, Central Research Lab, Kasturba Medical College, Manipal University, Manipal, 576104, India.
Lasers Med Sci. 2017 Dec;32(9):2081-2087. doi: 10.1007/s10103-017-2334-3. Epub 2017 Sep 30.
The advantage of using laser for assisted hatching in routine assisted reproductive technology (ART) practice is debatable. Recently, it has been shown that laser-manipulated mouse embryos had compromised genetic integrity. However, the impact of laser-assisted hatching (LAH) on the epigenetic integrity of the preimplantation embryos is not elucidated so far. Since continuous thermal stress on embryos was found to lower mRNA levels of de novo (bovine) methyl transferases in embryos, we hypothesize that thermal energy induced during LAH may alter the epigenetic signature through abnormal de novo methyl transferases (Dnmts) levels. Thus, using mouse model, we made an attempt to look into the expression of Dnmt3a and Dnmt3b in laser-manipulated embryos and their effects on global methylation. This experimental prospective study used mouse embryos from varying developmental stages (2-cell, 6-8-cell, and blastocyst) which were subjected to LAH using a 1480-nm diode laser. Two pulses of 350 μs frequency were applied to breach the zona pellucida, and then, embryos were assessed for the expression of two de novo methyl transferases (Dnmt3a and Dnmt3b) and LINE-1 (long interspersed element-1) methylation when LAH embryos developed to blastocyst stage. Results from this study have shown that blastocysts subjected to LAH at two-cell stage had significantly lower mRNA transcripts of Dnmt3a (P < 0.01) and Dnmt3b (P < 0.05) whereas LAH at six- to eight-cell and blastocyst stages did not affect the mRNA level significantly. On the other hand, LINE-1 methylation did not change significantly between LAH and control group in all the stages studied. These results suggest that two-cell-stage laser manipulation of embryos changes the mRNA level of Dnmts without affecting the global DNA methylation.
在常规辅助生殖技术(ART)实践中,使用激光进行辅助孵化的优势存在争议。最近有研究表明,经激光处理的小鼠胚胎的遗传完整性受到了损害。然而,迄今为止,激光辅助孵化(LAH)对植入前胚胎表观遗传完整性的影响尚未阐明。由于发现胚胎受到持续热应激会降低胚胎中从头(牛)甲基转移酶的mRNA水平,我们推测LAH过程中产生的热能可能通过异常的从头甲基转移酶(Dnmts)水平改变表观遗传特征。因此,我们使用小鼠模型,试图研究经激光处理的胚胎中Dnmt3a和Dnmt3b的表达及其对整体甲基化的影响。这项实验性前瞻性研究使用了来自不同发育阶段(2细胞、6 - 8细胞和囊胚)的小鼠胚胎,这些胚胎使用1480纳米二极管激光进行LAH处理。施加两个频率为350微秒的脉冲以穿透透明带,然后,当LAH胚胎发育到囊胚阶段时,评估胚胎中两种从头甲基转移酶(Dnmt3a和Dnmt3b)的表达以及LINE - 1(长散在核元件 - 1)甲基化情况。这项研究的结果表明,在2细胞阶段接受LAH处理的囊胚中,Dnmt3a(P < 0.01)和Dnmt3b(P < 0.05)的mRNA转录本显著降低,而在6 - 8细胞和囊胚阶段进行LAH处理则对mRNA水平没有显著影响。另一方面,在所有研究阶段,LAH组和对照组之间的LINE - 1甲基化没有显著变化。这些结果表明,对胚胎进行2细胞阶段的激光处理会改变Dnmts的mRNA水平,而不影响整体DNA甲基化。