Gupta Alisha, Singh Jaswant, Dufort Isabelle, Robert Claude, Dias Fernanda Caminha Faustino, Anzar Muhammad
Agriculture and Agri-food, Saskatoon Research and Development Center, Saskatoon, Saskatchewan, Canada.
Department of Veterinary Biomedical Sciences, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
PLoS One. 2017 Nov 2;12(11):e0187268. doi: 10.1371/journal.pone.0187268. eCollection 2017.
Cryopreservation is known for its marked deleterious effects on embryonic health. Bovine compact morulae were vitrified or slow-frozen, and post-warm morulae were cultured to the expanded blastocyst stage. Blastocysts developed from vitrified and slow-frozen morulae were subjected to microarray analysis and compared with blastocysts developed from unfrozen control morulae for differential gene expression. Morula to blastocyst conversion rate was higher (P < 0.05) in control (72%) and vitrified (77%) than in slow-frozen (34%) morulae. Total 20 genes were upregulated and 44 genes were downregulated in blastocysts developed from vitrified morulae (fold change ≥ ± 2, P < 0.05) in comparison with blastocysts developed from control morulae. In blastocysts developed from slow-frozen morulae, 102 genes were upregulated and 63 genes were downregulated (fold change ≥ ± 1.5, P < 0.05). Blastocysts developed from vitrified morulae exhibited significant changes in gene expression mainly involving embryo implantation (PTGS2, CALB1), lipid peroxidation and reactive oxygen species generation (HSD3B1, AKR1B1, APOA1) and cell differentiation (KRT19, CLDN23). However, blastocysts developed from slow-frozen morulae showed changes in the expression of genes related to cell signaling (SPP1), cell structure and differentiation (DCLK2, JAM2 and VIM), and lipid metabolism (PLA2R1 and SMPD3). In silico comparison between blastocysts developed form vitrified and slow-frozen morulae revealed similar changes in gene expression as between blastocysts developed from vitrified and control morulae. In conclusion, blastocysts developed form vitrified morulae demonstrated better post-warming survival than blastocysts developed from slow-frozen morulae but their gene expression related to lipid metabolism, steroidogenesis, cell differentiation and placentation changed significantly (≥ 2 fold). Slow freezing method killed more morulae than vitrification but those which survived up to blastocyst stage did not express ≥ 2 fold change in their gene expression as compared with blastocysts from control morulae.
冷冻保存因其对胚胎健康有显著的有害影响而闻名。将牛致密桑葚胚进行玻璃化冷冻或慢速冷冻,解冻后的桑葚胚培养至扩张囊胚阶段。对由玻璃化冷冻和慢速冷冻桑葚胚发育而来的囊胚进行微阵列分析,并与由未冷冻的对照桑葚胚发育而来的囊胚进行比较,以分析差异基因表达。对照(72%)和玻璃化冷冻(77%)桑葚胚的桑葚胚到囊胚转化率高于慢速冷冻(34%)的桑葚胚(P < 0.05)。与由对照桑葚胚发育而来的囊胚相比,由玻璃化冷冻桑葚胚发育而来的囊胚中共有20个基因上调,44个基因下调(倍数变化≥±2,P < 0.05)。在由慢速冷冻桑葚胚发育而来的囊胚中,102个基因上调,63个基因下调(倍数变化≥±1.5,P < 0.05)。由玻璃化冷冻桑葚胚发育而来的囊胚在基因表达上有显著变化,主要涉及胚胎着床(PTGS2、CALB1)、脂质过氧化和活性氧生成(HSD3B1、AKR1B1、APOA1)以及细胞分化(KRT19、CLDN23)。然而,由慢速冷冻桑葚胚发育而来的囊胚在与细胞信号传导(SPP1)、细胞结构和分化(DCLK2、JAM2和VIM)以及脂质代谢(PLA2R1和SMPD3)相关的基因表达上有变化。对由玻璃化冷冻和慢速冷冻桑葚胚发育而来的囊胚进行电子比较,发现其基因表达变化与由玻璃化冷冻和对照桑葚胚发育而来的囊胚之间的变化相似。总之,由玻璃化冷冻桑葚胚发育而来的囊胚解冻后的存活率高于由慢速冷冻桑葚胚发育而来的囊胚,但其与脂质代谢、类固醇生成、细胞分化和胎盘形成相关的基因表达发生了显著变化(≥2倍)。慢速冷冻法杀死的桑葚胚比玻璃化冷冻法多,但那些存活至囊胚阶段的桑葚胚与对照桑葚胚发育而来的囊胚相比,其基因表达变化未达到≥2倍。