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Effects of vascular endothelial growth factor on porcine preimplantation embryos produced by in vitro fertilization and somatic cell nuclear transfer

机译:血管内皮生长因子对体外受精和体细胞核移植产生的猪植入前胚胎的影响

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This study examined the effects of vascular endothelial growth factor (VEGF) on porcine embryos produced by in vitro fertilization (IVF) and somatic cell nuclear transfer (SCNT) at different developmental stages. Four sets of experiments were performed. In the first, supplementation of the in vitro culture medium with 5 ng/mL VEGF was suitable for porcine IVF embryo development, and the blastocyst formation rate was significantly higher than the control and other groups (57.73 +/- 6.78% (5 ng/mL VEGF) vs. 43.21 +/- 10.22% (control), 42.16 +/- 10.24% (50 ng/mL VEGF) and 41.91 +/- 11.74% (500 ng/mL VEGF); P < 0.05). The total cell number after supplementation with 5 ng/mL VEGF was significantly higher than the control and other groups (151.85 +/- 39.77 (5 ng/mL VEGF) vs. 100.00 +/- 34.43 (control), 91.2 +/- 31.51 (50 ng/mL VEGF), and 112.53 +/- 47.66 (500 ng/mL VEGF); P < 0.05). In the second experiment, when VEGF was added at different developmental stages of IVF derived embryos (early stage, days 1-3, late stage, days 4-7), the blastocyst formation rate and total cell number were significantly higher at the late stage (47.71 +/- 9.13% and 131.5 +/- 20.70, respectively) than in the control (34.32 +/- 7.44% and 85.50 +/- 20.41, respectively) and at the early stage (33.60 +/- 5.78% and 86.75 +/- 25.10, respectively; P < 0.05). There was no significant difference in the blastocyst development rate or total cell number between the whole culture period (days 1-7) and the late stage culture period after supplementation with 5 ng/mL VEGF (P > 0.05). In the third experiment, the cleavage rate was significantly higher when SCNT embryos were cultured with VEGF during the whole culture period than in the late stage (63.56 +/- 15.52% vs. 39.72 +/- 4.94%; P < 0.05), but there was no significant difference between the control and the early stage culture period (P > 0.05). The blastocyst formation rate was significantly higher at the late stage culture period with VEGF than at the early stage culture period (34.40 +/- 15.06% vs. (16.07 +/- 5.01%; P < 0.05). There was no significant difference in the total cell number between the groups (P > 0.05). In experiment 4, using real-time PCR, VEGF mRNA expression was detected in all the developmental stages of IVF and SCNT embryos, but the expression level varied according to the developmental stage. VEGF receptor, KDR mRNA was detected in all stages IVF and SCNT embryos. However, fit-1 mRNA was not expressed in all embryonic stages of IVF and SCNT embryos. These data suggest that VEGF supplementation at the late embryonic developmental stage might improve the developmental potential of both IVF and SCNT preimplantation porcine embryos through its receptors
机译:这项研究检查了血管内皮生长因子(VEGF)对体外受精(IVF)和体细胞核移植(SCNT)在不同发育阶段产生的猪胚胎的影响。进行四组实验。首先,在体外培养基中添加5 ng / mL VEGF适合于猪IVF胚胎发育,胚泡形成率显着高于对照组和其他组(57.73 +/- 6.78%(5 ng / mL mL VEGF)vs.43.21 +/- 10.22%(对照),42.16 +/- 10.24%(50 ng / mL VEGF)和41.91 +/- 11.74%(500 ng / mL VEGF); P <0.05)。补充5 ng / mL VEGF后的总细胞数显着高于对照组和其他组(151.85 +/- 39.77(5 ng / mL VEGF)与100.00 +/- 34.43(对照),91.2 +/- 31.51 (50 ng / mL VEGF)和112.53 +/- 47.66(500 ng / mL VEGF); P <0.05)。在第二个实验中,当在IVF衍生胚胎的不同发育阶段(早期,1-3天,晚期,4-7天)添加VEGF时,胚泡形成率和总细胞数在晚期显着增加。 (分别为47.71 +/- 9.13%和131.5 +/- 20.70)比对照组(分别为34.32 +/- 7.44%和85.50 +/- 20.41)和早期(33.60 +/- 5.78%和86.75)分别为+/- 25.10; P <0.05)。补充5 ng / mL VEGF后,整个培养期(第1-7天)与晚期培养期之间的胚泡发育速率或总细胞数无显着差异(P> 0.05)。在第三个实验中,在整个培养期间用VEGF培养SCNT胚胎时的裂解率显着高于后期(63.56 +/- 15.52%对39.72 +/- 4.94%; P <0.05),但是对照组和早期培养期之间无显着差异(P> 0.05)。用VEGF培养的胚囊形成率显着高于早期培养期(34.40 +/- 15.06%vs(16.07 +/- 5.01%; P <0.05)。组间总细胞数(P> 0.05)在实验4中,采用实时PCR检测IVF和SCNT胚胎所有发育阶段的VEGF mRNA表达,但表达水平随发育阶段而变化。在IVF和SCNT胚胎的所有阶段均检测到VEGF受体,KDR mRNA的表达,但是在IVF和SCNT胚胎的所有胚胎阶段均未表达fit-1 mRNA,这些数据表明胚胎发育后期补充VEGF可能促进胚胎发育。 IVF和SCNT植入前的猪胚胎通过其受体的潜力

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