控制性超促排卵对小鼠胎盘功能基因表达及胎鼠体质量的影响

Effects of controlled ovarian hyperstimulation on placental function gene expression and weight in mouse offspring

  • 摘要:
      背景  辅助生殖技术是治疗不孕症的主要手段,全球通过辅助生殖技术出生的婴儿已经超过800万。辅助生殖技术存在多种不良妊娠结局,影响着子代近期和远期的健康。
      目的  探讨控制性超促排卵对小鼠胎盘功能基因表达及胎儿体质量的影响。
      方法  将自然妊娠小鼠囊胚移植入自然交配假孕鼠(NC组,n=8)及超促排卵后假孕鼠(COH组,n=8)子宫内,以消除控制性超促排卵对卵母细胞、体外受精和体外胚胎培养等的影响,单独研究子宫内环境对胎盘功能基因及胎儿体质量的影响,并于妊娠18.5 d取胎鼠及胎盘称重,采用q-PCR技术检测胎盘生长相关印记基因的表达,采用Luminex液相悬浮芯片技术检测胎盘生长相关细胞因子变化。
      结果  与NC组比较,控制性超促排卵组小鼠胎鼠体质量降低,胎盘重量降低,胎盘效率降低(P<0.05)。控制性超促排卵组小鼠胎盘生长相关印记基因Igf-2、Peg3、H19、Mest、Cdkn1c、Mash2、Cd81、Plagl1、Zim1、Ube3a表达水平降低(P<0.05)。控制性超促排卵组小鼠胎盘生长相关细胞因子VEGF、PIGF-2、PDGF-BB、MMP-2、MMP-9、VEGFR2表达水平降低(P<0.05)。
      结论  控制性超促排卵可以降低小鼠胎盘生长相关印记基因的表达水平,降低胎盘生长相关细胞因子表达水平,降低胎鼠体质量。

     

    Abstract:
      Background  Assisted reproductive technology is the main treatment for infertility, more than 8 million babies have been born through it worldwide. While it has been associated with a variety of adverse pregnancy outcomes, which may affect the short- and long-term health of offspring.
      Objective  To investigate the effects of controlled ovarian hyperstimulation on placental function gene expression and fetal weight in mice.
      Methods  The blastocysts of naturally pregnant mice were transplanted into the uterus of naturally mating pseudopregnant mice (NC group, n=8) and pseudopregnant mice (COH group, n=8) after hyperovulation. In order to eliminate the confounders affecting the health of offspring, such as controlled ovarian hyperstimulation on oocytes, in vitro fertilization and in vitro embryo culture, the influence of uterine environment on placental function genes and fetal weight was studied separately. Fetal mice and placenta were taken and weighed at 18.5d of pregnancy. The expression of placenta growth-related imprinted genes was detected by q-PCR, and placenta growth-related genes were detected by Luminex liquid suspension chip technology.
      Results  Compared with the NC group, fetal weight, placental weight and placental efficiency decreased significantly in the controlled ovarian hyperstimulation group (P<0.05) and the expression levels of Igf-2, Peg3, H19, Mest, Cdkn1c, Mash2, Cd81, Plagl1, Zim1 and Ube3a also decreased in the controlled ovarian hyperstimulation group (P<0.05), so did the expression levels of placental growth-related cytokines VEGF, PIGF-2, PDGF-BB, MMP-2, MMP-9 and VEGFR2 (P<0.05).
      Conclusion  Controlled ovarian hyperstimulation can reduce the expression level of placental growth-related imprinted genes and placental growth-related cytokines, and decrease weight in offspring.

     

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