首页> 外文期刊>Biology of Reproduction: Offical Journal of the Society for the Study of Reproduction >In Vivo Effect of Leukemia Inhibitory Factor (LIF) and an Anti-LIF Polyclonal Antibody on Murine Embryo and Fetal Development Following Exposure at the Time of Transcervical Blastocyst Transfer.
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In Vivo Effect of Leukemia Inhibitory Factor (LIF) and an Anti-LIF Polyclonal Antibody on Murine Embryo and Fetal Development Following Exposure at the Time of Transcervical Blastocyst Transfer.

机译:宫颈抑制性囊胚转移时暴露后,白血病抑制因子(LIF)和抗LIF多克隆抗体对小鼠胚胎和胎儿发育的体内作用。

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Leukemia inhibitory factor (LIF) enhances in vitro murine preimplantation development in a time- and dose-dependent fashion. Knockout experiments have demonstrated that endometrial LIF is essential for in vivo murine implantation. We assessed the impact of LIF and an anti-LIF polyclonal antibody (pab) on in vivo development and developed a novel and successful nonsurgical method of embryo transfer for this species, a transcervical blastocyst transfer technique. The objectives of this study were to evaluate the effects of LIF and the anti-LIF pab on 1) implantation, resorption, pregnancy, and viability rates and 2) the overall structural and skeletal development. Two-cell embryos were recovered from superovulated mated donors, cultured to the expanded blastocyst stage, and transferred transcervically into pseudopregnant recipients. Exposure to 5000 U/ml LIF resulted in significant increases in implantation, pregnancy, and viability rates compared with controls. A similar dose of pab produced overall inhibitory effects with a significant decrease in implantation rate. Paradoxically, lower pab doses resulted in significantly increased viability rates. Exposure to LIF had no effect on fetoplacental development. However, pab treatments had variable but significant negative effects on placental length, ossification of the exoccipital bone, and vertebral space width compared with controls. Exposure of murine blastocysts to LIF at the time of transcervical transfer resulted in pronounced positive effects on implantation and pregnancy rates without affecting fetal development. A similar pab dose dramatically reduced implantation and pregnancy rates; at high and low doses, pab produced deleterious effects on placental and skeletal development.
机译:白血病抑制因子(LIF)以时间和剂量依赖的方式增强体外鼠植入前的发育。敲除实验证明子宫内膜LIF对于体内鼠类植入至关重要。我们评估了LIF和抗LIF多克隆抗体(pab)对体内发育的影响,并为该物种开发了一种新颖且成功的非手术胚胎移植方法,一种经子宫颈囊胚移植技术。这项研究的目的是评估LIF和抗LIF pab对1)植入,吸收,妊娠和存活率以及2)总体结构和骨骼发育的影响。从超排卵的交配供体中取出两细胞胚胎,将其培养至扩大的胚泡期,并经子宫颈转移至假孕受体中。与对照组相比,暴露于5000 U / ml LIF导致植入,妊娠和生存率显着增加。相似剂量的pab产生了总体抑制作用,植入率大大降低。矛盾的是,较低的pab剂量导致存活率显着提高。暴露于LIF对胎儿胎盘发育没有影响。然而,与对照相比,pab治疗对胎盘长度,枕骨骨化和椎间隙宽度具有可变但显着的负面影响。经宫颈转移时,鼠胚囊暴露于LIF会对植入和妊娠率产生明显的积极影响,而不会影响胎儿的发育。相似的pab剂量会大大降低植入率和怀孕率。无论高剂量还是低剂量,pab都会对胎盘和骨骼发育产生有害影响。

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