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白血病抑制因子可以替代着床期雌激素,对于诱导子宫进入接受着床状态至关重要,但对随后的胚胎发育并非必不可少。

Leukemia inhibitory factor can substitute for nidatory estrogen and is essential to inducing a receptive uterus for implantation but is not essential for subsequent embryogenesis.

作者信息

Chen J R, Cheng J G, Shatzer T, Sewell L, Hernandez L, Stewart C L

机构信息

Cancer and Developmental Biology Laboratory, ABL-Basic Research Program, NCI-Frederick Cancer Research and Development Center, Maryland 21702, USA.

出版信息

Endocrinology. 2000 Dec;141(12):4365-72. doi: 10.1210/endo.141.12.7855.

DOI:10.1210/endo.141.12.7855
PMID:11108244
Abstract

A stage critical in mammalian development is embryo implantation. At this point, the blastocyst establishes a close interaction with the uterine tissues, a step necessary for its continued embryonic development. In many mammalian species, including man, uterine expression of the cytokine, leukemia inhibitory factor (LIF) is coincident with the onset of implantation and in mice LIF is essential to this process. The reasons for implantation failure have not been established. Here we show in LIF-deficient mice that up to the onset of implantation, changes in uterine cell proliferation, hormone levels, blastocyst localization, as well as expression of lactoferrin and Muc-1, do not differ from wild-types. However, the uterus fails to respond to the presence of embryos or to artificial stimuli by decidualizing. In mice, implantation and decidualization are induced by nidatory estrogen. We show that uterine expression of LIF is up-regulated by estrogen and LIF can replace nidatory estrogen at inducing both implantation and decidualization in ovariectomized mice. Implantation of LIF-deficient embryos in the LIF-deficient females, with normal development to term is rescued by i.p. injection of LIF. Transient expression of LIF on D4 of pregnancy is therefore only required to induce a state of receptivity in the uterus permitting embryo implantation and decidualization. LIF is neither required by the embryo for development nor for the maintenance of pregnancy.

摘要

胚胎植入是哺乳动物发育过程中的一个关键阶段。此时,囊胚与子宫组织建立紧密的相互作用,这是其胚胎持续发育所必需的步骤。在包括人类在内的许多哺乳动物物种中,细胞因子白血病抑制因子(LIF)在子宫中的表达与植入的开始同时出现,并且在小鼠中LIF对这一过程至关重要。植入失败的原因尚未明确。在这里,我们在LIF基因缺陷的小鼠中发现,直到植入开始时,子宫细胞增殖、激素水平、囊胚定位以及乳铁蛋白和Muc-1的表达变化与野生型小鼠并无差异。然而,子宫无法通过蜕膜化对胚胎的存在或人工刺激做出反应。在小鼠中,植入和蜕膜化是由着床雌激素诱导的。我们发现,雌激素可上调子宫中LIF的表达,并且LIF能够在去卵巢小鼠中替代着床雌激素诱导植入和蜕膜化。通过腹腔注射LIF可挽救LIF基因缺陷雌性小鼠中LIF基因缺陷胚胎的植入,并使其正常发育至足月。因此,妊娠第4天短暂表达LIF仅用于诱导子宫处于允许胚胎植入和蜕膜化的接受状态。胚胎发育及维持妊娠过程均不需要LIF。

相似文献

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Leukemia inhibitory factor can substitute for nidatory estrogen and is essential to inducing a receptive uterus for implantation but is not essential for subsequent embryogenesis.白血病抑制因子可以替代着床期雌激素,对于诱导子宫进入接受着床状态至关重要,但对随后的胚胎发育并非必不可少。
Endocrinology. 2000 Dec;141(12):4365-72. doi: 10.1210/endo.141.12.7855.
2
Studies using the estrogen receptor alpha knockout uterus demonstrate that implantation but not decidualization-associated signaling is estrogen dependent.使用雌激素受体α基因敲除子宫的研究表明,着床而非蜕膜化相关信号传导是雌激素依赖性的。
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Dysregulation of EGF family of growth factors and COX-2 in the uterus during the preattachment and attachment reactions of the blastocyst with the luminal epithelium correlates with implantation failure in LIF-deficient mice.在胚泡与腔上皮的着床前和着床反应期间,子宫中表皮生长因子(EGF)家族生长因子和环氧化酶-2(COX-2)的失调与白血病抑制因子(LIF)缺陷小鼠的着床失败相关。
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Identification of genes regulated by leukemia-inhibitory factor in the mouse uterus at the time of implantation.着床时小鼠子宫中受白血病抑制因子调控的基因的鉴定。
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Endometrial glands are essential for blastocyst implantation and decidualization in the mouse uterus.子宫内膜腺体对于小鼠子宫中囊胚着床和蜕膜化是必不可少的。
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Blastocyst implantation depends on maternal expression of leukaemia inhibitory factor.囊胚着床依赖于白血病抑制因子的母体表达。
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Leukemia inhibitory factor ligand-receptor signaling is important for uterine receptivity and implantation in golden hamsters (Mesocricetus auratus).白血病抑制因子配体-受体信号传导对金黄地鼠(Mesocricetus auratus)的子宫接受性和着床很重要。
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Uterine expression of leukemia inhibitory factor coincides with the onset of blastocyst implantation.白血病抑制因子的子宫表达与胚泡着床的开始时间一致。
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Evidence for heterodimeric association of leukemia inhibitory factor (LIF) receptor and gp130 in the mouse uterus for LIF signaling during blastocyst implantation.白血病抑制因子(LIF)受体与gp130在小鼠子宫中形成异源二聚体关联以介导胚泡着床期间LIF信号传导的证据。
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