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囊胚着床依赖于白血病抑制因子的母体表达。

Blastocyst implantation depends on maternal expression of leukaemia inhibitory factor.

作者信息

Stewart C L, Kaspar P, Brunet L J, Bhatt H, Gadi I, Köntgen F, Abbondanzo S J

机构信息

Department of Cell and Developmental Biology, Roche Institute of Molecular Biology, Nutley, New Jersey 07110.

出版信息

Nature. 1992 Sep 3;359(6390):76-9. doi: 10.1038/359076a0.

DOI:10.1038/359076a0
PMID:1522892
Abstract

A critical point during mammalian pregnancy is the implantation of the blastocyst when the embryo attaches to the wall of the uterus. The autonomously developing preimplantation embryo then becomes dependent on the maternal environment for its continued development. Little is known about the regulation of implantation, except that a complex interaction between peptide and steroid hormones synchronizes the preparation of the uterus for implantation with the development of the embryo. Whether the implantation event is under maternal or embryonic control is also unclear (reviewed in refs 1, 2). We have previously shown that a cytokine, leukaemia inhibitory factor (LIF), is expressed in the uterine endometrial glands specifically on the fourth day of pregnancy. This burst of expression is under maternal control and always precedes implantation of the blastocyst. Here we report that transient expression of LIF in mice is essential for implantation. Females lacking a functional LIF gene are fertile, but their blastocysts fail to implant and do not develop. The blastocysts, however, are viable and, when transferred to wild-type pseudopregnant recipients, they can implant and develop to term.

摘要

哺乳动物怀孕过程中的一个关键点是囊胚着床,即胚胎附着于子宫壁之时。自主发育的着床前胚胎随后开始依赖母体环境以继续发育。除了肽类激素和甾体激素之间的复杂相互作用使子宫为着床所做的准备与胚胎发育同步外,关于着床的调控所知甚少。着床事件是受母体控制还是胚胎控制也尚不清楚(参考文献1、2中有综述)。我们之前已表明,一种细胞因子,即白血病抑制因子(LIF),在怀孕第4天特异性地在子宫内膜腺体中表达。这种表达的突然增加受母体控制,并且总是先于囊胚着床。在此我们报告,LIF在小鼠中的瞬时表达对着床至关重要。缺乏功能性LIF基因的雌性具有生育能力,但其囊胚无法着床且不能发育。然而,这些囊胚是有活力的,当移植到野生型假孕受体中时,它们能够着床并发育至足月。

相似文献

1
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。
Nature. 1992 Sep 3;359(6390):76-9. doi: 10.1038/359076a0.
2
Leukaemia inhibitory factor and the regulation of pre-implantation development of the mammalian embryo.白血病抑制因子与哺乳动物胚胎植入前发育的调控
Mol Reprod Dev. 1994 Oct;39(2):233-8. doi: 10.1002/mrd.1080390217.
3
Cloning of leukemia inhibitory factor (LIF) and its expression in the uterus during embryonic diapause and implantation in the mink (Mustela vison).水貂(鼬属)胚胎滞育和着床期间白血病抑制因子(LIF)的克隆及其在子宫中的表达
Mol Reprod Dev. 1998 Sep;51(1):13-21. doi: 10.1002/(SICI)1098-2795(199809)51:1<13::AID-MRD2>3.0.CO;2-Z.
4
A role for cytokines in early pregnancy.细胞因子在妊娠早期的作用。
Indian J Physiol Pharmacol. 1994 Jul;38(3):153-62.
5
Effects of leukaemia inhibitory factor on embryo implantation in the mouse.白血病抑制因子对小鼠胚胎着床的影响。
Cytokine. 2000 Nov;12(11):1676-82. doi: 10.1006/cyto.2000.0758.
6
[Expression of LIF gene during early development of mouse embryo].[白血病抑制因子基因在小鼠胚胎早期发育过程中的表达]
Shi Yan Sheng Wu Xue Bao. 1998 Mar;31(1):105-9.
7
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。
Proc Natl Acad Sci U S A. 1991 Dec 15;88(24):11408-12. doi: 10.1073/pnas.88.24.11408.
8
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。
Mol Endocrinol. 2000 Aug;14(8):1147-61. doi: 10.1210/mend.14.8.0498.
9
Dual control of LIF expression and LIF receptor function regulate Stat3 activation at the onset of uterine receptivity and embryo implantation.白血病抑制因子(LIF)表达和LIF受体功能的双重调控在子宫容受性和胚胎着床起始阶段调节信号转导和转录激活因子3(Stat3)的激活。
Proc Natl Acad Sci U S A. 2001 Jul 17;98(15):8680-5. doi: 10.1073/pnas.151180898. Epub 2001 Jul 3.
10
Temporal and spatial expression of leukemia inhibitory factor in rabbit uterus during early pregnancy.白血病抑制因子在兔早期妊娠子宫中的时空表达
Mol Reprod Dev. 1994 Jun;38(2):148-52. doi: 10.1002/mrd.1080380205.

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