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核因子-κB(NF-κB)和抑制因子-κB(IκB)在足月和早产时人胎膜及蜕膜中的定位。

Localization of nuclear factor-kappa B (NF kappa B) and inhibitory factor-kappa B (I kappa B) in human fetal membranes and decidua at term and preterm delivery.

作者信息

Yan X, Sun M, Gibb W

机构信息

Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, University of Ottawa, Ottawa, Ontario, Canada.

出版信息

Placenta. 2002 Apr;23(4):288-93. doi: 10.1053/plac.2002.0789.

Abstract

The human fetal membranes and decidua are thought to be involved in the onset of human parturition. These tissues produce and respond to various cytokines, which may be involved in preterm labour and possibly term labour. They also show increasing production of prostaglandins (PGs) with advancing gestation and labour. The expression of PGHS-2, a rate limiting enzyme in PG synthesis, is increased in the fetal membranes at labour. The gene for PGHS-2 and many of the cytokine genes (e.g. TNFalpha, IL-1, IL-6) are stimulated by the transcription factor NF kappa B. This factor is composed of two subunits, p50 and p65, which are localized in the cytoplasm bound to I kappa B. When activated I kappa B is metabolized, and p50, p65 translocate to the nucleus to activate various genes. The purpose of the present study was to examine the tissue and cellular distribution of p65 and I kappa B in the human fetal membranes and decidua throughout gestation. Term tissues were obtained prior to labour by elective caesarean section (n=10) or following vaginal delivery (n=10) and 10 preterm tissues were obtained following labour prior to 37 weeks gestation. None of the tissues had any evidence of infection. The immunoreactive NF kappa B and I kappa B were localized in the tissues. p65 protein was found in the nucleus and cytoplasm of cells in the amnion, chorion laeve and decidua. In the amnion and chorion laeve, no changes occurred in subcellular localization with advancing gestation or term labour. However, in the decidua, there was a marked increase in the nuclear localization of i.r. p 65 in tissues obtained at term when compared with tissues delivered preterm. In the case of I kappa B, it was localized to the cytoplasm of cells in all tissues and there was an increase i.r. I kappa B in decidua at term compared to preterm but no change occurred in the amnion or chorion. The increase in nuclear localization of p65 in the decidua that occurs with advancing gestation, highlights the potential importance of this factor in the regulation of parturition related genes in this tissue.

摘要

人类胎膜和蜕膜被认为与人类分娩的发动有关。这些组织产生并对多种细胞因子作出反应,这些细胞因子可能参与早产以及足月分娩。随着妊娠进展和分娩,它们还显示出前列腺素(PGs)的产生增加。PG合成中的限速酶PGHS-2在分娩时胎膜中的表达增加。PGHS-2基因和许多细胞因子基因(如TNFα、IL-1、IL-6)受转录因子NF-κB刺激。该因子由两个亚基p50和p65组成,它们定位于与IκB结合的细胞质中。激活时,IκB被代谢,p50、p65转位至细胞核以激活各种基因。本研究的目的是检查整个妊娠期人胎膜和蜕膜中p65和IκB的组织和细胞分布。足月组织在分娩前通过择期剖宫产获得(n = 10)或经阴道分娩后获得(n = 10),10例早产组织在妊娠37周前分娩后获得。所有组织均无感染迹象。免疫反应性NF-κB和IκB定位于组织中。p65蛋白在羊膜、平滑绒毛膜和蜕膜的细胞核和细胞质中均有发现。在羊膜和平滑绒毛膜中,随着妊娠进展或足月分娩,亚细胞定位无变化。然而,在蜕膜中,与早产时娩出的组织相比,足月时获得的组织中免疫反应性p65的核定位显著增加。就IκB而言,它定位于所有组织细胞的细胞质中,与早产相比,足月时蜕膜中免疫反应性IκB增加,但羊膜或绒毛膜中无变化。随着妊娠进展,蜕膜中p65核定位的增加突出了该因子在调节该组织中分娩相关基因方面的潜在重要性。

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