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首页> 外文期刊>International journal of colorectal disease. >Spatiotemporal pattern analysis of transcription factor 4 in the developing anorectum of the rat embryo with anorectal malformations.
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Spatiotemporal pattern analysis of transcription factor 4 in the developing anorectum of the rat embryo with anorectal malformations.

机译:大鼠胚胎发育期肛门直肠畸形的肛门直肠中转录因子4的时空模式分析。

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摘要

PURPOSE: As a member of the transcription factors family, transcription factor 4(Tcf4) is known to influence gene expression in endodermally derived tissues including lung, liver, pancreas, stomach, and intestine. However, it remained unknown if this capability is active during anorectal development in the normal and anorectal malformations (ARM) rat embryos. MATERIALS AND METHODS: In this study, ethylenethiourea (ETU)-induced ARM model was introduced to investigate the expression pattern of Tcf4 during anorectal development using immunohistochemical staining, reverse transcriptase polymerase chain reaction (RT-PCR), and Western blot analysis. RESULTS: Immunostaining revealed that Tcf4 expression showed space-dependent changes in the developing anorectum: in normal embryos, Tcf4 protein is initially expressed in the dorsal endoderm of urorectal septum (URS) and hindgut on embryonic day 13 (E13). Additionally, separate expression domain develops intensively on the dorsal CM on E14. On E15, positive cells are then detected in the fused tissue of URS, and prominently in the anal membrane. In the ARM embryos, however, the epithelium of the cloaca, URS, and anorectum was negative or faint for Tcf4. In Western blot and RT-PCR, time-dependent changes of Tcf4 protein and mRNA expression were remarkable during the anorectal development: on E14, E14.5, and E15, the expression level reached the peak; after E16, Tcf4 expression gradually decreased. In contrast, in ARM embryos, spatiotemporal expression of Tcf4 was imbalanced during the anorectal morphogenesis from E13 to E16. CONCLUSIONS: These data implied that the downregulation of Tcf4 at the time of cloacal separation into rectum and urethra might be related to the development of ARM.
机译:目的:作为转录因子家族的成员,已知转录因子4(Tcf4)影响内胚层衍生组织(包括肺,肝,胰腺,胃和肠)中的基因表达。但是,尚不清楚这种能力是否在正常和肛门直肠畸形(ARM)大鼠胚胎的肛门直肠发育过程中起作用。材料与方法:本研究引入亚乙基硫脲诱导的ARM模型,通过免疫组织化学染色,逆转录酶聚合酶链反应(RT-PCR)和Western blot分析研究Tcf4在肛门直肠发育过程中的表达模式。结果:免疫染色显示,Tcf4表达在发育中的肛门直肠中呈空间依赖性变化:在正常胚胎中,Tcf4蛋白最初在第13天(E13)在尿直肠隔(URS)的后内胚层和后肠表达。另外,单独的表达域在E14的背CM上集中发展。然后在E15上,在URS的融合组织中以及在肛门膜中显着检测到阳性细胞。然而,在ARM胚胎中,泄殖腔,URS和肛肠的上皮对Tcf4呈阴性或微弱。在蛋白质印迹和RT-PCR中,肛肠发育过程中Tcf4蛋白和mRNA表达随时间变化显着:在E14,E14.5和E15上,表达水平达到峰值; E16后,Tcf4表达逐渐降低。相反,在ARM胚胎中,从E13到E16的肛肠形态发生过程中Tcf4的时空表达不平衡。结论:这些数据暗示泄殖腔分离为直肠和尿道时Tcf4的下调可能与ARM的发展有关。

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