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大鼠胚胎肛门直肠畸形发育过程中转录因子4的时空模式分析

Spatiotemporal pattern analysis of transcription factor 4 in the developing anorectum of the rat embryo with anorectal malformations.

作者信息

Zhang Tao, Bai Yu Zuo, Wang Da Jia, Jia Hui Min, Yuan Zheng Wei, Wang Wei Lin

机构信息

Department of Pediatric Surgery, Shengjing Hospital China Medical University, Heping District, Shenyang 110004, People's Republic of China.

出版信息

Int J Colorectal Dis. 2009 Sep;24(9):1039-47. doi: 10.1007/s00384-009-0705-3. Epub 2009 Apr 22.

Abstract

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.

摘要

目的

作为转录因子家族的一员,已知转录因子4(Tcf4)会影响包括肺、肝、胰腺、胃和肠道在内的内胚层衍生组织中的基因表达。然而,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,这种能力是否活跃仍不清楚。

材料与方法

在本研究中,引入乙撑硫脲(ETU)诱导的ARM模型,采用免疫组织化学染色、逆转录聚合酶链反应(RT-PCR)和蛋白质印迹分析来研究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呈现空间依赖性变化:在正常胚胎中,Tcf4蛋白最初在胚胎第13天(E13)时表达于尿直肠隔(URS)的背侧内胚层和后肠。此外,在E14时,独立的表达域在背侧CM上强烈发展。在E15时,然后在URS的融合组织中检测到阳性细胞,并且在肛门膜中显著。然而,在ARM胚胎中,泄殖腔、URS和肛门直肠的上皮对Tcf4呈阴性或弱阳性。在蛋白质印迹和RT-PCR中,Tcf4蛋白和mRNA表达在肛门直肠发育过程中呈现时间依赖性变化:在E14、E14.5和E15时,表达水平达到峰值;在E16之后,Tcf4表达逐渐下降。相比之下,在ARM胚胎中,从E13到E16的肛门直肠形态发生过程中,Tcf4的时空表达失衡。

结论

这些数据表明,在泄殖腔分离为直肠和尿道时Tcf4的下调可能与ARM的发生有关。

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