Tang Xiao Bing, Zhang Tao, Wang Wei Lin, Yuan Zheng Wei, Bai Yu Zuo
Department of Pediatric Surgery, Shengjing Hospital, China Medical University, 36 Sanhao Street, Heping District, Shenyang, 110004, People's Republic of China.
Cell Tissue Res. 2014 Jul;357(1):83-90. doi: 10.1007/s00441-014-1858-0. Epub 2014 Apr 18.
The main aim of this study was to determine Cdx2 expression patterns during anorectal development in normal and anorectal malformation (ARM) embryos with a view to establishing the possible role of Cdx2 in ARM pathogenesis. ARM was induced with ethylenethiourea on the 10th gestational day (GD10) in rat embryos, and Cesarean deliveries were performed to harvest the embryos. The temporal and spatial expression of Cdx2 was evaluated in normal rat embryos (n = 303) and ARM embryos (n = 321) from GD13 to GD16. Immunohistochemical staining revealed that, in normal embryos, Cdx2 was mainly expressed on the epithelium of the urorectal septum (URS) and the hindgut on GD13. On GD14, Cdx2-immunopositive cells were extensively detected on the URS, hindgut, and cloacal membrane. On GD15, increased immunopositive tissue staining on the anal membrane was evident. In ARM embryos, the epithelium of the cloaca, URS, and anorectum were negative or faintly immunostaining for Cdx2. Analyses by Western blot and real-time reverse transcription plus the polymerase chain reaction revealed that, in the normal group, Cdx2 protein and mRNA expression showed time-dependent changes in the developing hindgut from GD13 to GD16. Upon the URS division of the cloaca into the primitive rectum and urogenital sinus (UGS) on GD15, Cdx2 expression began to decrease. Moreover, the Cdx2 expression level in the ARM group from GD13 to GD14 was significantly lower than that in the normal group (P < 0.05). In ARM embryos, an imbalance in the spatiotemporal expression of Cdx2 was noted during anorectal morphogenesis from GD13 to GD16. Downregulation of Cdx2 at the time of cloacal separation into the primitive rectum and UGS might thus be related to the development of ARM.
本研究的主要目的是确定正常胚胎和肛门直肠畸形(ARM)胚胎在肛门直肠发育过程中Cdx2的表达模式,以期明确Cdx2在ARM发病机制中的可能作用。在大鼠胚胎妊娠第10天(GD10)用乙硫脲诱导产生ARM,然后通过剖宫产获取胚胎。评估了从GD13到GD16正常大鼠胚胎(n = 303)和ARM胚胎(n = 321)中Cdx2的时空表达。免疫组织化学染色显示,在正常胚胎中,GD13时Cdx2主要表达于尿直肠隔(URS)和后肠的上皮。GD14时,在URS、后肠和泄殖腔膜上广泛检测到Cdx2免疫阳性细胞。GD15时,肛门膜上免疫阳性组织染色明显增加。在ARM胚胎中,泄殖腔、URS和肛门直肠的上皮对Cdx2呈阴性或弱阳性免疫染色。蛋白质免疫印迹分析以及实时逆转录聚合酶链反应分析显示,在正常组中,从GD13到GD16发育中的后肠内Cdx2蛋白和mRNA表达呈现时间依赖性变化。在GD15泄殖腔的URS分裂形成原始直肠和泌尿生殖窦(UGS)时,Cdx2表达开始下降。此外,ARM组从GD13到GD14的Cdx2表达水平显著低于正常组(P < 0.05)。在ARM胚胎中,从GD13到GD16的肛门直肠形态发生过程中,Cdx2的时空表达存在失衡。因此,在泄殖腔分离形成原始直肠和UGS时Cdx2的下调可能与ARM的发生有关。