Williams A K, Qi B Q, Beasley S W
Department of Paediatric Surgery, Christchurch Hospital, Christchurch School of Medicine, New Zealand.
J Pediatr Surg. 2000 Nov;35(11):1617-20. doi: 10.1053/jpsu.2000.18331.
BACKGROUND/PURPOSE: Recent work has shown that apoptosis is a key component of the normal development of the foregut. This study was designed to compare the patterns of apoptosis in the normal foregut with those in the fetus developing esophageal atresia and tracheoesophageal fistula (EA-TEF) using 3-dimensional reconstructive techniques.
Timed pregnant rats that received no treatment (control group) or received Adriamycin intraperitoneally (experimental group) had their embryos removed between days 11 and 14 of gestation. The embryos were sectioned serially and stained with H&E. Three-dimensional reconstructions were made of the foregut and areas of apoptosis were marked on them to facilitate analysis of apoptotic patterns.
Apoptosis was evident in control embryos in the region in which tracheoesophageal separation occurs from days 12 and 12.5. Experimental embryos showed no apoptosis until day 13 when apoptosis was observed immediately posterior to the foregut within the esophageal mesenchyme and in the laryngeal mesenchyme ventral to the foregut.
The pattern, timing and location of apoptosis in rats developing EA-TEF is abnormal. Our work indicates that it is actually a complete lack of apoptosis at the crucial stage of development that leads to this abnormality rather than an alteration in the patterning of apoptosis at this crucial time. The observation of apoptosis only within the mesenchyme raises the possibility that apoptosis in the foregut developing EA-TEF may be a reaction to that abnormal development rather than its cause.
背景/目的:近期研究表明,细胞凋亡是前肠正常发育的关键组成部分。本研究旨在运用三维重建技术,比较正常前肠与患食管闭锁及食管气管瘘(EA-TEF)胎儿的前肠细胞凋亡模式。
将未接受治疗的定时妊娠大鼠(对照组)或腹腔注射阿霉素的大鼠(实验组)在妊娠第11至14天取出胚胎。胚胎连续切片并进行苏木精-伊红染色。对前肠进行三维重建,并在其上标记细胞凋亡区域,以利于分析凋亡模式。
对照组胚胎在第12天和12.5天食管气管分离区域可见明显细胞凋亡。实验组胚胎直到第13天才出现细胞凋亡,此时在前肠后方的食管间充质以及前肠腹侧的喉间充质中观察到细胞凋亡。
患EA-TEF大鼠的细胞凋亡模式、时间和位置均异常。我们的研究表明,实际上是发育关键阶段完全缺乏细胞凋亡导致了这种异常,而非关键时期细胞凋亡模式的改变。仅在间充质内观察到细胞凋亡,这增加了患EA-TEF的前肠中细胞凋亡可能是对异常发育的一种反应而非其原因的可能性。