Department of Histology and Embryology, Shanxi Medical University, Taiyuan, China.
Dis Esophagus. 2012 Jan;25(1):10-6. doi: 10.1111/j.1442-2050.2011.01208.x. Epub 2011 May 19.
Muscularis externa of mouse esophagus is composed of two skeletal muscle layers in the adult. But less attention is paid to the histogenesis of the muscularis externa of the esophagus, and controversies still exist about the developmental process and the spatio-temporal expression characteristics of muscle-specific proteins during the development of esophageal muscularis externa. To further probe into the developmental pattern of muscularis externa of the mouse esophagus and the expression characteristics of different muscle-specific proteins, immunohistochemical and terminal deoxyribonucleotidyl transferase-mediated deoxyuridine triphosphate (dUTP)-digoxigenin nick-end labeling apoptotic staining methods are used to investigate the expression patterns of different muscle-specific proteins and to elucidate the relationship of these protein expressions with the development of muscularis externa of the mouse esophagus. Thus, an understanding of the developing esophageal muscularis externa may be important for developing therapeutic strategies for the treatment of human esophagus diseases. Serial sections of mouse embryos from embryonic day (ED) 12 to ED18, and full-length esophagi from postnatal first to 5th day were stained with monoclonal antibodies against α-smooth muscle actin (α-SMA), α-sarcomerical actin (α-SCA), desmin, and monoclonal anti-skeletal myosin (MHC), while apoptosis was determined using the terminal deoxyribonucleotidyl transferase-mediated dUTP-digoxigenin nick-end labeling assay. The expression of α-SMA was started at ED12. During the development of ED14-ED15, α-SMA positive cells were seen extending from the walls of left three, four, and six arch arteries toward the dorsal wall of esophagus. Stronger expression of α-SCA and desmin could be detected at ED14 and ED15, expression intensity in caudal segment and inner layer was stained stronger than that of cranial segment and outer layer, but after ED16, strong expression of α-SCA and desmin was found in the outer layer of muscularis externa. Expression of MHC was first detected in the outer layer of cranial segment of muscularis externa at ED17. At ED18, MHC had extended to the level of thyroid gland, staining intensity in the outer layer and cranial segment was stronger than that of inner layer and caudal segment. One to five days after birth, the thickness of the esophageal muscle layer was obviously increased. Most of the muscle cells in the cranial segment of esophagus showed strong expression of α-SCA and clear cross striations at higher magnification. With progression toward the caudal segment, expression intensity of α-SCA became weaker, but the expression intensity of desmin was the same at different levels of esophagus. The muscle fibers were arranged densely with high expression of MHC in the cranial segment. During the development of esophageal muscularis externa, few apoptotic cells were observed. α-SMA, α-SCA, desmin, and MHC show different expression patterns. The differentiation of outer layer of esophageal muscularis externa is quicker than that of inner layer, and the caudal segment is quicker than that of the cranial segment. Besides, apoptosis may not participate in the development of esophageal muscularis externa. The smooth muscle cells from arch arteries may participate in the development of esophageal muscularis externa.
鼠标食道的外肌由成年时的两层骨骼肌组成。但是,人们对外食道外肌的组织发生学关注较少,对于食道外肌发育过程中肌肉特异性蛋白的时空表达特征仍然存在争议。为了进一步探讨鼠标食道外肌的发育模式和不同肌肉特异性蛋白的表达特征,我们采用免疫组织化学和末端脱氧核苷酸转移酶介导的脱氧尿苷三磷酸(dUTP)-地高辛切口末端标记法检测不同肌肉特异性蛋白的表达模式,并阐明这些蛋白表达与鼠标食道外肌发育的关系。因此,了解发育中的食道外肌对于开发治疗人类食道疾病的治疗策略可能很重要。我们对来自胚胎期第 12 天(ED)至第 18 天的小鼠胚胎和出生后第 1 至第 5 天的全长食道进行了连续切片,并用抗α-平滑肌肌动蛋白(α-SMA)、α-横纹肌肌动蛋白(α-SCA)、结蛋白和抗骨骼肌肌球蛋白(MHC)的单克隆抗体进行染色,同时使用末端脱氧核苷酸转移酶介导的 dUTP-地高辛切口末端标记法检测细胞凋亡。α-SMA 的表达始于 ED12。在 ED14-ED15 发育期间,可见α-SMA 阳性细胞从左三、四、六弓动脉的壁向食道背壁延伸。在 ED14 和 ED15 可以检测到更强的α-SCA 和结蛋白表达,尾部和内层的染色强度比头部和外层强,但在 ED16 之后,外肌层中可以检测到强的α-SCA 和结蛋白表达。MHC 的表达在 ED17 时首次在外层的头部食道外肌中检测到。在 ED18 时,MHC 已经延伸到甲状腺水平,外层和头部的染色强度比内层和尾部强。出生后 1 至 5 天,食道肌层厚度明显增加。食道头部的大多数肌肉细胞都表现出强烈的α-SCA 表达,在高倍镜下显示出清晰的横纹。随着向尾部的推进,α-SCA 的表达强度减弱,但不同水平的食道中结蛋白的表达强度相同。头部的肌肉纤维排列密集,MHC 表达较高。在外食道外肌的发育过程中,观察到很少的凋亡细胞。α-SMA、α-SCA、结蛋白和 MHC 表现出不同的表达模式。食道外肌的外层分化比内层快,尾部比头部快。此外,凋亡可能不参与食道外肌的发育。弓动脉的平滑肌细胞可能参与食道外肌的发育。