Naka Takahiro, Yokose Satoshi
Division of Restorative Dentistry, Department of Conservative Dentistry, Ohu University School of Dentistry, 31-1, Misumido, Koriyama, Fukushima 963-8611, Japan.
Acta Histochem Cytochem. 2009 Apr 28;42(2):47-53. doi: 10.1267/ahc.08027. Epub 2009 Mar 31.
The development of mouse submandibular gland (SMG) begins at embryonic day 11.5-12 (E11.5-12), during which successive rounds of epithelial clefting and branching create complex epithelial tree-like structures. Homeobox genes regulate place-dependent morphogenesis, including epithelial-mesenchymal interactions, and control the expression patterns of signaling molecules. The Barx2 containing Homeobox exerts several key roles in development. Some studies have shown that the Barx2 plays important roles in the epithelial-mesenchymal interactions of organogenesis. However, the mechanisms of Barx2 associated with the development of SMG are obscure. In this study, we demonstrated for the first time the exact spatial and temporal Barx2 expression pattern in SMG epithelial tissue during development using immunohistochemical staining and Real-Time quantitative PCR. Barx2 was expressed in the nucleus of the epithelial cells located in the proliferative and differentiative regions of the developing SMG during the early development stages (E11.5-E13.5). After the E14.5-time period, the expression gradually decreased, and at E16.5, expression mostly disappeared despite the fact that evidence of cytodifferentiation, such as the appearance of proacinar cells, distinct lumen formation, and secretory products, was beginning to be observed. Results of Real-Time PCR demonstrated that the amount of Barx2 mRNA expression in SMG was maximal on E14.5, and gradually decreased by E18.5. These results indicate that Barx2 is associated with early stage epithelial tissue development, and can be a useful epithelial marker of the SMG during early developmental stages.
小鼠下颌下腺(SMG)的发育始于胚胎第11.5 - 12天(E11.5 - 12),在此期间,连续几轮的上皮裂隙形成和分支产生了复杂的上皮树状结构。同源盒基因调节位置依赖性形态发生,包括上皮 - 间充质相互作用,并控制信号分子的表达模式。含有同源盒的Barx2在发育中发挥着几个关键作用。一些研究表明,Barx2在器官发生的上皮 - 间充质相互作用中起重要作用。然而,与SMG发育相关的Barx2机制尚不清楚。在本研究中,我们首次使用免疫组织化学染色和实时定量PCR证明了发育过程中SMG上皮组织中Barx2的确切时空表达模式。在早期发育阶段(E11.5 - E13.5),Barx2在发育中的SMG增殖和分化区域的上皮细胞核中表达。在E14.5时期之后,表达逐渐下降,并且在E16.5时,尽管开始观察到细胞分化的证据,如前腺泡细胞的出现、明显的管腔形成和分泌产物,但表达大多消失。实时PCR结果表明,SMG中Barx2 mRNA表达量在E14.5时最高,并在E18.5时逐渐下降。这些结果表明,Barx2与早期上皮组织发育相关,并且在早期发育阶段可以作为SMG有用的上皮标记物。