Department of Oral and Maxillofacial Surgery, Nihon University School of Dentistry, 1-8-13 Kanda-Surugadai, Chiyoda-ku, Tokyo, 101-8310, Japan.
J Mol Histol. 2012 Dec;43(6):751-9. doi: 10.1007/s10735-012-9437-8. Epub 2012 Jul 17.
Our study immunohistochemically evaluated the localization patterns of small Rho GTPases and β-catenin during regeneration of the rat submandibular gland. After 7 days of obstruction, regenerating glands were collected at days 0, 3, 7, 11 and 14 after duct release to study regeneration. RhoA was detected strongly and RhoC was detected weakly in the cytoplasm of newly formed acinar cells from day 3 to 7, and both RhoA and RhoC at the basal site and cytoplasm were detected moderately from day 11 to 14. RhoB was detected strongly and moderately in the cytoplasm of newly formed and matured acinar cells, respectively, and detected strongly in duct-like structures (DLSs) and intercalated ducts (ICDs). Rac1 was detected at the cell-cell and subcellular region, but β-catenin was not observed in newly formed acinar cells. Rac1 immunolabeling gradually reduced, and the β-catenin staining pattern became stronger. p-Rac1, a phosphorylated form of Rac1, was observed in the cytoplasm of newly formed acinar cells. At apical and subcellular region of DLSs and ICDs, Rac1 and β-catenin were detected. These findings suggest that RhoA and RhoC might be involved in the actin cytoskeleton at the basolateral site of regenerating acinar cells, and RhoB might play a unique role in regenerating acinar cells and in DLSs and ICDs. Rac1 and β-catenin at the cell-cell region might play important roles in cell-cell adhesion and the differentiation of regenerating acinar cells, as well as actin reconstruction at apical and subcellular regions of DLSs and ICDs.
我们通过免疫组织化学方法研究了小 Rho GTPases 和β-连环蛋白在大鼠下颌下腺再生过程中的定位模式。在阻塞 7 天后,在导管释放后的第 0、3、7、11 和 14 天收集再生腺体,以研究再生。在第 3 至 7 天,新形成的腺泡细胞的细胞质中检测到强烈的 RhoA 和弱的 RhoC,而从第 11 至 14 天,基底和细胞质中均检测到中度的 RhoA 和 RhoC。RhoB 在新形成和成熟的腺泡细胞的细胞质中均被强烈和中度检测到,并且在管状结构(DLSs)和中间导管(ICDs)中被强烈检测到。Rac1 被检测到在细胞-细胞和亚细胞区域,但β-连环蛋白未在新形成的腺泡细胞中被检测到。Rac1 免疫标记逐渐减少,β-连环蛋白染色模式变得更强。磷酸化形式的 Rac1(p-Rac1)被观察到在新形成的腺泡细胞的细胞质中。在 DLSs 和 ICDs 的顶端和亚细胞区域,检测到 Rac1 和β-连环蛋白。这些发现表明,RhoA 和 RhoC 可能参与再生腺泡细胞的基底外侧部位的肌动蛋白细胞骨架,而 RhoB 可能在再生腺泡细胞和 DLSs 和 ICDs 中发挥独特作用。细胞-细胞区域的 Rac1 和β-连环蛋白可能在细胞-细胞黏附和再生腺泡细胞的分化中发挥重要作用,以及 DLSs 和 ICDs 的顶端和亚细胞区域的肌动蛋白重构。