Department of Pathology, Wakayama Medical University School of Medicine, Wakayama, Japan.
Department of Physiology, Wakayama Medical University School of Medicine, Wakayama, Japan.
Am J Pathol. 2019 Apr;189(4):773-783. doi: 10.1016/j.ajpath.2019.01.006. Epub 2019 Jan 19.
Smad3 has circadian expression; however, whether Smad3 affects the expression of clock genes is poorly understood. Here, we investigated the regulatory mechanisms between Smad3 and the clock genes Dec1, Dec2, and Per1. In Smad3 knockout mice, the amplitude of locomotor activity was decreased, and Dec1 expression was decreased in the suprachiasmatic nucleus, liver, kidney, and tongue compared with control mice. Conversely, Dec2 and Per1 expression was increased compared with that of control mice. In Smad3 knockout mice, immunohistochemical staining revealed that Dec1 expression decreased, whereas Dec2 and Per1 expression increased in the endothelial cells of the kidney and liver. In NIH3T3 cells, Smad3 overexpression increased Dec1 expression, but decreased Dec2 and Per1 expression. In a wound-healing experiment that used Smad3 knockout mice, Dec1 expression decreased in the basal cells of squamous epithelium, promoting wound healing of the mucosa. Finally, the migration and proliferation of Smad3 knockdown squamous carcinoma cells was suppressed by Dec1 overexpression but was promoted by Dec2 overexpression. Dec1 overexpression decreased E-cadherin and proliferating cell nuclear antigen expression, whereas these expression levels were increased by Dec2 overexpression. These results suggest Smad3 is relevant to circadian rhythm and regulates cell migration and proliferation through Dec1, Dec2, and Per1 expression.
Smad3 具有昼夜节律表达;然而,Smad3 是否影响时钟基因的表达尚不清楚。在这里,我们研究了 Smad3 与时钟基因 Dec1、Dec2 和 Per1 之间的调节机制。在 Smad3 敲除小鼠中,与对照组小鼠相比,其运动活性的振幅降低,并且在视交叉上核、肝脏、肾脏和舌中的 Dec1 表达降低。相反,Dec2 和 Per1 的表达与对照组相比增加。在 Smad3 敲除小鼠中,免疫组织化学染色显示 Dec1 表达减少,而肾脏和肝脏内皮细胞中的 Dec2 和 Per1 表达增加。在 NIH3T3 细胞中,Smad3 过表达增加 Dec1 表达,但减少 Dec2 和 Per1 表达。在使用 Smad3 敲除小鼠的伤口愈合实验中,鳞状上皮的基底细胞中 Dec1 表达减少,促进了黏膜的伤口愈合。最后,Dec1 过表达抑制 Smad3 敲低的鳞状癌细胞的迁移和增殖,但 Dec2 过表达促进其迁移和增殖。Dec1 过表达降低了 E-钙黏蛋白和增殖细胞核抗原的表达,而 Dec2 过表达则增加了这些表达水平。这些结果表明 Smad3 与昼夜节律有关,并通过 Dec1、Dec2 和 Per1 的表达来调节细胞迁移和增殖。