Mashima Hirosato, Watanabe Noboru, Sekine Masanari, Matsumoto Satohiro, Asano Takeharu, Yuhashi Kazuhito, Sagihara Noriyoshi, Urayoshi Shunsuke, Uehara Takeshi, Fujiwara Junichi, Ishii Takehiro, Tsuboi Rumiko, Miyatani Hiroyuki, Ohnishi Hirohide
Department of Gastroenterology, Saitama Medical Center, Jichi Medical University, Saitama 330-8503, Japan.
Department of Gastroenterology, Akita University Graduate School of Medicine, Akita 010-8543, Japan.
Biochem Biophys Rep. 2018 Jan 28;13:93-98. doi: 10.1016/j.bbrep.2018.01.003. eCollection 2018 Mar.
Intestinal homeostasis and the coordinated actions of digestion, absorption and excretion are tightly regulated by a number of gastrointestinal hormones. Most of them exert their actions through G-protein-coupled receptors. Recently, we showed that the absence of Gα/Gα signaling impaired the maturation of Paneth cells, induced their differentiation toward goblet cells, and affected the regeneration of the colonic mucosa in an experimental model of colitis. Although an immunohistochemical study showed that Gα/Gα were highly expressed in enterocytes, it seemed that enterocytes were not affected in Int-G/G double knock-out intestine. Thus, we used an intestinal epithelial cell line to examine the role of signaling through Gα/Gα in enterocytes and manipulated the expression level of Gα and/or Gα. The proliferation was inhibited in IEC-6 cells that overexpressed Gα/Gα and enhanced in IEC-6 cells in which Gα/Gα was downregulated. The expression of T-cell factor 1 was increased according to the overexpression of Gα/Gα. The expression of Notch1 intracellular cytoplasmic domain was decreased by the overexpression of Gα/Gα and increased by the downregulation of Gα/Gα. The relative mRNA expression of , a goblet cell marker, was elevated in a Gα/Gα knock-down experiment. Our findings suggest that Gα/Gα-mediated signaling inhibits proliferation and may support a physiological function, such as absorption or secretion, in terminally differentiated enterocytes.
肠道内环境稳态以及消化、吸收和排泄的协同作用受到多种胃肠激素的严格调控。它们中的大多数通过G蛋白偶联受体发挥作用。最近,我们发现在结肠炎实验模型中,Gα/Gα信号缺失会损害潘氏细胞的成熟,诱导其向杯状细胞分化,并影响结肠黏膜的再生。尽管一项免疫组织化学研究表明Gα/Gα在肠上皮细胞中高表达,但在Int-G/G双敲除肠道中肠上皮细胞似乎未受影响。因此,我们使用一种肠上皮细胞系来研究通过Gα/Gα在肠上皮细胞中的信号传导作用,并调控Gα和/或Gα的表达水平。在过表达Gα/Gα的IEC-6细胞中增殖受到抑制,而在Gα/Gα下调的IEC-6细胞中增殖增强。T细胞因子1的表达随着Gα/Gα的过表达而增加。Notch1细胞内胞质结构域的表达随着Gα/Gα的过表达而降低,随着Gα/Gα的下调而增加。在Gα/Gα敲低实验中,杯状细胞标志物的相对mRNA表达升高。我们的研究结果表明,Gα/Gα介导的信号传导抑制增殖,并可能在终末分化的肠上皮细胞中支持诸如吸收或分泌等生理功能。