Montufar-Solis Dina, Williams Alexander, Vigneswaran Nadarajah, Klein John R
Department of Diagnostic and Biomedical Sciences, School of Dentistry, University of Texas Health Science Center at Houston, Houston TX, USA.
Department of Diagnostic and Biomedical Sciences, School of Dentistry, University of Texas Health Science Center at Houston, Houston TX, USA.
Biochem Biophys Res Commun. 2017 Jan 29;483(1):590-595. doi: 10.1016/j.bbrc.2016.12.099. Epub 2016 Dec 21.
Roquin is an E3 ligase that regulates mRNA stability. Mice with a mutation in the Rc3h1 gene and Roquin protein, referred to as Roquin or sanroque mice, develop broad-spectrum chronic inflammatory conditions and autoimmune pathologies. Our laboratory recently reported that sanroque mice also develop extensive inflammation that is localized in the small intestine but is rare in the colon. Here, we demonstrate that small intestinal intraepithelial lymphocytes (IELs) are present in the epithelium of sanroque mice but that cell recoverability is low using standard extraction techniques even though lamina propria lymphocytes (LPLs) can be recovered in normal numbers. In studies aimed at characterizing T cell costimulatory markers and activation molecules on LPLs in sanroque mice, we identified Ly6C and 4-1BB (CD137) as being expressed at elevated levels on sanroque small intestinal LPLs, and we show that both of those subsets, in conjunction with cells expressing the KLRG1 T cell activation molecule, are sources of IL-17A, IFN-γ, and TNFα. TNFα was primarily produced by 4-1BB+, KLRG1-cells, but was also made by some 4-1BB-, KLRG1-cells, and 4-1BB-, KLRG1+ cells. These findings collectively suggest that the small intestinal inflammatory response in sanroque mice is driven, at least in part, by LPL activation through Ly6C and 4-1BB signaling, and they provide further evidence in support of using the sanroque mouse as an animal model of chronic small intestinal inflammation.
Roquin是一种调节mRNA稳定性的E3连接酶。Rc3h1基因和Roquin蛋白发生突变的小鼠,即Roquin或sanroque小鼠,会出现广谱慢性炎症和自身免疫性病变。我们实验室最近报道,sanroque小鼠还会在小肠出现广泛炎症,但在结肠中很少见。在这里,我们证明sanroque小鼠的小肠上皮内淋巴细胞(IELs)存在于上皮中,但即使固有层淋巴细胞(LPLs)能够正常数量回收,使用标准提取技术回收IELs细胞的能力也很低。在旨在表征sanroque小鼠LPLs上的T细胞共刺激标志物和激活分子的研究中,我们发现Ly6C和4-1BB(CD137)在sanroque小鼠小肠LPLs上的表达水平升高,并且我们表明这两个亚群,与表达KLRG1 T细胞激活分子的细胞一起,是IL-17A、IFN-γ和TNFα的来源。TNFα主要由4-1BB +、KLRG1 -细胞产生,但也由一些4-1BB -、KLRG1 -细胞和4-1BB -、KLRG1 +细胞产生。这些发现共同表明,sanroque小鼠的小肠炎症反应至少部分是由通过Ly6C和4-1BB信号传导的LPL激活驱动的,并且它们提供了进一步的证据支持将sanroque小鼠用作慢性小肠炎症的动物模型。