Department of Diagnostic and Biomedical Sciences, University of Texas Health Science Center School of Dentistry, Houston, Texas, United States of America.
PLoS One. 2013;8(2):e56436. doi: 10.1371/journal.pone.0056436. Epub 2013 Feb 25.
Roquin, an E3 ubiquitin ligase that localizes to cytosolic RNA granules, is involved in regulating mRNA stability and translation. Mice that have a M199R mutation in the Roquin protein (referred to as sanroque or Roquin(san/san) mice) develop autoimmune pathologies, although the extent to which these occur in the intestinal mucosa has not been determined. Here, we demonstrate that Roquin(san/san) mice reproducibly develop intestinal inflammation in the small intestine but not the colon. Similarly, mice generated in our laboratory in which the Roquin gene was disrupted by insertion of a gene trap cassette (Roquin(gt/gt) mice) had small intestinal inflammation that mimicked that of Roquin(san/san) mice. MLN cells in Roquin(san/san) mice consisted of activated proliferating T cells, and had increased numbers of CD44(hi) CD62L(lo) KLRG1(+) short-lived effector cells. Proportionally more small intestinal intraepithelial lymphocytes in Roquin(san/san) mice expressed the ICOS T cell activation marker. Of particular interest, small intestinal lamina propria lymphocytes in Roquin(san/san) mice consisted of a high proportion of Gr-1(+) T cells that included IL-17A(+) cells and CD8(+) IFN-γ(+) cells. Extensive cytokine dysregulation resulting in both over-expression and under-expression of chemotactic cytokines occurred in the ileum of Roquin(san/san) mice, the region most prone to the development of inflammation. These findings demonstrate that chronic inflammation ensues in the intestine following Roquin alteration either as a consequence of protein mutation or gene disruption, and they have implications for understanding how small intestinal inflammation is perpetuated in Crohn's disease (CD). Due to the paucity of animal models of CD-like pathophysiology in the small intestine, and because the primary gene/protein defects of the Roquin animal systems used here are well-defined, it will be possible to further elucidate the underlying genetic and molecular mechanisms that drive the disease process.
Roquin 是一种定位于细胞质 RNA 颗粒的 E3 泛素连接酶,参与调节 mRNA 的稳定性和翻译。在 Roquin 蛋白中具有 M199R 突变的小鼠(称为 sanroque 或 Roquin(san/san) 小鼠)会发展出自免疫病理学,但尚未确定这些病理学在肠道黏膜中的程度。在这里,我们证明 Roquin(san/san) 小鼠在小肠中可重复性地发展为肠道炎症,但不在结肠中。同样,我们实验室中通过插入基因陷阱盒破坏 Roquin 基因的小鼠(Roquin(gt/gt) 小鼠)也具有模仿 Roquin(san/san) 小鼠的小肠炎症。Roquin(san/san) 小鼠的 MLN 细胞由活化增殖的 T 细胞组成,并且具有更多数量的 CD44(hi) CD62L(lo) KLRG1(+) 短寿命效应细胞。Roquin(san/san) 小鼠的肠道上皮内淋巴细胞中比例更高的表达 ICOS T 细胞激活标记物。特别有趣的是,Roquin(san/san) 小鼠的小肠固有层淋巴细胞由高比例的 Gr-1(+) T 细胞组成,其中包括 IL-17A(+) 细胞和 CD8(+) IFN-γ(+) 细胞。Roquin(san/san) 小鼠的回肠中发生了广泛的细胞因子失调,导致趋化因子细胞因子的过度表达和表达不足,这是炎症最易发生的区域。这些发现表明,无论是由于蛋白质突变还是基因缺失导致 Roquin 改变,肠道都会随之发生慢性炎症,这对于理解克罗恩病 (CD) 中小肠炎症的持续存在具有重要意义。由于小肠中类似 CD 的病理生理学的动物模型很少,并且由于这里使用的 Roquin 动物系统的主要基因/蛋白缺陷定义明确,因此可以进一步阐明驱动疾病过程的潜在遗传和分子机制。