Division of Digestive Diseases, Emory University School of Medicine, Atlanta, Georgia.
Division of Digestive Diseases, Emory University School of Medicine, Atlanta, Georgia; Winship Cancer Institute, Emory University School of Medicine, Atlanta, Georgia; Atlanta Veterans Administration Medical Center, Decatur, Georgia.
Am J Pathol. 2018 Feb;188(2):353-366. doi: 10.1016/j.ajpath.2017.10.006. Epub 2017 Nov 9.
Intestinal epithelial cells form a barrier that is critical in protecting the host from the hostile luminal environment. Previously, we showed that lysophosphatidic acid (LPA) receptor 1 regulates proliferation of intestinal epithelial cells, such that the absence of LPA1 mitigates the epithelial wound healing process. This study provides evidence that LPA1 is important for the maintenance of epithelial barrier integrity. The epithelial permeability, determined by fluorescently labeled dextran flux and transepithelial resistance, is increased in the intestine of mice with global deletion of Lpar1, Lpar1 (Lpa1). Serum liposaccharide level and bacteria loads in the intestinal mucosa and peripheral organs were elevated in Lpa1 mice. Decreased claudin-4, caudin-7, and E-cadherin expression in Lpa1 mice further suggested defective apical junction integrity in these mice. Regulation of LPA1 expression in Caco-2 cells modulated epithelial permeability and the expression levels of junctional proteins. The increased epithelial permeability in Lpa1 mice correlated with increased susceptibility to an experimental model of colitis. This resulted in more severe inflammation and increased mortality compared with control mice. Treatment of Caco-2 cells with tumor necrosis factor-α and interferon-γ significantly increased paracellular permeability, which was blocked by cotreatment with LPA, but not LPA1 knockdown cells. Similarly, orally given LPA blocked tumor necrosis factor-mediated intestinal barrier defect in mice. LPA1 plays a significant role in maintenance of epithelial barrier in the intestine via regulation of apical junction integrity.
肠上皮细胞形成一道屏障,对于保护宿主免受腔道内恶劣环境的影响至关重要。此前我们已经证实,溶血磷脂酸(LPA)受体 1 调节肠上皮细胞的增殖,因此缺乏 LPA1 可减轻上皮细胞的伤口愈合过程。本研究提供了证据表明,LPA1 对于维持上皮屏障完整性非常重要。通过荧光标记的葡聚糖通量和跨上皮电阻来确定上皮通透性,发现 Lpar1 基因敲除(Lpar1)和 Lpar1 全身性缺失(Lpa1)的小鼠肠上皮通透性增加。Lpa1 小鼠血清中脂多糖水平和肠道黏膜及外周器官中的细菌载量升高。Lpa1 小鼠中 Claudin-4、Claudin-7 和 E-cadherin 的表达减少进一步表明这些小鼠的顶端连接完整性存在缺陷。Caco-2 细胞中 LPA1 表达的调节可调节上皮通透性和连接蛋白的表达水平。Lpa1 小鼠的上皮通透性增加与对结肠炎实验模型的易感性增加相关,与对照小鼠相比,其炎症更严重,死亡率更高。用肿瘤坏死因子-α和干扰素-γ处理 Caco-2 细胞可显著增加细胞旁通透性,而用 LPA 共同处理可阻断这种通透性增加,但用 LPA1 敲低细胞处理则不能阻断。同样,口服给予 LPA 可阻断肿瘤坏死因子介导的小鼠肠道屏障缺陷。LPA1 通过调节顶端连接的完整性在维持肠道上皮屏障中发挥重要作用。