Wright Karen, Rooney Nicholas, Feeney Mark, Tate Jeremy, Robertson Duncan, Welham Melanie, Ward Stephen
Department of Pharmacy and Pharmacology, University of Bath, UK.
Gastroenterology. 2005 Aug;129(2):437-53. doi: 10.1016/j.gastro.2005.05.026.
BACKGROUND & AIMS: Two G-protein-coupled cannabinoid receptors, termed CB1 and CB2, have been identified and several mammalian enteric nervous systems express CB1 receptors and produce endocannabinoids. An immunomodulatory role for the endocannabinoid system in gastrointestinal inflammatory disorders has been proposed and this study sought to determine the location of both cannabinoid receptors in human colon and to investigate epithelial receptor function.
The location of CB1 and CB2 receptors in human colonic tissue was determined by immunohistochemistry. Primary colonic epithelial cells were treated with both synthetic and endogenous cannabinoids in vitro, and biochemical coupling of the receptors to known signaling events was determined by immunoblotting. Human colonic epithelial cell lines were used in cannabinoid-binding studies and as a model for in vitro wound-healing experiments.
CB1-receptor immunoreactivity was evident in normal colonic epithelium, smooth muscle, and the submucosal myenteric plexus. CB1- and CB2-receptor expression was present on plasma cells in the lamina propria, whereas only CB2 was present on macrophages. CB2 immunoreactivity was seen in the epithelium of colonic tissue characteristic of inflammatory bowel disease. Cannabinoids enhanced epithelial wound closure either alone or in combination with lysophosphatidic acid through a CB1-lysophosphatidic acid 1 heteromeric receptor complex.
CB1 receptors are expressed in normal human colon and colonic epithelium is responsive biochemically and functionally to cannabinoids. Increased epithelial CB2-receptor expression in human inflammatory bowel disease tissue implies an immunomodulatory role that may impact on mucosal immunity.
已鉴定出两种G蛋白偶联大麻素受体,分别称为CB1和CB2,几种哺乳动物的肠神经系统表达CB1受体并产生内源性大麻素。有人提出内源性大麻素系统在胃肠道炎症性疾病中具有免疫调节作用,本研究旨在确定两种大麻素受体在人结肠中的位置,并研究上皮受体功能。
通过免疫组织化学确定CB1和CB2受体在人结肠组织中的位置。体外将原代结肠上皮细胞用合成和内源性大麻素处理,通过免疫印迹确定受体与已知信号事件的生化偶联。人结肠上皮细胞系用于大麻素结合研究,并作为体外伤口愈合实验的模型。
CB1受体免疫反应在正常结肠上皮、平滑肌和黏膜下肌间神经丛中明显。CB1和CB2受体表达存在于固有层浆细胞上,而巨噬细胞上仅存在CB2。在炎症性肠病特征性的结肠组织上皮中可见CB2免疫反应。大麻素单独或与溶血磷脂酸联合通过CB1-溶血磷脂酸1异源受体复合物增强上皮伤口闭合。
CB1受体在正常人结肠中表达,结肠上皮对大麻素具有生化和功能反应。人炎症性肠病组织中上皮CB2受体表达增加意味着可能影响黏膜免疫的免疫调节作用。