Sutherland Kate, Young Richard L, Cooper Nicole J, Horowitz Michael, Blackshaw L Ashley
Discipline of Physiology, School of Molecular and Biomedical Sciences, University of Adelaide, Australia.
Am J Physiol Gastrointest Liver Physiol. 2007 May;292(5):G1420-8. doi: 10.1152/ajpgi.00504.2006. Epub 2007 Feb 8.
Nutrient-evoked gastrointestinal reflexes are likely initiated by specialized epithelial cells located in the small intestine that detect luminal stimuli and release mediators that activate vagal endings. The G-protein alpha-gustducin, a key signal molecule in lingual taste detection, has been identified in mouse small intestine, where it may also subserve nutrient detection; however, the phenotype of alpha-gustducin cells is unknown. Immunohistochemistry was performed throughout the mouse small intestine for alpha-gustducin, enteroendocrine cell markers 5-HT and glucagon-like peptide-1 (GLP-1), and brush cell markers neuronal nitric oxide synthase and Ulex europaeus agglutinin-1 (UEA-1) lectin binding, singly, and in combination. alpha-Gustducin was expressed in solitary epithelial cells of the mid to upper villus, which were distributed in a regional manner with most occurring within the midjejunum. Here, 27% of alpha-gustducin cells colabeled for 5-HT and 15% for GLP-1; 57% of alpha-gustducin cells colabeled UEA-1, with no triple labeling. alpha-Gustducin cells that colabeled for 5-HT or GLP-1 were of distinct morphology and exhibited a different alpha-gustducin immunolabeling pattern to those colabeled with UEA-1. Neuronal nitric oxide synthase was absent from intestinal epithelium despite strong labeling in the myenteric plexus. We conclude that subsets of enteroendocrine cells in the midjejunum and brush cells (more generally distributed) are equipped to utilize alpha-gustducin signaling in mice. Intestinal taste modalities may be signaled by these enteroendocrine cells via the release of 5-HT, GLP-1, or coexpressed mediators or by brush cells via a nonnitrergic mediator in distinct regions of the intestine.
营养物质诱发的胃肠反射可能由位于小肠的特化上皮细胞启动,这些细胞检测肠腔刺激并释放激活迷走神经末梢的介质。G蛋白α-味导素是舌味觉检测中的关键信号分子,已在小鼠小肠中被鉴定出来,它在小肠中可能也参与营养物质的检测;然而,α-味导素细胞的表型尚不清楚。对小鼠整个小肠进行免疫组织化学检测,分别及联合检测α-味导素、肠内分泌细胞标志物5-羟色胺(5-HT)和胰高血糖素样肽-1(GLP-1),以及刷细胞标志物神经元型一氧化氮合酶和荆豆凝集素-1(UEA-1)凝集素结合情况。α-味导素在绒毛中上部的单个上皮细胞中表达,其分布具有区域特征,大多数位于空肠中部。在此处,27%的α-味导素细胞与5-HT共标记,15%与GLP-1共标记;57%的α-味导素细胞与UEA-1共标记,无三重标记。与5-HT或GLP-1共标记的α-味导素细胞具有独特的形态,并且与与UEA-1共标记的细胞呈现不同的α-味导素免疫标记模式。尽管肌间神经丛有强烈标记,但肠上皮中不存在神经元型一氧化氮合酶。我们得出结论,空肠中部的肠内分泌细胞亚群和刷细胞(分布更广泛)具备在小鼠中利用α-味导素信号传导的能力。肠道味觉模式可能由这些肠内分泌细胞通过释放5-HT、GLP-1或共表达的介质发出信号,或者由刷细胞通过肠道不同区域的非一氧化氮能介质发出信号。