Psichas Arianna, Tolhurst Gwen, Brighton Cheryl A, Gribble Fiona M, Reimann Frank
Metabolic Research Laboratories and MRC Metabolic Diseases Unit, Wellcome Trust-MRC Institute of Metabolic Science, University of Cambridge.
Metabolic Research Laboratories and MRC Metabolic Diseases Unit, Wellcome Trust-MRC Institute of Metabolic Science, University of Cambridge;
J Vis Exp. 2017 Apr 20(122):55687. doi: 10.3791/55687.
The gut is the largest endocrine organ of the body, with hormone-secreting enteroendocrine cells located along the length of the gastrointestinal epithelium. Despite their physiological importance, enteroendocrine cells represent only a small fraction of the epithelial cell population and in the past, their characterization has presented a considerable challenge resulting in a reliance on cell line models. Here, we provide a detailed protocol for the isolation and culture of mixed murine small intestinal cells. These primary cultures have been used to identify the signaling pathways underlying the stimulation and inhibition of gut peptide secretion in response to a number of nutrients and neuropeptides as well as pharmacological agents. Furthermore, in combination with the use of transgenic fluorescent reporter mice, we have demonstrated that these primary cultures become a powerful tool for the examination of fluorescently-tagged enteroendocrine cells at the intracellular level, using methods such as patch clamping and single-cell calcium and cAMP-FRET imaging.
肠道是人体最大的内分泌器官,沿胃肠道上皮全长分布着分泌激素的肠内分泌细胞。尽管它们具有重要的生理功能,但肠内分泌细胞仅占上皮细胞群体的一小部分,而且过去对它们的特性描述面临着相当大的挑战,导致人们依赖细胞系模型。在此,我们提供了一份详细的方案,用于分离和培养混合的小鼠小肠细胞。这些原代培养物已被用于确定在多种营养素、神经肽以及药物作用下,肠道肽分泌的刺激和抑制所涉及的信号通路。此外,结合使用转基因荧光报告小鼠,我们已经证明,这些原代培养物成为了一种强大的工具,可通过膜片钳、单细胞钙成像以及cAMP - FRET成像等方法,在细胞内水平检测荧光标记的肠内分泌细胞。