Unit of Signal Transduction and Gastrointestinal Cancer, Division of Digestive Diseases, Department of Medicine, CURE, Digestive Diseases Research Center, Molecular Biology Institute and Jonsson Comprehensive Cancer Center, David Geffen School of Medicine, University of California at Los Angeles, California 90095-1786, USA.
J Cell Physiol. 2010 Oct;225(1):73-83. doi: 10.1002/jcp.22198.
The extracellular Ca(2+)-sensing receptor (CaR) is increasingly implicated in the regulation of multiple cellular functions in the gastrointestinal tract, including secretion, proliferation and differentiation of intestinal epithelial cells. However, the signaling mechanisms involved remain poorly defined. Here we examined signaling pathways activated by the CaR, including Ca(2+) oscillations, in individual human colon epithelial cells. Single cell imaging of colon-derived cells expressing the CaR, including SW-480, HT-29, and NCM-460 cells, shows that stimulation of this receptor by addition of aromatic amino acids or by an elevation of the extracellular Ca(2+) concentration promoted striking intracellular Ca(2+) oscillations. The intracellular calcium oscillations in response to extracellular Ca(2+) were of sinusoidal pattern and mediated by the phospholipase C/diacylglycerol/inositol 1,4,5-trisphosphate pathway as revealed by a biosensor that detects the accumulation of diacylglycerol in the plasma membrane. The intracellular calcium oscillations in response to aromatic amino acids were of transient type, that is, Ca(2+) spikes that returned to baseline levels, and required an intact actin cytoskeleton, a functional Rho, Filamin A and the ion channel TRPC1. Further analysis showed that re-expression and stimulation of the CaR in human epithelial cells derived from normal colon and from colorectal adenocarcinoma inhibits their proliferation. This inhibition was associated with the activation of the signaling pathway that mediates the generation of sinusoidal, but not transient, intracellular Ca(2+) oscillations. Thus, these results indicate that the CaR can function in two signaling modes in human colonic epithelial cells offering a potential link between gastrointestinal responses and food/nutrients uptake and metabolism.
细胞外钙敏感受体(CaR)越来越多地参与胃肠道多种细胞功能的调节,包括肠道上皮细胞的分泌、增殖和分化。然而,涉及的信号机制仍未完全确定。在这里,我们研究了 CaR 激活的信号通路,包括单个结肠上皮细胞中的 Ca2+振荡。表达 CaR 的结肠衍生细胞(包括 SW-480、HT-29 和 NCM-460 细胞)的单细胞成像表明,通过添加芳香族氨基酸或升高细胞外 Ca2+浓度刺激该受体,可促进显著的细胞内 Ca2+振荡。细胞外 Ca2+响应的细胞内钙振荡呈正弦波模式,并通过检测质膜中二酰基甘油积累的生物传感器揭示,由 PLC/diacylglycerol/inositol 1,4,5-trisphosphate 途径介导。对芳香族氨基酸的响应的细胞内钙振荡为瞬时型,即 Ca2+ 尖峰恢复到基线水平,需要完整的肌动蛋白细胞骨架、功能性 Rho、Filamin A 和离子通道 TRPC1。进一步分析表明,在源自正常结肠和结直肠腺癌的人上皮细胞中重新表达和刺激 CaR 可抑制其增殖。这种抑制与介导产生正弦波但不产生瞬时细胞内 Ca2+振荡的信号通路的激活有关。因此,这些结果表明 CaR 可以在人结肠上皮细胞中以两种信号模式发挥作用,为胃肠道反应与食物/营养物质摄取和代谢之间提供了潜在联系。