Chen Tiane, Hubbard Ann, Murtazina Rakhilya, Price Jennifer, Yang Jianbo, Cha Boyoung, Sarker Rafiquel, Donowitz Mark
Department of Medicine, Division of Gastroenterology and Hepatology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Department of Medicine, Division of Gastroenterology and Hepatology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
J Cell Sci. 2014 Aug 15;127(Pt 16):3535-45. doi: 10.1242/jcs.149930. Epub 2014 Jun 13.
The intestinal brush border Na(+)/H(+) exchanger NHE3 is tightly regulated through changes in its endocytosis and exocytosis. Myosin VI, a minus-end-directed actin motor, has been implicated in endocytosis at the inter-microvillar cleft and during vesicle remodeling in the terminal web. Here, we asked whether myosin VI also regulates NHE3 movement down the microvillus. The basal NHE3 activity and its surface amount, determined by fluorometry of the ratiometric pH indicator BCECF and biotinylation assays, respectively, were increased in myosin-VI-knockdown (KD) Caco-2/Bbe cells. Carbachol (CCH) and forskolin (FSK) stimulated NHE3 endocytosis in control but not in myosin VI KD cells. Importantly, immunoelectron microscopy results showed that NHE3 was preferentially localized in the basal half of control microvilli but in the distal half in myosin VI KD cells. Treatment with dynasore duplicated some aspects of myosin VI KD: it increased basal surface NHE3 activity and prevented FSK-induced NHE3 endocytosis. However, NHE3 had an intermediate distribution along the microvillus (between that in myosin VI KD and untreated cells) in dynasore-treated cells. We conclude that myosin VI is required for basal and stimulated endocytosis of NHE3 in intestinal cells, and suggest that myosin VI also moves NHE3 down the microvillus.
肠道刷状缘Na(+)/H(+)交换蛋白NHE3通过其胞吞作用和胞吐作用的变化受到严格调控。肌球蛋白VI是一种向负端移动的肌动蛋白马达,已被证明参与微绒毛间裂的胞吞作用以及终末网中囊泡重塑过程。在此,我们探究肌球蛋白VI是否也调控NHE3沿微绒毛的移动。分别通过比率型pH指示剂BCECF的荧光测定法和生物素化分析确定,在肌球蛋白VI敲低(KD)的Caco-2/Bbe细胞中,基础NHE3活性及其表面含量均增加。在对照细胞中,卡巴胆碱(CCH)和福斯可林(FSK)可刺激NHE3的胞吞作用,但在肌球蛋白VI KD细胞中则无此作用。重要的是,免疫电子显微镜结果显示,NHE3在对照微绒毛的基部半段优先定位,但在肌球蛋白VI KD细胞中则位于远端半段。用dynasore处理可重现肌球蛋白VI KD的某些方面:它增加了基础表面NHE3活性,并阻止了FSK诱导的NHE3胞吞作用。然而,在dynasore处理的细胞中,NHE3沿微绒毛呈中间分布(介于肌球蛋白VI KD细胞和未处理细胞之间)。我们得出结论,肌球蛋白VI是肠道细胞中NHE3基础和刺激型胞吞作用所必需的,并表明肌球蛋白VI也使NHE3沿微绒毛移动。