Washington University School of Medicine, Department of Developmental Biology, 660 S. Euclid Avenue, St. Louis, MO 63110, USA.
J Neurophysiol. 2010 Dec;104(6):3439-50. doi: 10.1152/jn.00525.2010. Epub 2010 Jun 16.
Otopetrin 1 (OTOP1) is a multitransmembrane domain protein, which is essential for mineralization of otoconia, the calcium carbonate biominerals required for vestibular function, and the normal sensation of gravity. The mechanism driving mineralization of otoconia is poorly understood, but it has been proposed that supporting cells and a mechanism to maintain high concentrations of calcium are critical. Using Otop1 knockout mice and a utricular epithelial organ culture system, we show that OTOP1 is expressed at the apex of supporting cells and functions to increase cytosolic calcium in response to purinergic agonists, such as adenosine 5'-triphosphate (ATP). This is achieved by blocking mobilization of calcium from intracellular stores in an extracellular calcium-dependent manner and by mediating influx of extracellular calcium. These data support a model in which OTOP1 acts as a sensor of the extracellular calcium concentration near supporting cells and responds to ATP in the endolymph to increase intracellular calcium levels during otoconia mineralization.
耳石蛋白 1(OTOP1)是一种具有多个跨膜结构域的蛋白,对耳石的矿化、前庭功能所必需的碳酸钙生物矿化以及正常的重力感觉至关重要。耳石矿化的机制尚未完全阐明,但有研究提出,支持细胞及其维持高浓度钙的机制是关键。我们利用 Otop1 基因敲除小鼠和前庭上皮器官培养系统,证明 OTOP1 在支持细胞的顶端表达,并能在嘌呤能激动剂(如三磷酸腺苷,ATP)的刺激下增加细胞内钙。其实现方式是通过细胞外钙离子依赖的方式阻断细胞内钙库的钙动员,并介导细胞外钙内流。这些数据支持这样一种模型,即 OTOP1 作为支持细胞附近细胞外钙离子浓度的传感器,在耳石矿化过程中,对内淋巴中的 ATP 做出反应,以增加细胞内钙水平。