Minakata Toshiya, Inagaki Akira, Yamamura Aya, Yamamura Hisao, Sekiya Shinji, Murakami Shingo
Department of Otolaryngology, Head and Neck Surgery, Graduate School of Medical Sciences and Medical School, Nagoya City University, Nagoya, Japan.
Department of Physiology, Aichi Medical University, Nagakute, Japan.
Front Mol Neurosci. 2019 Jul 16;12:175. doi: 10.3389/fnmol.2019.00175. eCollection 2019.
Maintaining Ca homeostasis in lymphatic fluids is necessary for proper hearing. Despite its significance, the mechanisms that maintain the cochlear lymphatic Ca concentrations within a certain range are not fully clarified. We investigated the functional expression of calcium-sensing receptor (CaSR), which plays a pivotal role in sensing extracellular Ca concentrations for feedback regulations. Western blotting for CaSR revealed an approximately 130-kDa protein expression in cochlear tissue extracts and immunohistochemical analysis revealed its expression specifically in type I fibrocytes in the spiral ligament, fibrocytes in the supralimbal and limbal regions, the epithelium of the osseous spiral lamina, and the smooth muscle cells of the spiral modiolar arteries. Ca imaging demonstrated that extracellular Ca increased the levels of intracellular Ca in CaSR-expressing fibrocytes in the spiral ligament, and that this was suppressed by the CaSR inhibitor, NPS2143. Furthermore, hearing thresholds were moderately elevated by intracochlear application of the CaSR inhibitors NPS2143 and Calhex231, across a range of frequencies (8-32 kHz). These results demonstrate the functional expression of CaSR in the cochlear perilymphatic compartment. In addition, the elevated hearing thresholds that are achieved by inhibiting CaSR suggest this is a required mechanism for normal hearing, presumably by sensing perilymphatic Ca to stabilize Ca concentrations within a certain range. These results provide novel insight into the mechanisms regulating Ca homeostasis in the cochlea and provide a new perspective on cochlear physiology.
维持淋巴液中的钙稳态对于正常听力至关重要。尽管其意义重大,但将耳蜗淋巴液中的钙浓度维持在一定范围内的机制尚未完全阐明。我们研究了钙敏感受体(CaSR)的功能表达,该受体在感知细胞外钙浓度以进行反馈调节中起关键作用。对CaSR进行蛋白质印迹分析显示,在耳蜗组织提取物中有一个约130 kDa的蛋白质表达,免疫组织化学分析显示其特异性表达于螺旋韧带中的I型纤维细胞、上缘和边缘区域的纤维细胞、骨螺旋板的上皮以及螺旋蜗轴动脉的平滑肌细胞中。钙成像表明,细胞外钙可增加螺旋韧带中表达CaSR的纤维细胞内的钙水平,而这被CaSR抑制剂NPS2143所抑制。此外,通过在耳蜗内应用CaSR抑制剂NPS2143和Calhex231,在一系列频率(8 - 32 kHz)范围内,听力阈值会适度升高。这些结果证明了CaSR在耳蜗外淋巴间隙中的功能表达。此外,抑制CaSR导致听力阈值升高,这表明这是正常听力所需的机制,可能是通过感知外淋巴钙以将钙浓度稳定在一定范围内。这些结果为调节耳蜗钙稳态的机制提供了新的见解,并为耳蜗生理学提供了新的视角。