Shi Xiaorui
Department of Otolaryngology and Head and Neck Surgery, Oregon Hearing Research Center, Oregon Health and Science University, Portland, Oregon 97239-3098, USA. Institute of Microcirculation, Chinese Academy of MedicalSciences (CAMS) & Peking Union Medical College(PUMC), 5 Dong Dan San Tiao, Beijing, 100005, China.
Am J Pathol. 2009 May;174(5):1692-704. doi: 10.2353/ajpath.2009.080739. Epub 2009 Apr 6.
This study explored the effect of acoustic trauma on cochlear pericytes. Transmission electron microscopy revealed that pericytes on capillaries of the stria vascularis were closely associated with the endothelium in both control guinea pigs and mice. Pericyte foot processes were tightly positioned adjacent to endothelial cells. Exposure to wide-band noise at a level of 120 dB for 3 hours per day for 2 consecutive days produced a significant hearing threshold shift and structurally damaged blood vessels in the stria vascularis. Additionally, the serum protein, IgG, was observed to leak from capillaries of the stria vascularis, and pericytes lost their tight association with endothelial cells. Levels of the pericyte structural protein, desmin, substantially increased after noise exposure in both guinea pigs and mice with a corresponding increase in pericyte coverage of vessels. Increased expression levels of desmin were associated with the induction of hypoxia inducible factor (HIF)-1alpha and the up-regulation of vascular endothelial growth factor (VEGF). Inhibition of HIF-1alpha activity caused a decrease in VEGF expression levels in stria vascularis vessels. Blockade of VEGF activity with SU1498, a VEGF receptor inhibitor, significantly attenuated the expression of desmin in pericytes. These data demonstrate that cochlear pericytes are markedly affected by acoustic trauma and display an abnormal morphology. HIF-1alpha activation and VEGF up-regulation are important factors for the alteration of the pericyte structural protein desmin.
本研究探讨了声损伤对耳蜗周细胞的影响。透射电子显微镜显示,在对照豚鼠和小鼠中,血管纹毛细血管上的周细胞与内皮细胞紧密相连。周细胞足突紧密地位于内皮细胞相邻处。连续2天每天暴露于120 dB的宽带噪声3小时,导致显著的听力阈值偏移和血管纹结构受损的血管。此外,观察到血清蛋白IgG从血管纹的毛细血管中渗漏,周细胞与内皮细胞失去紧密联系。在豚鼠和小鼠中,噪声暴露后周细胞结构蛋白结蛋白的水平显著增加,血管周细胞覆盖率相应增加。结蛋白表达水平的增加与缺氧诱导因子(HIF)-1α的诱导和血管内皮生长因子(VEGF)的上调有关。抑制HIF-1α活性导致血管纹血管中VEGF表达水平降低。用VEGF受体抑制剂SU1498阻断VEGF活性,显著减弱了周细胞中结蛋白的表达。这些数据表明,耳蜗周细胞受到声损伤的显著影响,并呈现异常形态。HIF-1α激活和VEGF上调是周细胞结构蛋白结蛋白改变的重要因素。