Schrott A, Stephan K, Spoendlin H
Department of Otolaryngology, University of Innsbruck, Austria.
Eur Arch Otorhinolaryngol. 1990;247(1):8-11. doi: 10.1007/BF00240940.
Mutant animals with a particular type of cochlear pathology are an excellent model for studying the functional role of various cells of the cochlea. In homozygous WV/WV mutant mice we found a selective loss of outer hair cells as a constant defect with no progressive degeneration of the organ of Corti. The mice were followed throughout their lives and exhibited auditory brainstem responses that were elevated to about 50 dB SPL as compared to normal control animals. Sequential temporal bone studies showed that there was a selective loss of outer hair cells throughout the entire cochlea as seen in surface preparations. The inner hair cells were present in normal numbers and appeared to be essentially normal.
具有特定类型耳蜗病理的突变动物是研究耳蜗各种细胞功能作用的优秀模型。在纯合WV/WV突变小鼠中,我们发现外毛细胞选择性缺失是一个持续存在的缺陷,柯蒂氏器无进行性退变。对这些小鼠进行了终生跟踪,发现与正常对照动物相比,它们的听觉脑干反应升高至约50 dB SPL。颞骨的连续研究表明,如在表面标本中所见,整个耳蜗外毛细胞均有选择性缺失。内毛细胞数量正常,外观基本正常。