Zheng J L, Gao W Q
Department of Neuroscience, Genentech, Inc., South San Francisco, CA 94080, USA>
J Neurobiol. 1999 Apr;39(1):29-40.
Degeneration of hair cells and spiral ganglion neurons due to acoustic trauma and various ototoxins is a major cause of hearing loss. Although our previous study demonstrates that specific neurotrophins protect spiral ganglion neurons from ototoxic insult, they do not protect hair cells. In the present experiments, we used postnatal rat cochlear explant cultures to identify molecules that protect hair cells from ototoxic damage. Of 51 compounds examined, only concanavalin A (Con A) significantly protected hair cells from gentamicin. A dose-dependent study of Con A showed that maximal protection occurred at 100 nM. The protective effects of Con A on hair cells were confirmed with confocal microscopy and paraffin sectioning of the cultures. Several experiments were performed to examine the mechanism of protection by Con A. Incubation of Con A with gentamicin did not form a complex and coaddition of Con A and gentamicin to Escherichia coli cultures did not interfere with the antibiotic activity of gentamicin. However, Lyso-Tracker staining and gentamicin immunocytochemistry provided evidence that preincubation with Con A blocked gentamicin uptake into hair cells. Considered together, these findings may help elucidate the ototoxic mechanism of aminoglycoside antibiotics, and suggest that Con A may be of therapeutic value in prevention of aminoglycoside-induced hearing loss.
由于声学创伤和各种耳毒性药物导致的毛细胞和螺旋神经节神经元变性是听力损失的主要原因。尽管我们之前的研究表明特定的神经营养因子可保护螺旋神经节神经元免受耳毒性损伤,但它们并不能保护毛细胞。在本实验中,我们使用新生大鼠耳蜗外植体培养物来鉴定可保护毛细胞免受耳毒性损伤的分子。在所检测的51种化合物中,只有伴刀豆球蛋白A(Con A)能显著保护毛细胞免受庆大霉素的损伤。Con A的剂量依赖性研究表明,在100 nM时可达到最大保护效果。通过共聚焦显微镜和培养物石蜡切片证实了Con A对毛细胞的保护作用。进行了多项实验以研究Con A的保护机制。Con A与庆大霉素孵育未形成复合物,将Con A和庆大霉素共同添加到大肠杆菌培养物中也未干扰庆大霉素的抗菌活性。然而,溶酶体追踪染色和庆大霉素免疫细胞化学提供了证据,表明预先用Con A孵育可阻止庆大霉素进入毛细胞。综合考虑,这些发现可能有助于阐明氨基糖苷类抗生素的耳毒性机制,并表明Con A在预防氨基糖苷类药物导致的听力损失方面可能具有治疗价值。