Oda Y, Harada Y, Kasuga S, Hirakawa K, Yajin K
Department of Otolaryngology, Hiroshima University School of Medicine, Japan.
Acta Otolaryngol Suppl. 1995;519:238-43. doi: 10.3109/00016489509121914.
Morphological changes in utricular supporting cells in the guinea pig following streptomycin sulfate (SM) intoxication were investigated ultrastructurally in vitro, using an organ culture system. The intracellular structures of the supporting cells, such as the nucleus, mitochondria, and Golgi apparati were well preserved after 7 days in culture. After 10 and 14 days in culture, the supporting cells degenerated. The organ culture system was applied to ototoxicity studies on the supporting cells in utricular macula within 7 days after explanation. When the utricles were exposed to 3, 10 and 30 mg/ml of SM for 3 days, the number of granules in the supporting cells decreased markedly and the number of lysosomes increased daily. The lysosomes contained mitochondria, myeloid bodies, granules and vesicles. Acid phosphatase (AcPase) activity decreased in Golgi apparati and lysosomes. When the concentration of SM was reduced to 3 and 10 mg/ml, the damage to the supporting cells was less marked than that in cells exposed to 30 mg/ml. The supporting cells showed a dose-dependent response with respect to morphological damage. After 3 days culture with 30 mg/ml of SM, the specimens were subsequently cultured for 4 days in a medium without SM. After removal of SM from the medium, lysosomes decreased in number, and the granules and the endoplasmic reticulum showed a gradual increase. The AcPase activity was determined in both lysosomes and Golgi apparatus. This study revealed that the morphological changes in the supporting cells can be reversible.
利用器官培养系统,在体外对硫酸链霉素(SM)中毒后豚鼠椭圆囊支持细胞的形态学变化进行了超微结构研究。培养7天后,支持细胞的细胞核、线粒体和高尔基体等细胞内结构保存良好。培养10天和14天后,支持细胞发生退化。该器官培养系统应用于解剖后7天内椭圆囊斑支持细胞的耳毒性研究。当椭圆囊暴露于3、10和30mg/ml的SM中3天时,支持细胞中的颗粒数量明显减少,溶酶体数量每日增加。溶酶体含有线粒体、髓样小体、颗粒和囊泡。高尔基体和溶酶体中的酸性磷酸酶(AcPase)活性降低。当SM浓度降至3和10mg/ml时,对支持细胞的损伤不如暴露于30mg/ml的细胞明显。支持细胞在形态损伤方面呈现剂量依赖性反应。用30mg/ml的SM培养3天后,将标本随后在不含SM的培养基中培养4天。从培养基中去除SM后,溶酶体数量减少,颗粒和内质网逐渐增加。同时测定了溶酶体和高尔基体中的AcPase活性。本研究表明,支持细胞的形态学变化是可逆的。