Yamane H, Konishi K, Iguchi H, Nakagawa T, Shibata S, Takayama M, Nishimura K, Sunami K, Nakai Y
Department of Otorhinolaryngology, Osaka City University Medical School, Japan.
Acta Otolaryngol Suppl. 1998;538:7-11.
We examined the usefulness of the dye extrusion method for assessing cochlear hair cell death in guinea pigs. Unilateral temporal bones were incubated in sterile Dulbecco modified Eagle's medium for 1-6 h and then perfused with PBS/0.3% trypan blue to determine hair cell viability. Cells with nuclei stained with trypan blue were assumed to have died. The contralateral temporal bones of each animal were incubated with the same medium for 1-6 h and examined by transmission electron microscopy (TEM). This method revealed that hair cell viability under these conditions was maintained for at most 3 h. After incubation for more than 3 h, hair cell injury began and increased. After 6 h incubation, TEM revealed apoptotic death of outer hair cells. The results with this method agreed with the TEM findings. The dye extrusion method is simple, easy and useful for screening hair cell death in the cochlea under pathological conditions.
我们研究了染料排除法在评估豚鼠耳蜗毛细胞死亡中的实用性。将单侧颞骨在无菌的杜尔贝科改良伊格尔培养基中孵育1 - 6小时,然后用PBS/0.3%台盼蓝灌注以确定毛细胞活力。细胞核被台盼蓝染色的细胞被认为已经死亡。每只动物的对侧颞骨在相同培养基中孵育1 - 6小时,并通过透射电子显微镜(TEM)检查。该方法显示在这些条件下毛细胞活力最多维持3小时。孵育超过3小时后,毛细胞损伤开始并增加。孵育6小时后,TEM显示外毛细胞发生凋亡性死亡。该方法的结果与TEM的发现一致。染料排除法简单、易行,对于筛选病理条件下耳蜗中的毛细胞死亡很有用。