Rossman C M, Forrest J B, Ruffin R E, Newhouse M T
Am Rev Respir Dis. 1980 Jun;121(6):1011-6. doi: 10.1164/arrd.1980.121.6.1011.
We studied the ultrastructure and function of respiratory tract cilia in a group of patients with Kartagener's Syndrome, and compared the results with those from a group of subjects with unexplained histories of chronic bronchiectasis and bronchitis. Both patient groups lacked pulmonary and nasal mucociliary transport. On electron microscopic examination of nasal mucosal biopsy tissue, all patient specimens had abnormal cilia with a highly disorganized microtubular network, and a consistent absence of dynein arms. Cilia from both groups were immotile when viewed under direct phase contrast, but could be animated by the addition of 10(-6) g/ml of ATP or ATPase to the same degree of spontaneous motility seen in normal cilia. Immotile cilia syndrome clearly includes not only patients with Kartagener's syndrome, but also some patients with chronic bronchitis and bronchiectasis.
我们研究了一组患有卡塔格内综合征患者呼吸道纤毛的超微结构和功能,并将结果与一组有不明原因慢性支气管扩张和支气管炎病史的受试者的结果进行了比较。两组患者均缺乏肺和鼻黏膜纤毛运输功能。在对鼻黏膜活检组织进行电子显微镜检查时,所有患者标本的纤毛均异常,微管网络高度紊乱,且始终缺乏动力蛋白臂。在直接相差显微镜下观察,两组的纤毛均无运动能力,但加入10(-6) g/ml的ATP或ATP酶后,纤毛可被激活,达到与正常纤毛相同程度的自发运动。不动纤毛综合征显然不仅包括卡塔格内综合征患者,还包括一些慢性支气管炎和支气管扩张患者。