Ultrastructure of the bronchial epithelium in adult patients with cystic fibrosis.

H Gilljam, A M Motakefi, B Robertson, B Strandvik
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Abstract

The respiratory epithelium of large airways was studied in biopsy specimens obtained by bronchoscopy in seven patients with cystic fibrosis (CF). All but one of these patients were chronically colonised with Pseudomonas aeruginosa. Biopsy specimens were also obtained from the large airways of 10 control patients with or without signs of chronic bronchitis. All samples were studied by transmission electron microscopy. Morphometry was applied to assess the volume density of various cell types and intercellular spaces and for quantification of microvilli of ciliated cells. In CF patients, the average number of microvilli per ciliated cell was decreased by 17% compared to patients with chronic bronchitis and by 34% compared to patients with apparently normal bronchi (p less than 0.02, respectively), but otherwise no abnormalities were found. In particular, the volume density of goblet cells was not increased. Thus the ultrastructure of the airway epithelium may be nearly normal in CF, even in adult patients with chronic respiratory infection.

成人囊性纤维化患者支气管上皮的超微结构。
对7例囊性纤维化(CF)患者的支气管镜活检标本进行了大气道呼吸上皮的研究。除一人外,所有患者均长期感染铜绿假单胞菌。活检标本也从10例有或无慢性支气管炎症状的对照患者的大气道中获得。所有样品均采用透射电子显微镜进行研究。形态学测定法评估不同细胞类型和细胞间隙的体积密度,定量纤毛细胞的微绒毛。CF患者每个纤毛细胞的微绒毛平均数量比慢性支气管炎患者减少17%,比支气管明显正常患者减少34% (p均小于0.02),其他未见异常。特别是杯状细胞的体积密度没有增加。因此,CF患者的气道上皮超微结构可能几乎正常,即使是慢性呼吸道感染的成人患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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