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Freeze-fracture analysis of the respiratory cilia from the bronchial mucosa of a patient with primary ciliary dyskinesia.

作者信息

Lessner U, Breipohl W, Konietzko N, Rehn B

机构信息

Abteilung für Anatomie, Gesamthochschule Essen, BRD.

出版信息

Respiration. 1988;53(1):44-9. doi: 10.1159/000195395.

DOI:10.1159/000195395
PMID:3291032
Abstract

Respiratory cilia of the bronchial mucosa from a 5-year-old boy with clinical evidence of classical Kartagener's syndrome (situs inversus, bronchiectasis and sinusitis) were first examined by means of transmission electron microscopy for identification of the axonemal defects described as typical for primary ciliary dyskinesia (PCD). Additional oscillography was performed on the cilia in vitro, which showed absence of a coordinated ciliary beat frequency. After clear classification of the case as PCD, a freeze-fracture examination of the respiratory cilia was performed, which revealed a higher density of intramembrane particles on the outer fracture face (E-face) than on the inner fracture face (P-face). The results were discussed with regard to probable pathogenetic aspects on PCD.

摘要

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引用本文的文献

1
Freeze fracture study of airway epithelium from patients with primary ciliary dyskinesia.原发性纤毛运动障碍患者气道上皮的冷冻断裂研究
Thorax. 2002 Apr;57(4):363-5. doi: 10.1136/thorax.57.4.363.
2
Abnormal length of cilia--a cause of primary ciliary dyskinesia--a case report.纤毛长度异常——原发性纤毛运动障碍的一个病因——病例报告
Eur J Pediatr. 1992 Jan;151(1):73-5. doi: 10.1007/BF02073899.