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The Clara cell and pulmonary surfactant: A study using selective chemical ablation
Author(s) -
Cottrell R. C.,
Foster J. R.,
Pelling D.,
Herod I. A.,
Lee V. S.,
Purchase R.,
Bayley D.,
Miller K.
Publication year - 1984
Publication title -
cell biochemistry and function
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.933
H-Index - 61
eISSN - 1099-0844
pISSN - 0263-6484
DOI - 10.1002/cbf.290020404
Subject(s) - pulmonary surfactant , phospholipid , chemistry , chromatography , ultracentrifuge , jugular vein , cell , lung , pulmonary compliance , medicine , biochemistry , membrane
Administration of 3‐hydroxymethylfuran‐N‐ethylcarbamate (HFC) to female hamsters via the jugular vein under pentobarbitone anaesthetic at 20 mg per kg body weight produced pronounced necrosis of the Clara cells without apparent morphological effect on other cell types as judged by transmission electron microscope examination. The surfactant material recoverable by minimal lavage followed by purification by sucrose gradient ultracentrifugation increased, reaching a maximum around 48 h after treatment. At this time static pressure/volume measurements on isolated lungs indicated an increase in airway surface compliance. Lavageable surfactant phospholipid composition was examined by 31 P nuclear magnetic resonance (n.m.r.). The distribution of phospholipids between the various classes was unchanged by HFC treatment. No change in the total lung surfactant pool size was seen. These results are discussed in relation to the possible roles of the Clara cell in influencing airway surfactant levels.