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Research Article Free access | 10.1172/JCI114451

Pneumocystis carinii: inhibition of lung cell growth mediated by parasite attachment.

A H Limper and W J Martin 2nd

Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota 55905.

Find articles by Limper, A. in: PubMed | Google Scholar

Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota 55905.

Find articles by Martin, W. in: PubMed | Google Scholar

Published February 1, 1990 - More info

Published in Volume 85, Issue 2 on February 1, 1990
J Clin Invest. 1990;85(2):391–396. https://doi.org/10.1172/JCI114451.
© 1990 The American Society for Clinical Investigation
Published February 1, 1990 - Version history
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Abstract

Pneumocystis carinii pneumonia is a significant cause of mortality in immunocompromised patients. Current concepts suggest that attachment of P. carinii to alveolar epithelium is required for development of pneumonia. We examined the mechanism of P. carinii adherence to cultured A549 cells, a permanent cell line derived from human alveolar epithelium. P. carinii adherence was quantified by measuring attachment of 51Cr-labeled P. carinii to cultured A549 cells. After 8 h of incubation, 37.4 +/- 4.2% of P. carinii were adherent to A549 cells. In the presence of agents known to impair cytoskeletal function, including 10(-5) M cytochalasin B, 10(-5) M colchicine, and 10(-5) M trimethylcolchicinic acid (TMCA), adherence was decreased from 57.4 +/- 4.2% to 9.3 +/- 3.4%, 12.5 +/- 3.6%, and 21.5 +/- 3.6%, respectively (P less than 0.01, all comparisons). Secondly, we examined the effect of P. carinii on the function of A549 cells. P. carinii resulted in significant impairment of A549 cell growth, indicating P. carinii adversely affected the function of target lung cells. A P. carinii:A549 cell ratio of 50:1 resulted in 43.5 +/- 2.9% inhibition of A549 cell growth (P less than 0.001). Additionally, TMCA, which significantly prevented attachment of P. carinii, reversed the impairment of A549 cell growth. These data demonstrate that P. carinii attachment to cultured lung cells can be quantified, is dependent on intact cytoskeletal function and is necessary for impairment of lung cell replication.

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