|
|
||||||||
Guest Access | Sign In via User Name/Password |
|||||||||
Chest, Vol 89, 327-330, Copyright © 1986 by American College of Chest Physicians
ARTICLES |
P Wolf, C Hall and JP Kilbourn
In this investigation, the presence of calcitonin and calmodulin has been demonstrated in immunoperoxidase formalin-fixed, paraffin-embedded sections of lung from autopsy tissues of four patients who died as a result of complications resulting from their cystic fibrosis disease. Immunoreactive calcitonin has been stained and quantitated in solitary endocrine cells which are increased in number and staining intensity in cystic fibrosis lung when compared to COPD and normal lungs. Immunoreactive calmodulin has been demonstrated to be increased in cystic fibrosis lung when compared to COPD and normal lungs. Previously, increased calcitonin and calmodulin were identified in sputum from cystic fibrosis patients utilizing radioimmunoassay. The calcitonin and calmodulin may be associated with increased calcium in pulmonary secretions leading to selective colonization of the lung by a limited number of pathogenic bacteria and enhanced pulmonary infection.
This article has been cited by other articles:
![]() |
J. Pan, C. Bear, S. Farragher, E. Cutz, and H. Yeger Cystic Fibrosis Transmembrane Conductance Regulator Modulates Neurosecretory Function in Pulmonary Neuroendocrine Cell-Related Tumor Cell Line Models Am. J. Respir. Cell Mol. Biol., November 1, 2002; 27(5): 553 - 560. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Yeger, J. Pan, X. W. Fu, C. Bear, and E. Cutz Expression of CFTR and Cl{-} conductances in cells of pulmonary neuroepithelial bodies Am J Physiol Lung Cell Mol Physiol, September 1, 2001; 281(3): L713 - L721. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |