Chest ACCP Member Benefits
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     

Guest Access | Sign In via User Name/Password
This Article
Right arrow Full Text (PDF) Free
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Article Archive
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Wolf, P
Right arrow Articles by Kilbourn, J.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Wolf, P
Right arrow Articles by Kilbourn, J.

Chest, Vol 89, 327-330, Copyright © 1986 by American College of Chest Physicians


ARTICLES

Demonstration of calcitonin and calmodulin by immunoperoxidase in the cystic fibrosis lung

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:


Home page
Am. J. Respir. Cell Mol. Bio.Home page
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]


Home page
Am. J. Physiol. Lung Cell. Mol. Physiol.Home page
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
Copyright © 1986 by the American College of Chest Physicians.