AJP - Lung AJP: Heart and Circulatory Physiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


Am J Physiol Lung Cell Mol Physiol (August 24, 2007). doi:10.1152/ajplung.00103.2007
This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
293/5/L1163    most recent
00103.2007v1
Right arrow Alert me when this article is cited
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 Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Wyatt, T. A
Right arrow Articles by Romberger, D. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wyatt, T. A
Right arrow Articles by Romberger, D. J.
Submitted on March 16, 2007
Accepted on August 21, 2007

Feedlot dust stimulation of interleukin-6 and 8 requires protein kinase C-epsilon human bronchial epithelial cells

Todd A Wyatt1, Rebecca E Slager2, Jane DeVasure3, Brent W Auvermann4, Michael L Mulhern5, Susanna G. Von Essen3, Tracy Mathisen3, Anthony A Floreani3, and Debra J. Romberger1*

1 Internal Medicine-Pulmonary, University of Nebraska Medical Center, Omaha, Nebraska, United States; Research Service, Dept. of Veterans Affairs Medical Center, Omaha, Nebraska, United States
2 Internal Medicine-Pulmonary, University of Nebraska Medical Center, United States
3 Internal Medicine-Pulmonary, University of Nebraska Medical Center, Omaha, Nebraska, United States
4 Texas A&M Agricultural Research & Extension Center, Amarillo, Texas, United States
5 Genetics, Cell Biology, & Anatomy, University of Nebraska Medical Center, Omaha, Nebraska, United States

* To whom correspondence should be addressed. E-mail: dromberg{at}unmc.edu.

Individuals exposed to dusts from concentrated animal feeding operations report increased numbers of respiratory tract symptoms and bronchoalveolar lavage samples from such individuals demonstrate elevated lung inflammatory mediators, including interleukin (IL)-8 and IL-6. We previously found that exposure of bronchial epithelial cells to hog barn dusts resulted in a protein kinase C (PKC) -dependent increase in IL-6 and IL-8 release. We hypothesized that cattle feedlot dusts would also generate bronchial epithelial interleukin release in vitro. To test this, we used interleukin ELISAs and direct PKC isoform assays. We found that a dust extract from cattle feedlots (FLDE) augments PKC activity of human bronchial epithelial cells in vitro. A 5-10% dilution of FLDE stimulated a significant release of IL-6 and IL-8 at 6-24 hr in a PKC-dependent manner vs. control medium-treated cells. An increase in PKC alpha activity was observed with 1 hr of FLDE treatment and PKC epsilon activity was elevated at 6 hr FLDE exposure. The PKC alpha inhibitor, Go 6976, did not inhibit FLDE-stimulated IL-8 and IL-6 release. However, the PKC epsilon inhibitor, Ro 31-8220, effectively inhibited FLDE-stimulated IL-8 and IL-6 release. Inhibition of FLDE-stimulated IL-6 and IL-8 was confirmed in a dominant negative PKC epsilon expressing BEAS-2B cell line, but not observed in a PKC alpha dominant negative BEAS-2B cell line. These data support the hypothesis that FLDE exposure stimulates bronchial epithelial IL-8 and IL-6 release via a PKC epsilon-dependent pathway.




This article has been cited by other articles:


Home page
J. Pharmacol. Exp. Ther.Home page
K. M. Kassel, P. R. Dodmane, N. A. Schulte, and M. L. Toews
Lysophosphatidic Acid Induces Rapid and Sustained Decreases in Epidermal Growth Factor Receptor Binding via Different Signaling Pathways in BEAS-2B Airway Epithelial Cells
J. Pharmacol. Exp. Ther., June 1, 2008; 325(3): 809 - 817.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Visit Other APS Journals Online
Copyright © 2007 by the American Physiological Society.