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van Rijt, S.H. ; Keller, I.E. ; John, G. ; Kohse, K. ; Yildirim, A.Ö. ; Eickelberg, O. ; Meiners, S.

Acute cigarette smoke exposure impairs proteasome function in the lung.

Am. J. Physiol. Lung Cell Mol. Physiol. 303, L814-L823 (2012)
DOI PMC
Open Access Gold as soon as Publ. Version/Full Text is submitted to ZB.
van Rijt SH, Keller IE, John G, Kohse K, Yildirim AO, Eickelberg O, Meiners S. Acute cigarette smoke exposure impairs proteasome function in the lung. Am J Physiol Lung Cell Mol Physiol 303: L814-L823, 2012. First published September 7, 2012; doi:10.1152/ajplung.00128.2012.-Cigarette smoke mediates DNA damage, lipid peroxidation, and modification and misfolding of proteins, thereby inducing severe cellular damage. The ubiquitin proteasome system serves as the major disposal system for modified and misfolded proteins and is thus essential for proper cellular function. Its role in cigarette smoke-induced cell damage, however, is largely unknown. We hypothesized that the ubiquitin-proteasome system is involved in the degradation of cigarette smoke-damaged proteins and that cigarette smoke exposure impairs the proteasome itself. Here, we show that treatment of human alveolar epithelial cells with cigarette smoke extract (CSE) induced time-and dose-dependent cell death, a rise in intracellular reactive oxygen species, and increased levels of carbonylated and polyubiquitinated proteins. While high doses of CSE severely impaired all three proteasomal activities, low CSE concentrations significantly inhibited only the trypsin-like activity of the proteasome in alveolar and bronchial epithelial cells. Moreover, acute exposure of mice to cigarette smoke significantly impaired the trypsin-like activity by 25% in the lungs. Reduced proteasome activity was not due to transcriptional regulation of the proteasome. Notably, cigarette smoke exposure induced accumulation of polyubiquitinated proteins in the soluble and insoluble protein fraction of the lung. We show for the first time that acute exposure to cigarette smoke directly impairs proteasome activity in the lungs of mice and in human epithelial cells at low doses without affecting proteasome expression. Our results indicate that defective proteasomal protein quality control may exacerbate the detrimental effects of cigarette smoke in the lung.
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Publication type Article: Journal article
Document type Scientific Article
Keywords Ubiquitin Proteasome System ; Cigarette Smoke ; Protein Quality Control ; Oxidative Stress ; Chronic Obstructive Pulmonary Disease; OBSTRUCTIVE PULMONARY-DISEASE; OXIDATIVE STRESS; 20S PROTEASOME; ANTIGEN PRESENTATION; UBIQUITIN; DEGRADATION; INHIBITORS; SYSTEM; CARDIOMYOPATHIES; PROTEINS
Language english
Publication Year 2012
HGF-reported in Year 2012
ISSN (print) / ISBN 1040-0605
e-ISSN 1522-1504
Journal American Journal of Physiology - Lung Cellular and Molecular Physiology
Quellenangaben Volume: 303, Issue: 9, Pages: L814-L823 Article Number: , Supplement: ,
Publisher American Physiological Society
Publishing Place Bethesda, Md. [u.a.]
Reviewing status Peer reviewed
Institute(s) Institute of Lung Health and Immunity (LHI)
POF-Topic(s) 30202 - Environmental Health
Research field(s) Lung Research
PSP Element(s) G-501600-004
G-501600-001
G-505000-007
PubMed ID 22962013
DOI 10.1152/ajplung.00128.2012
WOS ID WOS:000310646200009
Scopus ID 84868358100
Erfassungsdatum 2012-11-29
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