Document Detail


Effects of anthrax lethal toxin on human primary keratinocytes.
MedLine Citation:
PMID:  19120626     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
AIMS: To investigate the effects of anthrax lethal toxin (LeTx) on human primary keratinocytes. METHODS AND RESULTS: We show here that human primary keratinocytes are resistant to LeTx-triggered cytotoxicity. All but one of the MEKs (mitogen-activated protein kinase kinases) are cleaved within 3 h, and the cleavage of MEKs in keratinocytes leads to their subsequent proteasome-mediated degradation at different rates. Moreover, LeTx reduced the concentration of several cytokines except RANTES in culture. CONCLUSIONS: Our results indicate that primary keratinocytes are resistant to LeTx cytotoxicity, and MEK cleavage does not correlate with LeTx cytotoxicity. Although LeTx is considered as an anti-inflammatory agent, it upregulates RANTES. SIGNIFICANCE AND IMPACT OF THE STUDY: According to a current view, the action of LeTx results in downregulation of the inflammatory response, as evidenced by diminished expression of several inflammatory biomarkers. Paradoxically, LeTx has been reported to attract neutrophils to cutaneous infection sites. This paper, which shows that RANTES, a chemoattractant for immune cells, is upregulated after exposure of keratinocytes to LeTx, although a number of other markers of the inflammatory response are downregulated. Our results might explain why the exposure of keratinocytes to LeTx results in the recruitment of neutrophils to cutaneous infection sites, while the expression of several inflammatory biomarkers is diminished.
Authors:
S S Koçer; M Matic; M Ingrassia; S G Walker; E Roemer; G Licul; S R Simon
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural    
Journal Detail:
Title:  Journal of applied microbiology     Volume:  105     ISSN:  1365-2672     ISO Abbreviation:  J. Appl. Microbiol.     Publication Date:  2008 Dec 
Date Detail:
Created Date:  2009-01-05     Completed Date:  2009-10-09     Revised Date:  2009-11-19    
Medline Journal Info:
Nlm Unique ID:  9706280     Medline TA:  J Appl Microbiol     Country:  England    
Other Details:
Languages:  eng     Pagination:  1756-67     Citation Subset:  IM    
Affiliation:
Department of Biochemistry and Cell Biology, State University of New York at Stony Brook, New York, NY 11794-8691, USA.
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MeSH Terms
Descriptor/Qualifier:
Animals
Antigens, Bacterial / pharmacology*,  toxicity*
Bacillus anthracis*
Bacterial Toxins / pharmacology*,  toxicity*
Biological Markers / metabolism
Chemokine CCL5 / metabolism
Cytokines / metabolism
Foreskin
Glycoproteins / pharmacology
Humans
Keratinocytes / drug effects*,  enzymology,  metabolism
Male
Mitogen-Activated Protein Kinase Kinases / metabolism*
Grant Support
ID/Acronym/Agency:
R21-AI53524/AI/NIAID NIH HHS
Chemical
Reg. No./Substance:
0/Antigens, Bacterial; 0/Bacterial Toxins; 0/Biological Markers; 0/Chemokine CCL5; 0/Cytokines; 0/Glycoproteins; 0/anthrax toxin; 0/calpain inhibitors; EC 2.7.12.2/Mitogen-Activated Protein Kinase Kinases

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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