Linked Life Data

19265148

Source:http://linkedlifedata.com/resource/pubmed/id/19265148

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2009-3-6
pubmed:abstractText
Gp91(phox)/NADPH oxidase (NOX) 2 is the main catalytic component of NOX, which mediates the phagocytic killing of ingested pathogens via the production of reactive oxygen species (ROS). However, Mycobacterium tuberculosis (Mtb) is relatively resistant to the microbicidal effects of ROS. Thus, the exact roles of NOX2 in the innate immune control against Mtb infection are not fully resolved. In this study, we show that NOX2 is essential for TLR2-dependent inflammatory responses and 1,25-dihydroxyvitamin D(3) (1,25D(3))-mediated antimicrobial activity against Mtb via cathelicidin expression. NOX2-null macrophages prominently abrogated Mtb-induced ROS production and inflammatory signaling activation in a TLR2-dependent manner. Mtb triggered a physical association between NOX2 and TLR2. In addition, the knockdown of NOX2 inhibited 1,25D(3)-triggered antimicrobial activity against viable Mtb through the modulation of cathelicidin expression in human macrophages. Treatment of NOX2 knocked down cells with cathelicidin restored the 1,25D(3)-induced antimicrobial effect, suggesting that the NOX2-dependent induction of cathelicidin in macrophages is part of a defensive strategy against Mtb. Furthermore, cathelicidin expression was required for the Mtb-induced release of ROS and the production of proinflammatory cytokines/chemokines, indicating a positive circuit of inflammation in response to Mtb. Our data collectively demonstrate a novel regulatory mechanism for TLR2-dependent innate responses to Mtb involving crosstalk between NOX2 and TLR2 and the expression of cathelicidin.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
1550-6606
pubmed:author
pubmed:issnType
Electronic
pubmed:day
15
pubmed:volume
182
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3696-705
pubmed:meshHeading
pubmed-meshheading:19265148-Amino Acid Sequence, pubmed-meshheading:19265148-Animals, pubmed-meshheading:19265148-Antimicrobial Cationic Peptides, pubmed-meshheading:19265148-Cell Line, pubmed-meshheading:19265148-Cell Line, Tumor, pubmed-meshheading:19265148-Cells, Cultured, pubmed-meshheading:19265148-Humans, pubmed-meshheading:19265148-Immunity, Innate, pubmed-meshheading:19265148-Inflammation Mediators, pubmed-meshheading:19265148-Macrophages, pubmed-meshheading:19265148-Membrane Glycoproteins, pubmed-meshheading:19265148-Mice, pubmed-meshheading:19265148-Mice, Inbred C3H, pubmed-meshheading:19265148-Mice, Inbred C57BL, pubmed-meshheading:19265148-Mice, Knockout, pubmed-meshheading:19265148-Molecular Sequence Data, pubmed-meshheading:19265148-Mycobacterium tuberculosis, pubmed-meshheading:19265148-NADPH Oxidase, pubmed-meshheading:19265148-Signal Transduction, pubmed-meshheading:19265148-Toll-Like Receptor 2
pubmed:year
2009
pubmed:articleTitle
NADPH oxidase 2 interaction with TLR2 is required for efficient innate immune responses to mycobacteria via cathelicidin expression.
pubmed:affiliation
Department of Microbiology, Infection Signaling Network Research Center, College of Medicine, Chungnam National University, Daejeon, South Korea.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't