| Src homology 3-interacting domain of Rv1917c of Mycobacterium tuberculosis induces selective maturation of human dendritic cells by regulating PI3K-MAPK-NF-kappaB signaling and drives Th2 immune responses. | |
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MedLine Citation:
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PMID: 20837474 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Mycobacterium tuberculosis, an etiological agent of pulmonary tuberculosis, causes significant morbidity and mortality worldwide. Pathogenic mycobacteria survive in the host by subverting host innate immunity. Dendritic cells (DCs) are professional antigen-presenting cells that are vital for eliciting immune responses to infectious agents, including pathogenic mycobacteria. DCs orchestrate distinct Th responses based on the signals they receive. In this perspective, deciphering the interactions of the proline-glutamic acid/proline-proline-glutamic acid (PE/PPE) family of proteins of M. tuberculosis with DCs assumes significant pathophysiological attributes. In this study, we demonstrate that Rv1917c (PPE34), a representative member of the proline-proline-glutamic-major polymorphic tandem repeat family, interacts with TLR2 and triggers functional maturation of human DCs. Signaling perturbations implicated a critical role for integrated cross-talk among PI3K-MAPK and NF-κB signaling cascades in Rv1917c-induced maturation of DCs. However, this maturation of DCs was associated with a secretion of high amounts of anti-inflammatory cytokine IL-10, whereas Th1-polarizing cytokine IL-12 was not induced. Consistent with these results, Rv1917c-matured DCs favored secretion of IL-4, IL-5, and IL-10 from CD4(+) T cells and contributed to Th2-skewed cytokine balance ex vivo in healthy individuals and in patients with pulmonary tuberculosis. Interestingly, the Rv1917c-skewed Th2 immune response involved induced expression of cyclooxygenase-2 (COX-2) in DCs. Taken together, these results indicate that Rv1917c facilitates a shift in the ensuing immunity toward the Th2 phenotype and could aid in immune evasion by mycobacteria. |
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Authors:
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Kushagra Bansal; Akhauri Yash Sinha; Devram Sampat Ghorpade; Shambhuprasad Kotresh Togarsimalemath; Shripad A Patil; Srini V Kaveri; Kithiganahalli Narayanaswamy Balaji; Jagadeesh Bayry |
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Publication Detail:
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Type: Journal Article; Research Support, Non-U.S. Gov't Date: 2010-09-13 |
Journal Detail:
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Title: The Journal of biological chemistry Volume: 285 ISSN: 1083-351X ISO Abbreviation: J. Biol. Chem. Publication Date: 2010 Nov |
Date Detail:
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Created Date: 2010-11-15 Completed Date: 2011-02-28 Revised Date: 2011-12-21 |
Medline Journal Info:
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Nlm Unique ID: 2985121R Medline TA: J Biol Chem Country: United States |
Other Details:
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Languages: eng Pagination: 36511-22 Citation Subset: IM |
Affiliation:
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Department of Microbiology and Cell Biology, Indian Institute of Science, Bangalore 560012, India. |
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| MeSH Terms | |
Descriptor/Qualifier:
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Antigens, Bacterial
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genetics,
metabolism* Bacterial Proteins / genetics, metabolism* Blotting, Western Cells, Cultured Cyclooxygenase 2 / genetics, metabolism Dendritic Cells / immunology*, metabolism* Enzyme-Linked Immunosorbent Assay Extracellular Signal-Regulated MAP Kinases / genetics, metabolism Fluorescent Antibody Technique Gene Expression Regulation Humans Mycobacterium tuberculosis / immunology, metabolism* NF-kappa B / genetics, metabolism* Phosphatidylinositol 3-Kinases / genetics, metabolism RNA, Messenger / genetics Reverse Transcriptase Polymerase Chain Reaction T-Lymphocytes Th2 Cells / immunology*, metabolism Tuberculosis / immunology, metabolism*, microbiology p38 Mitogen-Activated Protein Kinases / genetics, metabolism src Homology Domains |
| Chemical | |
Reg. No./Substance:
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0/Antigens, Bacterial; 0/Bacterial Proteins; 0/NF-kappa B; 0/RNA, Messenger; 0/Rv1917c protein, Mycobacterium tuberculosis; EC 1.14.99.1/Cyclooxygenase 2; EC 1.14.99.1/PTGS2 protein, human; EC 2.7.1.-/Phosphatidylinositol 3-Kinases; EC 2.7.11.24/Extracellular Signal-Regulated MAP Kinases; EC 2.7.11.24/p38 Mitogen-Activated Protein Kinases |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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