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Microbial heat shock protein 65 attenuates airway hyperresponsiveness and inflammation by modulating the function of dendritic cells

Authors
Shin, YS; Takeda, K; Shiraishi, Y; Jeong, YY; Domenico, J; Jia, Y; Han, J; Spallek, R; Singh, M; Lucas, JJ; Gelfand, EW
Citation
Journal of immunology (Baltimore, Md. : 1950), 189(7):3404-3410, 2012
Journal Title
Journal of immunology (Baltimore, Md. : 1950)
ISSN
0022-17671550-6606
Abstract
Heat shock proteins (HSPs), produced in response to stress, are suppressive in disease models. We previously showed that Mycobacterium leprae HSP65 prevented development of airway hyperresponsiveness and inflammation in mice. Our goal in this study was to define the mechanism responsible for the suppressive effects of HSP. In one in vivo approach, BALB/c mice were sensitized to OVA, followed by primary OVA challenges. Several weeks later, HSP65 was administered prior to a single, provocative secondary challenge. In a second in vivo approach, the secondary challenge was replaced by intratracheal instillation of allergen-pulsed bone marrow-derived dendritic cells (BMDCs). The in vitro effects of HSP65 on BMDCs were examined in coculture experiments with CD4(+) T cells. In vivo, HSP65 prevented the development of airway hyperresponsiveness and inflammation. Additionally, Th1 cytokine levels in bronchoalveolar lavage fluid were increased. In vitro, HSP65 induced Notch receptor ligand Delta1 expression on BMDCs, and HSP65-treated BMDCs skewed CD4(+) T cells to Th1 cytokine production. Thus, HSP65-induced effects on allergen-induced airway hyperresponsiveness and inflammation were associated with increased Delta1 expression on dendritic cells, modulation of dendritic cell function, and CD4(+) Th1 cytokine production.
MeSH terms
AnimalsBacterial Proteins/*physiologyBronchial Hyperreactivity/immunology/*pathology/*prevention & controlCells, CulturedChaperonin 60/*physiologyCoculture TechniquesCytokines/biosynthesisDendritic Cells/*immunology/*microbiology/pathologyDisease Models, AnimalFemaleInflammation/immunology/microbiology/*prevention & controlMiceMice, Inbred BALB CMycobacterium leprae/*immunologyOvalbumin/administration & dosage/immunologyTh1 Cells/immunology/microbiology/pathology
DOI
10.4049/jimmunol.1201138
PMID
22933632
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Allergy
AJOU Authors
신, 유섭
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