共 29 条
Role of caspase-1 in nuclear translocation of IL-37, release of the cytokine, and IL-37 inhibition of innate immune responses
被引:199
作者:
Bulau, Ana-Maria
[1
]
Nold, Marcel F.
[2
]
Li, Suzhao
[4
]
Nold-Petry, Claudia A.
[2
]
Fink, Michaela
[1
]
Mansell, Ashley
[3
]
Schwerd, Tobias
[1
]
Hong, Jaewoo
[5
]
Rubartelli, Anna
[6
]
Dinarello, Charles A.
[4
,7
]
Bufler, Philip
[1
]
机构:
[1] Univ Munich, Dr von Hauner Childrens Hosp, Dept Pediat, D-80337 Munich, Germany
[2] Monash Univ, Monash Inst Med Res, Ritchie Ctr, Melbourne, Vic 3168, Australia
[3] Monash Univ, Monash Inst Med Res, Ctr Innate Immun & Infect Dis, Melbourne, Vic 3168, Australia
[4] Univ Colorado, Aurora, CO 80045 USA
[5] Konkuk Univ, Dept Biomed Sci & Technol, Seoul 143701, South Korea
[6] Ist Sci Studio & Cura Tumori, Azienda Osped Univ San Martino, Ist Ricovero & Cura Carattere Sci, Cell Biol Unit, I-16132 Genoa, Italy
[7] Radboud Univ Nijmegen, Med Ctr, Dept Med, NL-6500 HB Nijmegen, Netherlands
来源:
基金:
美国国家卫生研究院;
英国医学研究理事会;
关键词:
NALP3;
INFLAMMASOME;
PROTEIN;
FAMILY;
MACROPHAGES;
ACTIVATION;
MATURATION;
IL-1-BETA;
SECRETION;
SIGIRR;
BETA;
D O I:
10.1073/pnas.1324140111
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
IL-37 is a fundamental inhibitor of innate immunity. Human IL-37 has a caspase-1 cleavage site and translocates to the nucleus upon LPS stimulation. Here, we investigated whether caspase-1 processing affects IL-37-mediated suppression of LPS-induced cytokines and the release from cells by analyzing a caspase-1 cleavage site mutant IL-37 (IL-37D20A). Nuclear translocation of IL-37D20A is significantly impaired compared with WT IL-37 in transfected cells. LPS-induced IL-6 was decreased in cells expressing WT IL-37 but not IL-37D20A. The function of IL-37 in transfected bone marrow-derived macrophages is nucleotide-binding oligomerization domain-like receptor family, pyrin domain containing 3 (NLRP3) inflammasome-dependent, because IL-37 transfection in apoptosis-associated speck-like protein containing a carboxyl-terminal caspase recruitment domain-and NLRP3-deficient cells does not reduce levels of IL-6 and IL-1 beta upon LPS stimulation. IL-37-expressing macrophages release both precursor and mature IL-37, but only the externalization of mature IL-37 was dependent on ATP. Precursor and mature IL-37 was also secreted from human dendritic cells and peripheral blood mononuclear cells. To determine whether IL-37 is active in the extracellular compartment, we pretreated IL-37 transgenic mice with IL-37-neutralizing antibodies before LPS challenge. In IL-37-expressing mice, neutralizing IL-37 antibodies reversed the suppression of LPS-induced serum IL-6. In contrast, the addition of neutralizing antibody did not reverse suppression of LPS-induced IL-6 in mouse macrophages transfected with IL-37. Although caspase-1 is required for nuclear translocation of intracellular IL-37 and for secretion of mature IL-37, the release of the IL-37 precursor is independent of caspase-1 activation. IL-37 now emerges as a dual-function cytokine with intra- and extracellular properties for suppressing innate inflammation.
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页码:2650 / 2655
页数:6
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