Immunoproteasomes Preserve Protein Homeostasis upon Interferon-Induced Oxidative Stress

被引:452
作者
Seifert, Ulrike [1 ]
Bialy, Lukasz P. [1 ]
Ebstein, Frederic [1 ]
Bech-Otschir, Dawadschargal [1 ]
Voigt, Antje [2 ]
Schroeter, Friederike [1 ]
Prozorovski, Timour [3 ]
Lange, Nicole [1 ]
Steffen, Janos [1 ]
Rieger, Melanie [1 ]
Kuckelkorn, Ulrike [1 ]
Aktas, Orhan [3 ]
Kloetzel, Peter-M. [1 ]
Krueger, Elke [1 ]
机构
[1] Charite, Inst Biochem CC2, D-13347 Berlin, Germany
[2] Charite, Med Klin Kardiol & Angiol CC13, D-10117 Berlin, Germany
[3] Univ Dusseldorf, Fac Med, Dept Neurol, D-40225 Dusseldorf, Germany
关键词
NEWLY SYNTHESIZED PROTEINS; CD8(+) T-CELLS; PROTEASOME SYSTEM; GAMMA-INTERFERON; HEAT-SHOCK; INDUCTION; DEGRADATION; UBIQUITIN; IMMUNITY; PATHWAY;
D O I
10.1016/j.cell.2010.07.036
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Interferon (IFN)-induced immunoproteasomes (i-proteasomes) have been associated with improved processing of major histocompatibility complex (MHC) class I antigens. Here, we show that i-proteasomes function to protect cell viability under conditions of IFN-induced oxidative stress. IFNs trigger the production of reactive oxygen species, which induce protein oxidation and the formation of nascent, oxidant-damaged proteins. We find that the ubiquitylation machinery is concomitantly upregulated in response to IFNs, functioning to target defective ribosomal products (DRiPs) for degradation by i-proteasomes. i-proteasome-deficiency in cells and in murine inflammation models results in the formation of aggresome-like induced structures and increased sensitivity to apoptosis. Efficient clearance of these aggregates by the enhanced proteolytic activity of the i-proteasome is important for the preservation of cell viability upon IFN-induced oxidative stress. Our findings suggest that rather than having a specific role in the production of class I antigens, i-proteasomes increase the peptide supply for antigen presentation as part of a more general role in the maintenance of protein homeostasis.
引用
收藏
页码:613 / 624
页数:12
相关论文
共 49 条
[21]   Aggresomes, inclusion bodies and protein aggregation [J].
Kopito, RR .
TRENDS IN CELL BIOLOGY, 2000, 10 (12) :524-530
[22]   Upregulation of immunoproteasomes by nitric oxide: Potential antioxidative mechanism in endothelial cells [J].
Kotamraju, S ;
Matalon, S ;
Matsunaga, T ;
Hickman-Davis, JM ;
Kalyanaraman, B .
FREE RADICAL BIOLOGY AND MEDICINE, 2006, 40 (06) :1034-1044
[23]   The components of the proteasome system and their role in MHC class I antigen processing [J].
Krüger, E ;
Kuckelkorn, U ;
Sijts, A ;
Kloetzel, PM .
REVIEWS OF PHYSIOLOGY, BIOCHEMISTRY AND PHARMACOLOGY, VOL 148, 2004, 148 :81-104
[24]   Dendritic cell aggresome-like induced structures are dedicated areas for ubiquitination and storage of newly synthesized defective proteins [J].
Lelouard, H ;
Ferrand, V ;
Marguet, D ;
Bania, J ;
Camosseto, V ;
David, A ;
Gatti, E ;
Pierre, P .
JOURNAL OF CELL BIOLOGY, 2004, 164 (05) :667-675
[25]   Regulation of translation is required for dendritic cell function and survival during activation [J].
Lelouard, Hugues ;
Schmidt, Enrico K. ;
Camosseto, Voahirana ;
Clavarino, Giovanna ;
Ceppi, Maurizio ;
Hsu, Hsiang-Ting ;
Pierre, Philippe .
JOURNAL OF CELL BIOLOGY, 2007, 179 (07) :1427-1439
[26]   Immunity by ubiquitylation: A reversible process of modification [J].
Liu, YC ;
Penninger, J ;
Karin, M .
NATURE REVIEWS IMMUNOLOGY, 2005, 5 (12) :941-952
[27]   Heat shock and oxygen radicals stimulate ubiquitin-dependent degradation mainly of newly synthesized proteins [J].
Medicherla, Balasubrahmanyam ;
Goldberg, Alfred L. .
JOURNAL OF CELL BIOLOGY, 2008, 182 (04) :663-673
[28]   Proteasome-independent functions of ubiquitin in endocytosis and signaling [J].
Mukhopadhyay, Debdyuti ;
Riezman, Howard .
SCIENCE, 2007, 315 (5809) :201-205
[29]   Immunoproteasome-deficient mice mount largely normal CD8+ T cell responses to lymphocytic choriomeningitis virus infection and DNA vaccination [J].
Nussbaum, AK ;
Rodriguez-Carreno, MP ;
Benning, N ;
Botten, J ;
Whitton, JL .
JOURNAL OF IMMUNOLOGY, 2005, 175 (02) :1153-1160
[30]   An oxidative mechanism of interferon induced priming of the Fas pathway in Fanconi anemia cells [J].
Pearl-Yafe, M ;
Halperin, D ;
Halevy, A ;
Kalir, H ;
Bielorai, B ;
Fabian, I .
BIOCHEMICAL PHARMACOLOGY, 2003, 65 (05) :833-842