Caught with their PAMPs down? The extracellular signalling actions of molecular chaperones are not due to microbial contaminants

被引:70
作者
Henderson, Brian [1 ]
Calderwood, Stuart K. [2 ]
Coates, Anthony R. M. [3 ]
Cohen, Irun [4 ]
van Eden, Willem [5 ]
Lehner, Thomas [6 ]
Pockley, A. Graham [7 ]
机构
[1] UCL, Div Microbial Dis, UCL Eastman Dent Inst, London WC1X 8LD, England
[2] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Dept Radiat Oncol, Boston, MA 02215 USA
[3] St Georges Univ London, Ctr Infect, Div Cellular & Mol Med, London SW17 ORE, England
[4] Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel
[5] Univ Utrecht, Inst Infect Dis & Immunol, NL-3584 CL Utrecht, Netherlands
[6] Guys Hosp, Kings Coll London, London SE1 9RT, England
[7] Univ Sheffield, Sch Med, Immunobiol Res Grp, Sheffield S10 2RX, S Yorkshire, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
Heat shock proteins; Endotoxin; Innate immunity; Adaptive immunity; Inflammation; Immunoregulation; HEAT-SHOCK PROTEINS; MYCOBACTERIUM-TUBERCULOSIS CHAPERONIN-60.1; STIMULATES BONE-RESORPTION; EARLY-PREGNANCY FACTOR; TUMOR-NECROSIS-FACTOR; T-CELLS RESPOND; DENDRITIC CELLS; ESCHERICHIA-COLI; CUTTING EDGE; CYTOKINE PRODUCTION;
D O I
10.1007/s12192-009-0137-6
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In recent years, it has been hypothesised that a new signalling system may exist in vertebrates in which secreted molecular chaperones form a dynamic continuum between the cellular stress response and corresponding homeostatic physiological mechanisms. This hypothesis seems to be supported by the finding that many molecular chaperones are released from cells and act as extracellular signals for a range of cells. However, this nascent field of biological research seems to suffer from an excessive criticism that the biological activities of molecular chaperones are due to undefined components of the microbial expression hosts used to generate recombinant versions of these proteins. In this article, a number of the proponents of the cell signalling actions of molecular chaperones take this criticism head-on. They show that sufficient evidence exists to support fully the hypothesis that molecular chaperones have cell-cell signalling actions that are likely to be part of the homeostatic mechanism of the vertebrate.
引用
收藏
页码:123 / 141
页数:19
相关论文
共 132 条
[21]   Immune modulation with high-dose heat-shock protein gp96: therapy of murine autoimmune diabetes and encephalomyelitis [J].
Chandawarkar, RY ;
Wagh, MS ;
Kovalchin, JT ;
Srivastava, P .
INTERNATIONAL IMMUNOLOGY, 2004, 16 (04) :615-624
[22]   LYMPHOCYTE-T CLONES ILLUMINATE PATHOGENESIS AND AFFECT THERAPY OF EXPERIMENTAL ARTHRITIS [J].
COHEN, IR ;
HOLOSHITZ, J ;
VANEDEN, W ;
FRENKEL, A .
ARTHRITIS AND RHEUMATISM, 1985, 28 (08) :841-845
[23]   Heat shock protein 60 activates B cells via the TLR4-MyD88 pathway [J].
Cohen-Sfady, M ;
Nussbaum, G ;
Pevsner-Fischer, M ;
Mor, F ;
Carmi, P ;
Zanin-Zhorov, A ;
Lider, O ;
Cohen, IR .
JOURNAL OF IMMUNOLOGY, 2005, 175 (06) :3594-3602
[24]   Inhibition of antigen-presenting cell function and stimulation of human peripheral blood mononuclear cells to express an antiinflammatory cytokine profile by the stress protein BiP - Relevance to the treatment of inflammatory arthritis [J].
Corrigall, VM ;
Bodman-Smith, MD ;
Brunst, M ;
Cornell, H ;
Panayi, GS .
ARTHRITIS AND RHEUMATISM, 2004, 50 (04) :1164-1171
[25]   The human endoplasmic reticulum molecular chaperone BiP is an autoantigen for rheumatoid arthritis and prevents the induction of experimental arthritis [J].
Corrigall, VM ;
Bodman-Smith, MD ;
Fife, MS ;
Canas, B ;
Myers, LK ;
Wooley, PH ;
Soh, C ;
Staines, NA ;
Pappin, DJC ;
Berlo, SE ;
van Eden, W ;
van der Zee, R ;
Lanchbury, JS ;
Panayi, GS .
JOURNAL OF IMMUNOLOGY, 2001, 166 (03) :1492-1498
[26]   JUVENILE CHRONIC ARTHRITIS - T-CELL REACTIVITY TO HUMAN HSP60 IN PATIENTS WITH A FAVORABLE COURSE OF ARTHRITIS [J].
DEGRAEFFMEEDER, ER ;
VANEDEN, W ;
RIJKERS, GT ;
PRAKKEN, BJ ;
KUIS, W ;
VOORHORSTOGINK, MM ;
VANDERZEE, R ;
SCHUURMAN, HJ ;
HELDERS, PJM ;
ZEGERS, BJM .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (03) :934-940
[27]   RECOGNITION OF HUMAN 60 KD HEAT-SHOCK PROTEIN BY MONONUCLEAR-CELLS FROM PATIENTS WITH JUVENILE CHRONIC ARTHRITIS [J].
DEGRAEFFMEEDER, ER ;
VANDERZEE, R ;
RIJKERS, GT ;
SCHUURMAN, HJ ;
KUIS, W ;
BIJLSMA, JWJ ;
ZEGERS, BJM ;
VANEDEN, W .
LANCET, 1991, 337 (8754) :1368-1372
[28]   Involvement of LOX-1 in dendritic cell-mediated antigen cross-presentation [J].
Delneste, Y ;
Magistrelli, G ;
Gauchat, JF ;
Haeuw, JF ;
Aubry, JP ;
Nakamura, K ;
Kawakami-Honda, N ;
Goetsch, L ;
Sawamura, T ;
Bonnefoy, JY ;
Jeannin, P .
IMMUNITY, 2002, 17 (03) :353-362
[29]   Testing the role of gp96 as peptide chaperone in antigen processing [J].
Demine, R ;
Walden, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (18) :17573-17578
[30]   Analysis of purified gp96 preparations from rat and mouse livers using 2-D gel electrophoresis and tandem mass spectrometry [J].
Fairburn, B. ;
Muthana, M. ;
Hopkinson, K. ;
Slack, L. K. ;
Mirza, S. ;
Georgiou, A. S. ;
Espigares, E. ;
Wong, C. ;
Pockley, A. G. .
BIOCHIMIE, 2006, 88 (09) :1165-1174