Microparticles as regulators of inflammation - Novel players of cellular crosstalk in the rheumatic diseases

被引:190
作者
Distler, JHW
Pisetsky, DS
Huber, LC
Kalden, JR
Gay, S
Distler, O
机构
[1] Univ Erlangen Nurnberg, Inst Clin Immunol & Rheumatol, Dept Internal Med 3, D-91054 Erlangen, Germany
[2] Univ Zurich Hosp, CH-8091 Zurich, Switzerland
[3] Duke Univ, Med Ctr, Durham, NC USA
[4] Durham VA Hosp, Durham, NC USA
来源
ARTHRITIS AND RHEUMATISM | 2005年 / 52卷 / 11期
关键词
D O I
10.1002/art.21350
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
As illustrated in Figure 5, microparticles represent novel signaling structures that can be generated during cell activation and apoptosis, 2 events fundamental to inflammation. These particles may serve to both induce and amplify inflammation and potentiate tissue damage in rheumatic disease. Furthermore, microparticles represent potentially useful biomarkers, since key cells in inflammation can be sampled from the blood, using cell surface markers to allow identification of individual cell types. Future studies will define the cell processes generating microparticles, the signaling pathways they induce, and their potential as targets for new therapies, based on either their formation or their triggering of downstream effects in inflammation. Once viewed as by-products of other cellular processes, microparticles are emerging as an exciting new element for information exchange during inflammation, with rheumatic disease as an important setting for their expression.
引用
收藏
页码:3337 / 3348
页数:12
相关论文
共 73 条
[21]   A novel P2X7 receptor activator, the human cathelicidin-derived peptide LL37, induces IL-1β processing and release [J].
Elssner, A ;
Duncan, M ;
Gavrilin, M ;
Wewers, MD .
JOURNAL OF IMMUNOLOGY, 2004, 172 (08) :4987-4994
[22]   Leukocyte-leukocyte interactions mediated by platelet microparticles under flow [J].
Forlow, SB ;
McEver, RP ;
Nollert, MU .
BLOOD, 2000, 95 (04) :1317-1323
[23]   SECRETORY PHOSPHOLIPASE A(2) GENERATES THE NOVEL LIPID MEDIATOR LYSOPHOSPHATIDIC ACID IN MEMBRANE MICROVESICLES SHED FROM ACTIVATED CELLS [J].
FOURCADE, O ;
SIMON, MF ;
VIODE, C ;
RUGANI, N ;
LEBALLE, F ;
RAGAB, A ;
FOURNIE, B ;
SARDA, L ;
CHAP, H .
CELL, 1995, 80 (06) :919-927
[24]  
FOX JEB, 1985, J BIOL CHEM, V260, P1060
[25]   Cellular microparticles: what are they bad or good for? [J].
Freyssinet, JM .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2003, 1 (07) :1655-1662
[26]   Activated polymorphonuclear neutrophils disseminate anti-inflammatory microparticles by ectocytosis [J].
Gasser, O ;
Schifferli, JA .
BLOOD, 2004, 104 (08) :2543-2548
[27]   Characterisation and properties of ectosomes released by human polymorphonuclear neutrophils [J].
Gasser, O ;
Hess, C ;
Miot, S ;
Deon, C ;
Sanchez, JC ;
Schifferli, JA .
EXPERIMENTAL CELL RESEARCH, 2003, 285 (02) :243-257
[28]  
GEMMELL CH, 1993, J BIOL CHEM, V268, P14586
[29]  
GILBERT GE, 1991, J BIOL CHEM, V266, P17261
[30]   Essential role for Ca2+ in regulation of IL-1β secretion by P2X7 nucleotide receptor in monocytes, macrophages, and HEK-293 cells [J].
Gudipaty, L ;
Munetz, J ;
Verhoef, PA ;
Dubyak, GR .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2003, 285 (02) :C286-C299