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Platelet-leukocyte deregulated interactions foster sterile inflammation and tissue damage in immune-mediated vessel diseases
被引:26
|作者:
Maugeri, Norma
[1
]
Baldini, Mattia
Ramirez, Giuseppe A.
Rovere-Querini, Patrizia
Manfredi, Angelo A.
机构:
[1] Univ Vita Salute San Raffaele, Autoimmun & Vasc Inflammat Unit, Milan, Italy
关键词:
GIANT-CELL ARTERITIS;
LONG PENTRAXIN PTX3;
CRANIAL ISCHEMIC COMPLICATIONS;
VASCULAR INFLAMMATION;
ACTIVATED PLATELETS;
HMGB1;
NEUTROPHILS;
CLEARANCE;
PROTEIN;
INNATE;
D O I:
10.1016/j.thromres.2011.12.001
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Platelets and leukocytes co-localize and interact at sites of vessel injury, haemorrhage, thrombosis and inflammation. Recent studies have highlighted the role of local cues in the interaction between the two cell populations, including the exposure of anionic phospholipids and the release of Damage Associated Molecular Patterns (DAMPs) by activated platelets, the release of the prototypical tissue pentraxin PTX3 by neutrophils, as well as the generation of polarized clusters of neutrophil beta(2) integrins. In turn, the reciprocal activatory cross-talk between platelets and leukocytes contributes to the generation of thrombo-inflammatory lesions and of vascular injury. Here we will discuss the implications of these results for the pathogenesis and the clinical features of self-sustaining immune-mediated vessel diseases. (C) 2011 Elsevier Ltd. All rights reserved.
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页码:267 / 273
页数:7
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