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Macrophage TLR4 and PAR2 Signaling: Role in Regulating Vascular Inflammatory Injury and Repair
被引:40
|作者:
Rayees, Sheikh
Rochford, Ian
Joshi, Jagdish Chandra
Joshi, Bhagwati
Banerjee, Somenath
Mehta, Dolly
[1
]
机构:
[1] Univ Illinois, Coll Med, Dept Pharmacol, Chicago, IL 60680 USA
来源:
FRONTIERS IN IMMUNOLOGY
|
2020年
/
11卷
基金:
美国国家卫生研究院;
关键词:
macrophage;
vascular permeability;
acute lung injury;
TLR4;
PAR2;
inflammation;
alveolar macrophages;
PROTEASE-ACTIVATED RECEPTORS;
PULMONARY ALVEOLAR PROTEINOSIS;
FLOW-CYTOMETRIC ANALYSIS;
NF-KAPPA-B;
COLONY-STIMULATING FACTOR;
TOLL-LIKE;
INTERSTITIAL MACROPHAGES;
ONTOGENIC DEVELOPMENT;
CHEMOKINE SYSTEM;
LUNG MACROPHAGES;
D O I:
10.3389/fimmu.2020.02091
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Macrophages play a central role in dictating the tissue response to infection and orchestrating subsequent repair of the damage. In this context, macrophages residing in the lungs continuously sense and discriminate among a wide range of insults to initiate the immune responses important to host-defense. Inflammatory tissue injury also leads to activation of proteases, and thereby the coagulation pathway, to optimize injury and repair post-infection. However, long-lasting inflammatory triggers from macrophages can impair the lung's ability to recover from severe injury, leading to increased lung vascular permeability and neutrophilic injury, hallmarks of Acute Lung Injury (ALI). In this review, we discuss the roles of toll-like receptor 4 (TLR4) and protease activating receptor 2 (PAR2) expressed on the macrophage cell-surface in regulating lung vascular inflammatory signaling.
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