Experimental Cardiology Laboratory, Cardiology, University Medical Center Utrecht, Utrecht, The Netherlands.
J Innate Immun. 2010;2(4):307-15. doi: 10.1159/000314270. Epub 2010 Apr 30.
Innate immunity is important in the pathogenesis and progression of cardiovascular disease. Innate immune cells express various pattern-recognition receptors, among which also Toll-like receptors (TLRs). TLRs occur in atherosclerotic lesions where they are triggered by both exogenous (bacterial and viral pathogens) and endogenous (tissue damage-associated) molecules. Several endogenous TLR activators are described in relation to atherosclerotic disease or ischemia-induced cardiac injury. Experimental animal models have proved the role of TLR endogenous activators in disease initiation and further development. Nowadays, researchers aim to unravel the exact mechanisms involved in the endogenous ligand-dependent TLR signaling and to discover new potential activators, released during pathological conditions such as atherosclerosis and related ischemic manifestations. This review provides an overview of the currently known endogenous molecules which trigger innate immunity via TLRs in cardiovascular disease.
先天免疫在心血管疾病的发病机制和进展中很重要。先天免疫细胞表达各种模式识别受体,其中也包括 Toll 样受体(TLR)。TLR 存在于动脉粥样硬化病变中,它们可被外源性(细菌和病毒病原体)和内源性(与组织损伤相关的)分子触发。与动脉粥样硬化疾病或缺血性心脏损伤相关,已有几种内源性 TLR 激活物被描述。实验动物模型已经证明了 TLR 内源性激活物在疾病起始和进一步发展中的作用。如今,研究人员旨在揭示内源性配体依赖性 TLR 信号转导中涉及的确切机制,并发现新的潜在激活物,这些激活物在动脉粥样硬化和相关缺血表现等病理条件下释放。这篇综述概述了目前已知的通过先天免疫中 TLR 触发心血管疾病的内源性分子。