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分子线索引导炎症反应。

Molecular cues guiding inflammatory responses.

机构信息

Departamento de Biología Vascular e Inflamación, Centro Nacional de Investigaciones Cardiovasculares, Melchor Fernández Almagro 3, 28029 Madrid, Spain.

出版信息

Cardiovasc Res. 2010 May 1;86(2):174-82. doi: 10.1093/cvr/cvq001. Epub 2010 Jan 6.

Abstract

Alarm signals generated at inflammatory foci reach the vascular lumen to attract immune cells towards the affected tissue. Different leucocyte subsets decipher and integrate these complex signals in order to make adequate decisions for their migration towards the inflamed tissue. Soluble cues (cytokines and chemokines) and membrane receptors in both endothelium and leucocytes orchestrate the coordinated recruitment of specific inflammatory cell subsets. All these molecules are spatio-temporally organized in specialized structures at the luminal side of endothelium and the leucocyte membrane or are generated as chemical gradients in the damaged tissue. Thus, the repertoire of chemokines and their receptors as well as adhesion molecules expressed by each leucocyte subset determine their recruitment for participation in specific inflammatory pathologies. Whenever inflammatory signals are altered or misprocessed, inflammation can become chronic, causing extensive tissue damage. To combat chronic inflammation and autoimmune diseases, novel therapeutic strategies attempt to silence the predominant signals in each inflammatory scenario. In this review, we provide a general overview of all these aspects related to the molecular regulation of leucocyte guidance in inflammatory responses.

摘要

炎症部位产生的警报信号到达血管腔,吸引免疫细胞向受影响的组织移动。不同的白细胞亚群对这些复杂信号进行解读和整合,以便对其向炎症组织的迁移做出适当的决策。可溶性线索(细胞因子和趋化因子)和内皮细胞和白细胞中的膜受体共同协调特定炎症细胞亚群的协调招募。所有这些分子都在血管内皮细胞腔侧和白细胞膜的特化结构中或在受损组织中作为化学梯度进行时空组织。因此,每种白细胞亚群表达的趋化因子及其受体和黏附分子决定了它们被招募来参与特定的炎症病理。一旦炎症信号发生改变或处理不当,炎症就可能变成慢性的,导致广泛的组织损伤。为了对抗慢性炎症和自身免疫性疾病,新的治疗策略试图沉默每种炎症情况下的主要信号。在这篇综述中,我们提供了与炎症反应中白细胞导向的分子调控相关的所有这些方面的概述。

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