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CCR7在星形胶质细胞中表达,在炎症损伤后上调。

CCR7 is expressed in astrocytes and upregulated after an inflammatory injury.

作者信息

Gomez-Nicola Diego, Pallas-Bazarra Noemí, Valle-Argos Beatriz, Nieto-Sampedro Manuel

机构信息

Neural Plasticity Group, Functional and Systems Neurobiology Department, Cajal Institute, CSIC, Avda Doctor Arce, 37, 28002, Madrid, Spain.

出版信息

J Neuroimmunol. 2010 Oct 8;227(1-2):87-92. doi: 10.1016/j.jneuroim.2010.06.018. Epub 2010 Jul 16.

Abstract

Neurodegenerative or autoimmune diseases are frequently regulated by chemokines and their receptors, controlling both glial activation and immune cell infiltration. CCL19 and CCL21 have been described to mediate crucial functions during CNS pathological states, regulating both immune cell traffic to the CNS and communication between glia and neurons. Here, we describe the expression pattern and cellular sources of CCR7, receptor of CCL19 and CCL21, in the normal mouse brain. Moreover, we found that CCR7 is upregulated in reactive astrocytes upon intracerebral LPS, regulating early glial reactivity through its ligands CCL19 and CCL21. Our results indicate that CCR7 is playing an important role for the intercellular communication during the inflammatory activation in the CNS.

摘要

神经退行性疾病或自身免疫性疾病常受趋化因子及其受体调控,控制着胶质细胞活化和免疫细胞浸润。CCL19和CCL21已被描述在中枢神经系统病理状态下介导关键功能,调节免疫细胞向中枢神经系统的迁移以及胶质细胞与神经元之间的通讯。在此,我们描述了CCL19和CCL21的受体CCR7在正常小鼠脑内的表达模式和细胞来源。此外,我们发现脑内注射脂多糖后,反应性星形胶质细胞中CCR7上调,通过其配体CCL19和CCL21调节早期胶质细胞反应性。我们的结果表明,CCR7在中枢神经系统炎症激活期间的细胞间通讯中发挥着重要作用。

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