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人少突胶质细胞上的CXC趋化因子受体:对多发性硬化症的影响

CXC chemokine receptors on human oligodendrocytes: implications for multiple sclerosis.

作者信息

Omari Kakuri M, John Gareth R, Sealfon Stuart C, Raine Cedric S

机构信息

Department of Pathology (Neuropathology), Albert Einstein College of Medicine, 1300 Morris Park Avenue, F-140, Bronx, NY 10461, USA.

出版信息

Brain. 2005 May;128(Pt 5):1003-15. doi: 10.1093/brain/awh479. Epub 2005 Mar 17.

Abstract

Subsequent to demyelination in multiple sclerosis, myelin repair occurs but, as lesions age, the ability to remyelinate diminishes. Molecular pathways underlying oligodendrocyte behaviour during CNS remyelination remain to be elucidated. In this study, we report for the first time constitutive expression of the CXC/alpha chemokine receptors, CXCR1, CXCR2 and CXCR3, on oligodendrocytes in normal adult human CNS tissue, the levels of which were upregulated in multiple sclerosis and other neurological diseases (OND). In addition, both immature (A2B5+/O4+) and more mature (CNPase+) human oligodendrocytes in vitro expressed the same three receptors. The respective ligands to CXCR1, CXCR2 and CXCR3 [i.e. CXCL8/IL-8, CXCL1/GRO-alpha and CXCL10/IP-10), were absent in CNS tissue from normals and subjects with OND, but were present at high levels on hypertrophic (reactive) astrocytes at the edge of active (but not silent) multiple sclerosis lesions. Astrocytes in vitro could be induced to express chemokines following stimulation with pro-inflammatory cytokines. CXCL8 and CXCL1 production by human astrocytes at both the RNA and protein levels could be induced by interleukin (IL)-1beta, while CXCL10 was induced by both IL-1beta and interferon-gamma. Since these cytokines are integral to inflammatory events occurring at the margins of active multiple sclerosis lesions, their upregulation in these regions may underlie the dynamics of chemokine expression observed herein. The simultaneous expression of different CXC chemokine receptors on oligodendrocytes, and their ligands on astrocytes around multiple sclerosis lesions, may bespeak novel functional roles for these immune system molecules in the recruitment of oligodendrocytes and remyelination.

摘要

在多发性硬化症发生脱髓鞘之后,髓鞘会进行修复,但是随着病灶的老化,重新髓鞘化的能力会下降。中枢神经系统(CNS)重新髓鞘化过程中少突胶质细胞行为的分子途径仍有待阐明。在本研究中,我们首次报道了CXC/α趋化因子受体CXCR1、CXCR2和CXCR3在正常成人人中枢神经系统组织中的少突胶质细胞上组成性表达,在多发性硬化症和其他神经疾病(OND)中其水平上调。此外,体外培养的未成熟(A2B5+/O4+)和更成熟(CNPase+)的人少突胶质细胞都表达这三种相同的受体。CXCR1、CXCR2和CXCR3各自的配体[即CXCL8/IL-8、CXCL1/GRO-α和CXCL10/IP-10]在正常人和OND患者的中枢神经系统组织中不存在,但在活动性(而非静止性)多发性硬化症病灶边缘的肥大(反应性)星形胶质细胞上高水平存在。体外培养的星形胶质细胞在用促炎细胞因子刺激后可被诱导表达趋化因子。人星形胶质细胞在RNA和蛋白质水平上产生CXCL8和CXCL1可被白细胞介素(IL)-1β诱导,而CXCL10可被IL-1β和干扰素-γ诱导。由于这些细胞因子是活动性多发性硬化症病灶边缘发生的炎症事件所必需的,它们在这些区域的上调可能是本文观察到的趋化因子表达动态变化的基础。少突胶质细胞上不同CXC趋化因子受体与多发性硬化症病灶周围星形胶质细胞上其配体的同时表达,可能表明这些免疫系统分子在少突胶质细胞募集和重新髓鞘化中具有新的功能作用。

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