趋化细胞因子、白细胞介素-8和MCAF发现以来的35年:历史概述。

IF 4.4 3区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Proceedings of the Japan Academy. Series B, Physical and Biological Sciences Pub Date : 2023-01-01 DOI:10.2183/pjab.99.014
Kouji Matsushima, Shigeyuki Shichino, Satoshi Ueha
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引用次数: 1

摘要

炎症是宿主对各种入侵刺激的防御反应,但过度和持续的炎症反应可引起组织损伤,从而导致不可逆的器官损伤和功能障碍。过度的炎症反应被认为与大多数人类疾病有关。炎症需要一种特殊类型的白细胞浸润到被侵犯的组织中。从历史上看,炎症过程中潜在的分子机制是一个谜,影响了炎症、免疫学和病理学领域的研究。然而,趋化因子(趋化因子)的开创性发现,单核细胞来源的中性粒细胞趋化因子(MDNCF;白细胞介素[IL]-8, CXCL8)和单核细胞趋化活化因子(MCAF);单核细胞趋化因子1 [MCP-1], CCL2)在20世纪80年代末终于使我们能够解决这个问题。在这篇综述中,我们提供了过去35年来趋化因子研究的历史概述。
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Thirty-five years since the discovery of chemotactic cytokines, interleukin-8 and MCAF: A historical overview.

Inflammation is a host defense response to various invading stimuli, but an excessive and persistent inflammatory response can cause tissue injury, which can lead to irreversible organ damage and dysfunction. Excessive inflammatory responses are believed to link to most human diseases. A specific type of leukocyte infiltration into invaded tissues is required for inflammation. Historically, the underlying molecular mechanisms of this process during inflammation were an enigma, compromising research in the fields of inflammation, immunology, and pathology. However, the pioneering discovery of chemotactic cytokines (chemokines), monocyte-derived neutrophil chemotactic factor (MDNCF; interleukin [IL]-8, CXCL8) and monocyte chemotactic and activating factor (MCAF; monocyte chemotactic factor 1 [MCP-1], CCL2) in the late 1980s finally enabled us to address this issue. In this review, we provide a historical overview of chemokine research over the last 35 years.

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来源期刊
CiteScore
6.60
自引率
0.00%
发文量
26
审稿时长
>12 weeks
期刊介绍: The Proceedings of the Japan Academy Ser. B (PJA-B) is a scientific publication of the Japan Academy with a 90-year history, and covers all branches of natural sciences, except for mathematics, which is covered by the PJA-A. It is published ten times a year and is distributed widely throughout the world and can be read and obtained free of charge through the world wide web.
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