[Understanding New Regulatory Mechanism of TCR Signal Transduction].

IF 0.3 4区 医学 Q4 PHARMACOLOGY & PHARMACY Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan Pub Date : 2024-01-01 DOI:10.1248/yakushi.23-00154-4
Jun-Ichi Kashiwakura, Tadashi Matsuda
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引用次数: 0

Abstract

Signal-transducing adaptor protein-2 (STAP-2) is a unique scaffold protein that regulates several immunological signaling pathways, including LIF/LIF receptor and LPS/TLR4 signals. STAP-2 is required for Fas/FasL-dependent T cell apoptosis and SDF-1α-induced T cell migration. Conversely, STAP-2 modulates integrin-mediated T cell adhesion, suggesting that STAP-2 is essential for several negative and positive T cell functions. However, whether STAP-2 is involved in T cell-antigen receptor (TCR)-mediated T cell activation is unknown. STAP-2 deficiency was recently reported to suppress TCR-mediated T cell activation by inhibiting LCK-mediated CD3ζ and ZAP-70 activation. Using STAP-2 deficient mice, it was demonstrated that STAP-2 is required for the pathogenesis of Propionibacterium acnes-induced granuloma formation and experimental autoimmune encephalomyelitis. Here, detailed functions of STAP-2 in TCR-mediated T cell activation, and how STAP-2 affects the pathogenesis of T cell-mediated inflammation and immune diseases, are reviewed.

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[了解 TCR 信号转导的新调控机制]。
信号转导适配蛋白-2(STAP-2)是一种独特的支架蛋白,可调节多种免疫信号通路,包括 LIF/LIF 受体和 LPS/TLR4 信号。STAP-2 是 Fas/FasL 依赖性 T 细胞凋亡和 SDF-1α 诱导的 T 细胞迁移所必需的。相反,STAP-2 可调节整合素介导的 T 细胞粘附,这表明 STAP-2 对 T 细胞的几种负性和正性功能都至关重要。然而,STAP-2 是否参与了 T 细胞-抗原受体(TCR)介导的 T 细胞活化尚不清楚。最近有报道称,STAP-2 的缺乏会抑制 LCK 介导的 CD3ζ 和 ZAP-70 的活化,从而抑制 TCR 介导的 T 细胞活化。利用 STAP-2 缺陷小鼠证明,STAP-2 在痤疮丙酸杆菌诱导的肉芽肿形成和实验性自身免疫性脑脊髓炎的发病机制中是必需的。在此,我们将详细介绍 STAP-2 在 TCR 介导的 T 细胞活化中的功能,以及 STAP-2 如何影响 T 细胞介导的炎症和免疫疾病的发病机制。
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CiteScore
0.60
自引率
0.00%
发文量
169
审稿时长
1 months
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