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丝状肌动蛋白参与设定肥大细胞脱颗粒的阈值。

Involvement of filamentous actin in setting the threshold for degranulation in mast cells.

作者信息

Tolarová Helena, Dráberová Lubica, Heneberg Petr, Dráber Petr

机构信息

Department of Signal Transduction, Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, Prague, Czech Republic.

出版信息

Eur J Immunol. 2004 Jun;34(6):1627-36. doi: 10.1002/eji.200424991.

Abstract

Previous studies using cytochalasins and latrunculin B, inhibitors of actin polymerization, showed that filamentous (F)-actin had a negative regulatory role in Fc epsilon receptor I (Fc epsilon RI) signaling. How F-actin is involved in regulating the activation of mast cells is unknown. In this study we investigated the role of F-actin in mast cell activation induced by aggregation of the glycosylphosphatidylinositol (GPI)-anchored proteins Thy-1 and TEC-21, and compared it to activation via Fc epsilon RI. Pretreatment of rat basophilic leukemia cells with latrunculin B inhibited the Thy-1-induced actin polymerization and elevated the Thy-1-mediated secretory and calcium responses. Inhibition of actin polymerization followed by Thy-1 aggregation resulted in an increased tyrosine phosphorylation of Syk, phospholipase C gamma (PLC gamma), Gab2 and linker for activation of T cells (LAT) adapters, and some other signaling molecules. Enzymatic activities of phosphatidylinositol 3-kinase, PLC gamma, and phosphatase SHP-2 were also up-regulated, but tyrosine phosphorylation of ezrin was inhibited. Similar changes were observed in Fc epsilon RI-activated cells. Significant changes in intracellular distribution, tyrosine phosphorylation, and/or enzymatic activities of signaling molecules occurred in latrunculin-pretreated cells before cell triggering. The combined data suggest that actin polymerization is critical for setting the thresholds for mast cell signaling via aggregation of both Fc epsilon RI and GPI-anchored proteins.

摘要

以往使用肌动蛋白聚合抑制剂细胞松弛素和拉春库林B进行的研究表明,丝状(F)-肌动蛋白在Fcε受体I(FcεRI)信号传导中具有负调节作用。F-肌动蛋白如何参与调节肥大细胞的活化尚不清楚。在本研究中,我们研究了F-肌动蛋白在糖基磷脂酰肌醇(GPI)锚定蛋白Thy-1和TEC-21聚集诱导的肥大细胞活化中的作用,并将其与通过FcεRI的活化进行比较。用拉春库林B预处理大鼠嗜碱性白血病细胞可抑制Thy-1诱导的肌动蛋白聚合,并提高Thy-1介导的分泌和钙反应。肌动蛋白聚合抑制后再进行Thy-1聚集导致Syk、磷脂酶Cγ(PLCγ)、Gab2和T细胞活化连接蛋白(LAT)衔接蛋白以及其他一些信号分子的酪氨酸磷酸化增加。磷脂酰肌醇3激酶、PLCγ和磷酸酶SHP-2的酶活性也上调,但埃兹蛋白的酪氨酸磷酸化受到抑制。在FcεRI活化的细胞中也观察到类似的变化。在细胞触发之前,拉春库林预处理的细胞中信号分子的细胞内分布、酪氨酸磷酸化和/或酶活性发生了显著变化。综合数据表明,肌动蛋白聚合对于通过FcεRI和GPI锚定蛋白聚集来设定肥大细胞信号传导的阈值至关重要。

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