STK10 regulates platelet function in arterial thrombosis and thromboinflammation

血小板 血小板活化 磷酸化 激酶 血小板疾病 免疫沉淀 细胞生物学 蛋白质磷酸化 血块回缩 化学 止血 蛋白激酶A 生物 分子生物学 磷脂酰肌醇 基因剔除小鼠 中性粒细胞胞外陷阱 内科学 信号转导 癌症研究 败血症 内分泌学 组织因子 蛋白激酶B 免疫学 细胞外 P-选择素 蛋白激酶C 血小板生成素 医学
作者
Y N Li,Hui Zhu,Yun Liu,Xiaoqian Li,Xiaoyue Zu,Chenyue Wang,Xiao‐Qi Xu,Yueyue Sun,Yue Dai,Jie Zhang,Shuang Chen,Huimin Jiang,Zhenyu Li,Lingyu Zeng,Kailin Xu,Jianlin Qiao
出处
期刊:Blood [Elsevier BV]
卷期号:147 (1): 73-86 被引量:6
标识
DOI:10.1182/blood.2025030134
摘要

ABSTRACT: Serine/threonine kinase 10 (STK10) is a member of the Ste20 family of serine/threonine kinases and regulates lymphocyte adhesion. Quantitative phosphoproteomic assay showed increased STK10 phosphorylation in activated platelets. However, its role in platelet function remains unclear. In our study, we investigated the expression and role of STK10 in platelet function. We first showed STK10 expression in human and mouse platelets. By establishing megakaryocyte/platelet-specific STK10 knockout mice, we found that the deletion of platelet STK10 impaired hemostasis and arterial thrombosis. Consistently, platelet aggregation, α-granule release, αIIbβ3 activation, procoagulant activity, spreading, and clot retraction were all reduced after the deletion of STK10. Quantitative phosphoproteomic assays revealed several dysregulated phosphoproteins, which were enriched in platelet activation and focal adhesion. Using immunoprecipitation coupled to mass spectrometry and protein phosphorylation profiles screening approaches, we identified that STK10 interacts with integrin-linked protein kinase (ILK) and the deletion of STK10 significantly reduced ILK phosphorylation (Ser343). A subsequent in vitro phosphorylation assay demonstrated that STK10 directly phosphorylated ILK at Ser343. In addition, the inhibition of calcium, protein kinase C, or phosphatidylinositol 3-kinase inhibited STK10 phosphorylation in activated platelets. Moreover, the deletion of platelet STK10 reduced platelet-neutrophil interactions, neutrophil accumulation, and neutrophil extracellular trap formation, ameliorated thromboinflammation, and increased the survival of sepsis mice. Furthermore, an increase in the activation of platelet STK10 and ILK was observed in sepsis mice and patients with sepsis. In conclusion, our study identifies a novel regulatory role of STK10 in platelet function, arterial thrombosis, and thromboinflammation, implying that it might be a potential target for the treatment of thrombotic or cardiovascular diseases.
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