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巨核细胞中α-辅肌动蛋白-1缺乏会导致血小板计数降低、血小板功能障碍和线粒体损伤。

α-Actinin-1 deficiency in megakaryocytes causes low platelet count, platelet dysfunction, and mitochondrial impairment.

作者信息

Lin Xiangjie, Gao Hanchen, Xin Min, Huang Jian, Li Xia, Zhou Yutong, Lv Keyu, Huang Xin, Wang Jinghan, Zhou Yulan, Cui Dawei, Fang Chao, Wu Lanlan, Shi Xiaofeng, Ma Zhixin, Qian Yu, Tong Hongyan, Dai Jing, Jin Jie, Huang Jiansong

机构信息

Department of Hematology, Zhejiang Key Laboratory for Precision Diagnosis and Treatment of Hematological Malignancies, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.

Department of Laboratory Medicine, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

出版信息

Blood Adv. 2025 Mar 11;9(5):1185-1201. doi: 10.1182/bloodadvances.2024014805.

Abstract

Cytoskeletal remodeling and mitochondrial bioenergetics play important roles in thrombocytopoiesis and platelet function. Recently, α-actinin-1 mutations have been reported in patients with congenital macrothrombocytopenia. However, the role and underlying mechanism of α-actinin-1 in thrombocytopoiesis and platelet function remain elusive. Using megakaryocyte (MK)-specific α-actinin-1 knockout (KO; PF4-Actn1-/-) mice, we demonstrated that PF4-Actn1-/- mice exhibited reduced platelet counts. The decreased platelet number in PF4-Actn1-/- mice was due to defects in thrombocytopoiesis. Hematoxylin and eosin staining and flow cytometry revealed a decrease in the number of MKs in the bone marrow of PF4-Actn1-/- mice. The absence of α-actinin-1 increased the proportion of 2 N-4 N MKs and decreased the proportion of 8 N-32 N MKs. Colony-forming unit-MK colony formation, the ratio of proplatelet formation-bearing MKs, and MK migration in response to stromal cell-derived factor-1 signaling were inhibited in PF4-Actn1-/- mice. Platelet spreading, clot retraction, aggregation, integrin αIIbβ3 activation, and CD62P exposure in response to various agonists were decreased in PF4-Actn1-/- platelets. Notably, PF4-Actn1-/- platelets inhibited calcium mobilization, reactive oxygen species (ROS) generation, and actin polymerization in response to collagen and thrombin. Furthermore, the PF4-Actn1-/- mice exhibited impaired hemostasis and thrombosis. Mechanistically, proteomic analysis of low-ploidy (2-4 N) and high-ploidy (≥8 N) PF4-Actn1-/- MKs revealed that α-actinin-1 deletion reduced platelet activation and mitochondrial function. PF4-Actn1-/- platelets and Actn1 KO 293T cells exhibited reduced mitochondrial membrane potential, mitochondrial ROS generation, mitochondrial calcium mobilization, and mitochondrial bioenergetics. Overall, in this study, we report that mice with α-actinin-1 deficiency in MKs exhibit low platelet count and impaired platelet function, thrombosis, and mitochondrial bioenergetics.

摘要

细胞骨架重塑和线粒体生物能量学在血小板生成和血小板功能中发挥着重要作用。最近,在先天性巨血小板减少症患者中报道了α-辅肌动蛋白-1突变。然而,α-辅肌动蛋白-1在血小板生成和血小板功能中的作用及潜在机制仍不清楚。利用巨核细胞(MK)特异性α-辅肌动蛋白-1基因敲除(KO;PF4-Actn1-/-)小鼠,我们证明PF4-Actn1-/-小鼠的血小板计数减少。PF4-Actn1-/-小鼠血小板数量减少是由于血小板生成缺陷所致。苏木精和伊红染色及流式细胞术显示PF4-Actn1-/-小鼠骨髓中MK数量减少。α-辅肌动蛋白-1的缺失增加了2N-4N MK的比例,降低了8N-32N MK的比例。PF4-Actn1-/-小鼠中集落形成单位-MK集落形成、含前血小板形成的MK比例以及MK对基质细胞衍生因子-1信号的迁移均受到抑制。PF4-Actn1-/-血小板对各种激动剂的血小板铺展、血块收缩、聚集、整合素αIIbβ3激活和CD62P暴露均减少。值得注意的是,PF4-Actn1-/-血小板在对胶原和凝血酶的反应中抑制钙动员、活性氧(ROS)生成和肌动蛋白聚合。此外,PF4-Actn1-/-小鼠的止血和血栓形成功能受损。从机制上讲,对低倍体(2-4N)和高倍体(≥8N)PF4-Actn1-/- MK进行蛋白质组学分析发现,α-辅肌动蛋白-1的缺失降低了血小板活化和线粒体功能。PF4-Actn1-/-血小板和Actn1基因敲除的293T细胞表现出线粒体膜电位降低、线粒体ROS生成减少、线粒体钙动员减少和线粒体生物能量学改变。总体而言,在本研究中,我们报道了MK中α-辅肌动蛋白-1缺乏的小鼠表现出血小板计数低以及血小板功能、血栓形成和线粒体生物能量学受损。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1770/11925533/0780172a22bf/BLOODA_ADV-2024-014805-ga1.jpg

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