12-脂氧合酶在调节巨核细胞成熟和血小板样颗粒产生中的作用

IF 3.4 3区 医学 Q1 HEMATOLOGY
Vanessa L. Gauvin , Marie-France N. Soucy , Jaël D. Richard , Kate A. Graham , Alexis J. Matthew , Mathieu P.A. Hébert , Jérémie A. Doiron , Mathieu Johnson , Eric P. Allain , David A. Barnett , Sandra Turcotte , Luc H. Boudreau
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引用次数: 0

摘要

巨核细胞是一种主要在骨髓中产生的髓样细胞,对于将血小板释放到血液中至关重要。通过血小板的产生,巨核细胞将自身的生物成分转移到这些细胞中,包括炎症酶。在这些酶中,12-脂氧合酶(12-LO)已被证明可以调节血小板活化并参与多种慢性炎症。然而,12-LO在巨核细胞成熟和随后血小板释放中的作用仍未被研究。本研究证明了12-LO表达在巨核细胞成熟和功能中的重要性。利用流式细胞术和荧光显微镜分析DAMI细胞的分化情况。通过Western blot分析和LC-MS/MS评估炎症酶谱。为了评估巨核细胞的功能,使用了血小板型12-LO敲除小鼠。DAMI细胞向成熟巨核细胞的分化导致表面标记物表达增加,血小板样颗粒产生增强,细胞增殖减少,细胞死亡增加。分化细胞中花生四烯酸的细胞膜释放量增加,12-LO、环氧化酶-1、血栓素合成酶等炎症酶表达增加。在这些细胞中,12(S)-羟基二碳四烯酸和血栓素的产生也增加。在缺乏12-LO表达(ALOX12−/−)的DAMI细胞中,我们发现与ALOX12+/+细胞相比,分化后CD41的表达没有差异。然而,缺乏12- lo的细胞产生较少的原血小板,因此产生较少的血小板样颗粒。在体内,12- lo缺陷小鼠的血小板计数与野生型小鼠相当,骨髓巨核细胞数量在两组之间保持一致。离体分析显示缺乏12-LO的巨核细胞产生较少的血小板。这些发现表明12-LO可能在巨核细胞功能中发挥调节作用,特别是在血小板形成和血小板释放中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The role of 12-lipoxygenase in regulating megakaryocyte maturation and platelet-like particles production

The role of 12-lipoxygenase in regulating megakaryocyte maturation and platelet-like particles production
Megakaryocytes, a type of myeloid cell primarily produced in the bone marrow, are essential for releasing platelets into the bloodstream. Through platelet production, megakaryocytes transfer their own biological content to these cells, including inflammatory enzymes. Amongst these enzymes, 12-lipoxygenase (12-LO) has been shown to modulate platelet activation and is involved in several chronic inflammatory conditions. However, the role of 12-LO in megakaryocyte maturation and the subsequent release of platelets remains uninvestigated. This study demonstrates the importance of 12-LO expression in megakaryocyte maturation and functions. Flow cytometry and fluorescence microscopy were utilized to analyze DAMI cell differentiation. Inflammatory enzyme profiles were assessed through Western blot analysis and LC-MS/MS. To evaluate megakaryocyte functionality, platelet-type 12-LO knockout mice were employed. Differentiation of DAMI cells into mature megakaryocytes resulted in increased surface marker expression, enhanced platelet-like particle production, reduced cell proliferation, and elevated cell death. The arachidonic acid release from cell membranes was increased in differentiated cells as well as the expression of several inflammatory enzymes such as 12-LO, cyclooxygenase-1 and thromboxane synthase. The production of 12(S)-hydroxyeicosatetraenoic acid and thromboxane was also increased in these cells. In DAMI cells deficient in 12-LO expression (ALOX12−/−), we found no difference in CD41 expression following differentiation compared to ALOX12+/+ cells. However, 12-LO-deficient cells produced fewer proplatelets and, consequently, fewer platelet-like particles. In vivo, platelet counts in 12-LO-deficient mice were comparable to those in wild-type mice, and the number of bone marrow megakaryocytes remained consistent between the groups. Ex vivo analysis revealed that megakaryocytes lacking 12-LO produced fewer platelets. These findings indicate that 12-LO may play a regulatory role in megakaryocyte function, particularly in proplatelet formation and platelet release.
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来源期刊
Thrombosis research
Thrombosis research 医学-外周血管病
CiteScore
14.60
自引率
4.00%
发文量
364
审稿时长
31 days
期刊介绍: Thrombosis Research is an international journal dedicated to the swift dissemination of new information on thrombosis, hemostasis, and vascular biology, aimed at advancing both science and clinical care. The journal publishes peer-reviewed original research, reviews, editorials, opinions, and critiques, covering both basic and clinical studies. Priority is given to research that promises novel approaches in the diagnosis, therapy, prognosis, and prevention of thrombotic and hemorrhagic diseases.
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