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血小板泛连接蛋白-1通道调节中性粒细胞的激活和迁移,但不影响腹主动脉瘤的进展。

Platelet pannexin-1 channels modulate neutrophil activation and migration but not the progression of abdominal aortic aneurysm.

作者信息

Metz Lisa Maria, Feige Tobias, de Biasi Larissa, Ehrenberg Agnes, Mulorz Joscha, Toska Laura Mara, Reusswig Friedrich, Quast Christine, Gerdes Norbert, Kelm Malte, Schelzig Hubert, Elvers Margitta

机构信息

Department of Vascular- and Endovascular Surgery, University Hospital Duesseldorf, Heinrich-Heine University, Duesseldorf, Germany.

Department of Cardiology, Pulmonology and Vascular Medicine, University Hospital Duesseldorf, Heinrich-Heine University, Duesseldorf, Germany.

出版信息

Front Mol Biosci. 2023 Mar 6;10:1111108. doi: 10.3389/fmolb.2023.1111108. eCollection 2023.

Abstract

Abdominal aortic aneurysm (AAA) is a common disease and highly lethal if untreated. The progressive dilatation of the abdominal aorta is accompanied by degradation and remodeling of the vessel wall due to chronic inflammation. Pannexins represent anion-selective channels and play a crucial role in non-vesicular ATP release to amplify paracrine signaling in cells. Thus, pannexins are involved in many (patho-) physiological processes. Recently, Panx1 channels were identified to be significantly involved in abdominal aortic aneurysm formation through endothelial derived Panx1 regulated inflammation and aortic remodeling. In platelets, Panx1 becomes activated following activation of glycoprotein (GP) VI. Since platelets play a role in cardiovascular diseases including abdominal aortic aneurysm, we analyzed the contribution of platelet Panx1 in the progression of abdominal aortic aneurysm. We detected enhanced Panx1 plasma levels in abdominal aortic aneurysm patients. In experimental abdominal aortic aneurysm using the pancreatic porcine elastase (PPE) mouse model, a major contribution of platelet Panx1 channels in platelet activation, pro-coagulant activity of platelets and platelet-mediated inflammation has been detected. In detail, platelets are important for the migration of neutrophils into the aortic wall induced by direct cell interaction and by activation of endothelial cells. Decreased platelet activation and inflammation did not affect ECM remodeling or wall thickness in platelet-specific Panx1 knock-out mice following PPE surgery. Thus, aortic diameter expansion at different time points after elastase infusion of the aortic wall was unaltered in platelet-specific Panx1 deficient mice suggesting that the modulation of inflammation alone does not affect abdominal aortic aneurysm formation and progression. In conclusion, our data strongly supports the role of platelets in inflammatory responses in abdominal aortic aneurysm Panx1 channels and adds important knowledge about the significance of platelets in abdominal aortic aneurysm pathology important for the establishment of an anti-platelet therapy for abdominal aortic aneurysm patients.

摘要

腹主动脉瘤(AAA)是一种常见疾病,若不治疗,致死率很高。腹主动脉的渐进性扩张伴随着由于慢性炎症导致的血管壁降解和重塑。泛连接蛋白代表阴离子选择性通道,在非囊泡性ATP释放以放大细胞旁分泌信号中起关键作用。因此,泛连接蛋白参与许多(病理)生理过程。最近,已确定Panx1通道通过内皮源性Panx1调节炎症和主动脉重塑,在腹主动脉瘤形成中起重要作用。在血小板中,糖蛋白(GP)VI激活后,Panx1被激活。由于血小板在包括腹主动脉瘤在内的心血管疾病中起作用,我们分析了血小板Panx1在腹主动脉瘤进展中的作用。我们检测到腹主动脉瘤患者的Panx1血浆水平升高。在使用猪胰弹性蛋白酶(PPE)小鼠模型的实验性腹主动脉瘤中,已检测到血小板Panx1通道在血小板激活、血小板促凝血活性和血小板介导的炎症中起主要作用。详细地说,血小板对于中性粒细胞通过直接细胞相互作用和内皮细胞激活诱导进入主动脉壁的迁移很重要。在PPE手术后,血小板特异性Panx1基因敲除小鼠中血小板激活和炎症的降低并不影响细胞外基质重塑或壁厚度。因此,在血小板特异性Panx1缺陷小鼠中,弹性蛋白酶注入主动脉壁后不同时间点的主动脉直径扩张未改变,这表明仅炎症调节并不影响腹主动脉瘤的形成和进展。总之,我们的数据有力地支持了血小板在腹主动脉瘤中炎症反应中Panx1通道的作用,并增加了关于血小板在腹主动脉瘤病理学中的重要性的重要知识,这对于为腹主动脉瘤患者建立抗血小板治疗很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f910/10025481/dd6f8c5f3873/fmolb-10-1111108-g001.jpg

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