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人类腹主动脉瘤中中性粒细胞募集的介质。

Mediators of neutrophil recruitment in human abdominal aortic aneurysms.

作者信息

Houard Xavier, Touat Ziad, Ollivier Véronique, Louedec Liliane, Philippe Monique, Sebbag Uriel, Meilhac Olivier, Rossignol Patrick, Michel Jean-Baptiste

机构信息

INSERM U698, Cardiovascular Haematology, Bio-Engineering and Remodelings, Paris 7 Denis Diderot University, Bichat-Claude Bernard Hospital, 46 rue Henri Huchard, F-75877 Paris Cedex 18, France.

出版信息

Cardiovasc Res. 2009 Jun 1;82(3):532-41. doi: 10.1093/cvr/cvp048. Epub 2009 Feb 5.

Abstract

AIMS

Neutrophils/platelet interactions are involved in abdominal aortic aneurysm (AAA). The intraluminal thrombus (ILT) is a human model of platelet/neutrophil interactions. The present study focused on mediators involved in neutrophil recruitment in AAA.

METHODS AND RESULTS

Conditioned media from luminal, intermediate, and abluminal layers of 29 human ILTs were analysed for neutrophil markers [elastase/alpha1-antitrypsin and MMP9/NGAL complexes, myeloperoxidase (MPO), and alpha-defensin peptides], RANTES, platelet factor 4 (PF4), and interleukin-8 (IL-8). Their time-dependent release into serum from clots generated in vitro and their plasma concentrations in AAA patients and controls were determined. Immunohistochemistry for neutrophils, platelets, IL-8, PF4, and RANTES on AAA sections was performed; and molecules involved in ILT neutrophil chemotactic function were analysed in vitro. Neutrophils and platelets colocalized in the luminal layer of the thrombus. Consistently, neutrophil markers and platelet-derived RANTES and PF4 were released predominantly by the luminal thrombus pole, where their concentrations were significantly correlated. The luminal ILT layer was also the main source of IL-8, whose immunostaining colocalized with neutrophils. All were also released time dependently from clots and were increased in plasma of AAA patients. Luminal ILT layers displayed potent neutrophil chemotactic activity in vitro, which was inhibited by RANTES- and IL-8-blocking antibodies as well as by reparixin, an antagonist of the IL-8 receptors CXCR1 and CXCR2.

CONCLUSION

Taken together, these results suggest that platelet-derived RANTES and neutrophil-derived IL-8 are involved in attracting neutrophils to the luminal layer of AAA ILT.

摘要

目的

中性粒细胞/血小板相互作用参与腹主动脉瘤(AAA)的发生发展。腔内血栓(ILT)是血小板/中性粒细胞相互作用的人体模型。本研究聚焦于AAA中参与中性粒细胞募集的介质。

方法与结果

分析了29例人类ILT的腔层、中层和腔外层的条件培养基中的中性粒细胞标志物[弹性蛋白酶/α1-抗胰蛋白酶和MMP9/NGAL复合物、髓过氧化物酶(MPO)和α-防御素肽]、RANTES、血小板因子4(PF4)和白细胞介素-8(IL-8)。测定了它们从体外形成的凝块中随时间释放到血清中的情况以及AAA患者和对照组血浆中的浓度。对AAA切片进行了中性粒细胞、血小板、IL-8、PF4和RANTES的免疫组织化学检测;并在体外分析了参与ILT中性粒细胞趋化功能的分子。中性粒细胞和血小板在血栓的腔层共定位。一致地,中性粒细胞标志物以及血小板衍生的RANTES和PF4主要由血栓腔层极释放,其浓度显著相关。腔层ILT也是IL-8的主要来源,其免疫染色与中性粒细胞共定位。所有这些物质也从凝块中随时间依赖性释放,并且在AAA患者的血浆中增加。腔层ILT在体外表现出强大的中性粒细胞趋化活性,RANTES和IL-8阻断抗体以及IL-8受体CXCR1和CXCR2的拮抗剂瑞帕霉素可抑制这种活性。

结论

综上所述,这些结果表明血小板衍生的RANTES和中性粒细胞衍生的IL-8参与将中性粒细胞吸引至AAA的ILT腔层。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1430/2682614/a242084456d5/cvp04801.jpg

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