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巨核细胞利用在体内类似足体的结构协同作用,穿透骨髓血窦的内皮屏障。

Megakaryocytes use in vivo podosome-like structures working collectively to penetrate the endothelial barrier of bone marrow sinusoids.

作者信息

Eckly Anita, Scandola Cyril, Oprescu Antoine, Michel Deborah, Rinckel Jean-Yves, Proamer Fabienne, Hoffmann David, Receveur Nicolas, Léon Catherine, Bear James E, Ghalloussi Dorsaf, Harousseau Gabriel, Bergmeier Wolfgang, Lanza Francois, Gaits-Iacovoni Frédérique, de la Salle Henri, Gachet Christian

机构信息

Université de Strasbourg, INSERM, EFS Grand Est, BPPS UMR-S 1255, FMTS, Strasbourg, France.

INSERM U1048, I2MC, Université Paul Sabatier, Toulouse, France.

出版信息

J Thromb Haemost. 2020 Nov;18(11):2987-3001. doi: 10.1111/jth.15024. Epub 2020 Aug 25.

Abstract

BACKGROUND

Blood platelets are anucleate cell fragments that prevent bleeding and minimize blood vessel injury. They are formed from the cytoplasm of megakaryocytes located in the bone marrow. For successful platelet production, megakaryocyte fragments must pass through the sinusoid endothelial barrier by a cell biology process unique to these giant cells as compared with erythrocytes and leukocytes. Currently, the mechanisms by which megakaryocytes interact and progress through the endothelial cells are not understood, resulting in a significant gap in our knowledge of platelet production.

OBJECTIVE

The aim of this study was to investigate how megakaryocytes interact and progress through the endothelial cells of mouse bone marrow sinusoids.

METHODS

We used a combination of fluorescence, electron, and three-dimensional microscopy to characterize the cellular events between megakaryocytes and endothelial cells.

RESULTS

We identified protrusive, F-actin-based podosome-like structures, called in vivo-MK podosomes, which initiate the formation of pores through endothelial cells. These structures present a collective and spatial organization through their interconnection via a contractile network of actomyosin, essential to regulate the endothelial openings. This ensures proper passage of megakaryocyte-derived processes into the blood circulation to promote thrombopoiesis.

CONCLUSION

This study provides novel insight into the in vivo function of podosomes of megakaryocytes with critical importance to platelet production.

摘要

背景

血小板是无核细胞碎片,可防止出血并将血管损伤降至最低。它们由位于骨髓中的巨核细胞的细胞质形成。为了成功产生血小板,与红细胞和白细胞相比,巨核细胞碎片必须通过这些巨细胞特有的细胞生物学过程穿过窦状内皮屏障。目前,尚不清楚巨核细胞与内皮细胞相互作用并穿过内皮细胞的机制,这导致我们对血小板生成的认识存在重大差距。

目的

本研究旨在探讨巨核细胞如何与小鼠骨髓窦状内皮细胞相互作用并穿过这些细胞。

方法

我们结合使用荧光显微镜、电子显微镜和三维显微镜来表征巨核细胞与内皮细胞之间的细胞事件。

结果

我们发现了基于F-肌动蛋白的突出的足体样结构,称为体内巨核细胞足体,它启动了穿过内皮细胞的孔隙形成。这些结构通过肌动球蛋白收缩网络相互连接,呈现出集体和空间组织,这对于调节内皮开口至关重要。这确保了巨核细胞衍生的突起正确进入血液循环以促进血小板生成。

结论

本研究为巨核细胞足体在体内的功能提供了新的见解,这对血小板生成至关重要。

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