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细胞外囊泡介导内皮细胞和血管平滑肌细胞之间的通讯。

Extracellular Vesicles Mediate Communication between Endothelial and Vascular Smooth Muscle Cells.

机构信息

Laboratory of Molecular Angiogenesis, GIGA Research Center, University of Liège, B34, 1 Avenue de l'Hôpital, 4000 Liège, Belgium.

Laboratory of Cell and Tissues Biology, GIGA Research Center, University of Liège, 1 Avenue de l'Hôpital, 4000 Liège, Belgium.

出版信息

Int J Mol Sci. 2021 Dec 28;23(1):331. doi: 10.3390/ijms23010331.

Abstract

The recruitment of pericytes and vascular smooth muscle cells (SMCs) that enwrap endothelial cells (ECs) is a crucial process for vascular maturation and stabilization. Communication between these two cell types is crucial during vascular development and in maintaining vessel homeostasis. Extracellular vesicles (EVs) have emerged as a new communication tool involving the exchange of microRNAs between cells. In the present study, we searched for microRNAs that could be transferred via EVs from ECs to SMCs and vice versa. Thanks to a microRNA profiling experiment, we found that two microRNAs are more exported in each cell type in coculture experiments: while miR-539 is more secreted by ECs, miR-582 is more present in EVs from SMCs. Functional assays revealed that both microRNAs can modulate both cell-type phenotypes. We further identified miR-539 and miR-582 targets, in agreement with their respective cell functions. The results obtained in vivo in the neovascularization model suggest that miR-539 and miR-582 might cooperate to trigger the process of blood vessel coverage by smooth muscle cells in a mature plexus. Taken together, these results are the first to highlight the role of miR-539 and miR-582 in angiogenesis and communication between ECs and SMCs.

摘要

周细胞和血管平滑肌细胞(SMCs)的募集是血管成熟和稳定的关键过程,这些细胞包裹着内皮细胞(ECs)。在血管发育和维持血管稳态过程中,这两种细胞类型之间的交流至关重要。细胞外囊泡(EVs)作为一种新的交流工具,涉及细胞间 microRNAs 的交换。在本研究中,我们搜索了可以通过 EVs 从 ECs 转移到 SMCs,反之亦然的 microRNAs。通过 microRNA 表达谱实验,我们发现两种 microRNAs 在共培养实验中在每种细胞类型中都有更多的外排:miR-539 更多地由 ECs 分泌,而 miR-582 在 SMCs 的 EVs 中更为丰富。功能测定表明,这两种 microRNAs 都可以调节两种细胞类型的表型。我们进一步鉴定了 miR-539 和 miR-582 的靶标,与它们各自的细胞功能一致。在新血管生成模型中的体内研究结果表明,miR-539 和 miR-582 可能共同作用,触发平滑肌细胞对成熟丛的血管覆盖过程。总之,这些结果首次强调了 miR-539 和 miR-582 在血管生成和 ECs 与 SMCs 之间的交流中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6400/8745747/02ede5543967/ijms-23-00331-g001.jpg

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