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基质硬度通过 Piezo1-YAP 信号轴调节巨噬细胞极化。

Matrix stiffness regulates macrophage polarisation via the Piezo1-YAP signalling axis.

机构信息

Department of Stomatology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

School of Stomatology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

出版信息

Cell Prolif. 2024 Aug;57(8):e13640. doi: 10.1111/cpr.13640. Epub 2024 Mar 31.

DOI:10.1111/cpr.13640
PMID:38556840
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11294424/
Abstract

Macrophages play a pivotal role in the immunological cascade activated in response to biomedical implants, which predetermine acceptance or rejection of implants by the host via pro- and anti-inflammatory polarisation states. The role of chemical signals in macrophage polarisation is well-established, but how physical cues regulate macrophage function that may play a fundamental role in implant-bone interface, remains poorly understood. Here we find that bone marrow-derived macrophages (BMDM) cultured on polyacrylamide gels of varying stiffness exhibit different polarisation states. BMDM are 'primed' to a pro-inflammatory M1 phenotype on stiff substrates, while to an anti-inflammatory M2 phenotype on soft and medium stiffness substrates. It is further observed that matrix stiffening increases Piezo1 expression, as well as leads to subsequent activation of the mechanotransduction signalling effector YAP, thus favouring M1 polarisation whilst suppressing M2 polarisation. Moreover, upon treatment with YAP inhibitor, we successfully induce macrophage re-polarisation to the M2 state within the implant site microenvironment, which in turn promotes implant osseointegration. Collectively, our present study thus characterises the critical role of the Piezo1-YAP signalling axis in macrophage mechanosensing and stiffness-mediated macrophage polarisation and provides cues for the design of immuno-modulatory biomaterials that can regulate the macrophage phenotype.

摘要

巨噬细胞在生物医学植入物激活的免疫级联反应中发挥关键作用,通过促炎和抗炎极化状态决定宿主对植入物的接受或排斥。化学信号在巨噬细胞极化中的作用已得到充分证实,但物理线索如何调节巨噬细胞功能,而这种功能可能在植入物-骨界面中起着基础性作用,目前仍知之甚少。在这里,我们发现,在不同硬度的聚丙烯酰胺凝胶上培养的骨髓来源的巨噬细胞(BMDM)表现出不同的极化状态。BMDM 在硬基底上被“预先”诱导为促炎的 M1 表型,而在软和中等硬度的基底上则被诱导为抗炎的 M2 表型。进一步观察到,基质变硬会增加 Piezo1 的表达,并导致随后机械转导信号效应物 YAP 的激活,从而有利于 M1 极化,同时抑制 M2 极化。此外,在用 YAP 抑制剂处理后,我们成功地诱导了植入部位微环境中巨噬细胞向 M2 状态的再极化,进而促进了植入物的骨整合。总的来说,本研究描述了 Piezo1-YAP 信号通路在巨噬细胞机械感知和刚度介导的巨噬细胞极化中的关键作用,并为设计可调节巨噬细胞表型的免疫调节生物材料提供了线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ff6/11294424/a288ad4a03a1/CPR-57-e13640-g006.jpg
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