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用于在微血管壁中实时追踪中性粒细胞的工程化微血管基底膜模拟物。

Engineered microvascular basement membrane mimetic for real-time neutrophil tracking in the microvascular wall.

作者信息

Morales Laura C, Kim Catherine D, Pan Yangang, Scheuring Simon, Gonzalez Anjelica L

机构信息

Department of Biomedical Engineering Yale University New Haven Connecticut USA.

Department of Anesthesiology Weill Cornell Medical College New York New York USA.

出版信息

Bioeng Transl Med. 2025 Mar 12;10(4):e70008. doi: 10.1002/btm2.70008. eCollection 2025 Jul.

DOI:10.1002/btm2.70008
PMID:40708981
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12284441/
Abstract

The microvascular basement membrane (mvBM) is crucial in maintaining vascular integrity and function and, therefore, key to the health of major organs. However, the complex nature and the intricate interplay of biochemical and biomechanical factors that regulate the mvBM functional dynamics make it difficult to study. Here, we present a novel and highly tunable in vitro model of the human mvBM, enabling a bottom-up approach to assemble a composite model of the microvascular wall and explore microvascular dynamics and interactions with circulating neutrophils in real time. An electrospun polyethylene glycol (PEG)-based fibrillar network mimics the mvBM with adjustable nanofiber diameter, orientation, and density. The fidelity of the model to the human mvBM's topography and mechanics was verified through second harmonic generation imaging and atomic force microscopy. PEG was functionalized with bioactive moieties to enable endothelial cell (EC) and pericyte (PC) attachment, through which neutrophil interactions with the microvascular wall model were observed. The model, coupled with 4D microscopy, revealed nuanced and dynamic neutrophil behavior when interacting with the microvascular wall, demonstrating its utility in characterizing cell-cell interactions. As such, the model can be employed in the exploration of inflammatory and microvascular-related diseases. Therefore, this innovative approach represents a significant advancement in vascular biology research, holding profound implications for understanding mvBM dynamics in both health and disease.

摘要

微血管基底膜(mvBM)对于维持血管完整性和功能至关重要,因此是主要器官健康的关键。然而,调节mvBM功能动态的生化和生物力学因素的复杂性质以及错综复杂的相互作用使得其难以研究。在此,我们提出了一种新型且高度可调的人mvBM体外模型,采用自下而上的方法构建微血管壁复合模型,并实时探索微血管动态以及与循环中性粒细胞的相互作用。基于静电纺丝聚乙二醇(PEG)的纤维网络模拟mvBM,具有可调节的纳米纤维直径、取向和密度。通过二次谐波产生成像和原子力显微镜验证了该模型与人mvBM的形貌和力学特性的保真度。PEG用生物活性部分进行功能化,以实现内皮细胞(EC)和周细胞(PC)的附着,通过这种方式观察中性粒细胞与微血管壁模型的相互作用。该模型与四维显微镜相结合,揭示了中性粒细胞与微血管壁相互作用时细微且动态的行为,证明了其在表征细胞间相互作用方面的实用性。因此,该模型可用于探索炎症和微血管相关疾病。所以,这种创新方法代表了血管生物学研究的重大进展,对理解健康和疾病状态下的mvBM动态具有深远意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ebc/12284441/325ce4ccf82b/BTM2-10-e70008-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ebc/12284441/91c12cbeae5c/BTM2-10-e70008-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ebc/12284441/52a1ac62d75f/BTM2-10-e70008-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ebc/12284441/ffdb45ab52a6/BTM2-10-e70008-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ebc/12284441/325ce4ccf82b/BTM2-10-e70008-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ebc/12284441/91c12cbeae5c/BTM2-10-e70008-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ebc/12284441/52a1ac62d75f/BTM2-10-e70008-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ebc/12284441/ffdb45ab52a6/BTM2-10-e70008-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ebc/12284441/325ce4ccf82b/BTM2-10-e70008-g001.jpg

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