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

IF 6.1 2区 医学 Q1 ENGINEERING, BIOMEDICAL
Laura C. Morales, Catherine D. Kim, Yangang Pan, Simon Scheuring, Anjelica L. Gonzalez
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引用次数: 0

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.
用于微血管壁中性粒细胞实时跟踪的工程微血管基膜模拟物
微血管基底膜(mvBM)在维持血管完整性和功能方面至关重要,因此对主要器官的健康至关重要。然而,调节mvBM功能动力学的生物化学和生物力学因素的复杂性和错综复杂的相互作用使其难以研究。在这里,我们提出了一种新颖的、高度可调的人类mvBM体外模型,使自下而上的方法能够组装微血管壁的复合模型,并实时探索微血管动力学及其与循环中性粒细胞的相互作用。一种基于聚乙二醇(PEG)的静电纺丝纤维网络模拟了mvBM,具有可调节的纳米纤维直径、取向和密度。通过二次谐波成像和原子力显微镜验证了该模型与人体mvBM的形貌和力学的保真度。PEG被生物活性部分功能化,使内皮细胞(EC)和周细胞(PC)能够附着,通过这种方式观察到中性粒细胞与微血管壁模型的相互作用。该模型与4D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而动态的行为,证明了其在表征细胞-细胞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。因此,这种创新的方法代表了血管生物学研究的重大进步,对理解mvBM在健康和疾病中的动态具有深远的意义。
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来源期刊
Bioengineering & Translational Medicine
Bioengineering & Translational Medicine Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
8.40
自引率
4.10%
发文量
150
审稿时长
12 weeks
期刊介绍: Bioengineering & Translational Medicine, an official, peer-reviewed online open-access journal of the American Institute of Chemical Engineers (AIChE) and the Society for Biological Engineering (SBE), focuses on how chemical and biological engineering approaches drive innovative technologies and solutions that impact clinical practice and commercial healthcare products.
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