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一层蛋白基微胶囊的刚度对树突状细胞摄取和内吞机制的影响。

Effect of the stiffness of one-layer protein-based microcapsules on dendritic cell uptake and endocytic mechanism.

机构信息

School of Ophthalmology and Optometry, Eye Hospital, School of Biomedical Engineering, Wenzhou Medical University, Wenzhou, Zhejiang Province, 325035, PR China.

Engineering Research Center of Clinical Functional Materials and Diagnosis & Treatment Devices of Zhejiang Province, Wenzhou Institute, University of Chinese Academy of Sciences (Wenzhou Institute of Biomaterials & Engineering), Wenzhou, Zhejiang Province, 325001, P. R. China.

出版信息

Biomater Sci. 2021 Dec 21;10(1):178-188. doi: 10.1039/d1bm01448j.

Abstract

Microcapsules are one of the most promising microscale drug carriers due to their facile fabrication, excellent deformability, and high efficacy in drug storage and delivery. Understanding the effects of their physicochemical properties (size, shape, rigidity, charge, surface chemistry, ) on both and performance is not only highly significant and interesting but also very challenging. Stiffness, an important design parameter, has been extensively explored in recent years, but how the rigidity of particles influences cellular internalization and uptake mechanisms remains controversial. Here, one-layered lysozyme-based microcapsules with well-controlled stiffness (modulus ranging from 3.49 ± 0.18 MPa to 26.14 ± 1.09 MPa) were prepared and used to investigate the effect of stiffness on the uptake process in dendritic cells and the underlying mechanism. The cellular uptake process and endocytic mechanism were investigated with laser scanning confocal microscopy, mechanism inhibitors, and pathway-specific antibody staining. Our data demonstrated that the stiffness of protein-based microcapsules could be a strong regulator of intracellular uptake and endocytic kinetics but had no obvious effect on the endocytic mechanism. We believe our results will provide a basic understanding of the intracellular uptake process of microcapsules and the endocytic mechanism and inspire strategies for the further design of potential drug delivery microcarriers.

摘要

微胶囊由于其易于制造、出色的变形能力以及在药物储存和输送方面的高效性,是最有前途的微尺度药物载体之一。了解其物理化学性质(大小、形状、刚性、电荷、表面化学等)对 和 性能的影响不仅非常重要和有趣,而且极具挑战性。近年来,刚性作为一个重要的设计参数得到了广泛的研究,但颗粒的刚性如何影响细胞内化和摄取机制仍存在争议。在这里,我们制备了具有良好可控刚度(模量范围为 3.49 ± 0.18 MPa 至 26.14 ± 1.09 MPa)的单层溶菌酶微胶囊,用于研究刚度对树突状细胞摄取过程的影响及其潜在机制。通过激光共聚焦显微镜、机制抑制剂和特异性抗体染色研究了细胞摄取过程和内吞机制。我们的数据表明,基于蛋白质的微胶囊的刚度可以强烈调节细胞内摄取和内吞动力学,但对内吞机制没有明显影响。我们相信,我们的研究结果将为微胶囊的细胞内摄取过程和内吞机制提供基本的了解,并为进一步设计潜在的药物输送微载体提供策略。

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