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通过细胞表面修饰控制细胞动力学

[Controlling Cell Dynamics by Cell-surface Modification].

作者信息

Higuchi Yuriko, Takafuji Yoshimasa

机构信息

Graduate School of Pharmaceutical Sciences, Kyoto University.

Faculty of Medicine, Kindai University.

出版信息

Yakugaku Zasshi. 2021;141(5):661-665. doi: 10.1248/yakushi.20-00219-6.

DOI:10.1248/yakushi.20-00219-6
PMID:33952748
Abstract

Although the concept of a drug delivery system (DDS) is usually applied to conventional drug therapy, it is also important for cell-based therapy. The surface manipulation of living cells represents a powerful tool for controlling cell behaviors in the body, such as enhancement of cell-cell interactions, targeted delivery of cells, and protection from immunological rejection. Functional groups, including amines, thiols, and carbonyls, offer excellent opportunities for chemical modification through the formation of covalent bonds with exogenous molecules. Non-natural reactive groups introduced by metabolic labeling were recently utilized for targeted chemical modification. On the other hand, noncovalent strategies are also available; two major examples are electrostatic interaction with a negative charge on the cell surface and hydrophobic insertion or interaction with the cell membrane. In this study, we analyzed factors affecting cell surface modifications using PEG-lipid and succeeded in enhancing the efficacy of modification by cyclodextrin. Then, mesenchymal stem cells (MSCs), whose therapeutic effect has been demonstrated at the clinical stage and which have been clinically used as a drug, were decorated with PEG-lipid conjugates having a targeted ligand such as peptide or scFv, which are recognized by ICAM1. The peptide or scFv decoration enhanced the cell adhesion of MSCs on cytokine treated-endothelial cells. This technique will prompt the targeted delivery of MSCs to intended therapy sites, and underscores the promise of cell surface engineering as a tool for improving cell-based therapy.

摘要

尽管药物递送系统(DDS)的概念通常应用于传统药物治疗,但它对基于细胞的治疗也很重要。活细胞的表面操控是控制体内细胞行为的有力工具,比如增强细胞间相互作用、细胞的靶向递送以及防止免疫排斥。包括胺基、巯基和羰基在内的官能团,为通过与外源性分子形成共价键进行化学修饰提供了绝佳机会。最近,通过代谢标记引入的非天然反应基团被用于靶向化学修饰。另一方面,非共价策略也可行;两个主要例子是与细胞表面负电荷的静电相互作用以及与细胞膜的疏水插入或相互作用。在本研究中,我们分析了使用聚乙二醇脂质(PEG-脂质)进行细胞表面修饰的影响因素,并成功通过环糊精提高了修饰效率。然后,用具有靶向配体(如肽或单链抗体片段(scFv))的PEG-脂质缀合物修饰间充质干细胞(MSC),这些配体可被细胞间黏附分子1(ICAM1)识别,MSC的治疗效果已在临床阶段得到证实,并且已作为一种药物临床使用。肽或scFv修饰增强了MSC在细胞因子处理的内皮细胞上的黏附。这项技术将促使MSC靶向递送至预期的治疗部位,并突出了细胞表面工程作为改善基于细胞治疗的工具的前景。

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