Suppr超能文献

利用基因工程改造的细胞膜衍生囊泡作为生物疗法。

Harnessing genetically engineered cell membrane-derived vesicles as biotherapeutics.

作者信息

Li Xiaohong, Wei Yuting, Zhang Zhirang, Zhang Xudong

机构信息

Shenzhen Key Laboratory for Systems Medicine in Inflammatory Diseases, School of Medicine, Sun Yat-Sen University, Shenzhen 518107, Guangdong, China.

Department of Pharmacology, Molecular Cancer Research Center, School of Medicine, Sun Yat-sen University, Shenzhen 518107, Guangdong, China.

出版信息

Extracell Vesicles Circ Nucl Acids. 2024 Jan 31;5(1):44-63. doi: 10.20517/evcna.2023.58. eCollection 2024.

Abstract

Cell membrane-derived vesicles (CMVs) are particles generated from living cells, including extracellular vesicles (EVs) and artificial extracellular vesicles (aEVs) prepared from cell membranes. CMVs possess considerable potential in drug delivery, regenerative medicine, immunomodulation, disease diagnosis, . owing to their stable lipid bilayer structure, favorable biocompatibility, and low toxicity. Although the majority of CMVs inherit certain attributes from the original cells, it is still difficult to execute distinct therapeutic functions, such as organ targeting, signal regulation, and exogenous biotherapeutic supplementation. Hence, engineering CMVs by genetic engineering, chemical modification, and hybridization is a promising way to endow CMVs with specific functions and open up novel vistas for applications. In particular, there is a growing interest in genetically engineered CMVs harnessed to exhibit biotherapeutics. Herein, we outline the preparation strategies and their characteristics for purifying CMVs. Additionally, we review the advances of genetically engineered CMVs utilized to target organs, regulate signal transduction, and deliver biomacromolecules and chemical drugs. Furthermore, we also summarize the emerging therapeutic applications of genetically engineered CMVs in addressing tumors, diabetes, systemic lupus erythematosus, and cardiovascular diseases.

摘要

细胞膜衍生囊泡(CMVs)是由活细胞产生的颗粒,包括细胞外囊泡(EVs)和由细胞膜制备的人工细胞外囊泡(aEVs)。由于其稳定的脂质双层结构、良好的生物相容性和低毒性,CMVs在药物递送、再生医学、免疫调节、疾病诊断等方面具有巨大潜力。尽管大多数CMVs继承了原始细胞的某些特性,但要实现独特的治疗功能,如器官靶向、信号调节和外源性生物治疗补充,仍然很困难。因此,通过基因工程、化学修饰和杂交对CMVs进行工程改造是赋予CMVs特定功能并开辟新应用前景的一种有前途的方法。特别是,人们对利用基因工程改造的CMVs来展示生物治疗药物的兴趣日益浓厚。在此,我们概述了纯化CMVs的制备策略及其特点。此外,我们回顾了用于器官靶向、调节信号转导以及递送生物大分子和化学药物的基因工程改造CMVs的研究进展。此外,我们还总结了基因工程改造CMVs在治疗肿瘤、糖尿病、系统性红斑狼疮和心血管疾病方面的新兴治疗应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea5c/11648408/71cc00d2aab5/evcna-5-1-44.fig.1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验