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靶向治疗用工程细胞外囊泡:膜修饰的原理与策略。

Targeted therapy using engineered extracellular vesicles: principles and strategies for membrane modification.

机构信息

National Clinical Research Center for Infectious Diseases, Shenzhen Third People's Hospital, Southern University of Science and Technology, Shenzhen, China.

Department of Orthopaedics, The Second Affiliated Hospital of Shenzhen University (People's Hospital of Shenzhen Baoan District), China, Shenzhen, 518000, China.

出版信息

J Nanobiotechnology. 2023 Sep 16;21(1):334. doi: 10.1186/s12951-023-02081-0.


DOI:10.1186/s12951-023-02081-0
PMID:37717008
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10505332/
Abstract

Extracellular vesicles (EVs) are 30-150 nm membrane-bound vesicles naturally secreted by cells and play important roles in intercellular communication by delivering regulatory molecules such as proteins, lipids, nucleic acids and metabolites to recipient cells. As natural nano-carriers, EVs possess desirable properties such as high biocompatibility, biological barrier permeability, low toxicity, and low immunogenicity, making them potential therapeutic delivery vehicles. EVs derived from specific cells have inherent targeting capacity towards specific cell types, which is yet not satisfactory enough for targeted therapy development and needs to be improved. Surface modifications endow EVs with targeting abilities, significantly improving their therapeutic efficiency. Herein, we first briefly introduce the biogenesis, composition, uptake and function of EVs, and review the cargo loading approaches for EVs. Then, we summarize the recent advances in surface engineering strategies of EVs, focusing on the applications of engineered EVs for targeted therapy. Altogether, EVs hold great promise for targeted delivery of various cargos, and targeted modifications show promising effects on multiple diseases.

摘要

细胞外囊泡 (EVs) 是由细胞自然分泌的 30-150nm 膜结合囊泡,通过向受体细胞传递调节分子(如蛋白质、脂质、核酸和代谢物),在细胞间通讯中发挥重要作用。作为天然的纳米载体,EVs 具有高生物相容性、生物屏障通透性、低毒性和低免疫原性等理想特性,使其成为有潜力的治疗性药物递送载体。特定细胞来源的 EVs 对特定细胞类型具有固有靶向能力,但对于靶向治疗的发展来说,这种靶向能力还不够理想,需要进一步提高。表面修饰赋予 EVs 靶向能力,显著提高了它们的治疗效率。本文首先简要介绍了 EVs 的生物发生、组成、摄取和功能,并综述了 EVs 的货物装载方法。然后,我们总结了 EVs 表面工程策略的最新进展,重点介绍了工程化 EVs 在靶向治疗中的应用。总之,EVs 在各种货物的靶向递送方面具有很大的应用潜力,而靶向修饰在多种疾病的治疗中显示出了很好的效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38b0/10505332/d78890528325/12951_2023_2081_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38b0/10505332/f0378b11077a/12951_2023_2081_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38b0/10505332/246e1b1b1320/12951_2023_2081_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38b0/10505332/2b91fc409a6a/12951_2023_2081_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38b0/10505332/d1795aeb0110/12951_2023_2081_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38b0/10505332/2f5aee568978/12951_2023_2081_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38b0/10505332/5f8142ae186c/12951_2023_2081_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38b0/10505332/b808ae4b8809/12951_2023_2081_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38b0/10505332/d78890528325/12951_2023_2081_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38b0/10505332/f0378b11077a/12951_2023_2081_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38b0/10505332/246e1b1b1320/12951_2023_2081_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38b0/10505332/2b91fc409a6a/12951_2023_2081_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38b0/10505332/d1795aeb0110/12951_2023_2081_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38b0/10505332/2f5aee568978/12951_2023_2081_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38b0/10505332/5f8142ae186c/12951_2023_2081_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38b0/10505332/b808ae4b8809/12951_2023_2081_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38b0/10505332/d78890528325/12951_2023_2081_Fig8_HTML.jpg

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Targeted therapy using engineered extracellular vesicles: principles and strategies for membrane modification.

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[10]
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本文引用的文献

[1]
Nanomaterials for mRNA-based therapeutics: Challenges and opportunities.

Bioeng Transl Med. 2023-1-29

[2]
Osteoclast-targeted delivery of anti-miRNA oligonucleotides by red blood cell extracellular vesicles.

J Control Release. 2023-6

[3]
Biomaterial-assisted targeted and controlled delivery of CRISPR/Cas9 for precise gene editing.

Biomater Sci. 2023-5-30

[4]
Mesenchymal Stem Cell-derived Exosomes: Novel Therapeutic Approach for Inflammatory Bowel Diseases.

Stem Cells Int. 2023-4-4

[5]
Cell-derived nanovesicle-mediated drug delivery to the brain: Principles and strategies for vesicle engineering.

Mol Ther. 2023-5-3

[6]
Extracellular Vesicles: The Next Generation Theranostic Nanomedicine for Inflammatory Bowel Disease.

Int J Nanomedicine. 2022

[7]
Chondrocyte-specific genomic editing enabled by hybrid exosomes for osteoarthritis treatment.

Theranostics. 2022

[8]
Designer Exosomes for Targeted Delivery of a Novel Therapeutic Cargo to Enhance Sorafenib-Mediated Ferroptosis in Hepatocellular Carcinoma.

Front Oncol. 2022-6-24

[9]
Cell-derived extracellular vesicles for CRISPR/Cas9 delivery: engineering strategies for cargo packaging and loading.

Biomater Sci. 2022-7-26

[10]
Eliciting anti-cancer immunity by genetically engineered multifunctional exosomes.

Mol Ther. 2022-9-7

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