Jinkui Wang, Mujie Li, Zhaoxia Zhang, Tao Mi, Junyi Luo, Dawei He
{"title":"基因工程糖基磷脂酰肌醇锚定抗gd2纳米体外泌体模拟物用于骨肉瘤的体外和体内靶向治疗","authors":"Jinkui Wang, Mujie Li, Zhaoxia Zhang, Tao Mi, Junyi Luo, Dawei He","doi":"10.1021/acsami.5c12922","DOIUrl":null,"url":null,"abstract":"This study focuses on the engineering of exosome mimetics (EMs) that are decorated with an antidisialoganglioside (GD2) nanobody for targeting osteosarcoma. We engineer the anti-GD2 nanobody coding vector into HEK-293T (293T) cells and fuse it with the decay-accelerating factor (DAF)-derived glycosylphosphatidylinositol (GPI) anchor signal peptide. The sequential extrusion method was used to produce the targeted EMs. These engineered GD2-targeted EMs (GD2-EMs) possess the same exosome markers as regular exosomes, are produced in large quantities, have a nanoscale size, and feature a surface anti-GD2 nanobody. Furthermore, they demonstrate increased internalization in osteosarcoma cells compared to unmodified EMs. In animal experiments using nude mice, the GD2-EMs exhibited superior tumor targeting, confirming their efficacy in vivo. In conclusion, the study successfully engineered anti-GD2 EMs, which showed promising results as a drug delivery system for osteosarcoma, indicating that engineering anti-GD2 EMs may be a viable approach for combating this disease.","PeriodicalId":5,"journal":{"name":"ACS Applied Materials & Interfaces","volume":"2 1","pages":""},"PeriodicalIF":8.2000,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Genetically Engineered Glycosylphosphatidylinositol-Anchored Anti-GD2 Nanobody-Exosome Mimetics for Targeted Osteosarcoma Therapy In Vitro and In Vivo\",\"authors\":\"Jinkui Wang, Mujie Li, Zhaoxia Zhang, Tao Mi, Junyi Luo, Dawei He\",\"doi\":\"10.1021/acsami.5c12922\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"This study focuses on the engineering of exosome mimetics (EMs) that are decorated with an antidisialoganglioside (GD2) nanobody for targeting osteosarcoma. We engineer the anti-GD2 nanobody coding vector into HEK-293T (293T) cells and fuse it with the decay-accelerating factor (DAF)-derived glycosylphosphatidylinositol (GPI) anchor signal peptide. The sequential extrusion method was used to produce the targeted EMs. These engineered GD2-targeted EMs (GD2-EMs) possess the same exosome markers as regular exosomes, are produced in large quantities, have a nanoscale size, and feature a surface anti-GD2 nanobody. Furthermore, they demonstrate increased internalization in osteosarcoma cells compared to unmodified EMs. In animal experiments using nude mice, the GD2-EMs exhibited superior tumor targeting, confirming their efficacy in vivo. In conclusion, the study successfully engineered anti-GD2 EMs, which showed promising results as a drug delivery system for osteosarcoma, indicating that engineering anti-GD2 EMs may be a viable approach for combating this disease.\",\"PeriodicalId\":5,\"journal\":{\"name\":\"ACS Applied Materials & Interfaces\",\"volume\":\"2 1\",\"pages\":\"\"},\"PeriodicalIF\":8.2000,\"publicationDate\":\"2025-10-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Materials & Interfaces\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1021/acsami.5c12922\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Materials & Interfaces","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1021/acsami.5c12922","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
Genetically Engineered Glycosylphosphatidylinositol-Anchored Anti-GD2 Nanobody-Exosome Mimetics for Targeted Osteosarcoma Therapy In Vitro and In Vivo
This study focuses on the engineering of exosome mimetics (EMs) that are decorated with an antidisialoganglioside (GD2) nanobody for targeting osteosarcoma. We engineer the anti-GD2 nanobody coding vector into HEK-293T (293T) cells and fuse it with the decay-accelerating factor (DAF)-derived glycosylphosphatidylinositol (GPI) anchor signal peptide. The sequential extrusion method was used to produce the targeted EMs. These engineered GD2-targeted EMs (GD2-EMs) possess the same exosome markers as regular exosomes, are produced in large quantities, have a nanoscale size, and feature a surface anti-GD2 nanobody. Furthermore, they demonstrate increased internalization in osteosarcoma cells compared to unmodified EMs. In animal experiments using nude mice, the GD2-EMs exhibited superior tumor targeting, confirming their efficacy in vivo. In conclusion, the study successfully engineered anti-GD2 EMs, which showed promising results as a drug delivery system for osteosarcoma, indicating that engineering anti-GD2 EMs may be a viable approach for combating this disease.
期刊介绍:
ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.