Yang Song, Zhu Haomiao, Jin Hongzhen, Wang Kun, Song Junna, Sun Na, Liu Yonghui, Yin Xiaona, Wang Rui, Wu Xiao, Liu Huadong, Zhang Chunling, Zhao Wei, Yu Fan
Qingdao Central Hospital, School of Health and Life Sciences, University of Health and Rehabilitation Sciences, No. 369, Qingdao National High-Tech Industrial Development Zone, Qingdao, 266113, China; State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, Key Laboratory of Molecular Drug Research and KLMDASR of Tianjin, Nankai University, No.38 Tongyan Road, Haihe Education Park, Tianjin, 300350, China.
State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, Key Laboratory of Molecular Drug Research and KLMDASR of Tianjin, Nankai University, No.38 Tongyan Road, Haihe Education Park, Tianjin, 300350, China; Department of Pharmacy, Qilu Hospital, Shandong University, No.107 Cultural West Road, Jinan, 250012, China.
Biomaterials. 2025 Aug;319:123208. doi: 10.1016/j.biomaterials.2025.123208. Epub 2025 Feb 24.
Exosomes derived from specific cells may be useful for targeted drug delivery, but tracking them in vivo is essential for their clinical application. However, their small size and complex structure challenge the development of exosome-tracking techniques, and traditional labeling methods are limited by weak affinity and potential toxicity. To address these issues, here we developed a novel bio-orthogonal labeling strategy based on phosphatidylinositol derivatives to fluorescently label exosomes from various human and mouse cell types. The different cell-derived exosomes revealed organ-specific distribution patterns and a favorable safety profile. Notably, 4T1 cell-derived exosomes specifically targeted the lungs. When used as drug carriers loaded with anti-inflammatory resveratrol, these exosomes showed significant therapeutic efficacy in mice with acute respiratory distress syndrome (ARDS), effectively reducing inflammatory responses, mitigating pulmonary fibrosis, and restoring lung tissue morphology and function. Our findings provide a novel exosome labeling strategy and an invaluable tool for their in vivo tracking and targeting screening, while exosomes that specifically target the lungs offer a potential therapeutic strategy for organ-specific diseases such as ARDS.
源自特定细胞的外泌体可能有助于靶向给药,但在体内追踪它们对于其临床应用至关重要。然而,它们的小尺寸和复杂结构对开发外泌体追踪技术构成挑战,并且传统的标记方法受到亲和力弱和潜在毒性的限制。为了解决这些问题,我们在此开发了一种基于磷脂酰肌醇衍生物的新型生物正交标记策略,以荧光标记来自各种人类和小鼠细胞类型的外泌体。不同细胞来源的外泌体显示出器官特异性分布模式和良好的安全性。值得注意的是,4T1细胞来源的外泌体特异性靶向肺部。当用作负载抗炎白藜芦醇的药物载体时,这些外泌体在急性呼吸窘迫综合征(ARDS)小鼠中显示出显著的治疗效果,有效减轻炎症反应,缓解肺纤维化,并恢复肺组织形态和功能。我们的研究结果为外泌体标记提供了一种新策略,并为其体内追踪和靶向筛选提供了宝贵工具,而特异性靶向肺部的外泌体为诸如ARDS等器官特异性疾病提供了一种潜在的治疗策略。