细胞外囊泡:肝纤维化的新兴治疗剂。

IF 4.8
Extracellular vesicles and circulating nucleic acids Pub Date : 2025-05-07 eCollection Date: 2025-01-01 DOI:10.20517/evcna.2025.08
Giulia Chiabotto, Armina Semnani, Elena Ceccotti, Stefania Bruno
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引用次数: 0

摘要

肝纤维化是一种进行性疾病,其特征是疤痕组织的过度积累,导致肝功能受损和潜在的肝硬化。尽管治疗策略取得了进步,但有效的抗纤维化治疗仍然是一个迫切的未满足的需求。最近的研究发现,由于细胞外囊泡(EVs)具有介导细胞间通讯和调节关键纤维化途径的能力,因此它是一种很有前景的治疗药物。本文旨在全面概述ev在不同的体外和体内肝纤维化模型中的治疗潜力,重点介绍其天然作用和其增强疗效的工程研究的最新进展。电动汽车可以来源于各种细胞来源,包括间充质基质细胞(MSCs)和肝驻留细胞。包括血清、母乳、细菌和植物在内的生物材料也可作为EV来源。其中,msc -EV具有显著的治疗潜力,可以通过炎症信号预处理、药物或基因工程来提高EV的质量和疗效。工程技术进一步扩展了电动汽车的应用,使其成为精确有效的药物输送载体。将药理化合物装入电动汽车,设计定制的电动汽车,以及制造电动汽车脂质体混合物等方法可以靶向递送到活化的肝星状细胞(hsc),这是纤维化进展的主要驱动因素。这些策略增强了基于ev的治疗的疗效。天然和工程EVs都能调节肝纤维化发展的关键途径,包括造血干细胞的激活、促纤维化基因的调节、细胞外基质沉积和程序性细胞死亡。此外,电动汽车调节免疫反应,培养有利于修复和再生的肝脏微环境。将电动汽车的自然再生特性与创新的工程策略相结合,为恢复肝功能提供了高度针对性的有效治疗方法,并解决了慢性肝病治疗的迫切未满足需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Extracellular vesicles: emerging therapeutic agents for liver fibrosis.

Liver fibrosis is a progressive condition characterized by excessive scar tissue buildup, leading to impaired liver function and potentially cirrhosis. Despite advancements in treatment strategies, effective anti-fibrotic therapies remain an urgent unmet need. Recent research has identified extracellular vesicles (EVs) as promising therapeutic agents due to their ability to mediate intercellular communication and regulate key fibrotic pathways. This review aims to provide a comprehensive overview of the therapeutic potential of EVs in different in vitro and in vivo models of hepatic fibrosis, focusing on their natural effects and recent advancements in their engineering for enhanced efficacy. EVs can be derived from various cellular sources, including mesenchymal stromal cells (MSCs) and liver-resident cells. Biological materials, including serum, breast milk, bacteria, and plants, also serve as EV sources. Among these, MSC-EVs stand out for their therapeutic potential, which can be significantly enhanced through preconditioning with inflammatory signals, pharmacological agents, or genetic engineering to improve EV quality and efficacy. Engineering techniques have further expanded EV applications, enabling their use as precise and effective drug-delivery vehicles. Approaches such as loading EVs with pharmacological compounds, designing customized EVs, and creating EV-liposome hybrids enable targeted delivery to activated hepatic stellate cells (HSCs), central drivers of fibrosis progression. These strategies enhance the efficacy of EV-based treatments. Both natural and engineered EVs regulate critical pathways of liver fibrosis development, including activation of HSCs, modulation of pro-fibrotic genes, extracellular matrix deposition, and programmed cell death. Additionally, EVs modulate immune responses, fostering a liver microenvironment conducive to repair and regeneration. Combining the natural regenerative properties of EVs with innovative engineering strategies provides highly targeted, effective treatment approaches to restore liver function and address the urgent unmet need for chronic liver disease therapies.

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