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细胞外囊泡生物发生的分子机制及其对定制细胞外囊泡设计的影响

Molecular Mechanisms of Extracellular Vesicle Biogenesis and Their Impact on the Design of Custom EVs.

作者信息

Carvalho Ferraz Luís, Pereira Paulo, Ferreira João Vasco

机构信息

iNOVA4Health, NOVA Medical School, Faculdade de Ciências Médicas, NMS|FCM, Universidade NOVA de Lisboa, Lisbon, 1169-056, Portugal.

出版信息

Adv Healthc Mater. 2025 Sep;14(23):e2501349. doi: 10.1002/adhm.202501349. Epub 2025 Jul 8.

Abstract

Extracellular Vesicles (EVs) are nanosized lipid-bound particles that are pivotal for intercellular communication and actively participate in diverse physiological processes, including immune modulation, proteostasis, and tissue repair. EVs have emerged as promising therapeutic targets and biomarkers because of their significant roles in the pathogenesis of diseases, including cancer, neurodegeneration, and cardiovascular disorders. Despite extensive research on EVs as diagnostic tools and mediators of cellular signaling, the fundamental mechanisms underlying their biogenesis remain unclear. Consequently, this understanding of how the composition of EVs dynamically changes in response to physiological and pathological conditions is often limited, leading to lower diagnostic utility and slower advancements in clinical interventions and EVs engineering. This review explores the intricate mechanisms underlying EVs biogenesis and payload selection, emphasizing how these processes vary across EVs subclasses, thereby underpinning their functional versatility. The biogenetic pathways are highlighted from the ectocytosis-driven generation of microvesicles and apoptotic body (ApoBDs) formation via membrane blebbing to the formation of exosomes within the endosomal compartments and their regulated release via exocytosis.

摘要

细胞外囊泡(EVs)是纳米级的脂质结合颗粒,对细胞间通讯至关重要,并积极参与多种生理过程,包括免疫调节、蛋白质稳态和组织修复。由于EVs在包括癌症、神经退行性疾病和心血管疾病在内的疾病发病机制中发挥着重要作用,它们已成为有前景的治疗靶点和生物标志物。尽管对EVs作为诊断工具和细胞信号传导介质进行了广泛研究,但其生物发生的基本机制仍不清楚。因此,对于EVs的组成如何响应生理和病理条件而动态变化的理解往往有限,导致诊断效用较低,临床干预和EVs工程的进展较慢。本综述探讨了EVs生物发生和货物选择的复杂机制,强调了这些过程在不同EVs亚类中的差异,从而支撑了它们的功能多样性。从通过膜泡形成的胞吐作用驱动的微泡生成和凋亡小体(ApoBDs)形成到内体区室内外泌体的形成及其通过胞吐作用的调节释放,突出了生物发生途径。

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