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脂滴与细胞外小囊泡:不止两个独立实体。

Lipid droplets and small extracellular vesicles: More than two independent entities.

作者信息

Genard Géraldine C, Tirinato Luca, Pagliari Francesca, Da Silva Jessica, Giammona Alessandro, Alquraish Fatema, Reyes Maria Parra, Bordas Marie, Marafioti Maria Grazia, Franco Simone Di, Janssen Jeannette, Garcia-Calderón Daniel, Hanley Rachel, Nistico Clelia, Fukasawa Yoshinori, Müller Torsten, Krijgsveld Jeroen, Todaro Matilde, Costanzo Francesco Saverio, Stassi Giorgio, Nessling Michelle, Richter Karsten, Maass Kendra K, Liberale Carlo, Seco Joao

机构信息

Division of Biomedical Physics in Radiation Oncology German Cancer Research Center (DKFZ) Heidelberg Germany.

Department of Experimental and Clinical Medicine, Nanotechnology Research Center University of Magna Graecia Catanzaro Italy.

出版信息

J Extracell Biol. 2024 Sep 10;3(9):e162. doi: 10.1002/jex2.162. eCollection 2024 Sep.

Abstract

Despite increasing knowledge about small extracellular vesicle (sEV) composition and functions in cell-cell communication, the mechanism behind their biogenesis remains unclear. Here, we reveal for the first time that sEV biogenesis and release into the microenvironment are tightly connected with another important organelle, Lipid Droplets (LDs). The correlation was observed in several human cancer cell lines as well as patient-derived colorectal cancer stem cells (CR-CSCs). Our results demonstrated that external stimuli such as radiation, pH, hypoxia or lipid-interfering drugs, known to affect the number of LDs/cell, similarly influenced sEV secretion. Importantly, through multiple omics data, at both mRNA and protein levels, we revealed RAB5C as a potential important molecular player behind this organelle connection. Altogether, the potential to fine-tune sEV biogenesis by targeting LDs could significantly impact the amount, cargos and properties of these sEVs, opening new clinical perspectives.

摘要

尽管人们对小细胞外囊泡(sEV)在细胞间通讯中的组成和功能的了解不断增加,但其生物发生背后的机制仍不清楚。在这里,我们首次揭示sEV的生物发生和释放到微环境中与另一个重要细胞器脂滴(LDs)紧密相连。在几种人类癌细胞系以及患者来源的结直肠癌干细胞(CR-CSCs)中都观察到了这种相关性。我们的结果表明,已知会影响每个细胞中LDs数量的外部刺激,如辐射、pH值、缺氧或脂质干扰药物,同样会影响sEV的分泌。重要的是,通过多个组学数据,在mRNA和蛋白质水平上,我们发现RAB5C是这种细胞器连接背后的一个潜在重要分子参与者。总之,通过靶向LDs来微调sEV生物发生的潜力可能会显著影响这些sEV的数量、货物和特性,开辟新的临床前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47ad/11386333/8bedb6c67215/JEX2-3-e162-g006.jpg

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