小泡
细胞外小泡
细胞生物学
免疫系统
线粒体
细胞内
细胞外
生物
细胞
微泡
化学
细胞器
核酸
小RNA
疾病
先天免疫系统
细胞外基质
生物化学
计算生物学
蛋白质组学
细胞室
胞外囊泡
细胞生长
细胞内寄生虫
作者
Rostyslav Horbay,Vasyl Syrvatka,Artem Bedzay,Mikaela van der Merwe,Dylan Burger,Shawn T. Beug
摘要
ABSTRACT According to the endosymbiotic theory of mitochondrial origin, an α‐proteobacterium entered a prokaryotic cell and, through symbiosis, evolved into the mitochondria—the powerhouse of the cell. Like other bacteria, the α‐proteobacteria generate their own extracellular vesicles (EVs), a trait that was passed onto the mitochondria, enabling them to generate mitochondria‐derived vesicles (MDVs). MDVs, similar to small EVs (sEVs), are vesicles ranging from 30 to 200 nm in diameter and carry cargo for degradation by lysosomes and peroxisomes. MDVs share several features with sEVs, including targeted cargo degradation, biogenesis, packaging into multivesicular bodies, nucleic acid and protein transportation, induction of immune responses, and surface antigen presentation. MDVs may also be released from the cell in a manner similar to sEVs, potentially influencing intercellular communication and immune responses. Furthermore, the presence of MDVs presents opportunities for early disease detection, including neurodegenerative disorders and cancer. In this review, we explore the differences and similarities between MDVs and EVs, including their roles in immunity.
科研通智能强力驱动
Strongly Powered by AbleSci AI