细胞源性微泡在干细胞研究和治疗中的新作用。

Jinlin Jiang, Xuyang Song
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摘要

微囊泡(Microvesicles, mv)或微颗粒是一种细胞外囊泡(extracellular vesicles, ev),在生理或病理条件下可由所有类型的细胞产生。mv的直径从100nm到1000nm不等。mv与外泌体不同,外泌体较小(20 nm ~ 100 nm),起源于多血管体[1]。MV生物发生总是与细胞生长、活化或凋亡有关。这一过程包括质膜的直接出芽和广泛的外部信号可以刺激细胞产生mv。刺激剂可以是物理应激(如剪切、缺氧和氧化应激)、生理激动剂(如凝血酶和TNFα)或非生理激活剂(如肉豆蔻酸酯和钙离子载体)。MV生成过程复杂,细胞采用多种机制,包括caspase激活、脂筏、细胞骨架重组等[2]。即使它们是由相同的亲本细胞产生但受到不同的刺激,mv在表面标记物表达、膜磷脂组成以及内部蛋白质和RNA谱方面也是异质的[2]。
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The emerging role of cell-derived microvesicles in stem cell research and therapy.
Microvesicles (MVs) or microparticles are one type of extracellular vesicles (EVs) which can be produced by all types of cells under physiological or pathological conditions. The diameter of MVs ranges from 100 nm to 1000 nm. MVs are different from exosomes which are smaller (20 nm 100 nm) and originate from multivescular bodies [1]. MV biogenesis is always associated with cell growth, activation or apoptosis. The process involves direct budding of plasma membrane and a wide range of external signals can stimulate cells to produce MVs. The stimulator can be physical stress (such as, shear, hypoxia and oxidative stress), physiological agonists (such as, thrombin and TNFα) or non-physiological activators (such as, phorbol myristate acetate and calcium ionophore). MV generation process is complex and multiples mechanisms have been employed by cells, including caspase activation, lipid rafts, cytoskeletal reorganization and so on [2]. MVs are heterogeneous with respect to their surface marker expression, membrane phospholipid composition, and internal protein and RNA repertoires even when they are produced by the same parent cells but with different stimulations [2].
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