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The origins and evolution of macropinocytosis

机译:大型细胞症的起源和演变

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摘要

In macropinocytosis, cells take up micrometre-sized droplets of medium into internal vesicles. These vesicles are acidified and fused to lysosomes, their contents digested and useful compounds extracted. Indigestible contents can be exocytosed. Macropinocytosis has been known for approaching 100 years and is described in both metazoa and amoebae, but not in plants or fungi. Its evolutionary origin goes back to at least the common ancestor of the amoebozoa and opisthokonts, with apparent secondary loss from fungi. The primary function of macropinocytosis in amoebae and some cancer cells is feeding, but the conserved processing pathway for macropinosomes, which involves shrinkage and the retrieval of membrane to the cell surface, has been adapted in immune cells for antigen presentation. Macropinocytic cups are large actin-driven processes, closely related to phagocytic cups and pseudopods and appear to be organized around a conserved signalling patch of PIP3, active Ras and active Rac that directs actin polymerization to its periphery. Patches can form spontaneously and must be sustained by excitable kinetics with strong cooperation from the actin cytoskeleton. Growth-factor signalling shares core components with macropinocytosis, based around phosphatidylinositol 3-kinase (PI3-kinase), and we suggest that it evolved to take control of ancient feeding structures through a coupled growth factor receptor.
机译:在大血细胞增生中,细胞将微米尺寸的培养基液滴到内部囊泡中。将这些囊泡酸化并融合到溶酶体中,其内容物消化和提取有用的化合物。难以消化的内容可以被吞噬。众所周知,宏观细胞增多作用于达到100年,并在Metazoa和Amoebae中描述,但不在植物或真菌中描述。它的进化起源至少回到了amoebozoa和Opisthokonts的共同祖先,具有明显的二次损失来自真菌。在AmoEbae和一些癌细胞中的麦仔植物症的主要功能是喂养,而是用于癌细胞收缩和对细胞表面的膜的癌细胞的保守加工途径已经适用于抗原呈递的免疫细胞。 Macropinytic Cups是大型肌动蛋白驱动的过程,与吞噬杯和假体密切相关,并且似乎在PIP3,活性RAS和活性RAC的保守信号贴片周围组织,其将肌动蛋白聚合指向其周边。斑块可以自发地形成,并且必须通过具有强大的肌动蛋白细胞骨架合作的激发动力学来维持。生长因子信号传导与大型细胞症共享核心组分,基于磷脂酰肌醇3-激酶(PI3-激酶),并表明它演变为通过偶联的生长因子受体控制古代饲养结构。

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