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在[具体情况未提及处]可见的50纳米游离囊泡不依赖于COPII。

The 50-nm Free Vesicles Visible in Are Not COPII-Dependent.

作者信息

Mironov Alexander A, Fusella Aurora, Beznoussenko Galina V

机构信息

Department of Cell Biology, IFOM ETS-The AIRC Institute of Molecular Oncology, Via Adamello, 16, 20139 Milan, Italy.

Department of Neurosciences, Imaging and Clinical Sciences & Centre for Advanced Studies and Technology, University "G. d'Annunzio" of Chieti-Pescara, 66013 Chieti, Italy.

出版信息

Curr Issues Mol Biol. 2025 May 7;47(5):336. doi: 10.3390/cimb47050336.

Abstract

According to the current dogma, ER-Golgi transport is mediated by COPII-coated vesicles. However, numerous contradictions have emerged in this field. In this study, we demonstrate that contains three distinct types of membrane spheres, with diameters of approximately 35-45 nm, 47-52 nm, and over 65 nm, respectively. The first type is Sso1-positive and primary associated with clathrin-positive endocytosis invaginations, which may function as exit sites for secretory soluble cargos. The second population is GOS1-positive and COPI-dependent. The third population represents secretory granules. Furthermore, we propose that several cornerstone studies supporting the COPII-vesicle model can have alternative interpretations. Our findings suggest that the predominant model of intracellular transport in is the "kiss-and-run" mechanism.

摘要

根据当前的理论,内质网-高尔基体运输由COPII包被的囊泡介导。然而,该领域已出现众多矛盾之处。在本研究中,我们证明[具体研究对象未给出]包含三种不同类型的膜球,直径分别约为35 - 45纳米、47 - 52纳米和超过65纳米。第一种类型为Sso1阳性,主要与网格蛋白阳性的内吞凹陷相关,可能作为分泌性可溶性货物的出口位点。第二种群体为GOS1阳性且依赖于COPI。第三种群体代表分泌颗粒。此外,我们提出,一些支持COPII囊泡模型的基础研究可能有其他解释。我们的研究结果表明,[具体研究对象未给出]中细胞内运输的主要模型是“吻-跑”机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec10/12110059/424ef53bfb85/cimb-47-00336-g001.jpg

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