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巨核细胞中界膜系统(DMS)的生物发生。

Biogenesis of the demarcation membrane system (DMS) in megakaryocytes.

机构信息

Unité mixte de recherche S949 Institut National de la Santé et de la Recherche Médicale, Université de Strasbourg, Etablissement Français du Sang-Alsace, Strasbourg, France;

出版信息

Blood. 2014 Feb 6;123(6):921-30. doi: 10.1182/blood-2013-03-492330. Epub 2013 Oct 23.

Abstract

The demarcation membrane system (DMS) in megakaryocytes forms the plasma membrane (PM) of future platelets. Using confocal microscopy, electron tomography, and large volume focused ion beam/scanning electron microscopy (FIB/SEM), we determined the sequential steps of DMS formation. We identified a pre-DMS that initiated at the cell periphery and was precisely located between the nuclear lobes. At all developmental stages, the DMS remained continuous with the cell surface. The number of these connections correlated well with the nuclear lobulation, suggesting a relationship with cleavage furrow formation and abortive cytokinesis. On DMS expansion, Golgi complexes assembled around the pre-DMS, and fusion profiles between trans-golgi network-derived vesicles and the DMS were observed. Brefeldin-A reduced DMS expansion, indicating that the exocytic pathway is essential for DMS biogenesis. Close contacts between the endoplasmic reticulum (ER) and the DMS were detected, suggesting physical interaction between the 2 membrane systems. FIB/SEM revealed that the DMS forms an intertwined tubular membrane network resembling the platelet open canalicular system. We thus propose the following steps in DMS biogenesis: (1) focal membrane assembly at the cell periphery; (2) PM invagination and formation of a perinuclear pre-DMS; (3) expansion through membrane delivery from Golgi complexes; and (4) ER-mediated lipid transfer.

摘要

巨核细胞中的界膜系统 (DMS) 形成未来血小板的质膜 (PM)。我们使用共聚焦显微镜、电子断层扫描、以及大体积聚焦离子束/扫描电子显微镜 (FIB/SEM),确定了 DMS 形成的连续步骤。我们发现了一个起始于细胞边缘的预 DMS,并且准确地位于核叶之间。在所有发育阶段,DMS 都与质膜保持连续。这些连接的数量与核叶裂很好地相关,这表明与胞质分裂沟的形成和失败有关。在 DMS 扩张时,高尔基复合体围绕预 DMS 组装,并且观察到源自高尔基网络衍生的小泡与 DMS 之间的融合谱。布雷非德菌素 A 减少了 DMS 的扩张,表明外显途径对于 DMS 的生物发生是必要的。内质网 (ER) 和 DMS 之间的紧密接触被检测到,这表明这两个膜系统之间存在物理相互作用。FIB/SEM 揭示了 DMS 形成类似于血小板开放小管系统的交织管状膜网络。因此,我们提出 DMS 生物发生的以下步骤:(1) 在细胞边缘的局部膜组装;(2) PM 内陷和核周预 DMS 的形成;(3) 通过来自高尔基复合体的膜传递进行扩张;和 (4) ER 介导的脂质转移。

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