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在受到趋化梯度作用的巨噬细胞内,高尔基体和微管组织中心的重新定向。

Reorientation of the Golgi apparatus and the microtubule-organizing center inside macrophages subjected to a chemotactic gradient.

作者信息

Nemere I, Kupfer A, Singer S J

出版信息

Cell Motil. 1985;5(1):17-29. doi: 10.1002/cm.970050103.

Abstract

Mouse peritoneal macrophages subjected to gradients of activated mouse serum were found by immunofluorescence observations to have their Golgi apparatus and their microtubule-organizing center largely oriented in the direction of the gradient. By analogy with similar results obtained with motile fibroblasts, it is proposed that these two organelles are rapidly and coordinately reoriented inside the macrophages in order to direct the insertion of new membrane mass, via vesicles derived from the Golgi apparatus, into the leading edge of the cell. Consistent with the importance of such membrane insertion to cell migration, we found that the ionophore monensin, an inhibitor of Golgi functions, inhibited cell motility in the chemostactic gradient. It was further shown that several inhibitors of chemotaxis (monensin, cytochalasin D, cycloheximide) did not inhibit the reorientation of the Golgi apparatus/microtubule-organizing center in cells exposed to a chemotactic gradient, and that the reorientation required extracellular Ca+2.

摘要

通过免疫荧光观察发现,置于活化小鼠血清梯度中的小鼠腹膜巨噬细胞,其高尔基体和微管组织中心在很大程度上沿梯度方向排列。与在运动性成纤维细胞中获得的类似结果相似,有人提出这两种细胞器在巨噬细胞内迅速且协调地重新定向,以便通过源自高尔基体的囊泡将新的膜物质插入细胞的前沿。与这种膜插入对细胞迁移的重要性一致,我们发现离子载体莫能菌素(一种高尔基体功能抑制剂)在趋化梯度中抑制细胞运动。进一步表明,几种趋化作用抑制剂(莫能菌素、细胞松弛素D、环己酰亚胺)并不抑制暴露于趋化梯度的细胞中高尔基体/微管组织中心的重新定向,且这种重新定向需要细胞外Ca+2。

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