Department of Cell Biology and Histology, Medical School, University of Murcia Murcia, Spain.
Front Endocrinol (Lausanne). 2013 Mar 28;4:41. doi: 10.3389/fendo.2013.00041. eCollection 2013.
In neuroendocrine cells, prohormones move from the endoplasmic reticulum to the Golgi complex (GC), where they are sorted and packed into secretory granules. The GC is considered the central station of the secretory pathway of proteins and lipids en route to their final destination. In most mammalian cells, it is formed by several stacks of cisternae connected by tubules, forming a continuous ribbon. This organelle shows an extraordinary structural and functional complexity, which is exacerbated by the fact that its architecture is cell type specific and also tuned by the functional status of the cell. It is, indeed, one the most beautiful cellular organelles and, for that reason, perhaps the most extensively photographed by electron microscopists. In recent decades, an exhaustive dissection of the molecular machinery involved in membrane traffic and other Golgi functions has been carried out. Concomitantly, detailed morphological studies have been performed, including 3D analysis by electron tomography, and the precise location of key proteins has been identified by immunoelectron microscopy. Despite all this effort, some basic aspects of Golgi functioning remain unsolved. For instance, the mode of intra-Golgi transport is not known, and two opposing theories (vesicular transport and cisternal maturation models) have polarized the field for many years. Neither of these theories explains all the experimental data so that new theories and combinations thereof have recently been proposed. Moreover, the specific role of the small vesicles and tubules which surround the stacks needs to be clarified. In this review, we summarize our current knowledge of the Golgi architecture in relation with its function and the mechanisms of intra-Golgi transport. Within the same framework, the characteristics of the GC of neuroendocrine cells are analyzed.
在神经内分泌细胞中,前激素从内质网移动到高尔基体复合体(GC),在那里它们被分拣并包装到分泌颗粒中。GC 被认为是蛋白质和脂质分泌途径的中央站,它们最终到达目的地。在大多数哺乳动物细胞中,它由几个堆叠的潴泡通过小管连接而成,形成一个连续的带状结构。这个细胞器具有非凡的结构和功能复杂性,这加剧了它的架构是细胞类型特异性的,并且还受到细胞功能状态的调节。它确实是最美丽的细胞器官之一,因此,也许是电子显微镜学家拍摄最多的细胞器。在最近几十年中,已经对涉及膜运输和其他高尔基体功能的分子机制进行了详尽的剖析。同时,还进行了详细的形态学研究,包括通过电子断层扫描进行 3D 分析,并通过免疫电子显微镜确定了关键蛋白的精确位置。尽管付出了所有这些努力,但高尔基体功能的一些基本方面仍然没有得到解决。例如,尚不清楚高尔基体内部运输的模式,并且两种对立的理论(小泡运输和潴泡成熟模型)多年来一直使该领域两极分化。这两个理论都不能解释所有的实验数据,因此最近提出了新的理论和它们的组合。此外,还需要阐明围绕堆叠的小泡和小管的特定作用。在这篇综述中,我们总结了我们目前对高尔基体结构与其功能和高尔基体内部运输机制的了解。在同一框架内,还分析了神经内分泌细胞的 GC 的特征。