Alterations of Golgi organization in Alzheimer's disease: A cause or a consequence?

Tissue Cell. 2017 Apr;49(2 Pt A):133-140. doi: 10.1016/j.tice.2016.11.007. Epub 2016 Nov 19.

Abstract

The Golgi apparatus is a central organelle of the secretory pathway involved in the post-translational modification and sorting of lipids and proteins. In mammalian cells, the Golgi apparatus is composed of stacks of cisternae organized in polarized manner, which are interconnected by membrane tubules to constitute the Golgi ribbon, located in the proximity of the centrosome. Besides the processing and transport of cargo, the Golgi complex is actively involved in the regulation of mitotic entry, cytoskeleton organization and dynamics, calcium homeostasis, and apoptosis, representing a signalling platform for the control of several cellular functions, including signalling initiated by receptors located at the plasma membrane. Alterations of the conventional Golgi organization are associated to many disorders, such as cancer or different neurodegenerative diseases. In this review, we examine the functional implications of modifications of Golgi structure in neurodegenerative disorders, with a focus on the role of Golgi fragmentation in the development of Alzheimer's disease. The comprehension of the mechanism that induces Golgi fragmentation and of its downstream effects on neuronal function have the potential to contribute to the development of more effective therapies to treat or prevent some of these disorders.

Keywords: Alzheimer’s disease; Golgi complex; Membrane trafficking; Neurodegeneration; Signalling.

Publication types

  • Review

MeSH terms

  • Alzheimer Disease / genetics*
  • Alzheimer Disease / pathology
  • Apoptosis / genetics
  • Calcium Signaling / genetics
  • Cell Membrane / genetics
  • Cell Membrane / ultrastructure
  • Golgi Apparatus / genetics*
  • Golgi Apparatus / pathology
  • Golgi Apparatus / ultrastructure
  • Humans
  • Neurons / metabolism
  • Neurons / pathology
  • Protein Processing, Post-Translational / genetics
  • Protein Transport / genetics*