Emerging Synaptic Molecules as Candidates in the Etiology of Neurological Disorders.

Neural Plast

Centro de Envejecimiento y Regeneración (CARE), Departamento de Biología Celular y Molecular, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile; Centre for Healthy Brain Ageing, School of Psychiatry, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia; Centro de Excelencia en Biomedicina de Magallanes (CEBIMA), Universidad de Magallanes, Punta Arenas, Chile.

Published: August 2017

AI Article Synopsis

  • Synapses are essential for neuron communication in the central nervous system and depend on specialized protein complexes for proper function and adaptability (synaptic plasticity).
  • There is a lack of understanding about how these proteins interact during important processes like brain development, learning, and memory.
  • Research shows a connection between synaptic proteins and various neurological disorders, including neurodevelopmental, neuropsychiatric, and neurodegenerative diseases, particularly focusing on proteins involved in cell adhesion, scaffolding, exocytosis, and neurotransmitter reception.

Article Abstract

Synapses are complex structures that allow communication between neurons in the central nervous system. Studies conducted in vertebrate and invertebrate models have contributed to the knowledge of the function of synaptic proteins. The functional synapse requires numerous protein complexes with specialized functions that are regulated in space and time to allow synaptic plasticity. However, their interplay during neuronal development, learning, and memory is poorly understood. Accumulating evidence links synapse proteins to neurodevelopmental, neuropsychiatric, and neurodegenerative diseases. In this review, we describe the way in which several proteins that participate in cell adhesion, scaffolding, exocytosis, and neurotransmitter reception from presynaptic and postsynaptic compartments, mainly from excitatory synapses, have been associated with several synaptopathies, and we relate their functions to the disease phenotype.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346360PMC
http://dx.doi.org/10.1155/2017/8081758DOI Listing

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