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Activation of RAGE leads to the release of glutamate from astrocytes and stimulates calcium signal in neurons

A. V. KamyninaResearch Center for Molecular Mechanisms of Aging and Age Related Diseases Moscow Institute of Physics and Technology (National Research University) Dolgoprudny RussiaNoemí EsterasDepartment of Clinical and Movement Neurosciences UCL Queen Square Institute of Neurology, Queen Square London UKDmitry O. KoroevShemyakin‐Ovchinnikov Institute of Bioorganic Chemistry RAS Moscow RussiaPlamena R. AngelovaDepartment of Clinical and Movement Neurosciences UCL Queen Square Institute of Neurology, Queen Square London UKO. M. VolpinaShemyakin‐Ovchinnikov Institute of Bioorganic Chemistry RAS Moscow RussiaAndrey Y. AbramovDepartment of Clinical and Movement Neurosciences UCL Queen Square Institute of Neurology, Queen Square London UK
2021en
ABI

Abstract

The receptor for advanced glycation end products (RAGE) is a signal receptor first shown to be activated by advanced glycation end products, but also by a variety of signal molecules, including pathological advanced oxidation protein products and β-amyloid. However, most of the RAGE activators have multiple intracellular targets, making it difficult to unravel the exact pathway of RAGE activation. Here, we show that the cell-impermeable RAGE fragment sequence (60-76) of the V-domain of the receptor is able to activate RAGE present on the plasma membrane of neurons and, preferentially, astrocytes. This leads to the exocytosis of vesicular glutamate transporter vesicles and the release of glutamate from astrocytes, which stimulate NMDA and AMPA/kainate receptors, resulting in calcium signals predominantly in neurons. Thus, we show a specific mechanism of RAGE activation by the RAGE fragment and propose a mechanism by which RAGE activation can contribute to the neuronal-astrocytic communication in physiology and pathology.

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