Protein quality control of -methyl-D-aspartate receptors.

Front Cell Neurosci

Department of Physiology and Biophysics, School of Medicine, Case Western Reserve University, Cleveland, OH, United States.

Published: July 2022

AI Article Synopsis

  • N-methyl-D-aspartate receptors (NMDARs) are important for excitatory signaling and synaptic development in the brain, typically formed by GluN1 and GluN2 subunits.
  • Variants in NMDAR genes are linked to several neurodevelopmental and psychiatric disorders, making proper receptor assembly and surface expression crucial for brain function.
  • The review discusses the mechanisms ensuring NMDAR assembly and trafficking, the impact of disease-related variants, and potential therapeutic strategies to improve NMDAR function in affected individuals.

Article Abstract

N-methyl-D-aspartate receptors (NMDARs) are glutamate-gated cation channels that mediate excitatory neurotransmission and are critical for synaptic development and plasticity in the mammalian central nervous system (CNS). Functional NMDARs typically form the heterotetrameric assembly of GluN1 and GluN2 subunits. Variants within genes are implicated in various neurodevelopmental and neuropsychiatric disorders. Due to the significance of NMDAR subunit composition for regional and developmental signaling at synapses, properly folded receptors must reach the plasma membrane for their function. This review focuses on the protein quality control of NMDARs. Specifically, we review the quality control mechanisms that ensure receptors are correctly folded and assembled within the endoplasmic reticulum (ER) and trafficked to the plasma membrane. Further, we discuss disease-associated variants that have shown disrupted NMDAR surface expression and function. Finally, we discuss potential targeted pharmacological and therapeutic approaches to ameliorate disease phenotypes by enhancing the expression and surface trafficking of subunits harboring disease-associated variants, thereby increasing their incorporation into functional receptors.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9352929PMC
http://dx.doi.org/10.3389/fncel.2022.907560DOI Listing

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