Auxiliary subunits: Shepherding AMPA receptors to the plasma membrane

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Abstract

Ionotropic glutamate receptors (iGluRs) are tetrameric ligand-gated cation channels that mediate excitatory signal transmission in the central nervous system (CNS) of vertebrates. The members of the iGluR subfamily of α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA) receptors (AMPARs) mediate most of the fast excitatory signal transmission, and their abundance in the postsynaptic membrane is a major determinant of the strength of excitatory synapses. Therefore, regulation of AMPAR trafficking to the postsynaptic membrane is an important constituent of mechanisms involved in learning and memory formation, such as long-term potentiation (LTP) and long-term depression (LTD). Auxiliary subunits play a critical role in the facilitation and regulation of AMPAR trafficking and function. The currently identified auxiliary subunits of AMPARs are transmembrane AMPA receptor regulatory proteins (TARPs), suppressor of lurcher (SOL), cornichon homologues (CNIHs), synapse differentiation-induced gene I (SynDIG I), cysteine-knot AMPAR modulating proteins 44 (CKAMP44), and germ cell-specific gene 1-like (GSG1L) protein. In this review we summarize our current knowledge of the modulatory influence exerted by these important but still underappreciated proteins. © 2014 by the authors; licensee MDPI, Basel, Switzerland.

Figures

  • Figure 1. (A) Phylogenetic tree of all tetraspanin-resembling four transmembrane domain-containing auxiliary subunits: type I TARPs (red), type II TARPs (orange), stg-1, stg-2, γ1, γ6, GSG1L, and claudin1 as a representative of the most closely related group of non-γ subunit proteins. (B) Phylogenetic tree of all non-tetraspanin-resembling auxiliary subunits with less than four transmembrane domains: CNIHs (blue), CNI, NETO, SOL-1, SynDIGI, SOL-2, CKAMP44. The ClustalW protein alignment was used for calculation and the Phylodendron program for the tree generation. Scale indicates number of exchanges per position along the branches connecting two proteins.
  • Figure 2. Schematic structures of iGluRs, TARPs, NETO, SOL-1, CNIH/CNI, CKAMP44, SynDIG1, and GSG1L.
  • Table 1. Modulation of AMPARs by TARPs; +, a positive modulation or interaction; −, a negative modulation; (+)/(−), possible or expected positive or negative modulation; 0, no modulation; ~, unclear/different results described; N/A, no data available. Contradictory results and observations are discussed in the text.
  • Table 2. Modulation of AMPARs by auxiliary subunits other than TARPs; +, a positive modulation or interaction; −, a negative modulation; (+)/(−), possible or expected positive or negative modulation; 0, no modulation; ~, unclear/different results described; N/A, no data available. Contradictory results and observations are discussed in the text. (des. = desensitization; deac. = deactivation).

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APA

Haering, S. C., Tapken, D., Pahl, S., & Hollmann, M. (2014, August 8). Auxiliary subunits: Shepherding AMPA receptors to the plasma membrane. Membranes. MDPI AG. https://doi.org/10.3390/membranes4030469

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