Claudin 24—A novel enhancer of AMPA receptor fidelity

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Authors: Tobias Strasdeit, Ehsan Amin, Sebastian Obst, Barbara Biermann, Thomas P. Newton, Simon Chris Kösters, Marten Schouwink, Sergey Fedotov, Javeria Shaukat, Subhrajit Bhattacharya, Muhammad Aslam, Max Anstötz
+10 more Faik Nadi Okka, Oscar Gabriel Sevillano Quispe, Pascal Bouvain, Julia Vedyashkin, Alexander I. Sobolevsky, Stephen F. Traynelis, Jakob von Engelhardt, Nadine Erlenhardt, Michael Hollmann, Nikolaj Klöcker
Cited by: 2
References: 55

Abstract

High-fidelity fast excitatory neurotransmission in the mammalian central nervous system is conducted by the AMPA receptor (AMPAR) subfamily of ionotropic glutamate receptors. AMPARs exist as complexes of the pore-lining α subunits GluA1-4 and a number of auxiliary subunits shaping their functional properties. The first discovered family of auxiliary subunits comprises the transmembrane AMPAR regulatory proteins (TARPs). Together with germ cell-specific gene 1-like (GSG1L), they belong to the PMP-22/EMP/MP20/claudin superfamily sharing substantial sequence homology and a 4-transmembrane domain (4-TMD) topology. Here, we identify the claudin Cldn24 as a novel AMPAR auxiliary subunit in cerebellar granule cells (CGCs). Specifically accelerating the recovery of desensitized receptors, Cldn24 counterbalances gating modulation of GluA by TARP-γ2 and GSG1L in CGCs and hence enables fast reactivation of native receptors. These features substantially expand the tuning properties of hitherto known AMPAR auxiliary subunits and render Cldn24 a powerful enhancer of AMPAR fidelity.

Fields of Study & Subjects

Barrier Structure and Function Studies Neuroscience and Neuropharmacology Research RNA regulation and disease

Publication details

Journal / source
Science Advances
Publisher
American Association for the Advancement of Science (AAAS)
Volume
12
Issue
10
Pages
eaeb0196–eaeb0196
Publication date
6 March 2026
Language
EN