Ubiquitin-dependent lysosomal targeting of GABA(A) receptors regulates neuronal inhibition.

Full Abstract

The strength of synaptic inhibition depends partly on the number of GABA(A) receptors (GABA(A)Rs) found at synaptic sites. The trafficking of GABA(A)Rs within the endocytic pathway is a key determinant of surface GABA(A)R number and is altered in neuropathologies, such as cerebral ischemia. However, the molecular mechanisms and signaling pathways that regulate this trafficking are poorly understood. Here, we report the subunit specific lysosomal targeting of synaptic GABA(A)Rs. We demonstrate that the targeting of synaptic GABA(A)Rs into the degradation pathway is facilitated by ubiquitination of a motif within the intracellular domain of the gamma2 subunit. Blockade of lysosomal activity or disruption of the trafficking of ubiquitinated cargo to lysosomes specifically increases the efficacy of synaptic inhibition without altering excitatory currents. Moreover, mutation of the ubiquitination site within the gamma2 subunit retards the lysosomal targeting of GABA(A)Rs and is sufficient to block the loss of synaptic GABA(A)Rs after anoxic insult. Together, our results establish a previously unknown mechanism for influencing inhibitory transmission under normal and pathological conditions.

Author information

Author/s: Arancibia-Cárcamo, I Lorena (IL); Yuen, Eunice Y (EY); Muir, James (J); Lumb, Michael J (MJ); Michels, Guido (G); Saliba, Richard S (RS); Smart, Trevor G (TG); Yan, Zhen (Z); Kittler, Josef T (JT); Moss, Stephen J (SJ);

Affiliation: Department of Neuroscience, Physiology, and Pharmacology, University College London, Gower Street, London, WC1E 6BT, United Kingdom.

Grants: NS047478 (Agency:NINDS NIH HHS) ; NS048045 (Agency:NINDS NIH HHS) ; NS051195 (Agency:NINDS NIH HHS) ; NS054900 (Agency:NINDS NIH HHS) ; NS056359 (Agency:NINDS NIH HHS) ; (Agency:Medical Research Council)

Journal and publication information

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

Journal: Proceedings of the National Academy of Sciences of the United States of America (Proc Natl Acad Sci U S A), published in United States. (Language: eng)

Reference: 2009-Oct; vol 106 (issue 41) : pp 17552-7

Dates: Created 2009/10/15; Completed 2009/11/03; Revised 2009/11/06;

PMID: 19815531, status: MEDLINE (last retrieval date: 11/9/2009, IMS Date: )

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