التفاصيل البيبلوغرافية
| العنوان: |
Ubiquitin-dependent lysosomal targeting of GABAA receptors regulates neuronal inhibition. |
| المؤلفون: |
Lorena Arancibia-Cârcamo, I., Yuen, Eunice Y., Muir, James, Lumb, Michael J., Michels, Guido, Saliba, Richard S., Smart, Trevor G., Zhen Yan, Kittler, Josef T., Moss, Stephen J. |
| المصدر: |
Proceedings of the National Academy of Sciences of the United States of America; 10/13/2009, Vol. 106 Issue 41, p17552-17557, 6p |
| مصطلحات موضوعية: |
UBIQUITIN, AMINO acids, BUTYRIC acid, NEURAL transmission, CEREBRAL ischemia, LYSOSOMES, ION channels |
| مستخلص: |
The strength of synaptic inhibition depends partly on the number of GABAA receptors (GABAARS) found at synaptic sites. The trafficking of GABAARS within the endocytic pathway is a key determinant of surface GABAAR 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 GABAARs. We demonstrate that the targeting of synaptic GABAARs into the degradation pathway is facilitated by ubiquitination of a motif within the intracellular domain of the y2 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 γ2 subunit retards the lysosomal targeting of GABAARs and is sufficient to block the loss of synaptic GABAARs after anoxic insult. Together, our results establish a previously unknown mechanism for influencing inhibitory transmission under normal and pathological conditions. [ABSTRACT FROM AUTHOR] |
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| قاعدة البيانات: |
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