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First published online 25 May 2004
doi: 10.1242/jcs.01153
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Research Article |
Department of Biological Sciences, National Sun Yat-Sen University, Kaohsiung City 804, Taiwan
* Author for correspondence (e-mail: netliou{at}mail.nsysu.edu.tw)
Accepted 12 February 2004
Although the long-term effects of all-trans retinoic acid (RA) on neuronal growth and differentiation have been intensively studied, nothing is known about its effect on synaptic transmission. Here we show that RA rapidly and specifically enhances the spontaneous acetylcholine release at developing neuromuscular synapses in Xenopus cell culture using whole-cell patch-clamp recording. Acute addition of RA dose-dependently and reversibly enhances the frequency of spontaneous synaptic currents (SSCs). Application of the lipophilic RA analogue all-trans retinol or RA metabolites produced by light-induced decomposition failed to provoke similar changes in SSC frequency, indicating the specificity of RA-induced facilitation of spontaneous transmitter release. Protein synthesis inhibitors anisomycin or cycloheximide had no effect on RA-induced SSC frequency facilitation. Treating cells with pan RA receptor (RAR) selective agonist or RARß-selective agonist, but not RAR
-, RAR
- or retinoid X receptor (RXR)-selective agonists, mimicked the action of RA. These results suggest that RA acts through the activation of RARß, to induce a rapid, non-genomic increase in the frequency of spontaneous transmitter release at developing neuromuscular synapses.
Key words: Retinoic acid, Non-genomic, Transmitter release, Neuromuscular junction, Development
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J.-C. Liou, S.-Y. Ho, M.-R. Shen, Y.-P. Liao, W.-T. Chiu, and K.-H. Kang A rapid, nongenomic pathway facilitates the synaptic transmission induced by retinoic acid at the developing synapse J. Cell Sci., October 15, 2005; 118(20): 4721 - 4730. [Abstract] [Full Text] [PDF] |
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