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Phosphorylation of cysteine string protein-α up-regulates the frequency of cholinergic waves via starburst amacrine cells

During the first postnatal week in rodents, cholinergic retinal waves initiate in starburst amacrine cells (SACs), propagating to retinal ganglion cells (RGCs) and visual centers, essential for visual circuit refinement. By modulating exocytosis in SACs, dynamic changes in the protein kinase A (PKA)...

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Autores principales: Chen, Ching-Feng, Wo, Rita R., Huang, Chien-Ting, Cheng, Tzu-Lin, Lu, Juu-Chin, Wang, Chih-Tien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9107963/
https://www.ncbi.nlm.nih.gov/pubmed/35543445
http://dx.doi.org/10.1017/S0952523822000013
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author Chen, Ching-Feng
Wo, Rita R.
Huang, Chien-Ting
Cheng, Tzu-Lin
Lu, Juu-Chin
Wang, Chih-Tien
author_facet Chen, Ching-Feng
Wo, Rita R.
Huang, Chien-Ting
Cheng, Tzu-Lin
Lu, Juu-Chin
Wang, Chih-Tien
author_sort Chen, Ching-Feng
collection PubMed
description During the first postnatal week in rodents, cholinergic retinal waves initiate in starburst amacrine cells (SACs), propagating to retinal ganglion cells (RGCs) and visual centers, essential for visual circuit refinement. By modulating exocytosis in SACs, dynamic changes in the protein kinase A (PKA) activity can regulate the spatiotemporal patterns of cholinergic waves. Previously, cysteine string protein-α (CSPα) is found to interact with the core exocytotic machinery by PKA-mediated phosphorylation at serine 10 (S10). However, whether PKA-mediated CSPα phosphorylation may regulate cholinergic waves via SACs remains unknown. Here, we examined how CSPα phosphorylation in SACs regulates cholinergic waves. First, we identified that CSPα1 is the major isoform in developing rat SACs and the inner plexiform layer during the first postnatal week. Using SAC-specific expression, we found that the CSPα1-PKA-phosphodeficient mutant (CSP-S10A) decreased wave frequency, but did not alter the wave spatial correlation compared to control, wild-type CSPα1 (CSP-WT), or two PKA-phosphomimetic mutants (CSP-S10D and CSP-S10E). These suggest that CSPα-S10 phosphodeficiency in SACs dampens the frequency of cholinergic waves. Moreover, the level of phospho-PKA substrates was significantly reduced in SACs overexpressing CSP-S10A compared to control or CSP-WT, suggesting that the dampened wave frequency is correlated with the decreased PKA activity. Further, compared to control or CSP-WT, CSP-S10A in SACs reduced the periodicity of wave-associated postsynaptic currents (PSCs) in neighboring RGCs, suggesting that these RGCs received the weakened synaptic inputs from SACs overexpressing CSP-S10A. Finally, CSP-S10A in SACs decreased the PSC amplitude and the slope to peak PSC compared to control or CSP-WT, suggesting that CSPα-S10 phosphodeficiency may dampen the speed of the SAC-RGC transmission. Thus, via PKA-mediated phosphorylation, CSPα in SACs may facilitate the SAC-RGC transmission, contributing to the robust frequency of cholinergic waves.
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spelling pubmed-91079632022-05-26 Phosphorylation of cysteine string protein-α up-regulates the frequency of cholinergic waves via starburst amacrine cells Chen, Ching-Feng Wo, Rita R. Huang, Chien-Ting Cheng, Tzu-Lin Lu, Juu-Chin Wang, Chih-Tien Vis Neurosci Research Article During the first postnatal week in rodents, cholinergic retinal waves initiate in starburst amacrine cells (SACs), propagating to retinal ganglion cells (RGCs) and visual centers, essential for visual circuit refinement. By modulating exocytosis in SACs, dynamic changes in the protein kinase A (PKA) activity can regulate the spatiotemporal patterns of cholinergic waves. Previously, cysteine string protein-α (CSPα) is found to interact with the core exocytotic machinery by PKA-mediated phosphorylation at serine 10 (S10). However, whether PKA-mediated CSPα phosphorylation may regulate cholinergic waves via SACs remains unknown. Here, we examined how CSPα phosphorylation in SACs regulates cholinergic waves. First, we identified that CSPα1 is the major isoform in developing rat SACs and the inner plexiform layer during the first postnatal week. Using SAC-specific expression, we found that the CSPα1-PKA-phosphodeficient mutant (CSP-S10A) decreased wave frequency, but did not alter the wave spatial correlation compared to control, wild-type CSPα1 (CSP-WT), or two PKA-phosphomimetic mutants (CSP-S10D and CSP-S10E). These suggest that CSPα-S10 phosphodeficiency in SACs dampens the frequency of cholinergic waves. Moreover, the level of phospho-PKA substrates was significantly reduced in SACs overexpressing CSP-S10A compared to control or CSP-WT, suggesting that the dampened wave frequency is correlated with the decreased PKA activity. Further, compared to control or CSP-WT, CSP-S10A in SACs reduced the periodicity of wave-associated postsynaptic currents (PSCs) in neighboring RGCs, suggesting that these RGCs received the weakened synaptic inputs from SACs overexpressing CSP-S10A. Finally, CSP-S10A in SACs decreased the PSC amplitude and the slope to peak PSC compared to control or CSP-WT, suggesting that CSPα-S10 phosphodeficiency may dampen the speed of the SAC-RGC transmission. Thus, via PKA-mediated phosphorylation, CSPα in SACs may facilitate the SAC-RGC transmission, contributing to the robust frequency of cholinergic waves. Cambridge University Press 2022-05-11 /pmc/articles/PMC9107963/ /pubmed/35543445 http://dx.doi.org/10.1017/S0952523822000013 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
spellingShingle Research Article
Chen, Ching-Feng
Wo, Rita R.
Huang, Chien-Ting
Cheng, Tzu-Lin
Lu, Juu-Chin
Wang, Chih-Tien
Phosphorylation of cysteine string protein-α up-regulates the frequency of cholinergic waves via starburst amacrine cells
title Phosphorylation of cysteine string protein-α up-regulates the frequency of cholinergic waves via starburst amacrine cells
title_full Phosphorylation of cysteine string protein-α up-regulates the frequency of cholinergic waves via starburst amacrine cells
title_fullStr Phosphorylation of cysteine string protein-α up-regulates the frequency of cholinergic waves via starburst amacrine cells
title_full_unstemmed Phosphorylation of cysteine string protein-α up-regulates the frequency of cholinergic waves via starburst amacrine cells
title_short Phosphorylation of cysteine string protein-α up-regulates the frequency of cholinergic waves via starburst amacrine cells
title_sort phosphorylation of cysteine string protein-α up-regulates the frequency of cholinergic waves via starburst amacrine cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9107963/
https://www.ncbi.nlm.nih.gov/pubmed/35543445
http://dx.doi.org/10.1017/S0952523822000013
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