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  4. Synaptotagmin I Regulates Patterned Spontaneous Activity in the Developing Rat Retina via Calcium Binding to the C2AB Domains
 
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Synaptotagmin I Regulates Patterned Spontaneous Activity in the Developing Rat Retina via Calcium Binding to the C2AB Domains

Journal
PLoS ONE
Journal Volume
7
Journal Issue
10
Date Issued
2012-10-16
Author(s)
Chiang, Chung Wei
Chen, Yu Chieh
Lu, Juu Chin
Hsiao, Yu Tien
Chang, Che Wei
Huang, Pin Chien
Chang, Yu Tzu
Chang, Payne Y.
CHIH-TIEN WANG  
DOI
10.1371/journal.pone.0047465
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/412522
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84867617097&doi=10.1371%2fjournal.pone.0047465&partnerID=40&md5=b363f03024d1198f48be0d86bfa8aafe
URL
https://api.elsevier.com/content/abstract/scopus_id/84867617097
Abstract
Background: In neonatal binocular animals, the developing retina displays patterned spontaneous activity termed retinal waves, which are initiated by a single class of interneurons (starburst amacrine cells, SACs) that release neurotransmitters. Although SACs are shown to regulate wave dynamics, little is known regarding how altering the proteins involved in neurotransmitter release may affect wave dynamics. Synaptotagmin (Syt) family harbors two Ca2+-binding domains (C2A and C2B) which serve as Ca2+ sensors in neurotransmitter release. However, it remains unclear whether SACs express any specific Syt isoform mediating retinal waves. Moreover, it is unknown how Ca2+ binding to C2A and C2B of Syt affects wave dynamics. Here, we investigated the expression of Syt I in the neonatal rat retina and examined the roles of C2A and C2B in regulating wave dynamics. Methodology/Principal Findings: Immunostaining and confocal microscopy showed that Syt I was expressed in neonatal rat SACs and cholinergic synapses, consistent with its potential role as a Ca2+ sensor mediating retinal waves. By combining a horizontal electroporation strategy with the SAC-specific promoter, we specifically expressed Syt I mutants with weakened Ca2+-binding ability in C2A or C2B in SACs. Subsequent live Ca2+ imaging was used to monitor the effects of these molecular perturbations on wave-associated spontaneous Ca2+ transients. We found that targeted expression of Syt I C2A or C2B mutants in SACs significantly reduced the frequency, duration, and amplitude of wave-associated Ca2+ transients, suggesting that both C2 domains regulate wave temporal properties. In contrast, these C2 mutants had relatively minor effects on pairwise correlations over distance for wave-associated Ca2+ transients. Conclusions/Significance: Through Ca2+ binding to C2A or C2B, the Ca2+ sensor Syt I in SACs may regulate patterned spontaneous activity to shape network activity during development. Hence, modulating the releasing machinery in presynaptic neurons (SACs) alters wave dynamics. © 2012 Chiang et al.
Other Subjects
calcium ion; mutant protein; synaptotagmin I; animal cell; animal tissue; article; calcium binding; cholinergic synapse; confocal microscopy; controlled study; dynamics; electroporation; evoked somatosensory response; gene transfer; immunohistochemistry; kinetics; newborn; nonhuman; promoter region; protein domain; protein expression; rat; regulatory mechanism; retina development; Animals; Calcium; Cholinergic Neurons; Gene Expression Regulation; Protein Binding; Protein Interaction Domains and Motifs; Rats; Receptors, AMPA; Retina; Synapses; Synaptic Transmission; Synaptotagmin I
Publisher
PUBLIC LIBRARY SCIENCE
Type
journal article
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journal.pone.0047465.PDF

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(MD5):6eb9d13d9a89e622c86ac183db74b99e

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