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Inhibitory Synapse Formation in a Co-culture Model Incorporating GABAergic Medium Spiny Neurons and HEK293 Cells Stably Expressing GABAA Receptors
被引:14
作者:
Brown, Laura E.
[1
]
Fuchs, Celine
[1
]
Nicholson, Martin W.
[1
]
Stephenson, F. Anne
[1
]
Thomson, Alex M.
[1
]
Jovanovic, Jasmina N.
[1
]
机构:
[1] UCL, Sch Pharm, London WC1E 6BT, England
来源:
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS
|
2014年
/
93期
关键词:
Neuroscience;
Issue;
93;
Developmental neuroscience;
synaptogenesis;
synaptic inhibition;
co-culture;
stable cell lines;
GABAergic;
medium spiny neurons;
HEK 293 cell line;
SUBUNIT;
LOCALIZATION;
PHARMACOLOGY;
NEUROLIGINS;
MATURATION;
NEUREXINS;
SUBTYPES;
BRAIN;
D O I:
10.3791/52115
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Inhibitory neurons act in the central nervous system to regulate the dynamics and spatio-temporal co-ordination of neuronal networks. GABA (Upsilon-aminobutyric acid) is the predominant inhibitory neurotransmitter in the brain. It is released from the presynaptic terminals of inhibitory neurons within highly specialized intercellular junctions known as synapses, where it binds to GABA(A) receptors (GABA(A)Rs) present at the plasma membrane of the synapse-receiving, postsynaptic neurons. Activation of these GABA-gated ion channels leads to influx of chloride resulting in postsynaptic potential changes that decrease the probability that these neurons will generate action potentials. During development, diverse types of inhibitory neurons with distinct morphological, electrophysiological and neurochemical characteristics have the ability to recognize their target neurons and form synapses which incorporate specific GABA(A)Rs subtypes. This principle of selective innervation of neuronal targets raises the question as to how the appropriate synaptic partners identify each other. To elucidate the underlying molecular mechanisms, a novel in vitro co-culture model system was established, in which medium spiny GABAergic neurons, a highly homogenous population of neurons isolated from the embryonic striatum, were cultured with stably transfected HEK293 cell lines that express different GABA(A)R subtypes. Synapses form rapidly, efficiently and selectively in this system, and are easily accessible for quantification. Our results indicate that various GABA(A)R subtypes differ in their ability to promote synapse formation, suggesting that this reduced in vitro model system can be used to reproduce, at least in part, the in vivo conditions required for the recognition of the appropriate synaptic partners and formation of specific synapses. Here the protocols for culturing the medium spiny neurons and generating HEK293 cells lines expressing GABA(A)Rs are first described, followed by detailed instructions on how to combine these two cell types in co-culture and analyze the formation of synaptic contacts.
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