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New light on cortical neuropeptides and synaptic network plasticity
被引:21
|作者:
Smith, Stephen J.
[1
]
Hawrylycz, Michael
[1
]
Rossier, Jean
[2
]
Sumbul, Uygar
[1
]
机构:
[1] Allen Inst Brain Sci, 615 Westlake Ave N, Seattle, WA 98109 USA
[2] Sorbonne Univ, Neurosci Paris Seine, Paris, France
关键词:
NEURONAL CELL-TYPES;
MOLECULAR-BASIS;
DIVERSITY;
TRANSMISSION;
ARCHITECTURE;
RECEPTORS;
EVOLUTION;
D O I:
10.1016/j.conb.2020.04.002
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Neuropeptides, members of a large and evolutionarily ancient family of proteinaceous cell-cell signaling molecules, are widely recognized as extremely potent regulators of brain function and behavior. At the cellular level, neuropeptides are known to act mainly via modulation of ion channel and synapse function, but functional impacts emerging at the level of complex cortical synaptic networks have resisted mechanistic analysis. New findings from single-cell RNA-seq transcriptomics now illuminate intricate patterns of cortical neuropeptide signaling gene expression and new tools now offer powerful molecular access to cortical neuropeptide signaling. Here we highlight some of these new findings and tools, focusing especially on prospects for experimental and theoretical exploration of peptidergic and synaptic networks interactions underlying cortical function and plasticity.
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页码:176 / 188
页数:13
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