葛根素
抑制性突触后电位
神经油
突触
生物
兴奋性突触后电位
神经肽
加巴能
小胶质细胞
神经科学
星形胶质细胞
细胞生物学
中枢神经系统
生物化学
氨基酸
甘氨酸
炎症
免疫学
甘氨酸受体
作者
Tetsuya Takano,John T. Wallace,Katherine T. Baldwin,Alicia Purkey,Akiyoshi Uezu,Jamie L. Courtland,Erik J. Soderblom,Tomomi Shimogori,Patricia F. Maness,Çağla Eroğlu,Scott H. Soderling
出处
期刊:Nature
[Nature Portfolio]
日期:2020-11-11
卷期号:588 (7837): 296-302
被引量:167
标识
DOI:10.1038/s41586-020-2926-0
摘要
Perisynaptic astrocytic processes are an integral part of central nervous system synapses1,2; however, the molecular mechanisms that govern astrocyte-synapse adhesions and how astrocyte contacts control synapse formation and function are largely unknown. Here we use an in vivo chemico-genetic approach that applies a cell-surface fragment complementation strategy, Split-TurboID, and identify a proteome that is enriched at astrocyte-neuron junctions in vivo, which includes neuronal cell adhesion molecule (NRCAM). We find that NRCAM is expressed in cortical astrocytes, localizes to perisynaptic contacts and is required to restrict neuropil infiltration by astrocytic processes. Furthermore, we show that astrocytic NRCAM interacts transcellularly with neuronal NRCAM coupled to gephyrin at inhibitory postsynapses. Depletion of astrocytic NRCAM reduces numbers of inhibitory synapses without altering glutamatergic synaptic density. Moreover, loss of astrocytic NRCAM markedly decreases inhibitory synaptic function, with minor effects on excitation. Thus, our results present a proteomic framework for how astrocytes interface with neurons and reveal how astrocytes control GABAergic synapse formation and function.
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