Phase separation at the synapse

被引:177
作者
Chen, Xudong [1 ]
Wu, Xiandeng [1 ]
Wu, Haowei [1 ]
Zhang, Mingjie [1 ,2 ]
机构
[1] Hong Kong Univ Sci & Technol, Div Life Sci, State Key Lab Mol Neurosci, Hong Kong, Peoples R China
[2] Hong Kong Univ Sci & Technol, Ctr Syst Biol & Human Hlth, Hong Kong, Peoples R China
关键词
POSTSYNAPTIC DENSITY PROTEINS; DOG CEREBRAL-CORTEX; ACTIVE ZONE; NEUROTRANSMITTER RELEASE; EXCITATORY SYNAPSES; DENDRITIC SPINES; CA2+ CHANNELS; LIQUID-PHASE; DOMAINS; SYNGAP;
D O I
10.1038/s41593-019-0579-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Phase separation is emerging as a versatile means for cellular sub-compartment formation. Chen et al. review recent advances of dense synaptic assembly formation via phase separation and discuss implications of phase separation in synaptic physiology. Emerging evidence indicates that liquid-liquid phase separation, the formation of a condensed molecular assembly within another diluted aqueous solution, is a means for cells to organize highly condensed biological assemblies (also known as biological condensates or membraneless compartments) with very broad functions and regulatory properties in different subcellular regions. Molecular machineries dictating synaptic transmissions in both presynaptic boutons and postsynaptic densities of neuronal synapses may be such biological condensates. Here we review recent developments showing how phase separation can build dense synaptic molecular clusters, highlight unique features of such condensed clusters in the context of synaptic development and signaling, discuss how aberrant phase-separation-mediated synaptic assembly formation may contribute to dysfunctional signaling in psychiatric disorders, and present some challenges and opportunities of phase separation in synaptic biology.
引用
收藏
页码:301 / 310
页数:10
相关论文
共 111 条
[1]   How to Make an Active Zone: Unexpected Universal Functional Redundancy between RIMs and RIM-BPs [J].
Acuna, Claudio ;
Liu, Xinran ;
Sudhof, Thomas C. .
NEURON, 2016, 91 (04) :792-807
[2]   RIM-BPs Mediate Tight Coupling of Action Potentials to Ca2+-Triggered Neurotransmitter Release [J].
Acuna, Claudio ;
Liu, Xinran ;
Gonzalez, Aneysis ;
Suedhof, Thomas C. .
NEURON, 2015, 87 (06) :1234-1247
[3]   Synaptic Vesicle Pools and Dynamics [J].
Alabi, AbdulRasheed A. ;
Tsien, Richard W. .
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2012, 4 (08)
[4]   Rapid Dispersion of SynGAP from Synaptic Spines Triggers AMPA Receptor Insertion and Spine Enlargement during LTP [J].
Araki, Yoichi ;
Zeng, Menglong ;
Zhang, Mingjie ;
Huganir, Richard L. .
NEURON, 2015, 85 (01) :173-189
[5]   Review Progress in Ostwald ripening theories and their applications to nickel-base superalloys - Part I: Ostwald ripening theories [J].
Baldan, A .
JOURNAL OF MATERIALS SCIENCE, 2002, 37 (11) :2171-2202
[6]   Biomolecular condensates: organizers of cellular biochemistry [J].
Banani, Salman F. ;
Lee, Hyun O. ;
Hyman, Anthony A. ;
Rosen, Michael K. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2017, 18 (05) :285-298
[7]   PROTEINS OF POSTSYNAPTIC DENSITY [J].
BANKER, G ;
CHURCHILL, L ;
COTMAN, CW .
JOURNAL OF CELL BIOLOGY, 1974, 63 (02) :456-465
[8]   INTERACTIONS OF SYNAPSIN-I WITH SMALL SYNAPTIC VESICLES - DISTINCT SITES IN SYNAPSIN-I BIND TO VESICLE PHOSPHOLIPIDS AND VESICLE PROTEINS [J].
BENFENATI, F ;
BAHLER, M ;
JAHN, R ;
GREENGARD, P .
JOURNAL OF CELL BIOLOGY, 1989, 108 (05) :1863-1872
[9]   SYNAPTIC VESICLE-ASSOCIATED CA2+/CALMODULIN-DEPENDENT PROTEIN KINASE-II IS A BINDING-PROTEIN FOR SYNAPSIN-I [J].
BENFENATI, F ;
VALTORTA, F ;
RUBENSTEIN, JL ;
GORELICK, FS ;
GREENGARD, P ;
CZERNIK, AJ .
NATURE, 1992, 359 (6394) :417-420
[10]   Spine Dynamics: Are They All the Same? [J].
Berry, Kalen P. ;
Nedivi, Elly .
NEURON, 2017, 96 (01) :43-55