| Literature DB >> 33524541 |
Feng Chen1, Huiyi Chen1, Yanting Chen1, Wenyan Wei2, Yuanhong Sun3, Lu Zhang4, Lili Cui5, Yan Wang6.
Abstract
The communication between neurons constitutes the basis of all neural activities, and synaptic vesicle exocytosis is the fundamental biological event that mediates most communication between neurons in the central nervous system. The SNARE complex is the core component of the protein machinery that facilitates the fusion of synaptic vesicles with presynaptic terminals and thereby the release of neurotransmitters. In synapses, each release event is dependent on the assembly of the SNARE complex. In recent years, basic research on the SNARE complex has provided a clearer understanding of the mechanism underlying the formation of the SNARE complex and its role in vesicle formation. Emerging evidence indicates that abnormal expression or dysfunction of the SNARE complex in synapse physiology might contribute to abnormal neurotransmission and ultimately to synaptic dysfunction. Clinical research using postmortem tissues suggests that SNARE complex dysfunction is correlated with various neurological diseases, and some basic research has also confirmed the important role of the SNARE complex in the pathology of these diseases. Genetic and pharmacogenetic studies suggest that the SNARE complex and individual proteins might represent important molecular targets in neurological disease. In this review, we summarize the recent progress toward understanding the SNARE complex in regulating membrane fusion events and provide an update of the recent discoveries from clinical and basic research on the SNARE complex in neurodegenerative, neuropsychiatric, and neurodevelopmental diseases.Entities:
Keywords: Neurodegenerative diseases; Neurodevelopmental diseases; Neuropsychiatric diseases; SNARE
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Year: 2021 PMID: 33524541 DOI: 10.1016/j.phrs.2021.105469
Source DB: PubMed Journal: Pharmacol Res ISSN: 1043-6618 Impact factor: 7.658