Journal
JOURNAL OF MOLECULAR CELL BIOLOGY
Volume 11, Issue 8, Pages 688-702Publisher
OXFORD UNIV PRESS
DOI: 10.1093/jmcb/mjz042
Keywords
ATP11B; synaptic plasticity; glutamate receptors; MAPK14 signaling pathway
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Funding
- National Natural Science Foundation of China [31500827, 81471162, 61873156, QD2015033]
- Science and Technology Commission of Shanghai [14JC1402400]
- Natural Science Foundation of Shanghai [17ZR1409900]
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Synaptic plasticity is known to regulate and support signal transduction between neurons, while synaptic dysfunction contributes to multiple neurological and other brain disorders; however, the specific mechanism underlying this process remains unclear. In the present study, abnormal neural and dendritic morphology was observed in the hippocampus following knockout of Atp11b both in vitro and in vivo. Moreover, ATP11B modified synaptic ultrastructure and promoted spine remodeling via the asymmetrical distribution of phosphatidylserine and enhancement of glutamate release, glutamate receptor expression, and intracellular Ca2+ concentration. Furthermore, experimental results also indicate that ATP11B regulated synaptic plasticity in hippocampal neurons through the MAPK14 signaling pathway. In conclusion, our data shed light on the possible mechanisms underlying the regulation of synaptic plasticity and lay the foundation for the exploration of proteins involved in signal transduction during this process.
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