Laboratory of Molecular Neural Biology, School of Life Sciences, Shanghai University, Shanghai, China.
School of Computer Engineering and Science, Shanghai University, Shanghai, China.
J Mol Cell Biol. 2019 Aug 19;11(8):688-702. doi: 10.1093/jmcb/mjz042.
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.
突触可塑性已知可以调节和支持神经元之间的信号转导,而突触功能障碍导致多种神经和其他脑疾病;然而,该过程的具体机制尚不清楚。在本研究中,无论是在体外还是体内,Atp11b 敲除后均观察到海马体中的神经和树突形态异常。此外,ATP11B 通过不对称分布的磷脂酰丝氨酸和增强谷氨酸释放、谷氨酸受体表达和细胞内 Ca2+浓度来修饰突触超微结构并促进脊柱重塑。此外,实验结果还表明,ATP11B 通过 MAPK14 信号通路调节海马神经元的突触可塑性。总之,我们的数据揭示了调节突触可塑性的可能机制,并为探索该过程中参与信号转导的蛋白质奠定了基础。