MET receptor tyrosine kinase promotes the generation of functional synapses in adult cortical circuits

被引:0
|
作者
Cui, Yuehua [1 ]
Ma, Xiaokuang [1 ]
Wei, Jing [1 ]
Chen, Chang [1 ]
Shakir, Neha [1 ]
Guirram, Hitesch [1 ]
Dai, Zhiyu [2 ]
Anderson, Trent [1 ]
Ferguson, Deveroux [1 ]
Qiu, Shenfeng [1 ]
机构
[1] Univ Arizona, Coll Med Phoenix, Basic Med Sci, Phoenix, AZ 85004 USA
[2] Univ Arizona, Coll Med Phoenix, Dept Med, Phoenix, AZ USA
关键词
aging; circuit connectivity; cortical circuits; molecular mechanisms; neural regeneration; neurodegeneration; synapses; HEPATOCYTE GROWTH-FACTOR; MULTIFUNCTIONAL DOCKING SITE; CRITICAL PERIOD PLASTICITY; ALZHEIMERS-DISEASE; LONG-TERM; SYNAPTIC PLASTICITY; C-MET; NATURAL OLIGOMERS; DENDRITIC GROWTH; MOUSE NEOCORTEX;
D O I
10.4103/NRR.NRR-D-23-01471
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Loss of synapse and functional connectivity in brain circuits is associated with aging and neurodegeneration, however, few molecular mechanisms are known to intrinsically promote synaptogenesis or enhance synapse function. We have previously shown that MET receptor tyrosine kinase in the developing cortical circuits promotes dendritic growth and dendritic spine morphogenesis. To investigate whether enhancing MET in adult cortex has synapse regenerating potential, we created a knockin mouse line, in which the human MET gene expression and signaling can be turned on in adult (10-12 months) cortical neurons through doxycycline-containing chow. We found that similar to the developing brain, turning on MET signaling in the adult cortex activates small GTPases and increases spine density in prefrontal projection neurons. These findings are further corroborated by increased synaptic activity and transient generation of immature silent synapses. Prolonged MET signaling resulted in an increased alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid/N-methyl-D-aspartate (AMPA/NMDA) receptor current ratio, indicative of enhanced synaptic function and connectivity. Our data reveal that enhancing MET signaling could be an interventional approach to promote synaptogenesis and preserve functional connectivity in the adult brain. These findings may have implications for regenerative therapy in aging and neurodegeneration conditions.
引用
收藏
页码:1431 / 1444
页数:14
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