Nucleoporin Nup358 Downregulation Tunes the Neuronal Excitability in Mouse Cortical Neurons

被引:1
|
作者
Martinez-Rojas, Vladimir A. [1 ,4 ]
Pischedda, Francesca [2 ]
Romero-Maldonado, Isabel [3 ]
Khalaf, Bouchra [2 ,5 ]
Piccoli, Giovanni [2 ]
Macchi, Paolo [2 ]
Musio, Carlo [1 ]
机构
[1] Natl Res Council CNR, Inst Biophys IBF, Via Sommar 18, I-38123 Trento, Italy
[2] Univ Trento, Dept Cellular Computat & Integrat Biol CIBIO, Via Sommar 9, I-38123 Trento, Italy
[3] Univ Autonoma Mexico UNAM, Inst Cellular Physiol, Ciudad Univ, Mexico City 04510, Mexico
[4] CINVESTAV, Dept Physiol Biophys & Neurosci, Mexico City 07360, Mexico
[5] Sunnybrook Res Inst, Toronto, ON M4N 3M5, Canada
来源
LIFE-BASEL | 2023年 / 13卷 / 09期
关键词
nucleoporins; ion channels; membrane excitability; voltage-gated sodium channels; neuronal activity; neurodegenerative disease; patch-clamp; NUCLEAR-PORE COMPLEX; PROTEINS; RANBP2;
D O I
10.3390/life13091791
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Nucleoporins (NUPs) are proteins that comprise the nuclear pore complexes (NPCs). The NPC spans the nuclear envelope of a cell and provides a channel through which RNA and proteins move between the nucleus and the cytoplasm and vice versa. NUP and NPC disruptions have a great impact on the pathophysiology of neurodegenerative diseases (NDDs). Although the downregulation of Nup358 leads to a reduction in the scaffold protein ankyrin-G at the axon initial segment (AIS) of mature neurons, the function of Nup358 in the cytoplasm of neurons remains elusive. To investigate whether Nup358 plays any role in neuronal activity, we downregulated Nup358 in non-pathological mouse cortical neurons and measured their active and passive bioelectrical properties. We identified that Nup358 downregulation is able to produce significant modifications of cell-membrane excitability via voltage-gated sodium channel kinetics. Our findings suggest that Nup358 contributes to neuronal excitability through a functional stabilization of the electrical properties of the neuronal membrane. Hypotheses will be discussed regarding the alteration of this active regulation as putatively occurring in the pathophysiology of NDDs.
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页数:13
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