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1.
Journal of Zhejiang University. Medical sciences ; (6): 12-18, 2019.
Artículo en Chino | WPRIM | ID: wpr-775260

RESUMEN

OBJECTIVE@#To investigate the mechanism of congenital paramyotonia caused by human skeletal muscle voltage-gated sodium channel hNav1.4 mutant I1363T.@*METHODS@#The conservation of the mutant site were detecled by using amino acid sequence alignment; the C-terminal mCherry fusion hNav1.4 was constructed, and the expression and distribution of wild type and hNav1.4 mutant I1363T were determined by confocal microscopy; the steady-state activation, fast inactivation and window current of wild type and hNav1.4 mutant I1363T were examined by whole-cell patch clamp.@*RESULTS@#Alignment of the amino acid sequences revealed that Ile1363 is highly conserved in human sodium channels. There was no significant difference in expression level and distribution between wild type and I1363T. Although no significant differences were observed between I1363T mutant and wild type in the activation upon channel gating, the of voltage-dependence of fast inactivation of I1363T mutant[(-59.01±0.26) mV] shifted 9 mV towards depolarization as compared with wild type[(-68.03±0.34) mV], and the slope factor of voltage-dependence curve increased to (5.24±0.23) mV, compared with (4.55±0.21) mV of the wild type. Moreover, I1363T showed the larger window current than that of the wild type.@*CONCLUSIONS@#I1363T causes the defect in fast inactivation of hNav1.4, which may increase the excitability of muscle cells and be responsible for myotonia. The increased window current of I1363T may result in an increase of inward Na+ current, could subsequently inactivate the channels and lead to loss of excitability and paralysis.


Asunto(s)
Humanos , Perfilación de la Expresión Génica , Activación del Canal Iónico , Genética , Músculo Esquelético , Mutación , Genética , Análisis de Secuencia de Proteína
2.
Journal of Zhejiang University. Medical sciences ; (6): 34-38, 2019.
Artículo en Chino | WPRIM | ID: wpr-775257

RESUMEN

As a non-invasive approach, sonogenetics is applied to control neuronal activity. The mechanosensitive channel(MSC), which has low threshold of responding to ultrasound, may be the alternative solution. Sonogenetics is the technique that activates the MSC expressed in targeted neurons by low intensity ultrasound, thus achieve the neuromodulation. In this review, we introduce the mechanosensitive channel of large conductance, transient receptor potential, channels of the two-pore-domain potassium family, Piezo and the recent progress on their application in sonogenetics.


Asunto(s)
Fenómenos Biomecánicos , Canales Iónicos , Metabolismo , Neuronas , Ondas Ultrasónicas
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