Une Mutation De KCNT1 Associée à L'épilepsie Améliore L'excitabilité Des Neurones Dérivés De iPSC Humains En Augmentant Les Courants De KNa Lâches

Une Mutation De KCNT1 Associée à L'épilepsie Améliore L'excitabilité Des Neurones Dérivés De iPSC Humains En Augmentant Les Courants De KNa Lâches

septembre 15, 2019 0 Par admin

Translating…

Featured ArticleResearch Articles, Neurobiology of Disease

Imran H. Quraishi, Shani Stern, Kile P. Mangan, Yalan Zhang, Syed R. Ali, Michael R. Mercier, Maria C. Marchetto, Michael J. McLachlan, Eugenia M. Jones, Fred H. Gage and Leonard K. Kaczmarek

Journal of Neuroscience 11 September 2019, 39 (37) 7438-7449; DOI: https://doi.org/10.1523/JNEUROSCI.1628-18.2019

Loading

Abstract

Mutations in the KCNT1 (Slack, KNa1.1) sodium-activated potassium channel produce severe epileptic encephalopathies. Expression in heterologous systems has shown that the disease-causing mutations give rise to channels that have increased current amplitude. It is not known, however, whether such gain of function occurs in human neurons, nor whether such increased KNa current is expected to suppress or increase the excitability of cortical neurons. Using genetically engineered human induced pluripotent stem cell (iPSC)-derived neurons, we have now found that sodium-dependent potassium currents are increased several-fold in neurons bearing a homozygous P924L mutation. In current-clamp recordings, the increased KNa current in neurons with the P924L mutation acts to shorten the duration of action potentials and to increase the amplitude of the afterhyperpolarization that follows each action potential. Strikingly, the number of action potentials that were evoked by depolarizing currents as well as maximal firing rates were increased in neurons expressing the mutant channel. In networks of spontaneously active neurons, the mean firing rate, the occurrence of rapid bursts of action potentials, and the intensity of firing during the burst were all increased in neurons with the P924L Slack mutation. The feasibility of an increased KNa current to increase firing rates independent of any compensatory changes was validated by numerical simulations. Our findings indicate that gain-of-function in Slack KNa channels causes hyperexcitability in both isolated neurons and in neural networks and occurs by a cell-autonomous mechanism that does not require network interactions.

SIGNIFICANCE STATEMENT KCNT1 mutations lead to severe epileptic encephalopathies for which there are no effective treatments. This study is the first demonstration that a KCNT1 mutation increases the Slack current in neurons. It also provides the first explanation for how this increased potassium current induces hyperexcitability, which could be the underlining factor causing seizures.

View Full Text

Log in through your institution

If your organization uses OpenAthens, you can log in using your OpenAthens username and password.

To check if your institution is supported, please see this list.

Contact your library for more details.

Pay Per Article – You may access this article (from the computer you are currently using) for 1 day for US$35.00

Regain Access – You can regain access to a recent Pay per Article purchase if your access period has not yet expired.


Huile de CBD peut aider avec l’épilepsie. Visite HuileCBD.be


 
/>Lire la suite