Job ID: 53322
PhD Student position: Electrophysiology (in vivo/ex vivo/in vitro) and behaviour: rescue of NaV1.2/SCN2A sodium channel in neurodevelopmental disorders
Position: Ph.D. Student
Deadline: 31 July 2021
Employment Start Date: 1 October 2021
Contract Length: 3 years
City: Valbonne - Sophia Antipolis
Institution: CNRS and University Cote d'Azur
Department: Institute of Molecular and Cellular Pharmacology (IPMC)
Voltage-gated Na+ channels (NaV) are essential for generation and propagation of action potentials (APs), and mutations of the NaV1.2 isoform (SCN2A gene) cause neurodevelopmental disorders with a remarkably large clinical spectrum. In particular, numerous NaV1.2 mutations cause severe late infantile-childhood neurodevelopmental disorders (LICND) with onset between 3 months and few years of age: a) developmental and epileptic encephalopathies (DEE) with various degrees of autism spectrum disorder (ASD) and intellectual disability (ID) b) severe ASD without epilepsy, c) severe ID without epilepsy & d) schizophrenia without epilepsy. Notably, recent large-scale human genetic studies have indicated that NaV1.2 mutations are among those that show the strongest association with ASD. It has been proposed that LICND mutations induce reduction of NaV1.2 function, but mechanisms linking reduced NaV1.2 function to clinical phenotypes are not completely understood yet. In addition, we have identified a novel pathological mechanism for mutations causing LICND with severe ASD, leading to a larger loss of NaV1.2 function. Importantly, there are no effective treatments for LICND and there are no NaV1.2 enhancers available for increasing its function. We aim to: 1) develop and test drugs and strategies for counteracting reduced NaV1.2 function (targeting also the novel mechanism that we identified), which could be used to treat severe LICND; 2) study pathological mechanisms and effects of treatments in vitro, ex vivo and in vivo.
– Methods. Electrophysiology in transfected cells and brain slices (patch-clamp) and in vivo (video-EEG, LFP), behavioral studies, pharmacological experiments and AAV viral delivery; use a new conditional gene targeted mouse model that we have generated (which carries a NaV1.2 human mutation causing the new pathological mechanism that we have identified); use of cre-lox mouse models. A novel sodium imaging techniques to optically record sodium currents will be used in collaboration with Marco Canepari (University of Grenoble).
Our group has long lasting expertise in the study of the pathophysiology of ion channels and neuronal excitability, and all the tools and techniques are available. The group is part of the Institute of Molecular and Cellular Pharmacology (IPMC; www.ipmc.cnrs.fr), which is affiliated to the Université Côte d’Azur (UCA; http://univ-cotedazur.fr) and the French National Center for Scientific Research (CNRS; http://www.cnrs.fr/), and has state of the art shared research facilities; it is located in the technological park of Sophia Antipolis (https://www.sophia-antipolis.fr/en/), in the French Riviera, near Nice.
A pre-selection will be made according to CV, letter of recommendation and results obtained in the Master program.Salary according to CNRS standards: around 1450 €/month net (health insurance is paid).
Contact: Massimo Mantegazza, IPMC, CNRS and Université Côte d’Azur, 660 Route des Lucioles, 06560 Valbonne-Sophia Antipolis, France email@example.com Tel.+33 493953425
– Mantegazza M., Cestèle S and Catterall W.A. (2021) Sodium Channelopathies of Skeletal Muscle and Brain. Physiological Reviews. https://doi.org/10.1152/physrev.00025.2020
– Chever O. et al. (2020) GABAergic neurons and NaV1.1 channel hyperactivity: a novel neocortex-specific mechanism of Cortical Spreading Depression. bioRxiv 2020.03.14.991158; Preprint. https://doi.org/10.1101/2020.03.14.991158
– Lena I. and Mantegazza M. (2019) Nav1.2 haploinsufficiency in Scn2a knock-out mice causes an autistic-like phenotype attenuated with age. Scientific Reports 9(1):12886. https://doi.org/10.1038/s41598-019-49392-7
– Salgueiro-Pereira et al. (2019) A two-hit story: seizures and genetic mutation interaction sets phenotype severity in SCN1A epilepsies. Neurobiology of Disease 125:31-44. https://www.ncbi.nlm.nih.gov/pubmed/30659983
– Terragni B. et al. (2018) Post-translational dysfunctions in channelopathies of the nervous system. Neuropharmacology 132:31-42. https://www.ncbi.nlm.nih.gov/pubmed/28571716
– Mantegazza M. et al. (2010) Voltage-gated sodium channels as therapeutic targets in epilepsy and other neurological disorders.
Lancet Neurology. 9(4):413-424. Review. https://www.ncbi.nlm.nih.gov/pubmed/20298965