Contribution of neuronal subtypes to the neural representation of social interaction in control versus autistic mice
Position
Post-doc
Published Date
23 mars 2022
12 avr. 2022
Until filled
Application
poster
Application deadline
Keywords
Calcium imaging; awake behaving mice; social memory; quantitative analysis
The role
Behavioral studies have shown that mice can form social memories, i.e., to remember familiar conspecifics. Optogenetic studies have demonstrated that assemblies of neurons in hippocampal ventral CA1 (vCA1) constitute a primary site of social memory. However, vCA1 contains a diversity of neuronal cell types with diverse functions and cellular targets, and the identity(ies) of cell types involved in social interaction remains unresolved. This postdoc project aims at determining which vCA1 cell types encode social interaction and how this encoding is performed. We will combine intersectional genetics and optogenetics with a last-generation miniature microscope to record and manipulate the calcium dynamics — as a proxy for neuronal activity — of different vCA1 cell types in awake mice during a social interaction task. State-of-the-art computational methods will quantitatively correlate mouse behavior and neural activity to disentangle and model encoding of social interaction at both single cell and population levels.
The role
Behavioral studies have shown that mice can form social memories, i.e., to remember familiar conspecifics. Optogenetic studies have demonstrated that assemblies of neurons in hippocampal ventral CA1 (vCA1) constitute a primary site of social memory. However, vCA1 contains a diversity of neuronal cell types with diverse functions and cellular targets, and the identity(ies) of cell types involved in social interaction remains unresolved. This postdoc project aims at determining which vCA1 cell types encode social interaction and how this encoding is performed. We will combine intersectional genetics and optogenetics with a last-generation miniature microscope to record and manipulate the calcium dynamics — as a proxy for neuronal activity — of different vCA1 cell types in awake mice during a social interaction task. State-of-the-art computational methods will quantitatively correlate mouse behavior and neural activity to disentangle and model encoding of social interaction at both single cell and population levels.
Requirements
The candidate should be enthusiastic, creative and ambitious, have good communication skills and be eager to learn. A Ph.D. with experience in computer science is required. Affection for neuroscience is preferred. Note: exception can be made for candidates who have not studied computer science if the candidate can prove coding skills.
Application procedure
All applications must be done through the CENTURI portal at this address: https://centuri-livingsystems.org/application-form-pdp2022-04/
Questions can be addressed to Antoine de Chevigny or to Léo Guignard by email with the mention [Job-2022] in the title.
Antoine de Chevigny: antoine.de-chevigny@inserm.fr
Léo Guignard: leo.guignard@univ-amu.fr
Selection process and calendar
Call open for applications until April 13th
Interviews of shortlisted candidates by the evaluation committee: June 15 or 16.
The pre-selection process will be based on qualifications and expertise reflected on the candidates CV and motivation letter. It will be merit-based. All candidates will be informed whether they have been pre-selected or not.
Location
Léo Guignard and Antoine de Chevigny labs