In our lab, we study the structural and functional properties of neocortical and striatal microcircuits, as well the interactions between these two brain areas (cortico-striatal pathway).
We use electrophysiological, anatomical, and imaging techniques in slices and in vivo, as well as computational methods in order to reveal the intricate organization of neurons and their synaptic connections. Our aim is to unravel the functional microcircuitry underlying sensorimotor processing in health and disease.
The Neocortex and Basal Ganglia are two brain regions involved in sensorimotor processing, and are tightly linked to each other via the cortico-striatal pathway. In order to understand the function of these brain regions, how they integrate sensory input and generate the appropriate motor output, it is essential to have a deep knowledge of their respective microcircuits.
Example of a simultaneous patch clamp recording from 4 striatal neurons. Stimulation of one striatal interneuron (Fast Spiking cell) evokes inhibitory responses in neighboring medium spiny neurons (MSNs) of both direct and indirect projections types (right). These responses are monosynaptic GABAergic IPSPs acting as a feedforward inhibitory pathway.
Stimulation of a layer 5 pyramidal cell (PC) evokes disynaptic inhibitory responses in neighboring PCs. These responses are mediated by GABAergic Martinotti cells.
Karolinska Institutet Campus Solna
Biomedicum, Quarter B4
Solnavägen 9, SE-171 65 Stockholm
Our lab uses electrophysiological, morphological, optogenetic, and computational methods to study neural microcircuits in the neocortex and basal-ganglia. In particular we are interested in the dynamic properties of neuronal microcircuits underlying sensory and motor processing.
We study the dynamic interactions between different types of excitatory and inhibitory neurons in order to unravel the way neural networks are structured and dynamically orchestrated.
Postdoc candidates should have a strong neuroscience background with documented experience in patch-clamp recording and/or in vivo electrophysiology. Knowledge of neuroanatomy, imaging, and computer programming are highly advantageous.
The project will involve in vivo patch-clamp recordings and calcium imaging in cortex and striatum. Funding is guaranteed for the first 2 years and may be extended according to progress and available funding.