Firing-rate based network modeling of the dLGN circuit: Effects of cortical feedback on spatiotemporal response properties of relay cells
Metadatos
Mostrar el registro completo del ítemAutor
Mobarhan, Milad Hobbi; Halnes, Geir; Martínez-Cañada, Pablo; Hafting, Torkel; Fyhn, Marianne; Einevoll, Gaute T.Editorial
Plos One
Fecha
2018-05-17Referencia bibliográfica
Mobarhan MH, Halnes G, Martínez-Cañada P, Hafting T, Fyhn M, Einevoll GT (2018) Firing-rate based network modeling of the dLGN circuit: Effects of cortical feedback on spatiotemporal response properties of relay cells. PLoS Comput Biol 14(5): e1006156. https://doi.org/10.1371/journal.pcbi.1006156
Patrocinador
Research Council of Norway (Digital Life) and the Government of Spain, FPU program (FPU13/01487, EST15/00055)Resumen
Visually evoked signals in the retina pass through the dorsal geniculate nucleus (dLGN) on
the way to the visual cortex. This is however not a simple feedforward flow of information:
there is a significant feedback from cortical cells back to both relay cells and interneurons in
the dLGN. Despite four decades of experimental and theoretical studies, the functional role
of this feedback is still debated. Here we use a firing-rate model, the extended difference-of-Gaussians (eDOG) model, to explore cortical feedback effects on visual responses of dLGN
relay cells. For this model the responses are found by direct evaluation of two- or threedimensional
integrals allowing for fast and comprehensive studies of putative effects of different
candidate organizations of the cortical feedback. Our analysis identifies a special
mixed configuration of excitatory and inhibitory cortical feedback which seems to best
account for available experimental data. This configuration consists of (i) a slow (long-delay)
and spatially widespread inhibitory feedback, combined with (ii) a fast (short-delayed) and
spatially narrow excitatory feedback, where (iii) the excitatory/inhibitory ON-ON connections
are accompanied respectively by inhibitory/excitatory OFF-ON connections, i.e. following a
phase-reversed arrangement. The recent development of optogenetic and pharmacogenetic
methods has provided new tools for more precise manipulation and investigation of the
thalamocortical circuit, in particular for mice. Such data will expectedly allow the eDOG
model to be better constrained by data from specific animal model systems than has been
possible until now for cat. We have therefore made the Python tool pyLGN which allows for
easy adaptation of the eDOG model to new situations.