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Mendoza, A. J.

Publications and source records attributed to Mendoza, A. J..

2 recordsLinked to original sources

Electrical coupling within thalamocortical networks cumulatively reduces cortical correlation to sensory inputs

Thalamocortical (TC) cells relay sensory information to the cortex, as well as driving their own feedback inhibition through collateral excitation of the thalamic reticular nucleus (TRN). The GABAergic cells of the TRN are extensively coupled through electrical synapses. While electrical synapses are most often noted for their roles in synchronizing rhythmic forms of neuronal activity, they are also positioned to modulate responses to transient information flow across and throughout the brain, although this effect is seldom explored. Here we sought to understand how electrical synapses embedded within a network of TRN neurons regulate the processing of ongoing sensory inputs during relay from thalamus to cortex. We used Hodgkin-Huxley point models to construct a network of a 9 TC and 9 TRN cells, with one cortical output neuron summing the TC activity. Each pair of TC and TRN cells was reciprocally coupled by chemical synapses. TRN cells were each electrically coupled to two neighboring cells, forming a ring topology. TC cells received synaptic inputs in sequence, with intervals between inputs varying from 10 to 50 ms across simulations. This architecture and sequence of inputs allowed us to assess the functional radius of an electrical synapse by comparing the cumulative effects of each additional TRN electrical synapse on the responses of the TRN and TC cells and the cortical output. Effects of electrical synapses on TRN cell activity were strongest for smaller intervals between inputs, and cumulative with additional synapses. In contrast, effects in TC neurons were strongest for larger intervals between inputs and also increased with coupling strength. Coupling within TRN modulated cortical integration of TC inputs by unexpectedly increasing response rates, duration and reducing spike correlation to the input sequence that was presented to the TC layer. Thus, embedded TRN electrical synapses exert powerful influence on thalamocortical relay, in a cumulative manner. These results highlight the multi-synaptic influences of electrically coupled cells and reinforce that they should be included in more complex and realistic networks of the brain.

neuroscience↗

Cell-specific inhibitory modulation of sound processing in the auditory thalamus.

Inhibition plays an important role in controlling the flow and processing of auditory information throughout the central auditory pathway, yet how inhibitory circuits shape auditory processing in the medial geniculate body (MGB), the key region in the auditory thalamus, is poorly understood. The MGB gates the flow of auditory information to the auditory cortex, and it is inhibited largely by the thalamic reticular nucleus (TRN). The TRN contains two major classes of inhibitory neurons: parvalbumin (PVTRN)-positive and somatostatin (SSTTRN)-positive neurons. PV and SST neurons have been shown to play differential roles in controlling sound responses in auditory cortex. In the somatosensory and visual subregions of the TRN, PVTRN and SSTTRN neurons exhibit anatomical and functional differences. However, it remains unknown whether and how PVTRN and SSTTRN neurons differ in their anatomical projections from the TRN to the auditory thalamus, and whether and how they differentially modulate activity in the MGB. We find that PVTRN and SSTTRN neurons exhibit differential projection patterns within the auditory thalamus: PVTRN neurons predominantly project to ventral MGB, whereas SSTTRN neurons project to the dorso-medial regions of MGB. Optogenetic inactivation of PVTRN neurons bidirectionally modulated sound-evoked activity in MGB, increasing firing in 29% of MGB neurons, while suppressing firing in 41%. In contrast, inactivating SSTTRN neurons largely suppressed tone-evoked activity in MGB neurons. Cell type-specific computational models identified candidate circuit mechanisms for generating the differential effects of TRN inactivation on MGB sound responses. These distinct inhibitory pathways within the auditory thalamus reveal cell type-specific organization of thalamic inhibition in auditory computation.

neuroscience↗