All incoming auditory, visual and somatosensory information is relayed through the thalamus to the cerebral cortex, which, during wakefulness, is responsible for transforming these sensory inputs into a spatio-temporal pattern of neuronal activity that gives rise to an internal representation of the external world. These representations are a crucial component of our conscious experience. Understanding how incoming information from the thalamus gives rise to cortical activity is therefore essential for understanding both normal and pathological states of consciousness, such as schizophrenia or autism, when internal representations appear to go awry. Although they are only a minority of all cortical neurons, GABA-releasing inhibitory interneurons play a crucial role in these transformations. By providing both feedforward and feedback inhibition, inhibitory interneurons restrict electrical activity in the majority excitatory neurons to a precisely tuned response in time and in space. Therefore, understanding how sensory representations are generated requires a detailed knowledge of the identity and properties of the GABAergic neurons and synapses which mediate feedforward and feedback inhibition, and of their responses to incoming sensory information, but such knowledge is still lacking. The two largest and best studied inhibitory subtypes are """"""""fast spiking"""""""" interneurons and somatostatin-containing interneurons. Previous studies suggested that feedforward inhibition is mediated exclusively by fast-spiking cells. In contrast, we showed in the previous grant period that both subtypes of interneurons mediate feedforward inhibition, but do so under very different stimulation regimes: fast- spiking interneurons will fire in response to a transient stimulus, while somatostatin- containing interneurons will fire in response to a sustained input. During the current grant period, we will use electrophysiological and pharmacological methods to elucidate the biophysical basis for these striking differences in response properties, and we will use novel genetically modified strains of mice to test the roles of each interneuron subtype in shaping responses of cortical neurons to incoming sensory information from the thalamus.
All incoming sensory information is relayed through the thalamus to the cerebral cortex, which transforms these sensory inputs into a spatio-temporal pattern of neuronal activity that underlies our conscious experience. Understanding these thalamocortical transformations is therefore essential for understanding both normal and pathological states of consciousness, such as autism or schizophrenia, when internal representations appear to go awry. In this project we will study the crucial, but little-understood role played by specific subtypes of inhibitory neurons in shaping cortical responses to incoming information.
|Hu, Hang; Agmon, Ariel (2016) Differential Excitation of Distally versus Proximally Targeting Cortical Interneurons by Unitary Thalamocortical Bursts. J Neurosci 36:6906-16|
|Hu, Hang; Agmon, Ariel (2015) Properties of precise firing synchrony between synaptically coupled cortical interneurons depend on their mode of coupling. J Neurophysiol 114:624-37|
|Hu, Hang; Cavendish, John Z; Agmon, Ariel (2013) Not all that glitters is gold: off-target recombination in the somatostatin-IRES-Cre mouse line labels a subset of fast-spiking interneurons. Front Neural Circuits 7:195|
|Agmon, Ariel (2012) A novel, jitter-based method for detecting and measuring spike synchrony and quantifying temporal firing precision. Neural Syst Circuits 2:5|
|Ma, Yunyong; Hu, Hang; Agmon, Ariel (2012) Short-term plasticity of unitary inhibitory-to-inhibitory synapses depends on the presynaptic interneuron subtype. J Neurosci 32:983-8|
|Hu, Hang; Ma, Yunyong; Agmon, Ariel (2011) Submillisecond firing synchrony between different subtypes of cortical interneurons connected chemically but not electrically. J Neurosci 31:3351-61|
|Tan, Zhenjun; Hu, Hang; Huang, Z Josh et al. (2008) Robust but delayed thalamocortical activation of dendritic-targeting inhibitory interneurons. Proc Natl Acad Sci U S A 105:2187-92|