Browsing by Author "Yao, Xiaoyang"
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Item Open Access Gap Junctions Contribute to Differential Light Adaptation across Direction-Selective Retinal Ganglion Cells.(Neuron, 2018-10) Yao, Xiaoyang; Cafaro, Jon; McLaughlin, Amanda J; Postma, Friso R; Paul, David L; Awatramani, Gautam; Field, Greg DDirection-selective ganglion cells (DSGCs) deliver signals from the retina to multiple brain areas to indicate the presence and direction of motion. Delivering reliable signals in response to motion is critical across light levels. Here we determine how populations of DSGCs adapt to changes in light level, from moonlight to daylight. Using large-scale measurements of neural activity, we demonstrate that the population of DSGCs switches encoding strategies across light levels. Specifically, the direction tuning of superior (upward)-preferring ON-OFF DSGCs becomes broader at low light levels, whereas other DSGCs exhibit stable tuning. Using a conditional knockout of gap junctions, we show that this differential adaptation among superior-preferring ON-OFF DSGCs is caused by connexin36-mediated electrical coupling and differences in effective GABAergic inhibition. Furthermore, this adaptation strategy is beneficial for balancing motion detection and direction estimation at the lower signal-to-noise ratio encountered at night. These results provide insights into how light adaptation impacts motion encoding in the retina.Item Open Access Motion Processing in Direction Selective Retinal Ganglion Cells through Dynamic Environments(2018) Yao, XiaoyangDirection selective ganglion cells (DSGCs) signal the presence and direction of motion from the retina to multiple brain areas. Reliably signaling motion is critical through dynamic environments, including contrasts and light levels. This dissertation examines how direction-selective responses are reliably generated across stimulus contrasts, and how populations of DSGCs adapt to changes in light level, spanning moonlight to daylight. In Chapter 2, I describe the development of a functional classification method to identify and classify DSGCs. In Chapter 3, I show how NMDA-dependent synapses improve direction coding in DSGCs at threshold contrasts. In Chapter 4, I describe changes in DSGC responses across light levels, and how these adaptive changes depend on cell types. Chapter 5 focuses on two mechanisms that contribute to this cell type-dependent adaptation: connexin36-mediated electrical coupling and differences in effective GABAergic inhibition. In Chapter 6, I show with a simulation of DSGC activity based on data that this adaptation strategy is beneficial for balancing motion detection and direction estimation at the lower signal-to-noise encountered at night.
Item Open Access "Silent" NMDA Synapses Enhance Motion Sensitivity in a Mature Retinal Circuit.(Neuron, 2017-12) Sethuramanujam, Santhosh; Yao, Xiaoyang; deRosenroll, Geoff; Briggman, Kevin L; Field, Greg D; Awatramani, Gautam BRetinal direction-selective ganglion cells (DSGCs) have the remarkable ability to encode motion over a wide range of contrasts, relying on well-coordinated excitation and inhibition (E/I). E/I is orchestrated by a diverse set of glutamatergic bipolar cells that drive DSGCs directly, as well as indirectly through feedforward GABAergic/cholinergic signals mediated by starburst amacrine cells. Determining how direction-selective responses are generated across varied stimulus conditions requires understanding how glutamate, acetylcholine, and GABA signals are precisely coordinated. Here, we use a combination of paired patch-clamp recordings, serial EM, and large-scale multi-electrode array recordings to show that a single high-sensitivity source of glutamate is processed differentially by starbursts via AMPA receptors and DSGCs via NMDA receptors. We further demonstrate how this novel synaptic arrangement enables DSGCs to encode direction robustly near threshold contrasts. Together, these results reveal a space-efficient synaptic circuit model for direction computations, in which "silent" NMDA receptors play critical roles.