Molecular identification of wide-field amacrine cells in mouse retina that encode stimulus orientation.

Silvia J Park, Wanyu Lei, John Pisano, Andrea Orpia, Jacqueline Minehart,Joseph Pottackal,Christin Hanke-Gogokhia, Thomas E Zapadka,Cheryl Clarkson-Paredes,Anastas Popratiloff,Sarah E Ross,Joshua H Singer,Jonathan B Demb

bioRxiv : the preprint server for biology(2023)

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摘要
Visual information processing is sculpted by a diverse group of inhibitory interneurons in the retina called amacrine cells. Yet, for most of the >60 amacrine cell types, molecular identities and specialized functional attributes remain elusive. Here, we developed an intersectional genetic strategy to target a group of wide-field amacrine cells (WACs) in mouse retina that co-express the transcription factor Bhlhe22 and the Kappa Opioid Receptor (KOR; B/K WACs). B/K WACs feature straight, unbranched dendrites spanning over 0.5 mm (∼15° visual angle) and produce non-spiking responses to either light increments or decrements. Two-photon dendritic population imaging reveals Ca 2+ signals tuned to the physical orientations of B/K WAC dendrites, signifying a robust structure-function alignment. B/K WACs establish divergent connections with multiple retinal neurons, including unexpected connections with non-orientation-tuned ganglion cells and bipolar cells. Our work sets the stage for future comprehensive investigations of the most enigmatic group of retinal neurons: WACs.
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