Molecular identification of wide-field amacrine cells in mouse retina that encode stimulus orientation.
Silvia J ParkWanyu LeiJohn PisanoAndrea OrpiaJacqueline MinehartJoseph PottackalChristin Hanke-GogokhiaThomas E ZapadkaCheryl Clarkson-ParedesAnastas PopratiloffSarah E RossJoshua H SingerJonathan B DembPublished in: bioRxiv : the preprint server for biology (2023)
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.
Keyphrases
- induced apoptosis
- cell cycle arrest
- transcription factor
- optic nerve
- physical activity
- stem cells
- oxidative stress
- healthcare
- cell death
- signaling pathway
- mesenchymal stem cells
- machine learning
- gene expression
- chronic pain
- mass spectrometry
- pain management
- bone marrow
- genome wide
- single molecule
- toll like receptor
- photodynamic therapy
- protein kinase
- fluorescence imaging