Biology subjects

Kappel, J. M.

Publications and source records attributed to Kappel, J. M..

3 recordsLinked to original sources

bioRxiv2026

Fine ultrastructural organization of glomerular neuropil in the developing zebrafish olfactory bulb

Across animal phyla, odor information is represented in the first olfactory processing center by combinatorial activation of discrete glomeruli. To examine how this organization of olfactory processing channels emerges during development we combined 2-photon calcium imaging, volume electron microscopy, and large-scale automated neuron reconstruction in zebrafish larvae. We focused on a developmental stage (130 hours post fertilization) when the olfactory bulb (OB) is structured into ~16 large neuropil regions referred to as protoglomeruli but most glomeruli are not yet differentiated. Our ultrastructural reconstructions revealed that protoglomeruli are organized into smaller units referred to as microglomeruli, each of which is defined by a distinct set of mitral cells with overlapping, spatially confined dendritic arbors. Neighboring microglomeruli were innervated by distinct subsets of sensory axons and activity was more highly correlated among mitral cells associated with the same microglomerulus than across microglomeruli of the same or different protoglomeruli. These results reveal a precise subcellular organization of the neuropil in the developing OB into distinct processing channels, indicating that the layout of the adult glomerular array is established already early in development.

neuroscience↗

bioRxiv2024

Positional information drives distinct traits in transcriptomically identified neuronal types

Neuronal phenotypic traits such as morphology, connectivity, and function are dictated, to a large extent, by a specific combination of differentially expressed genes. Clusters of neurons in transcriptomic space correspond to distinct cell types and in some cases (e. g., C. elegans neurons1 and retinal ganglion cells2-4) have been shown to share morphology and function. The zebrafish optic tectum is composed of a spatial array of neurons that transforms visual inputs into motor outputs. While the visuotopic map is continuous, subregions of the tectum are functionally specialized5,6. To uncover the cell-type architecture of the tectum, we transcriptionally profiled its neurons, revealing more than 60 cell types that are organized in distinct anatomical layers. We then measured the visual responses of thousands of tectal neurons by two-photon calcium imaging and matched them with their transcriptional profile. Furthermore, we characterized the morphologies of transcriptionally identified neurons using specific transgenic lines. Surprisingly, we found that neurons that are transcriptionally similar can diverge functionally and morphologically. Incorporating the spatial coordinates of neurons within the tectal volume revealed functionally and morphologically defined anatomical subclusters within individual transcriptomic clusters. Our findings demonstrate that extrinsic, position-dependent factors expand the phenotypic repertoire of genetically similar neurons.

neuroscience↗

bioRxiv2021

Visual recognition of social signals by a tecto-thalamic neural circuit

Social affiliation emerges from individual-level behavioral rules that are driven by conspecific signals1-5. Long-distance attraction and short-distance repulsion, for example, are rules that jointly set a preferred inter-animal distance in swarms6-8. However, little is known about their perceptual mechanisms and executive neuronal circuits3. Here we trace the neuronal response to self-like biological motion9,10 (BM), a visual trigger for affiliation in developing zebrafish2,11. Unbiased activity mapping and targeted volumetric two-photon calcium imaging revealed 19 activity hotspots distributed throughout the brain and clustered BM-tuned neurons in a multimodal, socially activated nucleus of the dorsal thalamus (DT). Individual DT neurons encode fish-like local acceleration but are insensitive to global or continuous motion. Electron microscopic reconstruction of DT neurons revealed synaptic input from the optic tectum (TeO/superior colliculus) and projections into nodes of the conserved social behavior network12,13. Chemogenetic ablation of the TeO selectively disrupted DT responses to BM and social attraction without affecting short-distance repulsion. Together, we discovered a tecto-thalamic pathway that drives a core network for social affiliation. Our findings provide an example of visual social processing, and dissociate neuronal control of attraction from repulsion during affiliation, thus revealing neural underpinnings of collective behavior.

neuroscience↗