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Hewitt, M. N.

Publications and source records attributed to Hewitt, M. N..

2 recordsLinked to original sources

Data-Driven 3D Shape Analysis Reveals Cell Shape-Fate Relationships in Zebrafish Lateral Line Neuromast

Cell shape is a powerful readout of cell state, fate, and function. With the advent of sophisticated microscopes, image segmentation algorithms, and numerical shape representations, it is becoming more feasible to study cell shape in developing tissues. However, few studies have analyzed cell shape in three dimensions in living, intact organisms. Here, we took advantage of the favorable imaging qualities of zebrafish lateral line neuromasts to generate a dataset of high resolution images with labeled cells and nuclei. Using a custom Python-based workflow, we performed semi-automated, 3D cell and nucleus segmentation. We then used spherical harmonics and principal components analysis to distill neuromast cell and nuclear shape variation into several interpretable, biologically meaningful parameters. We found that neuromast cell and nuclear shapes vary with cell location and identity. The distinction between hair cells and support cells was discrete and accounted for much of the variation in neuromast cell and nucleus shape, which allowed us to train classifiers to predict hair cell identity from cell and nucleus shape features. Using markers for support cell subpopulations, we found that support cell subtypes also had different shapes from each other; however, shape features did not distinguish as sharply between support cell subtypes, suggesting that support cells vary continuously in shape. To investigate the effects of genetic perturbation that results in loss of a cell type on neuromast cell shape, we examined atoh1a mutants that lack hair cells. We found that neuromasts from atoh1a mutants lacked the cell shape phenotype associated with hair cells, but did not exhibit a mutant-specific cell shape. Our results demonstrate the utility of using 3D cell shape features to characterize, compare, and classify cells in a living, developing organism.

developmental biology↗

Dermal appendage-dependent patterning of zebrafish atoh1a+ Merkel cells

Touch system function requires precise interactions between specialized skin cells and somatosensory axons, as exemplified by the vertebrate mechanosensory Merkel cell-neurite complex. Development and patterning of Merkel cells and associated neurites during skin organogenesis remains poorly understood, partly due to the in utero development of mammalian embryos. Here, we discover Merkel cells in the zebrafish epidermis and identify Atonal homolog 1a (Atoh1a) as a marker of zebrafish Merkel cells. We show that zebrafish Merkel cells derive from basal keratinocytes, express neurosecretory and mechanosensory machinery, extend actin-rich microvilli, and complex with somatosensory axons, all hallmarks of mammalian Merkel cells. Merkel cells populate all major adult skin compartments, with region-specific densities and distribution patterns. In vivo photoconversion reveals that Merkel cells undergo steady loss and replenishment during skin homeostasis. Merkel cells develop concomitant with dermal appendages along the trunk, and preventing dermal appendage formation reduces Merkel cell density by affecting both cell differentiation and maintenance. By contrast, altering dermal appendage morphology changes the distribution, but not density, of Merkel cells. Overall, our studies provide insights into touch system maturation during skin organogenesis and establish zebrafish as an experimentally accessible in vivo model for the study of Merkel cell biology.

developmental biology↗