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Horstmeyer, R. W.

Publications and source records attributed to Horstmeyer, R. W..

2 recordsLinked to original sources

Hydrostatic pressure shapes and canalizes semicircular canal morphology to ensure vestibular function

How tissues acquire reproducible shapes to support their function is a fundamental question in developmental biology. Zebrafish semicircular canals form when epithelial pillars partition the lumen of the otic vesicle, the embryonic precursor of the inner ear, into the tubes that sense head rotation for balance. We show that hydrostatic pressure generated by the inflating otic vesicle shapes pillar geometry. Acute vesicle deflation shortens and broadens pillars, whereas pharmacologically induced inflation elongates and narrows them, effects captured by a physical model that treats the vesicle as a pressurized viscoelastic shell. Pillars initially form with variable curvature, but continued vesicle expansion drives them toward a common, straight geometry, a process accelerated by inflation and blocked by deflation. We identify Wnt signaling as crucial for sustaining this pressure by maintaining epithelial barrier integrity. Its disruption impairs pillar geometry and vestibular-dependent swimming behavior. Together, these findings identify hydrostatic pressure as a critical physical mechanism that canalizes tissue geometry to ensure robust organ formation and function.

developmental biology↗

Gigapixel behavioral and neural activity imaging with a novel multi-camera array microscope

The dynamics of living organisms are organized across many spatial scales. However, current cost-effective imaging systems can measure only a subset of these scales at once. We have created a scalable multi-camera array microscope (MCAM) that enables comprehensive high-resolution recording from multiple spatial scales simultaneously, ranging from cellular structures to large-group behavioral dynamics. By collecting data from up to 96 cameras, we computationally generate gigapixel-scale images and movies with a field of view over hundreds of square centimeters at 5um sensitivity. This allows us to observe the behavior and fine anatomical features of numerous freely moving model organisms on multiple spatial scales, including larval zebrafish, fruit flies, nematodes, carpenter ants, and slime mold. The MCAM architecture allows stereoscopic tracking of the z-position of organisms using the overlapping field of view from adjacent cameras. Further, we demonstrate the ability to acquire dual color fluorescence video of multiple freely moving zebrafish, recording neural activity via ratiometric calcium imaging. Overall, the MCAM provides a powerful platform for investigating cellular and behavioral processes across a wide range of spatial scales by removing the bottlenecks imposed by single-camera image acquisition systems.

bioengineering↗