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Imaging cellular activity simultaneously across all organs of a vertebrate reveals body-wide circuits
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Imaging cellular activity simultaneously across all organs of a vertebrate reveals body-wide circuits

Virginia M. S. Ruetten, Wei Zheng, Igor Siwanowicz +29 more
September 2025
 ·
bioRxiv
 ·
DOI 
10.1101/2025.08.20.670374
94
%
Reproducible
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This paper passed independent validation.
QED's automated review checked the evidence supporting each claim, the statistical methods, and whether the results are reproducible from the data provided.

It ranks in the top 1% of preprints assessed in Neuroscience this quarter.
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Why this is interesting

By achieving simultaneous whole-body, single-cell functional imaging in a vertebrate, this work shatters the organ-centric boundaries of classical physiology, revealing emergent coordination principles—kidney waves, ependymal oscillations, brainstem-controlled blood redistribution—invisible to any prior method.

Author perspective

What is the most important insight, discovery, or finding from your paper that you would like other scientists to know?
“

Physiology and disease don't respect organ boundaries, yet we mostly study the body one tissue at a time, searching under streetlights. WHOLISTIC expands the light, imaging cellular activity across a whole living vertebrate at once, letting the biology reveal which cellular players matter, then tracing, from their shared dynamics, functional circuits that link them. For drug screening, rather than chasing a compound's effects one tissue at a time, you capture them body-wide, on-target and off, in a single recording at cellular resolution.

”
Virginia M. S. Ruetten

QED claims analysis

Summary

WHOLISTIC enables simultaneous imaging of cellular calcium dynamics across all organs of transparent vertebrates, revealing previously unknown body-wide coordination patterns including state-dependent ependymal cell oscillations during motor quiescence, novel muscle synergies with distinct neural control, brain-body circuits mediating organ-specific responses, and rapid brainstem-controlled blood flow redistribution during hypoxic stress that prioritizes oxygen delivery to essential tissues over visceral organs.

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Main Claim 1 –

WHOLISTIC Images Body-Wide Cellular Calcium Dynamics in Vertebrates

Supporting evidence

  • WHOLISTIC Detects Novel Chondrocyte Cold and Meningeal Ketamine Responses
Main Claim 2 –

Cervical-Epaxial Muscles Synchronize with Abdominal Muscles

Supporting evidence

  • Ependymal Calcium Responses Scale with Motor Event Intensity
Main Claim 3 –

WHOLISTIC Plus Optogenetics Enables Causal Brain-Body Circuit Testing

Main Claim 4 –

Ependymal Cells Oscillate Ultraslowly During Motor Quiescence

Supporting evidence

  • Ependymal Projections Form Midline Sheets and Ensheathe Commissural Axons

Abstract

All cells in an animal collectively ensure, moment-to-moment, the survival of the whole organism in the face of environmental stressors. Physiology seeks to elucidate the intricate network of interactions that sustain life, which often span multiple organs, cell types, and timescales, but a major challenge lies in the inability to simultaneously record time-varying cellular activity throughout the entire body.

We developed WHOLISTIC (WHole Organism Live Imaging System for recording Tissue and IntraCellular activity), a method to image second-timescale, time-varying intracellular dynamics across cell-types of the vertebrate body. By advancing and integrating volumetric fluorescence microscopy, machine learning, and pancellular transgenic expression of calcium sensors in transparent young Danio rerio (zebrafish) and with proof of concept in adult Danionella, the method enables real-time recording of cellular dynamics across the organism. Calcium is a universal intracellular messenger, with a large array of cellular processes depending on changes in calcium concentration across varying time-scales, making it an ideal proxy of cellular activity.

Using this platform to screen the dynamics of most cells in the body, we discovered unexpected responses of specific cell types to stimuli, such as chondrocyte reactions to cold, meningeal responses to ketamine, and state-dependent activity, such as oscillatory ependymal-cell activity during periods of extended motor quiescence. At the organ scale, the method uncovered pulsating traveling waves along the kidney nephron. At the multi-organ scale, we uncovered muscle synergies and independencies, as well as muscle-organ interactions. Integration with optogenetics allowed us to all-optically determine the causal direction of brain-body interactions. At the whole-organism scale, the method captured the rapid brainstem-controlled redistribution of blood flow across the body.

Finally, we advanced Whole-Body Expansion Microscopy to provide ground-truth molecular and ultrastructural anatomical context, explaining the spatiotemporal structure of activity captured by WHOLISTIC. Together, these innovations establish a new paradigm for systems biology, bridging cellular and organismal physiology, with broad implications for both fundamental research and drug discovery.

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