
Engineering systems and experimental workflows to back-engineer brain structure and function at the @eboyden3 lab (MIT) 🐟🧠-🔬🧪-🤖&⚕️
Cambridge, MA
Joined August 2010
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Panos Symvoulidis retweeted
MIT researchers have invented a new microscope that can image electrical activity in neurons distributed across the brain of an entire organism. Professor @eboyden3, the senior author of the study, holds a joint appointment in Media Arts and Sciences (the academic program at the Media Lab) and @mcgovernmit.
news.mit.edu/2026/high-speed…
Nature
Imaging cellular activity across all organs reveals body-wide circuits
nature.com/articles/s41586-0…
Panos Symvoulidis retweeted
Thrilled to receive an #ERCStG for BIO-CACHE! We’re engineering cellular flight recorders to log transient biological events in living cells over time. 🙏 to
@ERC_Research, reviewers and panel members, mentors and students! Want to build cellular black boxes? DMs are open! 🧬✈️
Panos Symvoulidis retweeted
Voltage imaging across the zebrafish brain at 200.8Hz, achieved by optimizing a remote-scanning light-sheet microscope. @eboyden3
nature.com/articles/s41592-0…
Panos Symvoulidis retweeted
Hiring for research scientists in expansion chemistry and optical physiology at mindspan.org with
@eboyden3.bsky.social, Yongxin Zhao, Xue Han. Tools to analyze the human brain. We are into compiling arxiv.org/abs/2603.25713. We are into cutting edge technology.
Panos Symvoulidis retweeted
MIT researchers have invented a new microscope that can image electrical activity in neurons distributed across the brain of an entire organism — in this case, the experimental model Danio rerio (zebrafish). Professor @eboyden3, the senior author of the study, holds a joint appointment in Media Arts and Sciences (the academic program at the Media Lab) and @mcgovernmit. The study was published in @naturemethods.
vist.ly/5ff7b
Panos Symvoulidis retweeted
📢Our new study is out! An example of collaboration in science @IreneFaravelli & @BolanosAnton had the vision and perseverance to ask how far human brain tissue could develop outside the brain and followed that question for more than five years. Congrats to the team!🧠⏳
📢Thrilled to announce that the 2nd piece of work from my postdoc at @Arlottalab is out in @Nature! This has been a huge co-lead effort with my friend @IreneFaravelli 👩🔬👩🔬🤝
Link: nature.com/articles/s41586-0…
👇🧵
Panos Symvoulidis retweeted
Imagine watching electrical activity sweep across an entire #brain in near real time. @MIT has details on a new high-speed #microscopy technique that scans a zebrafish brain 200 times per second, revealing how neurons across regions respond and interact: bit.ly/4zf8p7H
Panos Symvoulidis retweeted
High-speed microscopy reveals electrical activity across the brain. New technique, demonstrated in zebrafish, could help scientists learn how the entire brain works as a whole. picower.mit.edu/news/high-sp… #neuroscience
Panos Symvoulidis retweeted
The study published today in @naturemethods 👉nature.com/articles/s41592-0…
Panos Symvoulidis retweeted
Engineers in Ed Boyden's lab have developed a microscope that captures electrical activity across an entire zebrafish brain at millisecond speed—revealing how neurons coordinate as an emergent whole. mcgovern.mit.edu/2026/08/14/…
Panos Symvoulidis retweeted
MIT researchers including Prof. @eboyden3, who holds a joint appointment in Media Arts and Sciences (the academic program at the Media Lab) and @mcgovernmit, have developed a technique called “implosion carving.” It allows researchers to imprint features throughout a hydrogel using photopatterning, and then shrink it to about 1/2,000 of its original volume, creating tiny 3D photonic devices with features small enough to channel visible light. The new work builds on “implosion fabrication,” which Prof. Boyden’s lab developed in 2018. news.mit.edu/2026/powerful-s…
Panos Symvoulidis retweeted
The first whole-body single-cell atlas of an adult vertebrate is here.
Using the miniature transparent fish Danionella cerebrum, researchers generated the first whole-body single-cell transcriptomic atlas of an adult vertebrate, profiling 607,000+ cells across the entire organism and integrating scRNA-seq with MERFISH spatial transcriptomics. Beyond cataloging cell types, the atlas uncovers conserved positional memory programs, reveals how adult neurons are organized by developmental origin rather than neurotransmitter identity, and maps regenerative dynamics following brain injury.
Key findings
• Constructed a whole-body atlas of 607,370 cells, identifying 40 major tissue classes and nearly 100 neural cell types spanning the central and peripheral nervous systems.
• Combined single-cell RNA sequencing with 500-gene MERFISH to spatially localize cell types throughout the entire adult vertebrate body.
• Adult connective tissue retains embryonic positional information, including persistent HOX gene expression and conserved appendage-patterning programs (e.g., TBX5, TBX4, PITX1, LMX1B) in adult fins.
• Comparative analyses reveal that neuronal transcriptomes are organized primarily by brain region/developmental origin, rather than neurotransmitter identity—an organizing principle shared with mammals.
• Molecular signatures indicate mosaic paedomorphosis, with adult Danionella retaining both larval- and adult-like transcriptional programs across multiple tissues.
• Time-resolved single-cell profiling after telencephalic injury defines sequential regenerative programs involving radial glial activation, immune remodeling, neurogenesis, and neuronal maturation, providing a roadmap of vertebrate brain regeneration.
Why it matters
This resource establishes Danionella cerebrum as a uniquely powerful vertebrate model for systems biology. Its miniature, transparent body makes organism-wide molecular mapping feasible, enabling future studies of aging, regeneration, neural circuits, disease, pharmacology, and evolution at single-cell resolution. The atlas also provides one of the most comprehensive references yet for understanding vertebrate cell diversity and tissue organization.
#SingleCell #SpatialTranscriptomics #MERFISH #Danionella #CellAtlas #Neuroscience #Regeneration #StemCells #DevelopmentalBiology #Evolution
Panos Symvoulidis retweeted
We further demonstrate that our framework works in real-world settings on a 200 MP Samsung ISOCELL HP2 prototype. For both object tracking and scene text recognition tasks, our sensor attention policy reproduces the smooth pursuit and saccadic scanpaths seen in simulations, achieving 200 MP bandwidth-efficient sensing under real-world conditions with sensor noise.
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Panos Symvoulidis retweeted
Should have posted about this before, but my Cleo simulator paper got published in JNeurosci!
Take a look if you want to simulate advanced opto/ephys experiments at a medium (point neuron) level of realism.
jneurosci.org/content/46/1/e…
Panos Symvoulidis retweeted
Early iSOAR 5D movie of membrane and mitochondria dynamics over 3 hrs at 3 min intervals in the head of a zebrafish embryo 6 dpf, covering a 300 x 1000 um FOV at 193 x 193 x 550 nm resolution (0.8 TB total).
Ever wonder why we decide to build a new microscope and how we go about it? For the last lecture this semester of the graduate microscopy class Na, Gokul, and I teach at Cal, I spoke on our developing iSOAR microscope, a swept HILO design with adaptive optics and structured illumination. iSOAR is designed to produce the petabytes of high resolution 5D videos of subcellular dynamics in zebrafish we need to train the multimodal vision models at the heart of our Cell Observatory Initiative. We still have some work to do, but the scopes are coming along nicely.
It's an exciting time at the Observatory, so if you're experienced and looking for a job in zebrafish transgenics, ultra-high throughput image processing, or the development of 5D spatiotemporal foundation models for interpreting the insane dynamic complexity of living matter, we'd love to hear from you. ([email protected], [email protected]).
Panos Symvoulidis retweeted
🧠 When the imaging protocol masks real biology: In a new iScience paper, Dirkx et al. address a subtle but important problem in human iPSC-derived neuronal cultures. Fluo-4 AM dye-based Ca²⁺ imaging is widely used to monitor neuronal activity, but the associated imaging medium exchange can disrupt the spontaneous synchronized network bursts that mark neuronal maturation. In other words, the workflow itself may alter the biology you want to measure.
To show that the issue comes from the imaging procedure itself, the authors used the MaxTwo HD-MEA system as a gold-standard functional reference. MaxTwo recordings showed that fresh imaging medium abolishes synchronized bursting while leaving overall firing intact, whereas re-applying each well’s own conditioned imaging medium preserves spontaneous bursting much more faithfully after dye loading.
This was more than a technical optimization. In agreement with the MaxWell HD-MEA ground truth, the team could still detect the expected hyperexcitable network phenotype in a KCNQ2-related epilepsy model with calcium imaging. A simple workflow change, but a meaningful step forward for functional phenotyping, disease modeling, and drug screening when single-cell spatial resolution matters.
👉 Read the full publication here – mxwbio.com/resources/iscienc…
👏 Congratulations to Nina Dirkx, Bob Asselbergh, Peter Verstraelen, Jonas Van Lent, Els De Vriendt, Vincent Timmerman, Winnok H. De Vos, and Sarah Weckhuysen from the VIB Center for Molecular Neurology, the University of Antwerp, and University Hospital Antwerp, Antwerp, Belgium.
Panos Symvoulidis retweeted
Excited to share my latest preprint on bioRxiv!
Synthetic 3D fluorescence organoid images with exact ground-truth masks for training deep learning models + testing pipelines before real data.
doi.org/10.64898/2026.04.16.…
#microscopy #Biotech #DrugDiscovery
Panos Symvoulidis retweeted
📷 Expansion microscopy turns 11 — and our comprehensive Primer is now live in @MethodsPrimers ! A decade of ExM, 1000+ papers, and still accelerating. Co-authored with the father of the field, @eboyden3 , + Ha Vo & Rong Xu. 📷 Free to read: rdcu.be/fdQPH
Panos Symvoulidis retweeted
Preprint out arguing that we should build the techology to translate (compile) molecularly annotated connectomes into dynamics. I think this is incredibly important. arxiv.org/abs/2603.25713


























