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Dr. Ranmal Samarasinghe in the lab.
Photo Credit: Elena Zhukova, UCLA Broad Stem Cell Research Center
Scientific Frontline: Extended "At a Glance" Summary: Stem Cell-Derived Brain Assembloids
The Core Concept: Stem cell-derived brain assembloids are lab-grown, three-dimensional models of simplified human neural circuits capable of generating coordinated electrical rhythms. Researchers recently utilized these models to successfully reproduce the slow, sweeping electrical brain waves characteristic of general anesthesia.
Key Distinction/Mechanism: Unlike animal brains or two-dimensional flat cell cultures, assembloids allow researchers to isolate and manipulate interconnected human neural circuits in a highly controlled environment. When exposed to the anesthetic propofol, individual neurons within the model become markedly quieter, but their collective activity synchronizes to produce the large electrical waves associated with an anesthetized brain, proving this phenomenon requires only a minimal cortical circuit rather than deeper structures like the thalamus.
Origin/History: Researchers at the University of California, Los Angeles published findings in the British Journal of Anaesthesia, marking the first time human brain assembloids successfully reproduced the electrical hallmarks of general anesthesia.
Major Frameworks/Components:
- Induced Pluripotent Stem Cells: Adult cells that have been reprogrammed into a stem cell-like state to grow specific neural tissue.
- Tri-Cellular Composition: The integration of excitatory neurons (which transmit signals), inhibitory neurons (which restrain activity), and glial cells (which provide support functions).
- Cortical Circuit Synchrony: The mechanism by which anesthetics bind to specific cellular receptors, quieting individual neurons while synchronizing the broader network's rhythm.
- Electroencephalogram (EEG) Signatures: The measurable slow, broad electrical brain waves that indicate an unconscious state.
Branch of Science: Neuroscience, Stem Cell Biology, Neurobiology, and Anesthesiology.
Future Application: These models provide a platform for screening new anesthetic drugs, determining individual patient sensitivities to anesthesia, and investigating complex conditions that severely alter brain dynamics, such as epilepsy, coma, and traumatic brain injury.
Why It Matters: This advancement bridges a major gap in clinical neuroscience by offering an ethical, human-based model that directly links molecular-level cellular changes with whole-brain electrical patterns. It allows researchers to build functional neural circuits from the ground up to investigate profound alterations in human consciousness.
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| Representative image of a developing human cortex-like organoid. In this study, these organoids were later fused with interneuron-producing organoids to form the assembloids used for electrophysiological recordings. Credits: Immunohistochemistry by Emily Duncan and imaging by Dr. Adrianna Carrasco of the Samarasinghe Lab |
Every day, hundreds of thousands of people undergo general anesthesia, trusting they'll drift into unconsciousness and wake safely after surgery. Yet despite decades of use, scientists still don't fully understand how anesthetic drugs reshape the brain's electrical activity to produce unconsciousness.
Studying the brain’s response to anesthesia has been difficult: in living humans, there’s no safe way to study the brain cell by cell, and in animals, the drugs act on many different brain regions at once, making it hard to isolate where the effects arise.
Now, UCLA researchers have shown for the first time that human stem cell-derived brain assembloids—tiny, three-dimensional models that recreate simplified human brain circuits—can reproduce the electrical changes seen during general anesthesia. Their findings were just published in the British Journal of Anaesthesia.
These new findings demonstrate that brain assembloids can serve as a human model for investigating how molecular changes inside brain cells shape large-scale patterns of electrical activity.
“We’re excited about these models’ potential not just for studying anesthesia, but as a tool we can use more broadly to understand how brain networks become disrupted in other disorders that profoundly alter brain dynamics like traumatic brain injury,” said senior author Dr. Ranmal Samarasinghe, an assistant professor of neurology and member of the UCLA Broad Stem Cell Research Center.
Scientists have long understood two pieces of the anesthesia puzzle: that drugs such as propofol bind to specific receptors on neurons, and what an anesthetized brain looks like on an electroencephalogram, or EEG.
“We’ve known what these drugs bind to for a long time, and we’ve known what happens at the level of the whole brain,” Dr. Daniel Toker, first author of the paper and a project scientist in Samarasinghe’s lab, said. “What we've been missing is a human model that lets us connect those two scales.”
Assembloids help close that gap. Unlike neurons grown flat in a lab dish, which are among the models that have previously been used in these types of studies, the assembloids contain interconnected circuits that produce coordinated electrical activity. And unlike animal brains, they let researchers isolate and manipulate those circuits in a controlled human system.
Slow Waves, Quiet Neurons
Created from induced pluripotent stem cells—adult cells that have been reprogrammed into a stem cell-like state—the assembloids combine three types of brain cells: excitatory neurons, which transmit signals; inhibitory neurons, which restrain activity; and glial cells, which play multiple roles in brain function. Together, these cells form circuits capable of generating coordinated rhythms similar to those in the human brain.
To test whether the models could capture the effects of anesthesia, the team exposed them to propofol. Because assembloids more closely resemble the developing fetal brain than the mature adult brain, it was unclear whether they would respond the same way.
But they did. Researchers found that the assembloids developed the broad, slow brain waves characteristic of anesthesia, even as the electrical activity of individual neurons grew markedly quieter.
Those two changes may sound contradictory, but together they capture one of anesthesia's defining features.
“It’s a little counterintuitive,” Toker said. “Individual neurons become less active, but the overall brain waves become larger, because many neurons begin changing their activity in synchrony.”
Toker compares the effect to a football stadium. If thousands of spectators are all holding separate conversations, a single microphone picks up little more than background noise. But if everyone falls quiet and then claps together every few seconds, those synchronized bursts become impossible to miss. In much the same way, anesthesia quiets individual neurons while synchronizing activity across the network, producing the large, slow waves seen on an EEG.
The team confirmed that the response depended on the biological mechanisms identified in decades of animal research. Blocking the receptors targeted by propofol eliminated the effect, and simpler models lacking inhibitory neurons failed to produce the characteristic waves.
The findings also speak to a longstanding debate over whether these signatures require input from the thalamus, a deep brain structure that relays signals to the cortex. Because assembloids contain no thalamus yet still reproduced the pattern, the results show that a minimal cortical circuit can be sufficient on its own.
A Platform Beyond Anesthesia
Beyond advancing scientists’ understanding of anesthesia, the study also expands what researchers can investigate using brain assembloids.
Because assembloids are built from human cells and can be precisely manipulated in the laboratory, researchers can now investigate how specific genes, cell types, and signaling pathways shape coordinated brain activity—questions that have been difficult or impossible to study directly in people.
The model could also help screen candidate drugs and examine why patients differ in their sensitivity to anesthesia, including the rare cases of unintentional awareness during surgery.
More broadly, by showing that a lab-grown human brain model can shift between distinct states of electrical activity, the study opens a new way to investigate how human brain circuits generate—and change—their activity.
“What makes brain assembloids so powerful is that you build the circuit from the ground up and decide what goes into it,” Toker said. “Because we're building it ourselves, we have a real chance to understand what shapes the brain activity we see in patients under anesthesia and across different conditions from coma to traumatic brain injury to epilepsy.”
Funding: This research was supported by the National Institutes of Health, CURE Epilepsy, the International SCN8A Alliance, the Simons Foundation, the UCLA Intellectual and Developmental Disabilities Research Center, a UCLA Broad Stem Cell Research Center Innovation Award, the In Memory of Christina Louise George Fund, and the Michael R. Bloomberg Revocable Trust.
Published in journal: British Journal of Anaesthesia
Title: Human brain assembloids as a model of anaesthetic-induced neural dynamics in vitro
Authors: Daniel Toker, Colin M. McCrimmon, Qing Cao, Anandita Pandey, Asia Guzman, Anjana Shriram, Andrew Hudson, Martin M. Monti, and Ranmal A. Samarasinghe
Source/Credit: University of California, Los Angeles / Health | Tiare Dunlap
Edited by: Scientific Frontline
Reference Number: ns100226_01
