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RESEARCH HIGHLIGHT
A neuronal basis for mental imagery
Stephen M. Fleming1,2,3
✉
and Nadine Dijkstra4
© The Author(s) under exclusive licence to Center for Excellence in Molecular Cell Science, Chinese Academy of Sciences 2026
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Cell Research (2026) 0:1–2; https://doi.org/10.1038/s41422-026-01260-6
Wadia et al. provide rare single-neuron evidence that mental
imagery reactivates a perceptual code in the human ventral
temporal cortex, with a substantial subset of object-tuned
neurons showing shared tuning across seeing and imagining.
By characterizing neuronal activity in a feature space derived
from a deep neural network, the study demonstrates
that imagery recapitulates the structure of perceptual
representations.
When sitting at our desks in the depths of the British winter, it is
tempting to call to mind an image of a Mediterranean holiday: the
warm sun on our faces, a cool drink in hand. This ability to
internally activate mental representations — to create and
recombine a range of previous experiences — is thought to
undergird artistic and creative endeavours and is a central feature
of planning and autobiographical memory. Conversely, overactive
mental imagery may contribute to psychological disturbances
including hallucinations and intrusive memories.
The neural basis of mental imagery has been at the core of the
imagery debate — is the format of imagery more perception-like
(iconic) or language-like (propositional)?1,2 Neuroimaging research
has made progress on this question, showing that mental imagery
co-opts or reactivates neuronal resources used for perception.3
One consequence of this architecture is that damage to these
brain areas can lead to problems not only with visual perception,
but also with imagination.4 Some have taken these findings to
suggest that the imagery debate is now resolved.5
However, overlap at the level of non-invasive recordings such as
fMRI or EEG does not reveal overlap at a neuronal or circuit level. It
is possible that imagery is subserved by activation of separate or
parallel circuitry located in similar cortical regions. Addressing this
question is critical for our understanding of mental imagery as a
psychological phenomenon — is it really recruiting the same
resources as when we perceive the outside world? Or does it only
seem that way?
This is where the study by Wadia and colleagues breaks new
ground in mental imagery research.6 The authors recorded single
neurons in human epilepsy patients (implanted with electrodes
for clinical purposes) while they viewed and subsequently
imagined objects. Focusing on neurons recorded from the ventral
temporal cortex (VTC), the authors built a computational model in
which neuronal activations were hypothesized to track one of 50
principal components of a low-dimensional feature space
(obtained by passing the images through a deep convolutional
neural network, AlexNet). In keeping with previous research,7 this
feature space provided a good account of the VTC neuronal
activity — so good, in fact, that a linear combination of neuronal
activations was sufficient to reconstruct the object that participants were looking at.
They then asked what happened in the brain when people were
asked to imagine, rather than perceive, those same objects.
Strikingly, a similar perceptual neuronal code was reactivated
when imagining the objects — with ~40% of the object-tuned
VTC neurons recorded during perception being reactivated by
imagery. Notably, a computational account of the sensory code
was important for understanding the type of reactivation induced
by mental imagery. By tracking activation in a latent feature space,
Wadia and colleagues were able to provide more secure inference
that the same computation is recapitulated during imagination,
rather than detecting reactivation at the level of neuronal activity
alone. Furthermore, they were able to show that a visual code was
a better explanation of the activation patterns than a semantic
code. These results help imagery research move beyond simply
asking whether a brain area is active, to an understanding of how
its activity supports perception and imagery. It also showcases the
importance of convergent evidence from both non-invasive brain
imaging and studies of single-unit activity.
Several questions emerge for future investigation. First of all,
what are the mechanisms that allow the visual code to be
harnessed in such a precise way? During perception, activation in
the visual cortex is ultimately caused by bottom-up signals from
the retina. In contrast, during imagery, these bottom-up signals
are absent by definition. It is remarkable that such a nuanced and
complex code can be recruited at will, by an instruction to
imagine. How exactly can information from memory be combined
to generate these rich visual representations in a purely top-down
manner?
Second, what supports the vividness or subjective force of
mental imagery? This question could be asked by supplementing
instructions to imagine simple objects with subjective ratings of
imagery vividness. Other studies have noted that people with
aphantasia — a lack of reported mental imagery experience —
can nevertheless activate similar brain areas, and share a capacity
to perform tasks that rely on perceptual reactivation, such as visual
working memory.8,9 One possibility is that the same neuronal code
is reactivated in both aphantasia and imagery, but that downstream regions (e.g., in the prefrontal cortex) fail to metacognitively access that information in aphantasia.10 Alternatively, a
recent study showed that there are subtle differences in the way
that visual representations are instantiated in people with
aphantasia, suggesting that the exact format of the neuronal
code during imagery might play a role in whether it reaches
awareness.11
1
Department of Experimental Psychology and Institute of Cognitive Neuroscience, University College London, London, UK. 2Max Planck UCL Centre for Computational Psychiatry
and Ageing Research, University College London, London, UK. 3CIFAR Program in Brain, Mind and Consciousness, Toronto, ON, Canada. 4Department of Imaging Neuroscience,
University College London, London, UK. ✉email: stephen.fl
[email protected]
S.M. Fleming and N. Dijkstra
2
Finally, it remains unknown how the brain solves the “reality
monitoring” problem — the problem of distinguishing between
perceived and imagined sensory activities. Wadia and colleagues
showed that a decoder could be trained to distinguish perceived
and imagined objects from only a small number of VTC neurons
— implying that there is sufficient information for reality
monitoring within the VTC. However, it is unclear what exactly
drives this classification. The 40% shared neurons between
imagery and perception most likely provides a lower bound on
the amount of overlap due to noise in the neuronal measurement,
the selection of the computational mode (...truncated)