Alessandro Gozzi Profile picture
May 2 10 tweets 5 min read
Task-free fMRI is governed by high-amplitude BOLD coactivations (termed "CAPs"). But how do these patterns emerge and what do they mean?
New collaborative work conceived by #Diego_Fasoli and #Stefano_Panzeri provides possible explanations 👉tinyurl.com/2p8un5kp

🧵1/n Image
In this work, we developed a large-scale network model of the mouse cortex that combines *directed* axonal connectivity (👉tinyurl.com/mryub799) with *non-linear* firing rate dynamics.

PS: “we” in this thread mostly stands for “Diego & Stefano”

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Our model reproduces remarkably well (ρ = 0.55) the topography of empirical 🐁 rsfMRI activity: simulated data show robust inter-hemispheric symmetry, and delineate well-characterized network systems of the mouse such a default-mode network, latero-cortical system etcetera.

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What about CAPs? Recurrently connected neural networks like the one we used here exhibit attractor dynamics: we thus hypothesized that attractor dynamics may exist in real-world rsfMRI timeseries & that the emergence & features of CAPs may be related to observed attractors

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We thus analyzed the dynamics of our model numerically and expressed model attractors as patterns of rsfMRI activity. Notably, most attractors we found had symmetric anatomy and emerged in spatially-opposed pairs, recapitulating topography of real-world mouse fMRI CAPs!

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These results suggest that CAPs are a manifestations of whole-cortex attractor dynamics of the kind we describe in our model!
Remarkably, this rich dynamics emerges only when using a *directed* axonal connectome, and is lost after connectome symmetrization (think of DTI...)

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In the paper we also tested and measured many other features. An interesting finding is for example the ability of our model to predict very well the "fMRI connectivity" anticorrelation observed upon global signal regression..

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..& the observation that state attractors from the model (as well as those in real fMRI data) encompass transient non-homotopic states (in spite of a highly symmetric connectome) a finding reflecting "Spontaneous Symmetry Breaking" (this one being for hardcore physicists😆)

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In conclusion, our work adds novel concepts and predictions to existing whole-brain modelling of rsfMRI activity, relating the emergence of high-amplitude cofluctuation patterns (e.g. CAPs) to cortico-cortical attractor dynamics.

9/n
Very grateful to Diego and Stefano for involving us in this study (and patiently explaining their findings in lay terms to me - hope my summary here makes sense!), @ColettaLudovico @danielgb_87 for help with connectome and CAPs, plus @ERC_Research and all funding agencies

10/10

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More from @Gozzi_Ale

Oct 19, 2021
Out today in @NatureComms our 🐁+👨work where we show that in #Autism
➡️(mTOR-related) excess of synapses causes aberrant fronto-striatal activity
➡️ this signature can be decoded in human fMRI scans, defining an identifiable autism subtype
@IITalk
1/4
tinyurl.com/265xy8ha
An important implication of our work is that it unifies two major pathological domains that in #Autism had long been regarded as distinct i.e. synaptic pathology & macroscale dysconnectivity

An expanded account of our results was reported here
➡️

2/4
All our previous results hold. We have now just added further evidence that Tsc2 mice lack major white matter/myelin alterations, further implicating synaptic pathology as cause for our findings, and documented that human findings are robust to multiple denoising strategies

3/4
Read 4 tweets
Oct 16, 2020
Can we ‘see’ #autism in the brain? And is there a specific brain signature for the condition?

This is what we found by comparing brain connectivity maps across 16 mouse autism models
➡️tinyurl.com/yxfu2gzn

➡️Majestically led 👏👏👏by @Valerio_Zerbi @NCMLabETH

Thread 1/n
Autism is diagnosed based on behavior - but is this condition associated with a specific brain signature of circuit dysfunction?
Despite decades of work, brain imaging has failed to identify such signature as we have evidence of under-connectivity... tinyurl.com/y5uxoe3s

2/n
.....over-connectivity....
linkinghub.elsevier.com/retrieve/pii/S…

3/n
Read 14 tweets
Oct 9, 2020
#Autism is often associated with an excess of synapses:
but how does this trait affect large-scale circuit function?

Here's what we found by modelling autism-related pruning deficits across-species🧠🐭
➡️tinyurl.com/y2yfj74o

By @MarcoPagani1985 @mvlombardo & al.

Thread 1/n
Postmortem investigations in idiopathic #Autism have consistently revealed an excess of excitatory synapses
tinyurl.com/y57cc4r5
tinyurl.com/y59mdffp
tinyurl.com/y3t64yfe

2/n
Seminal work form the #Sulzer_Lab @Columbia has shown that postmortem synaptic surplus in #Autism is associated with hyperactive mTOR signalling
➡️this is a molecular pathway often dysregulated in autism and a key point of convergence of many autism-risk genes

3/n
Read 19 tweets
Aug 7, 2020
Wondering whether axonal input *drives* fMRI-based functional connectivity? Us too!

Here is what we found using #chemogenetic deconstruction of rsfMRI in the mouse🐁🐭

➡️Cortical silencing results in paradoxical fMRI overconnectivity tinyurl.com/yy269j92

Thread below 1/n
Computational and empirical evidence suggest that structural and functional connectivity are robustly related

➡️ this recent review from @richardfbetzel @misicbata summarizes it all tinyurl.com/yyy5u3zm

2/n
⚠️A key prediction of structurally based models of fMRI coupling is that *inactivation* of a brain node would result in reduced rsfMRI connectivity with its targets⚠️

But is that really the case?

3/n
Read 19 tweets
May 15, 2020
**New preprint from the lab**

Regional, layer and cell-class specific connectivity of the mouse default mode network tinyurl.com/yddanw5w

Conceived & majestically led by @DrJigsaww @harrisjuliea @AllenInstitute

Thread covering DMN basics + implications of findings
1/n 👇
What is the Default Mode Network (DMN)?

👉Network identified in human PET/fMRI studies
👉Active and strongly synchronized during rest
👉Desynchronized by goal-oriented tasks
👉Encompasses associative cortices - Prefrontal, Cingulate, Retrosplenial, Parietal, Temporal

2/n
Why study the DMN?

👉Most prominent large-scale network of human brain
👉Pivotal substrate for higher-order cognitive and social functions
👉Key point of vulnerability for autism, schizophrenia, Alzhemier's and other brain disorders (seminal feature review below)

3/n
Read 13 tweets

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