How neurons in the mouse neocortex form billions of connections
Researchers at EPFL’s Blue Brain Project, a Swiss brain research Initiativehave combined two high profile, large-scale datasets to produce something completely new –a first draft model of the rules guiding neuron-to-neuron connectivity of a whole mouse neocortex. Based on these rules, they were able to generate statistical instances of the micro-connectome of 10 million neurons, a model spanning five orders of magnitude and containing 88 billion synaptic connections that will serve as the basis of the world’s largest-scale simulations of detailed neural circuits.
Identifying the connections across all neurons in every region of the neocortex
The structure of synaptic connections between neurons shapes their activity and function. Measuring a comprehensive snapshot of this so-called connectome has so far only been accomplished within tiny volumes, smaller than the head of a pin. For larger volumes, the long-range connectivity, formed by bundles of extremely thin but long fibers, has only been studied for small numbers of individual neurons, which is far from a complete picture. Alternatively, it has been studied at the macro-scale, a ‘zoomed-out’ view of average features that does not provide single-cell resolution.
In a paper published in Nature Communications, the Blue Brain researchers have shown that the trick lies in combining these two views. By integrating data from two recent datasets – the Allen Mouse Brain Connectivity Atlas and Janelia MouseLight – the researchers identified some of the key rules that dictate which individual neurons can form connections over large distances within the neocortex. This was possible because the two datasets complemented each other in terms of entirety of the neocortex and the cellular resolution provided.
Emergence of a surprisingly complex structure at single-cell resolution
Building on their previous work in modelling local brain circuits, the researchers were then able to parameterize these principles of neocortical connectivity and generate statistical connectome instances compatible with them. When they studied the resulting structure, they found something fascinating; at cellular resolution, a surprisingly complex structure that had so far only been seen between neighboring neurons now also tied together neurons in different regions and at opposite ends of the brain. This was comparable to a rule of self-similarity that has been previously found in the human brain (MRI data) and predicts that it extends all the way down to the level of individual neurons.
“This made me re-think how I think about these long-range connections”, reveals lead researcher Michael Reimann. “They have been depicted as these blunt cables, connecting or synchronizing whole brain regions. But maybe there is more to them, more specific targeting of individual neurons. And this is what we learned from just a few, relatively course-grained principles. I expect that with improved methods we will find more in the future.”
Openly accessible connectome can serve as a powerful null model to compare experimental findings
“We have completed such a first-draft connectome of mouse neocortex by using an improved version of our previously published circuit building pipeline (Markram et al., 2015),” explains Michael Reimann. “It has been improved to place neurons in brain-atlas defined 3d spaces instead of hexagonal prisms, taking into account the geometry and cellular composition of individual brain regions. The composition was based on data from the open source Blue Brain Cell Atlas. Further constraints were derived from other openly accessible datasets. Additional constraints that are so far unknown are likely to limit long-range connectivity even more. To start a process of iterative refinement, we made the model and data available to the public. The parameterized constraints on projection strength, mapping, layer profiles and individual axon targeting (i.e. the projection recipe), as well as stochastic instantiations of whole-neocortex micro-connectomes can be found under https://portal.bluebrain.epfl.ch/resources/models/mouse-projections”.
This openly accessible connectome can serve as a powerful null model to compare experimental findings to and as a substrate for whole-brain simulations of detailed neural networks. Sparse connection matrices of several instances of the predicted null model of neocortical long-range connectivity have also been publicly available as this result actively demonstrates thepower of making datasets available to the public.
Further advancing the case for Simulation
The simulation (in-silico) method allowed the scientists to target volumes several orders of magnitude smaller, than would be possible with experimental methods (Gămănut et al., 2018), right down to the innervation of individual neurons with sub-cellular resolution. Going forward, this will allow the simulation of the electrical activity of individual neurons, entire regions or of the entire neocortex.
“This paper builds upon Blue Brain’s earlier work on evaluating morphological constraints on connectivity, ‘Morphological Diversity Strongly Constrains Synaptic Connectivity and Plasticity’,(Cerebral Cortex, 2017) and ‘Reconstruction and Simulation of Neocortical Microcircuitry’ (Cell 2015) explains Blue Brain Founder and Director Prof. Henry Markram. “The findings enable us continue our simulation experiments at an exponentially increasing rate meaning, we can now build biologically accurate brain models of bigger and bigger brain regions and at a higher and higher resolution thereby further advancing the case for simulation”.
Reimann, M.W., Gevaert, M., Shi, Y., Lu, H., Markram, H., and Muller, E. A null model of the mouse whole-neocortex micro-connectome. Nature Communications 29 August 2019. https://doi.org/10.1038/s41467-019-11630-x
For more information, please contact Blue Brain Communications Manager – [email protected]
This study was supported by general funding to the Blue Brain Project from the Swiss government’s ETH Board of the Swiss Federal Institutes of Technology and by support to BBP as one of its research centers by the École polytechnique fédérale de Lausanne.
Blue Brain would like to thank the Allen Institute for Brain Science and the Janelia MouseLight project for the datasets they have made available.