Computational Neuroscience: Building a mathematical model of the brain

Automatic leveraging of information in a hippocampal neuron database to generate mathematical models should help foster interactions between experimental and computational neuroscientists.
  1. Frances Skinner  Is a corresponding author
  1. Division of Clinical and Computational Neuroscience, Krembil Brain Institute, University Health Network and Department of Physiology, University of Toronto, Canada

The amount of data that can be gathered about the human brain has been growing exponentially in recent years, but it could be argued that relatively little progress has been made in actually understanding how the brain works. While there may be sociological and philosophical reasons for this lack of progress (see, for example, Thompson, 2021), a main reason is the low level of interactions between the experimental and theoretical/modeling communities in neuroscience (Marder, 2015). Bridging this divide will be difficult because it requires researchers on both sides to leave their comfort zones and learn more about each other’s work, including the constraints that both sides work under. If not, there is a risk that the results of beautiful experiments, or the outputs of thoughtful models, will not be fully appreciated by everyone working in that particular field of neuroscience.

Where does one begin when trying to build a mathematical model of a biological system? In the case of the brain, besides deciding which region of the brain one wants to model and being clear about the goals of the study (Shou et al., 2015), choices need to be made about the level of abstraction. Understanding how the brain works, in both health and disease, requires studying neural circuits at the level of the cell, particularly as neurological diseases are cell-specific (see, for example, Gallo et al., 2020). Furthermore, many studies have made it abundantly clear that circuit function cannot be understood without a greater understanding of the individual cell types making up the circuit (see, for example, Daur et al., 2016 regarding the stomatogastric nervous system). Indeed, when considering a theoretical basis for biology, it is often argued that the correct level of abstraction is the cell (Brenner, 2010).

Hippocampome.org is a database that contains a vast amount of information about the different types of neuronal cells found in the hippocampus – a region of the brain that has major roles in learning and memory – in rodents. The first version of the database contained information on 122 types of neuronal cells based on the shapes of their axons and dendrites, their main neurotransmitters, and various molecular and biophysical properties (Wheeler et al., 2015). Subsequent versions of the database included information on a range of topics including the physiology of the synapses that connect neurons and the electrical behaviour of various neurons.

Now, in eLife, Giorgio Ascoli and colleagues at George Mason University – including Diek Wheeler as first author – present Hippocampome.org v2.0, which enables users to automatically build models that can be used to simulate the electrical behaviour of networks of neurons (Wheeler et al., 2024). Moreover, Hippocampome.org v2.0 includes data and information on over 50 new neuron types. Now, with the click of a button, a user can choose the region (or regions) of the hippocampus they are interested in and the cell types they would like to include in their model, and Hippocampome.org v2.0 will build a model in which the properties of the individual cells and their connections are based on experimental data from multiple research papers. Furthermore, the data come with important metadata (such as the age of the animals), so users can evaluate the values of the various parameters that are included in any model. Indeed, the richness of the data is such that some researchers have been able to make discoveries by applying data-mining techniques to Hippocampome.org (Sanchez-Aguilera et al., 2021).

Deciding how much detail to include in a model is a non-trivial consideration, but it is naturally dependent on the question being asked and the availability of experimental data. Choosing to represent each neuron by a single compartment, rather than including its structure and properties, and using a relatively simple mathematical model called an Izhikevich model (Izhikevich, 2003) to describe the spiking process is both sensible and necessary. Izhikevich models can encompass many, if not all, of the firing properties of biological cells, and although more complex neuron models exist – such as conductance-based models that include ion-channel types – they would make an already complex ‘automated network model building’ challenge even more complex.

With Hippocampome.org v2.0 in hand, it is now possible to start bridging the gap between theory and experiment without having to make a heroic effort to parse the experimental literature. That is, theoretical ’bones’ can be given experimental ‘meat’, as Wheeler et al. demonstrate in simulations of grid cells. Essentially, this resource can be used to bind hypothesis-driven and data-driven modeling (Eriksson et al., 2022).

To truly understand how the brain works, and to help the many individuals suffering from brain disorders, there needs to be stronger collaborations between experimentalists and modellers. This new resource developed by Wheeler et al. provides a practical path towards this outcome.

References

    1. Brenner S
    (2010) Sequences and consequences
    Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences 365:207–212.
    https://doi.org/10.1098/rstb.2009.0221

Article and author information

Author details

  1. Frances Skinner

    Frances Skinner is in the Division of Clinical and Computational Neuroscience, Krembil Brain Institute, University Health Network and the Department of Physiology, University of Toronto, Toronto, Canada

    For correspondence
    frances.skinner@gmail.com
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0001-7819-4202

Publication history

  1. Version of Record published: February 28, 2024 (version 1)

Copyright

© 2024, Skinner

This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

Metrics

  • 2,530
    views
  • 254
    downloads
  • 0
    citations

Views, downloads and citations are aggregated across all versions of this paper published by eLife.

Download links

A two-part list of links to download the article, or parts of the article, in various formats.

Downloads (link to download the article as PDF)

Open citations (links to open the citations from this article in various online reference manager services)

Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)

  1. Frances Skinner
(2024)
Computational Neuroscience: Building a mathematical model of the brain
eLife 13:e96231.
https://doi.org/10.7554/eLife.96231

Further reading

    1. Neuroscience
    Salima Messaoudi, Ada Allam ... Isabelle Caille
    Research Article

    The fragile X syndrome (FXS) represents the most prevalent form of inherited intellectual disability and is the first monogenic cause of autism spectrum disorder. FXS results from the absence of the RNA-binding protein FMRP (fragile X messenger ribonucleoprotein). Neuronal migration is an essential step of brain development allowing displacement of neurons from their germinal niches to their final integration site. The precise role of FMRP in neuronal migration remains largely unexplored. Using live imaging of postnatal rostral migratory stream (RMS) neurons in Fmr1-null mice, we observed that the absence of FMRP leads to delayed neuronal migration and altered trajectory, associated with defects of centrosomal movement. RNA-interference-induced knockdown of Fmr1 shows that these migratory defects are cell-autonomous. Notably, the primary Fmrp mRNA target implicated in these migratory defects is microtubule-associated protein 1B (MAP1B). Knocking down MAP1B expression effectively rescued most of the observed migratory defects. Finally, we elucidate the molecular mechanisms at play by demonstrating that the absence of FMRP induces defects in the cage of microtubules surrounding the nucleus of migrating neurons, which is rescued by MAP1B knockdown. Our findings reveal a novel neurodevelopmental role for FMRP in collaboration with MAP1B, jointly orchestrating neuronal migration by influencing the microtubular cytoskeleton.

    1. Biochemistry and Chemical Biology
    2. Neuroscience
    Maximilian Nagel, Marco Niestroj ... Marc Spehr
    Research Article

    In most mammals, conspecific chemosensory communication relies on semiochemical release within complex bodily secretions and subsequent stimulus detection by the vomeronasal organ (VNO). Urine, a rich source of ethologically relevant chemosignals, conveys detailed information about sex, social hierarchy, health, and reproductive state, which becomes accessible to a conspecific via vomeronasal sampling. So far, however, numerous aspects of social chemosignaling along the vomeronasal pathway remain unclear. Moreover, since virtually all research on vomeronasal physiology is based on secretions derived from inbred laboratory mice, it remains uncertain whether such stimuli provide a true representation of potentially more relevant cues found in the wild. Here, we combine a robust low-noise VNO activity assay with comparative molecular profiling of sex- and strain-specific mouse urine samples from two inbred laboratory strains as well as from wild mice. With comprehensive molecular portraits of these secretions, VNO activity analysis now enables us to (i) assess whether and, if so, how much sex/strain-selective ‘raw’ chemical information in urine is accessible via vomeronasal sampling; (ii) identify which chemicals exhibit sufficient discriminatory power to signal an animal’s sex, strain, or both; (iii) determine the extent to which wild mouse secretions are unique; and (iv) analyze whether vomeronasal response profiles differ between strains. We report both sex- and, in particular, strain-selective VNO representations of chemical information. Within the urinary ‘secretome’, both volatile compounds and proteins exhibit sufficient discriminative power to provide sex- and strain-specific molecular fingerprints. While total protein amount is substantially enriched in male urine, females secrete a larger variety at overall comparatively low concentrations. Surprisingly, the molecular spectrum of wild mouse urine does not dramatically exceed that of inbred strains. Finally, vomeronasal response profiles differ between C57BL/6 and BALB/c animals, with particularly disparate representations of female semiochemicals.