In this era of complete genomes, our knowledge of neuroanatomical circuitry remains surprisingly sparse. Such knowledge is critical, however, for both basic and clinical research into brain function. Here we advocate for a concerted effort to fill this gap, through systematic, experimental mapping of neural circuits at a mesoscopic scale of resolution suitable for comprehensive, brainwide coverage, using injections of tracers or viral vectors. We detail the scientific and medical rationale and briefly review existing knowledge and experimental techniques. We define a set of desiderata, including brainwide coverage; validated and extensible experimental techniques suitable for standardization and automation; centralized, open-access data repository; compatibility with existing resources; and tractability with current informatics technology. We discuss a hypothetical but tractable plan for mouse, additional efforts for the macaque, and technique development for human. We estimate that the mouse connectivity project could be completed within five years with a comparatively modest budget.
Citation: Bohland JW, Wu C, Barbas H, Bokil H, Bota M, et al. (2009) A Proposal for a Coordinated Effort for the Determination of Brainwide Neuroanatomical Connectivity in Model Organisms at a Mesoscopic Scale. PLoS Comput Biol 5(3): e1000334. doi:10.1371/journal.pcbi.1000334
Editor: Olaf Sporns, Indiana University, United States of America
Published: March 27, 2009
Copyright: © 2009 Bohland et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This paper is a result of discussions at the 2007 and 2008 Brain Architecture Project Banbury Center Meetings, funded by the W. M. Keck Foundation. The sponsors had no role in the conception or preparation of this manuscript.
Competing interests: The authors have declared that no competing interests exist.
The defining architectural feature of the nervous system is that it forms a circuit. Unlike other tissues or organs, it is the patterns of axonal connections between neurons that determine the functioning of the brain. Nevertheless, more than a decade after Francis Crick and Ted Jones bemoaned the “Backwardness of Human Neuroanatomy ,” our empirical knowledge about neuroanatomical connectivity in model organisms, including the mammalian species most widely used in biomedical research, remains surprisingly sparse. Efforts to manually curate neuroanatomical knowledge from the literature currently provide information about the reported presence or absence of ~10% of all possible long-range projections between the roughly 500 identified brain regions in the rat  (Figure 1). While this number does not represent a comprehensive survey of the literature, it is clear that many possible projections have not yet been studied using modern tracing methods. In addition, the standard level of data analysis and presentation provides only a qualitative view of the known projections. Such paucity of empirical knowledge stands in contrast to the complete genomes now available for many organisms.
This matrix shows information that has thus far been curated about projections between 486 discrete brain regions in the rat brain. Non-white entries indicate connections for which data are available. Black entries indicate the absence of a connection, and colored entries indicate reported connections of varying strength. The overall sparsity of this matrix (10.45% filled) is reflective of our lack of a unified understanding of brain connectivity in model organisms.
Here we argue the case for a coordinated effort across the neuroscience community to comprehensively determine neuroanatomical connectivity at a brainwide level in model organisms including the mouse, macaque, and eventually human. We discuss the important issues of resolution and rationale and survey the state of current knowledge and available techniques, then offer a basic outline for an experimental program and associated informatics requirements. The Allen Brain Atlas (ABA) for gene expression in the mouse  has demonstrated both the power of scaling up standardized techniques in neuroanatomical research and the feasibility of brainwide approaches. Numerous followup efforts to genome projects are also under way at various levels leading up to the phenotype. Time is therefore ripe for brainwide connectivity projects, to modernize neuroanatomical research, and to fill perhaps the largest lacuna in our knowledge about nervous system structure. The purpose of this article, which has resulted from discussions with a large and varied working group of experts, is to provide motivation and background for readers interested in brainwide connectivity projects, estimate resource requirements by analyzing a feasible scenario, recommend directions for such projects, and provide a platform for further discussions. The issues discussed here are likely to be relevant in implementing such a project through any combination of centralized and distributed efforts.
The Mesoscopic Level of Resolution
It is clear that there exists some degree of nonrandom organization of the interconnections in the nervous system at multiple scales, including individual neurons, groups of neurons, architectonic regions and subcortical nuclei, and functional systems. Macroscopic brain organization, at the level of entire structural–functional systems and major fiber bundles, is somewhat understood but provides an insufficient description of the overall architecture. However, for complex vertebrate brains it is not currently technologically feasible to determine brainwide connectivity at the level of individual synapses. Further, while a statistical description is possible at this microscopic resolution, correspondence cannot be expected between individual brains described at the level of all synapses of all neurons. Significantly more invariance can be expected at a mesoscopic level where co-localized groups of neurons, perhaps of the same type or sharing common organizational features, are considered together as a unit, and projection patterns from these neuronal groups are studied over macroscopic distances. This level of connectivity is well-suited to aid our understanding of specific mental functions. A comprehensive mesoscopic wiring diagram, if available, would supply a meaningful skeleton that can be further augmented by the statistical characterization of microcircuitry at a finer scale (e.g., single neurons or cortical columns).
The existence and nature of invariant connectivity patterns across individual brains is itself a topic of research that can be addressed within a large-scale connectivity project. There is adequate evidence for mesoscopic architectural invariance in the form of cyto-, chemo-, and myelo-architectonically defined brain regions and from spatial gene expression patterns to proceed. In addition, however, a brainwide project executed with calculated redundancy will make it possible to empirically define the extent of such invariance. Further, if input and output connections are methodically determined along an appropriate anatomical grid, it should be possible to delineate the mesoscopic projection patterns in brain space without imposing a system of discrete anatomical parcels defined a priori.
The availability of mesoscopic circuit diagrams for model nervous systems would impact neuroscience research at nearly all levels. Because connectivity underlies nervous system function, any lack of such knowledge impedes the achievement of comprehensive understanding, even if complete information was present about cytoarchitecture, neuronal cell types, gene expression profiles, or other structural considerations. Furthermore, the connectional architecture of the nervous system—the connectivity phenotype—is a critical missing link between genotype and behavioral phenotype; the simultaneous availability of comprehensive genomic and neuroanatomical information will greatly narrow this gap. The scientific rationale can be further sharpened by examining the role of circuitry in experimental and theoretical approaches to the nervous system.
Experimental design in electrophysiological studies can be improved by explicit consideration of connectivity. For example, without any reference to underlying connectivity it is difficult to interpret measured physiological activity or the effects of microstimulation. Studies that consider the internal dynamics of the brain, including studies of selective attention, often make arguments about top-down or bottom-up processes, which are ultimately contingent on neuroanatomical information that is frequently deficient. Likewise, the lack of empirical constraints on neural network models remains an Achilles heel of that subject area, and such theoretical research would benefit greatly from added knowledge of connectional brain architecture.
Many comparative and evolutionary studies have also suffered from a phrenological emphasis on changes in morphological characteristics and relative sizes of parts of the nervous system, with less consideration of connectivity. Knowledge of the mesoscopic circuit diagrams for multiple model organisms will greatly advance comparative and evolutionary neuroanatomy, as has been the case for comparative and evolutionary genomics. This is highlighted by recent advances in understanding the relation between avian and mammalian brains. Purely structural considerations, such as the presence of a layered cortex in mammals, had led to incorrect homological identification of avian telencephalic structures with mammalian basal ganglia. Connectivity considerations have led to a profound revision of this view, leading to a new nomenclature for avian brain compartments .
Neurological and neuropsychiatric disorders are responsible for approximately 30% of the total burden of illness in the United States, according to the World Health Organization's estimated Disability Adjusted Life Years (DALYs) for 2002 (http://www.who.int/healthinfo/global_burden_disease/en/index.html). The dominant paradigms for understanding such disorders have involved focal lesions, widespread neurodegeneration, vascular compromise, and neurotransmitter dysregulation, with circuit considerations playing a comparatively minor role. It has long been known, however, that disruptions in neural connectivity can underlie human brain disease ,. In disorders with no identified genetic component (e.g., traumatic brain injury or infectious disease), dysfunction arises directly from a disruption of the normal circuit. For those with heritable susceptibility effects, genetic polymorphism and cellular processes play a greater role, but anatomical circuits remain critical to understanding symptoms and developing therapies. In Parkinson disease, for example, drug and stimulation-based therapeutic interventions do not occur at the cellular lesion site, but rather are contingent on understanding interactions within the extra-pyramidal motor system . Incomplete knowledge of this circuitry potentially holds back development of therapies for both Parkinson and Huntington diseases, despite a reasonably complete understanding of the genetic etiology of the latter.
There is growing evidence that aberrant wiring plays a central role in the etiology, pathophysiology, and symptomatology of schizophrenia , autism , and dyslexia . Patients with autism and other pervasive developmental disorders are observed to have reductions in the size of the corpus callosum , and in long-range frontal/temporal functional connectivity –. Autism is thought to be highly heritable and polygenic , and a number of mouse genetic models have been developed. The ability to compare the connectivity phenotypes of different mouse models with wild-type mice could yield important clues regarding the common pathways for generating the behavioral phenotype. Currently, however, the baseline connectivity data required to make such data-driven comparisons is lacking. If connectivity phenotypes can be established for autism and other disorders, these can assist in screening for drug development and more accurate subtyping of psychiatric diagnoses.
The importance of circuit considerations for differentially characterizing disorders such as major depression, anxiety, and obsessive–compulsive disorders, and substance (including nicotine) addiction is beginning to be recognized. These illnesses are considered disorders of the affective circuitry underlying emotion and motivated behaviors, which spans the brainstem, hypothalamus, frontal and cingulate cortices, and basal cortical nuclei ,. Knowledge of affective circuits is substantially poorer than of sensory–motor circuitry, despite disorders of the former resulting in a much greater burden of illness. Determining connectivity in these systems will allow the development of objective diagnostic tools, and may also yield cross-mammalian emotional endophenotypes to guide new conceptualizations of core psychiatric syndromes and aid drug discovery . The development of animal models that mimic neuropsychiatric disorders at the circuit rather than behavioral level may also facilitate new therapeutic strategies. Furthermore, neuropsychiatric disorders likely result from pathologies at the system level, with complex genetic, epigenetic, and environmental factors combining to impact the neural circuitry. Systems-level knowledge, including neuroanatomic connectivity, may thus prove crucial in better understanding results from, for example, genomewide association studies. Analogously, the importance of incorporating knowledge from cellular systems biology (e.g., by grouping genes into pathways) has been recognized in other domains.
What Is Being Proposed?
We propose a concerted experimental effort to comprehensively determine brainwide mesoscale neuronal connectivity in model organisms. Our proposal is to employ existing neuroanatomical methods, including tracer injections and viral gene transfer, which have been sufficiently well-established and are appropriately scalable for deployment at this level. The first and primary objective is to apply these methods in a standardized, high-throughput experimental program to fully map the mesoscale wiring diagram for the mouse brain and, following the model of successful genome projects, to rapidly make the results and digitized primary data publicly accessible. The second objective is to collate and, where possible, digitize existing experimental data from the macaque, and to pursue targeted experiments using standardized protocols to plug key gaps in our knowledge of primate brain connectivity. Additionally, we argue for similar efforts in other model organisms and for the pursuit of experimental methods that can be used in postmortem human brain tissue.
The projects may be carried out in a distributed manner by coordinating efforts at multiple experimental laboratories making use of uniform experimental protocols, or in a more centralized way by creating one or a few dedicated sites. Here we outline the properties of a large-scale connectivity mapping project that are seen as essential, and some that are desirable but not required. The required attributes are as follows.
- Brainwide coverage at a mesoscopic resolution. The experimental technique must be applicable in all brain systems, cortical and subcortical. It should not be applicable only to specific cell types; if the technique is used to target specific cells, it must be capable of targeting any cell group.
- Validated and extensible experimental techniques. The experimental methods must be well-characterized and, to the extent possible, validated. The false positive rate should be especially low. The techniques must be amenable to high-throughput application; the individual steps for sample preparation, injection, histology, detection, and data analysis should be stereotyped and of limited complexity.
- Centralized, open-access data repository. The data collected from such an effort must be made freely available to all researchers from a centralized data repository. This includes raw image data, processed summary data, and metadata.
- Compatibility with existing neuroanatomical resources. The results of this project must be interpretable with respect to existing datasets. For example, creating ties to the ABA , existing connectivity databases (Table 1), and other atlas projects (e.g., –) is imperative.
- Tractability with current informatics technology. The data collected and maintained in the repository must be suitable to be analyzed and stored using existing informatics techniques and available technology, allowing for predictable growth in both methods and hardware.
Additional characteristics that would enhance the project's impact include the following.
- Availability of detailed anatomical information. The ability to characterize various additional properties of the observed projection patterns would be beneficial. This might include classification of the neuronal cell types and neurotransmitters involved, laminar origins and terminations of projections in stratified structures, receptor information, cell density estimates in the origin and termination areas, morphological properties of the axons and/or dendritic arbors, and statistical characterization of topography and convergence or divergence patterns of projections.
- Reconstruction of projection trajectories. In addition to the origins and terminations of projections, it would be valuable to determine their spatial trajectories. Such data would be particularly useful, for example, in understanding the impact of white matter lesions.
- Compatibility with high-resolution methods for targeted investigations. While the primary imaging data should be obtained with light microscopy, electron microscopy or other high-resolution imaging methods could enable more detailed study of particular systems, provided the experimental protocols remain compatible with such techniques.
- Characterization of intersubject variability. As discussed above, quantifying the variability of observed connectivity patterns would be valuable. This would require additional informatics methods and a substantially larger number of experiments than needed for estimating a single “map.”
Where Are We Now?
Assessing the extent of current connectivity knowledge in various species is difficult because virtually all aspects of previous reports, including the specifics of animals used, experimental methodology, anatomical nomenclature, and presentation of results have varied across studies and laboratories. Furthermore, published data often include only processed results in the form of prose, tables, and schematic illustrations, while primary materials including original tissue sections sit on laboratory shelves.
A small number of public repositories for connectivity information are available (see Table 1), including two major efforts to manually curate reports for specific species. The CoCoMac (Collations of Connectivity data on the Macaque Brain) database catalogs axonal tracing studies from the monkey literature , (approximately 400 literature reports detailing ~2,800 tracer injections), while the Brain Architecture Management System (BAMS) focuses on the rat , (328 references describing about 43,000 reported connections). Both systems organize connections based on discrete brain regions identified by the original authors according to a particular map or anatomical parcellation and use inference engines ,, to attempt to reconcile results across different parcellation schemes and nomenclature systems. These reconciliation processes possess considerable uncertainties, and the data remain very sparse; thus, any comprehensive picture of brain connectivity is not currently possible from such resources. The FACCS (Functional Anatomy of the Cerebro–Cerebellar System) database  is a strong effort to map connectivity data into a common spatial framework, but is currently limited in scope to the rat cerebrocerebellar system. Our understanding of the overall architecture of model nervous systems is currently limited to very simple organisms such as the nematode Caenorhabditis elegans .
Much of our theoretical knowledge of human brain connectivity comes from either very old sources  or from inference from varied reports in other species. Bürgel et al.  have developed a probabilistic atlas localizing major fiber bundles based on myelin staining in postmortem human brains, but these maps are very coarse and lack specificity in terms of termination zones. New technological developments such as diffusion-weighted magnetic resonance imaging (MRI) and computational techniques based on correlations in measured time series provide non-invasive methods for inferring some aspects of brain connectivity, but these methods necessarily require validation and should be complemented with more direct measurements. While an experimental program for the precise mapping of connectivity patterns in the human nervous system will require additional technological development, we are well-positioned to push forward with a systematic high-throughput experimental program for model organisms using mostly existing methods.
A Survey of Available Techniques
Reviews of the history  and application of various techniques for determining anatomical connectivity can be found elsewhere ,, and a further survey is presented in Text S1. Here we elaborate on methodologies suitable for the proposed experimental program.
Neuronal tracers allow injected molecules to be distributed within intact living neurons through active intra-axonal transport mechanisms. Tracer substances (see Text S1 for further details and properties) can be described by their preferred direction of transport, although labeling is often not exclusively unidirectional. Importantly, the majority of neuronal tracers can only be transported within a cell and do not cross the synapse; their utility in revealing the connectivity between brain areas is in tracing projection neurons either from axon terminals to potentially distant cell bodies, or vice versa. Retrograde transport (from axon terminal to cell body) is used to label the cells projecting to a particular target region, while anterograde transport (from cell bodies to axon terminals) allows for labeling the projection terminal regions of a cell or group of cells.
Modern “conventional” tracers yield strong, high-resolution labeling of fine processes, and can often be used in combination with one another, with histochemical techniques, genetic markers, light or electron microscopy, and a variety of delivery mechanisms. While there are many tracers that may prove suitable in a large-scale connectivity mapping project, phaseolus vulgaris–leucoagglutinin (PHA-L)  and high molecular weight (10 kDa) biotinylated dextran amines (BDA) ,, both of which have now been used extensively and are transported primarily in the anterograde direction over sufficiently long distances, are strong candidates for high-throughput use. Either tracer can also be used in conjunction with a second high-resolution tracer such as cholera toxin subunit B (CTB) , which is transported primarily in the retrograde direction, in a multiple labeling protocol ,. Such multi-tracer methods allow a single experiment to be used to probe the inputs and outputs for a particular injection site at a relatively low additional cost in the detection process.
Some tracer substances, and in particular neurotropic viruses such as rabies virus  and the alpha herpes viruses ,, can be transported transneuronally to label either presynaptic or postsynaptic cells. Viruses enter first-order neurons, replicate, and are transferred at or near the synapse to second-order cells where replication occurs again, thus continuing a self-amplification process. Viral spread, however, has a variable time course (which depends on projection strength), thus often making, for example, differentiation of weak first-order and strong second-order projections difficult, although this problem may be alleviated by using genetically engineered viruses that cross only a single synapse .
Replication-incompetent viral vectors engineered from adeno-associated virus (AAV), lentivirus, herpesvirus, and others can be used to drive high expression of fluorescent proteins as anterograde and retrograde tracers. These methods can have higher sensitivity than conventional tracer methods –. In addition, the number and types of infected neurons can be characterized, facilitating the pooling of data across multiple experiments. These viral reagents can be used in combination with transgenic mouse lines to label specific cell types –. It is clear that these and other genetic techniques will continue to gain prominence in neuroanatomy .
How Will We Get There?
The first and primary phase of our proposal is to systematically map mesoscale connectivity in the mouse brain using standardized methods to label neuronal projections in combination with optical microscopy. The mouse, as opposed to rat, is the preferred rodent model due to its increasing use in neuroscience , the ease of use of transgenic methods, and the availability of large-scale spatial gene expression data in the brain ,. Accordingly, results from the mouse will be readily reconcilable with existing data, and new anatomical methods should be quickly applicable, supplying diverse information to supplement the initial experiments. A sample workflow, timeline, and cost estimates for a comprehensive mouse connectivity project are included in Text S2. We estimate that the complete mouse project can be completed in five years at a total cost of less than US$20 million, using five replicated experimental pipelines, each consisting of uniform experimental equipment with technicians implementing standardized protocols. Increasing the number of pipelines would proportionately reduce the timeline.
The proposed protocol calls for systematic injections of conventional tracers and/or viral vectors in the young adult mouse, age-matched and weight-matched to an existing stereotaxic brain atlas. The ABA has established a standard by using male, 56-day-old C57BL/6J mice , and this group has developed a corresponding anatomical reference atlas that is a reasonable choice to be adopted for this project. It is vital that the mouse strains, ages, and atlases used are common across the project. Furthermore, all surgical procedures, injection methods, histological techniques, and experimental apparatus should be uniform to reduce variability in results. The use of motorized stereotaxic manipulators with encoded positions relative to standard landmarks, and the incorporation of automation where possible within the experimental protocols will greatly aid this task. Equipment is now available for automated or semi-automated scanning and digitization of labeled sections at submicron resolution using fluorescence or bright field microscopy (see Text S1) and will form a critical piece of the experimental pipeline. Digitized images will be transferred into a distributed data-processing pipeline for automated analysis of the experimental results and entry into a public database.
The project will necessitate further development of algorithms to reliably extract wiring information from digitized images, and to bring data from different sections and animals into register with one another. Photomicrographs from an individual animal must be registered in 3D while accounting for tissue distortions, a process that can be improved by acquiring low-resolution reference block face images prior to cutting each section . Detection of labeled cell bodies or clusters of cells and 3D registration to a Nissl-based atlas are problems that have been previously addressed on a large scale, for example, in the ABA . Detection of labeled axonal segments is somewhat more challenging, and typically relies on (sometimes software-assisted) manual tracing, but progress has been made toward providing automated, quantitative estimates of axon length and density ,. Importantly, the objective of the analysis stream need not be to reconstruct individual neurons, but rather to detect and quantify labeled areas outside of the injection site and represent those data in a common framework (see also ).
A high-throughput investigation in primates, on the scale proposed for mouse, is not feasible. Primate experiments are tremendously more costly, and the monkey brain is considerably larger, more complex, and more variable than mouse. It is therefore of critical importance that: 1) results from previous connectivity studies in primates are carefully curated from the existing literature, leveraging ongoing efforts such as CoCoMac ,; 2) efforts are made to systematically digitize slides that remain available from previous studies following such efforts as BrainMaps.org ; and 3) targeted experiments using standardized protocols are put in place that yield maximal data to validate and “fill in” the mesoscopic connectivity matrix for the macaque. See Text S3 for further details for a proposed primate connectivity project.
The success of the proposed efforts will hinge on the ability to coordinate activities across laboratories while maintaining quality control, to automate the analysis of acquired data, to store both raw and processed data, and to make the integrated results reliably available to different user groups through intuitive interfaces. Management of the large-scale dataset will require significant computational equipment and informatics expertise, some of which is likely to be distributed across multiple sites. The scope of the proposed project demands a customized laboratory information management system (LIMS) to organize and track tasks and materials within and across sites. Much can be learned from the informatics procedures carried out at the Allen Institute for Brain Science  and from the significant data-sharing efforts in genomics and bioinformatics ,.
A major challenge is to develop an appropriate structured database to store the results of injection experiments, digitized legacy data, and associated metadata. In the CoCoMac and BAMS databases, the underlying data model of anatomy is discrete; that is, each “connection” is associated with a pair of discrete brain sites. Through systematic injections, and by preserving and storing primary image data, it is possible for the underlying data to be represented in analog form. Spatial databases  as used in geographical information systems and, in some cases, neuroscience  provide many of the necessary tools once the underlying data model (e.g., coordinate system) has been established. Anatomical parcellations based on different atlases may then be probabilistically registered to this coordinate space to enable the representation of the full connectivity data in the form of connectivity graphs or matrices, with “nodes” defined by the particular parcellation. The SumsDB database (http://sumsdb.wustl.edu/sums), for example, includes a surface-based macaque atlas containing many anatomical partitioning schemes registered to a common spatial framework, along with maps of neuronal connectivity from retrograde tracer injections registered from individual subjects to the atlas . Representation in the continuous space additionally allows for a post-hoc analysis that solves for the partitioning of brain space that best follows the connectivity patterns observed in the data.
Technology Development and Evaluation for Human Studies
The ultimate goal of our proposal to experimentally map brainwide connectivity patterns is to arrive at a comprehensive understanding of the architecture of the human brain. A much-improved partial understanding can be obtained from the proposed efforts in mouse and macaque, and a proposal has been made for a human connectivity project that would rely primarily on neuroimaging techniques . Still, resources should be devoted to developing classical neuroanatomical techniques that are viable for humans. There have been sporadic efforts to increase the speed of action for lipophilic carbocyanine dyes when used in fixed postmortem human tissue ,, and these and other efforts should be studied further. Additionally, imaging methods including diffusion tensor imaging and diffusion spectrum imaging, as well as computational techniques for the assessment of “functional” or “effective” connectivity  can be validated by supplementing tracer studies in macaque with MRI data acquisition in the same animals. Such efforts are essential to ultimately reversing the backwardness of human neuroanatomy.
The largest current gap that exists between the genotype and phenotype in neuroscience is at the level of brain connectivity. There is thus enormous potential value in the acquisition of comprehensive, unified connectivity maps in model organisms. We have proposed a concerted effort within the neuroscience community to determine these connectivity patterns brainwide at the tractable yet representative mesoscopic scale, first in the mouse and followed by additional efforts for the macaque and eventually humans. The mouse proposal is based on existing methods, scaled up, and standardized for high-throughput experimentation. This effort would be complementary to, and would provide “scaffolding” for, additional anatomical projects using different emerging technologies, and can be integrated with existing resources such as the ABA to probe various levels of structural and functional organization. Examination of a potential project plan demonstrates that such an effort would be relatively inexpensive in terms of both money and time (see Text S2) compared with its potential value in neuroscience and biomedicine. If successful, similar projects could be undertaken for model organisms including vertebrates such as rat, zebrafish, zebra finch, and chick, and invertebrates such as jellyfish, flatworms, and drosophila, enabling comparative neuroanatomical studies that are currently well beyond reach.
While the principal objective of the proposed project is to characterize and make available a “wiring diagram,” the public availability of raw data is vital to allow researchers to form their own, perhaps more detailed, interpretation of the individual results. Technological advances have only recently made it feasible to capture and store the voluminous raw image data at submicron resolution, and to serve these images over the Web. The spirit of collaboration and open data access requisite in this proposal is also currently reflected in increasing proportions within the neuroscience community and within funding agencies, as reflected, for example, in the NIH Blueprint for Neuroscience Research  and in international neuroinformatics initiatives . Thus, we may be at a point in time that makes a project of this sort uniquely feasible. Realizing the vision put forth here will require additional planning, input from the community, and financial support. Moreover, eventually determining the connectivity matrix for human will require additional technical development. The hope, however, is that this proposal has made both the importance and the viability of brainwide connectivity projects apparent, and that we can move from planning to action on a short timescale.
Survey of methods relevant for determining neuronal connectivity. To supplement the discussion provided in the main article, here we provide a brief general overview of experimental methods for determining and imaging neuronal connection patterns.
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Example workflow, informatics requirements, timeline, and cost estimates for mouse connectivity project. Here we describe in greater detail a possible experimental pipeline and data analysis workflow for a systematic study of mesoscale mouse brain connectivity using neuroanatomical tracers.
(1.43 MB PDF)
Brief proposal for primate connectivity project. We describe an approach to better understand connectivity in the macaque brain that includes collating and digitizing existing materials as well as implementing specifically targeted experiments with standard protocols.
(0.15 MB PDF)
This paper was prepared as part of the Brain Architecture Project at Cold Spring Harbor Laboratory, following discussions at the 2007 and 2008 Banbury Center meetings with a working group of scientists who are listed alphabetically as middle authors. P. Mitra, L. Swanson, J. Doyle, H. Breiter, and C. Allen were instrumental in the planning and assembly of the Brain Architecture Project.
- 1. Crick F, Jones E (1993) Backwardness of human neuroanatomy. Nature 361: 109–110.
- 2. Bota M, Swanson LW (2007) Online workbenches for neural network connections. J Comp Neurol 500: 807–814.
- 3. Lein ES, Hawrylycz MJ, Ao N, Ayres M, Bensinger A, et al. (2007) Genome-wide atlas of gene expression in the adult mouse brain. Nature 445: 168–176.
- 4. Jarvis ED, Gunturkun O, Bruce L, Csillag A, Karten H, et al. (2005) Avian brains and a new understanding of vertebrate brain evolution. Nat Rev Neurosci 6: 151–159.
- 5. Geschwind N (1965) Disconnexion syndromes in animals and man. I. Brain 88: 237–294.
- 6. Wernicke K (1977) The Aphasia Symptom-Complex: A Psychological Study on an Anatomical Basis. In: Eggert G, editor. Wernicke's Works on Aphasia. The Hague: Mouton. pp. 92–117.
- 7. Johnson MD, Miocinovic S, McIntyre CC, Vitek JL (2008) Mechanisms and targets of deep brain stimulation in movement disorders. Neurotherapeutics 5: 294–308.
- 8. Bullmore ET, Frangou S, Murray RM (1997) The dysplastic net hypothesis: an integration of developmental and dysconnectivity theories of schizophrenia. Schizophr Res 28: 143–156.
- 9. Frith U (2001) Mind blindness and the brain in autism. Neuron 32: 969–979.
- 10. Démonet JF, Taylor MJ, Chaix Y (2004) Developmental dyslexia. Lancet 363: 1451–1460.
- 11. Egaas B, Courchesne E, Saitoh O (1995) Reduced size of corpus callosum in autism. Arch Neurol 52: 794–801.
- 12. Hardan AY, Minshew NJ, Keshavan MS (2000) Corpus callosum size in autism. Neurology 55: 1033–1036.
- 13. Castelli F, Frith C, Happe F, Frith U (2002) Autism, Asperger syndrome and brain mechanisms for the attribution of mental states to animated shapes. Brain 125: 1839–1849.
- 14. Just MA, Cherkassky VL, Keller TA, Minshew NJ (2004) Cortical activation and synchronization during sentence comprehension in high-functioning autism: evidence of underconnectivity. Brain 127: 1811–1821.
- 15. Murias M, Webb SJ, Greenson J, Dawson G (2007) Resting state cortical connectivity reflected in EEG coherence in individuals with autism. Biol Psychiatry 62: 270–273.
- 16. Folstein S (1996) Twin and adoption studies in child and adolescent psychiatric disorders. Curr Opin Pediatr 8: 339–347.
- 17. Panksepp J (1998) Affective neuroscience: The foundations of human and animal emotions. New York: Oxford University Press.
- 18. Breiter HC, Gasic GP (2004) A general circuitry processing reward/aversion information and its implications for neuropsychiatric illness. In: Gazzaniga M, editor. The Cognitive Neurosciences III. Cambridge: MIT Press. pp. 1043–1065.
- 19. Panksepp J (2006) Emotional endophenotypes in evolutionary psychiatry. Prog Neuropsychopharmacol Biol Psychiatry 30: 774–784.
- 20. Gustafson C, Bug WJ, Nissanov J (2007) NeuroTerrain—a client-server system for browsing 3D biomedical image data sets. BMC Bioinformatics 8: 40.
- 21. MacKenzie-Graham A, Jones ES, Shattuck DW, Dinov ID, Bota M, et al. (2003) The informatics of a C57BL/6J mouse brain atlas. Neuroinformatics 1: 397–410.
- 22. Visel A, Thaller C, Eichele G (2004) GenePaint.org: an atlas of gene expression patterns in the mouse embryo. Nucleic Acids Res 32: D552–D556.
- 23. Kotter R (2004) Online retrieval, processing, and visualization of primate connectivity data from the CoCoMac database. Neuroinformatics 2: 127–144.
- 24. Stephan KE, Kamper L, Bozkurt A, Burns GA, Young MP, et al. (2001) Advanced database methodology for the Collation of Connectivity data on the Macaque brain (CoCoMac). Philos Trans R Soc Lond B Biol Sci 356: 1159–1186.
- 25. Bota M, Dong HW, Swanson LW (2003) From gene networks to brain networks. Nat Neurosci 6: 795–799.
- 26. Bota M, Dong HW, Swanson LW (2005) Brain architecture management system. Neuroinformatics 3: 15–48.
- 27. Kotter R, Wanke E (2005) Mapping brains without coordinates. Philos Trans R Soc Lond B Biol Sci 360: 751–766.
- 28. Stephan KE, Zilles K, Kotter R (2000) Coordinate-independent mapping of structural and functional data by objective relational transformation (ORT). Philos Trans R Soc Lond B Biol Sci 355: 37–54.
- 29. Bjaalie JG, Leergaard TB, Lillehaug S, Odeh F, Moene IA, et al. (2005) Database and tools for analysis of topographic organization and map transformations in major projection systems of the brain. Neuroscience 136: 681–695.
- 30. White JG, Southgate E, Thomson JN, Brenner S (1986) The Structure of the Nervous System of the Nematode Caenorhabditis elegans. Philos Trans R Soc Lon Ser B Biol Sci 314: 1–340.
- 31. Dejerine J (1895) Anatomie des centres nerveux. Paris: Rueff.
- 32. Burgel U, Amunts K, Hoemke L, Mohlberg H, Gilsbach JM, et al. (2006) White matter fiber tracts of the human brain: three-dimensional mapping at microscopic resolution, topography and intersubject variability. Neuroimage 29: 1092–1105.
- 33. Schmahmann JD, Pandya DN (2007) Cerebral white matter—historical evolution of facts and notions concerning the organization of the fiber pathways of the brain. J Hist Neurosci 16: 237–267.
- 34. Kobbert C, Apps R, Bechmann I, Lanciego JL, Mey J, et al. (2000) Current concepts in neuroanatomical tracing. Prog Neurobiol 62: 327–351.
- 35. Vercelli A, Repici M, Garbossa D, Grimaldi A (2000) Recent techniques for tracing pathways in the central nervous system of developing and adult mammals. Brain Res Bull 51: 11–28.
- 36. Gerfen CR, Sawchenko PE (1984) An anterograde neuroanatomical tracing method that shows the detailed morphology of neurons, their axons and terminals: immunohistochemical localization of an axonally transported plant lectin, Phaseolus vulgaris leucoagglutinin (PHA-L). Brain Res 290: 219–238.
- 37. Reiner A, Veenman CL, Medina L, Jiao Y, Del Mar N, et al. (2000) Pathway tracing using biotinylated dextran amines. J Neurosci Methods 103: 23–37.
- 38. Veenman CL, Reiner A, Honig MG (1992) Biotinylated dextran amine as an anterograde tracer for single- and double-labeling studies. J Neurosci Methods 41: 239–254.
- 39. Luppi PH, Fort P, Jouvet M (1990) Iontophoretic application of unconjugated cholera toxin B subunit (CTb) combined with immunohistochemistry of neurochemical substances: a method for transmitter identification of retrogradely labeled neurons. Brain Res 534: 209–224.
- 40. Coolen LM, Jansen HT, Goodman RL, Wood RI, Lehman MN (1999) A new method for simultaneous demonstration of anterograde and retrograde connections in the brain: co-injections of biotinylated dextran amine and the beta subunit of cholera toxin. J Neurosci Methods 91: 1–8.
- 41. Lanciego JL, Luquin MR, Guillen J, Gimenez-Amaya JM (1998) Multiple neuroanatomical tracing in primates. Brain Res Brain Res Protoc 2: 323–332.
- 42. Kelly RM, Strick PL (2000) Rabies as a transneuronal tracer of circuits in the central nervous system. J Neurosci Methods 103: 63–71.
- 43. Aston-Jones G, Card JP (2000) Use of pseudorabies virus to delineate multisynaptic circuits in brain: opportunities and limitations. J Neurosci Methods 103: 51–61.
- 44. Ekstrand MI, Enquist LW, Pomeranz LE (2008) The alpha-herpesviruses: molecular pathfinders in nervous system circuits. Trends Mol Med 14: 134–140.
- 45. Wickersham IR, Lyon DC, Barnard RJ, Mori T, Finke S, et al. (2007) Monosynaptic restriction of transsynaptic tracing from single, genetically targeted neurons. Neuron 53: 639–647.
- 46. Grinevich V, Brecht M, Osten P (2005) Monosynaptic pathway from rat vibrissa motor cortex to facial motor neurons revealed by lentivirus-based axonal tracing. J Neurosci 25: 8250–8258.
- 47. Hattox AM, Priest CA, Keller A (2002) Functional circuitry involved in the regulation of whisker movements. J Comp Neurol 442: 266–276.
- 48. Miyashita E, Keller A, Asanuma H (1994) Input–output organization of the rat vibrissal motor cortex. Exp Brain Res 99: 223–232.
- 49. Atasoy D, Aponte Y, Su HH, Sternson SM (2008) A FLEX switch targets Channelrhodopsin-2 to multiple cell types for imaging and long-range circuit mapping. J Neurosci 28: 7025–7030.
- 50. Davidson BL, Breakefield XO (2003) Viral vectors for gene delivery to the nervous system. Nat Rev Neurosci 4: 353–364.
- 51. DeFalco J, Tomishima M, Liu H, Zhao C, Cai X, et al. (2001) Virus-assisted mapping of neural inputs to a feeding center in the hypothalamus. Science 291: 2608–2613.
- 52. Callaway EM (2005) A molecular and genetic arsenal for systems neuroscience. Trends Neurosci 28: 196–201.
- 53. Lin JM, Bohland JW, Andrews P, Burns GA, Allen CB, et al. (2008) An analysis of the abstracts presented at the annual meetings of the Society for Neuroscience from 2001 to 2006. PLoS ONE 3: e2052. doi:10.1371/journal.pone.0002052.
- 54. Toga AW, Banerjee PK (1993) Registration revisited. J Neurosci Methods 48: 1–13.
- 55. Ng L, Pathak SD, Kuan C, Lau C, Dong H, et al. (2007) Neuroinformatics for genome-wide 3D gene expression mapping in the mouse brain. IEEE-ACM Transactions on Computational Biology and Bioinformatics 4: 382–393.
- 56. Broser PJ, Erdogan S, Grinevich V, Osten P, Sakmann B, et al. (2008) Automated axon length quantification for populations of labelled neurons. J Neurosci Methods 169: 43–54.
- 57. Lillehaug S, Oyan D, Leergaard TB, Bjaalie JG (2002) Comparison of semi-automatic and automatic data acquisition methods for studying three-dimensional distributions of large neuronal populations and axonal plexuses. Network 13: 343–356.
- 58. Bjaalie JG, Leergaard TB (2006) Three-dimensional computerized reconstruction from serial sections: cells populations, regions, and whole brain. In: Zaborszky L, Wouterlood FG, Lanciego JL, editors. Neuroanatomical Tract Tracing: Molecules, Neurons, & Systems. New York: Springer. pp. 530–565.
- 59. Mikula S, Trotts I, Stone JM, Jones EG (2007) Internet-enabled high-resolution brain mapping and virtual microscopy. Neuroimage 35: 9–15.
- 60. Benson DA, Karsch-Mizrachi I, Lipman DJ, Ostell J, Wheeler DL (2007) GenBank. Nucleic Acids Res 35: D21–D25.
- 61. Stein L, Sternberg P, Durbin R, Thierry-Mieg J, Spieth J (2001) WormBase: network access to the genome and biology of Caenorhabditis elegans. Nucleic Acids Res 29: 82–86.
- 62. Güting RH (1994) An introduction to spatial database systems. The VLDB Journal The International Journal on Very Large Data Bases 3: 357–399.
- 63. Van Essen DC, Dierker DL (2007) Surface-based and probabilistic atlases of primate cerebral cortex. Neuron 56: 209–225.
- 64. Van Essen DC, Harwell J, Hanlon D, Dickson J (2005) Surface-based atlases and a database of cortical structure and function. In: Koslow SH, Subramaniam S, editors. Databasing the Brain: From Data to Knowledge (Neuroinformatics). John Wiley & Sons. pp. 369–388.
- 65. Sporns O, Tononi G, Kotter R (2005) The human connectome: A structural description of the human brain. PLoS Comput Biol 1: e42.
- 66. Sparks DL, Lue LF, Martin TA, Rogers J (2000) Neural tract tracing using Di-I: a review and a new method to make fast Di-I faster in human brain. J Neurosci Methods 103: 3–10.
- 67. Swift MJ, Crago PE, Grill WM (2005) Applied electric fields accelerate the diffusion rate and increase the diffusion distance of DiI in fixed tissue. J Neurosci Methods 141: 155–163.
- 68. Horwitz B (2003) The elusive concept of brain connectivity. Neuroimage 19: 466–470.
- 69. Baughman RW, Farkas R, Guzman M, Huerta MF (2006) The National Institutes of Health Blueprint for Neuroscience Research. J Neurosci 26: 10329–10331.
- 70. Bjaalie JG, Grillner S (2007) Global neuroinformatics: the International Neuroinformatics Coordinating Facility. J Neurosci 27: 3613–3615.
- 71. Markram H, Luo X, Silberberg G, Toledo-Rodriguez M, Gupta A (2005) The Neocortical Microcircuit Database. In: Koslow SH, Subramaniam S, editors. Databasing the Brain: From Data to Knowledge (Neuroinformatics). Hoboken, NJ: John Wiley & Sons. pp. 327–342.
- 72. Oishi K, Zilles K, Amunts K, Faria A, Jiang H, et al. (2008) Human brain white matter atlas: identification and assignment of common anatomical structures in superficial white matter. Neuroimage 43: 447–457.