1
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Brain-wide analysis of the supraspinal connectome reveals anatomical correlates to functional recovery after spinal injury

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          The supraspinal connectome is essential for normal behavior and homeostasis and consists of numerous sensory, motor, and autonomic projections from brain to spinal cord. Study of supraspinal control and its restoration after damage has focused mostly on a handful of major populations that carry motor commands, with only limited consideration of dozens more that provide autonomic or crucial motor modulation. Here, we assemble an experimental workflow to rapidly profile the entire supraspinal mesoconnectome in adult mice and disseminate the output in a web-based resource. Optimized viral labeling, 3D imaging, and registration to a mouse digital neuroanatomical atlas assigned tens of thousands of supraspinal neurons to 69 identified regions. We demonstrate the ability of this approach to clarify essential points of topographic mapping between spinal levels, measure population-specific sensitivity to spinal injury, and test the relationships between region-specific neuronal sparing and variability in functional recovery. This work will spur progress by broadening understanding of essential but understudied supraspinal populations.

          Related collections

          Most cited references101

          • Record: found
          • Abstract: found
          • Article: not found

          A mesoscale connectome of the mouse brain.

          Comprehensive knowledge of the brain's wiring diagram is fundamental for understanding how the nervous system processes information at both local and global scales. However, with the singular exception of the C. elegans microscale connectome, there are no complete connectivity data sets in other species. Here we report a brain-wide, cellular-level, mesoscale connectome for the mouse. The Allen Mouse Brain Connectivity Atlas uses enhanced green fluorescent protein (EGFP)-expressing adeno-associated viral vectors to trace axonal projections from defined regions and cell types, and high-throughput serial two-photon tomography to image the EGFP-labelled axons throughout the brain. This systematic and standardized approach allows spatial registration of individual experiments into a common three dimensional (3D) reference space, resulting in a whole-brain connectivity matrix. A computational model yields insights into connectional strength distribution, symmetry and other network properties. Virtual tractography illustrates 3D topography among interconnected regions. Cortico-thalamic pathway analysis demonstrates segregation and integration of parallel pathways. The Allen Mouse Brain Connectivity Atlas is a freely available, foundational resource for structural and functional investigations into the neural circuits that support behavioural and cognitive processes in health and disease.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            A Designer AAV Variant Permits Efficient Retrograde Access to Projection Neurons

            Efficient retrograde access to projection neurons for the delivery of sensors and effectors constitutes an important and enabling capability for neural circuit dissection. Such an approach would also be useful for gene therapy, including the treatment of neurodegenerative disorders characterized by pathological spread through functionally connected and highly distributed networks. Viral vectors, in particular, are powerful gene delivery vehicles for the nervous system, but all available tools suffer from inefficient retrograde transport or limited clinical potential. To address this need, we applied in vivo directed evolution to engineer potent retrograde functionality into the capsid of adeno-associated virus (AAV), a vector that has shown promise in neuroscience research and the clinic. A newly evolved variant, rAAV2-retro, permits robust retrograde access to projection neurons with efficiency comparable to classical synthetic retrograde tracers and enables sufficient sensor/effector expression for functional circuit interrogation and in vivo genome editing in targeted neuronal populations. VIDEO ABSTRACT.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              mScarlet: a bright monomeric red fluorescent protein for cellular imaging

              An extremely bright, truly monomeric RFP, mScarlet, is described that outperforms existing RFPs in diverse labeling applications, especially in FRET with ratiometric imaging.
                Bookmark

                Author and article information

                Contributors
                Role: Reviewing Editor
                Role: Senior Editor
                Journal
                eLife
                Elife
                eLife
                eLife
                eLife Sciences Publications, Ltd
                2050-084X
                15 July 2022
                2022
                : 11
                : e76254
                Affiliations
                [1 ] Department of Biomedical Sciences, Marquette University ( https://ror.org/04gr4te78) Milwaukee United States
                [2 ] Department of Neurological Surgery, University of Miami ( https://ror.org/02dgjyy92) Miami United States
                [3 ] Helen and Robert Appel Alzheimer's Disease Research Institute, Cornell University ( https://ror.org/05bnh6r87) New York United States
                CNRS Université de Bordeaux ( https://ror.org/02feahw73) France
                Emory University ( https://ror.org/03czfpz43) United States
                CNRS Université de Bordeaux ( https://ror.org/02feahw73) France
                CNRS Université de Bordeaux ( https://ror.org/02feahw73) France
                Université Paris-Saclay, CNRS ( https://ror.org/02feahw73) France
                University of Louisville ( https://ror.org/01ckdn478) United States
                Author information
                https://orcid.org/0000-0001-8041-5561
                https://orcid.org/0000-0003-3668-3694
                https://orcid.org/0000-0003-1974-6366
                https://orcid.org/0000-0001-9345-6688
                Article
                76254
                10.7554/eLife.76254
                9345604
                35838234
                577ac1c2-fc2c-434a-8c17-630bc2b32646
                © 2022, Wang et al

                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.

                History
                : 09 December 2021
                : 12 July 2022
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100000002, National Institutes of Health;
                Award ID: R01NS083983
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100012641, The Bryon Riesch Paralysis Foundation;
                Award Recipient :
                Funded by: The Miami Project to Cure Paralysis;
                Award Recipient :
                Funded by: The Buoniconti fund;
                Award Recipient :
                Funded by: State of Florida Red Light Camera Fund;
                Award Recipient :
                The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
                Categories
                Research Article
                Neuroscience
                Custom metadata
                Three-dimensional imaging and automated, brain-wide cell counting yield new insight into the diversity of neurons that connect the brain to the spinal cord and their different sensitivity to spinal cord damage.

                Life sciences
                supraspinal neurons,spinal cord injury,adeno-associated virus,digital neuroanatomical atlas,tissue clearing,3d visualization,mouse

                Comments

                Comment on this article