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      Enriched conditioning expands the regenerative ability of sensory neurons after spinal cord injury via neuronal intrinsic redox signaling

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          Abstract

          Overcoming the restricted axonal regenerative ability that limits functional repair following a central nervous system injury remains a challenge. Here we report a regenerative paradigm that we call enriched conditioning, which combines environmental enrichment (EE) followed by a conditioning sciatic nerve axotomy that precedes a spinal cord injury (SCI). Enriched conditioning significantly increases the regenerative ability of dorsal root ganglia (DRG) sensory neurons compared to EE or a conditioning injury alone, propelling axon growth well beyond the spinal injury site. Mechanistically, we established that enriched conditioning relies on the unique neuronal intrinsic signaling axis PKC-STAT3-NADPH oxidase 2 (NOX2), enhancing redox signaling as shown by redox proteomics in DRG. Finally, NOX2 conditional deletion or overexpression respectively blocked or phenocopied enriched conditioning-dependent axon regeneration after SCI leading to improved functional recovery. These studies provide a paradigm that drives the regenerative ability of sensory neurons offering a potential redox-dependent regenerative model for mechanistic and therapeutic discoveries.

          Abstract

          Pre conditioning injury or environmental enrichment have been shown to promote axon regeneration. Here the authors show that environmental enrichment, combined with preconditioning injury promotes regeneration via a redox signalling dependent mechanism.

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          The PRIDE database and related tools and resources in 2019: improving support for quantification data

          Abstract The PRoteomics IDEntifications (PRIDE) database (https://www.ebi.ac.uk/pride/) is the world’s largest data repository of mass spectrometry-based proteomics data, and is one of the founding members of the global ProteomeXchange (PX) consortium. In this manuscript, we summarize the developments in PRIDE resources and related tools since the previous update manuscript was published in Nucleic Acids Research in 2016. In the last 3 years, public data sharing through PRIDE (as part of PX) has definitely become the norm in the field. In parallel, data re-use of public proteomics data has increased enormously, with multiple applications. We first describe the new architecture of PRIDE Archive, the archival component of PRIDE. PRIDE Archive and the related data submission framework have been further developed to support the increase in submitted data volumes and additional data types. A new scalable and fault tolerant storage backend, Application Programming Interface and web interface have been implemented, as a part of an ongoing process. Additionally, we emphasize the improved support for quantitative proteomics data through the mzTab format. At last, we outline key statistics on the current data contents and volume of downloads, and how PRIDE data are starting to be disseminated to added-value resources including Ensembl, UniProt and Expression Atlas.
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            Targeted neurotechnology restores walking in humans with spinal cord injury

            Spinal cord injury leads to severe locomotor deficits or even complete leg paralysis. Here we introduce targeted spinal cord stimulation neurotechnologies that enabled voluntary control of walking in individuals who had sustained a spinal cord injury more than four years ago and presented with permanent motor deficits or complete paralysis despite extensive rehabilitation. Using an implanted pulse generator with real-time triggering capabilities, we delivered trains of spatially selective stimulation to the lumbosacral spinal cord with timing that coincided with the intended movement. Within one week, this spatiotemporal stimulation had re-established adaptive control of paralysed muscles during overground walking. Locomotor performance improved during rehabilitation. After a few months, participants regained voluntary control over previously paralysed muscles without stimulation and could walk or cycle in ecological settings during spatiotemporal stimulation. These results establish a technological framework for improving neurological recovery and supporting the activities of daily living after spinal cord injury.
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              Histone acetylation and transcriptional regulatory mechanisms.

              K Struhl (1998)
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                Author and article information

                Contributors
                s.di-giovanni@imperial.ac.uk
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                21 December 2020
                21 December 2020
                2020
                : 11
                : 6425
                Affiliations
                [1 ]GRID grid.7445.2, ISNI 0000 0001 2113 8111, Division of Neuroscience, Department of Brain Sciences, , Imperial College London, ; London, UK
                [2 ]GRID grid.13097.3c, ISNI 0000 0001 2322 6764, British Heart Foundation Centre, School of Cardiovascular Medicine and Sciences, James Black Centre, , King’s College London, ; London, UK
                [3 ]GRID grid.26790.3a, ISNI 0000 0004 1936 8606, Miami Project to Cure Paralysis, Center for Computational Sciences, , University of Miami, ; Miami, FL 33136 USA
                [4 ]GRID grid.7839.5, ISNI 0000 0004 1936 9721, Functional Proteomics, Faculty of Medicine, , Goethe University, ; Frankfurt, Germany
                [5 ]GRID grid.10392.39, ISNI 0000 0001 2190 1447, Laboratory for NeuroRegeneration and Repair, Center for Neurology, Hertie Institute for Clinical Brain Research, , University of Tuebingen, ; Tuebingen, Germany
                Author information
                http://orcid.org/0000-0001-6795-2688
                http://orcid.org/0000-0002-7139-8090
                http://orcid.org/0000-0003-1568-5965
                http://orcid.org/0000-0003-3550-7576
                http://orcid.org/0000-0003-1633-5318
                http://orcid.org/0000-0002-9751-8054
                http://orcid.org/0000-0003-3154-5399
                Article
                20179
                10.1038/s41467-020-20179-z
                7752916
                33349630
                174da9a8-15c9-417a-96f1-454c7a4c7343
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 24 February 2020
                : 6 November 2020
                Funding
                Funded by: FundRef https://doi.org/10.13039/501100000265, RCUK | Medical Research Council (MRC);
                Funded by: FundRef https://doi.org/10.13039/501100000833, Rosetrees Trust;
                Funded by: FundRef https://doi.org/10.13039/100012066, Wings for Life (Wings for Life United Kingdom);
                Categories
                Article
                Custom metadata
                © The Author(s) 2020

                Uncategorized
                neuroscience,spinal cord injury
                Uncategorized
                neuroscience, spinal cord injury

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