Proteomic Analysis of the Spatio-temporal Based Molecular Kinetics of Acute Spinal Cord Injury Identifies a Time- and Segment-specific Window for Effective Tissue Repair. Devaux, S., Cizkova, D., Quanico, J., Franck, J., Nataf, S., Pays, L., Hauberg-Lotte, L., Maass, P., Kobarg, J. H., Kobeissy, F., Meriaux, C., Wisztorski, M., Slovinska, L., Blasko, J., Cigankova, V., Fournier, I., & Salzet, M. Mol Cell Proteomics, 15(8):2641–70, 2016. ![Proteomic Analysis of the Spatio-temporal Based Molecular Kinetics of Acute Spinal Cord Injury Identifies a Time- and Segment-specific Window for Effective Tissue Repair [link]](https://bibbase.org/img/filetypes/link.svg "link")
Paper doi abstract bibtex Spinal cord injury (SCI) represents a major debilitating health issue with a direct socioeconomic burden on the public and private sectors worldwide. Although several studies have been conducted to identify the molecular progression of injury sequel due from the lesion site, still the exact underlying mechanisms and pathways of injury development have not been fully elucidated. In this work, based on OMICs, 3D matrix-assisted laser desorption ionization (MALDI) imaging, cytokines arrays, confocal imaging we established for the first time that molecular and cellular processes occurring after SCI are altered between the lesion proximity, i.e. rostral and caudal segments nearby the lesion (R1-C1) whereas segments distant from R1-C1, i.e. R2-C2 and R3-C3 levels coexpressed factors implicated in neurogenesis. Delay in T regulators recruitment between R1 and C1 favor discrepancies between the two segments. This is also reinforced by presence of neurites outgrowth inhibitors in C1, absent in R1. Moreover, the presence of immunoglobulins (IgGs) in neurons at the lesion site at 3 days, validated by mass spectrometry, may present additional factor that contributes to limited regeneration. Treatment in vivo with anti-CD20 one hour after SCI did not improve locomotor function and decrease IgG expression. These results open the door of a novel view of the SCI treatment by considering the C1 as the therapeutic target.
@article{devaux_proteomic_2016,
title = {Proteomic {Analysis} of the {Spatio}-temporal {Based} {Molecular} {Kinetics} of {Acute} {Spinal} {Cord} {Injury} {Identifies} a {Time}- and {Segment}-specific {Window} for {Effective} {Tissue} {Repair}},
volume = {15},
issn = {1535-9484 (Electronic) 1535-9476 (Linking)},
url = {http://www.ncbi.nlm.nih.gov/pubmed/27250205},
doi = {10.1074/mcp.M115.057794},
abstract = {Spinal cord injury (SCI) represents a major debilitating health issue with a direct socioeconomic burden on the public and private sectors worldwide. Although several studies have been conducted to identify the molecular progression of injury sequel due from the lesion site, still the exact underlying mechanisms and pathways of injury development have not been fully elucidated. In this work, based on OMICs, 3D matrix-assisted laser desorption ionization (MALDI) imaging, cytokines arrays, confocal imaging we established for the first time that molecular and cellular processes occurring after SCI are altered between the lesion proximity, i.e. rostral and caudal segments nearby the lesion (R1-C1) whereas segments distant from R1-C1, i.e. R2-C2 and R3-C3 levels coexpressed factors implicated in neurogenesis. Delay in T regulators recruitment between R1 and C1 favor discrepancies between the two segments. This is also reinforced by presence of neurites outgrowth inhibitors in C1, absent in R1. Moreover, the presence of immunoglobulins (IgGs) in neurons at the lesion site at 3 days, validated by mass spectrometry, may present additional factor that contributes to limited regeneration. Treatment in vivo with anti-CD20 one hour after SCI did not improve locomotor function and decrease IgG expression. These results open the door of a novel view of the SCI treatment by considering the C1 as the therapeutic target.},
number = {8},
journal = {Mol Cell Proteomics},
author = {Devaux, S. and Cizkova, D. and Quanico, J. and Franck, J. and Nataf, S. and Pays, L. and Hauberg-Lotte, L. and Maass, P. and Kobarg, J. H. and Kobeissy, F. and Meriaux, C. and Wisztorski, M. and Slovinska, L. and Blasko, J. and Cigankova, V. and Fournier, I. and Salzet, M.},
year = {2016},
keywords = {Animal, Animals, Biomarkers/*metabolism, Cytokines/*metabolism, Disease Models, Humans, Mass, Matrix-Assisted Laser Desorption-Ionization/methods, Protein Array Analysis, Protein Interaction Maps, Proteomics/*methods, Rats, Spectrometry, Spinal Cord Injuries/*metabolism, Time Factors},
pages = {2641--70},
}
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