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T cell deficiency in spinal cord injury: altered locomotor recovery and whole-genome transcriptional analysis

Overview of attention for article published in BMC Neuroscience, November 2015
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Title
T cell deficiency in spinal cord injury: altered locomotor recovery and whole-genome transcriptional analysis
Published in
BMC Neuroscience, November 2015
DOI 10.1186/s12868-015-0212-0
Pubmed ID
Authors

David Satzer, Catherine Miller, Jacob Maxon, Joseph Voth, Christina DiBartolomeo, Rebecca Mahoney, James R. Dutton, Walter C. Low, Ann M. Parr

Abstract

T cells undergo autoimmunization following spinal cord injury (SCI) and play both protective and destructive roles during the recovery process. T cell-deficient athymic nude (AN) rats exhibit improved functional recovery when compared to immunocompetent Sprague-Dawley (SD) rats following spinal cord transection. In the present study, we evaluated locomotor recovery in SD and AN rats following moderate spinal cord contusion. To explain variable locomotor outcome, we assessed whole-genome expression using RNA sequencing, in the acute (1 week post-injury) and chronic (8 weeks post-injury) phases of recovery. Athymic nude rats demonstrated greater locomotor function than SD rats only at 1 week post-injury, coinciding with peak T cell infiltration in immunocompetent rats. Genetic markers for T cells and helper T cells were acutely enriched in SD rats, while AN rats expressed genes for Th2 cells, cytotoxic T cells, NK cells, mast cells, IL-1a, and IL-6 at higher levels. Acute enrichment of cell death-related genes suggested that SD rats undergo secondary tissue damage from T cells. Additionally, SD rats exhibited increased acute expression of voltage-gated potassium (Kv) channel-related genes. However, AN rats demonstrated greater chronic expression of cell death-associated genes and less expression of axon-related genes. Immunostaining for macrophage markers revealed no T cell-dependent difference in the acute macrophage infiltrate. We put forth a model in which T cells facilitate early tissue damage, demyelination, and Kv channel dysregulation in SD rats following contusion SCI. However, compensatory features of the immune response in AN rats cause delayed tissue death and limit long-term recovery. T cell inhibition combined with other neuroprotective treatment may thus be a promising therapeutic avenue.

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The data shown below were compiled from readership statistics for 50 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 2 4%
Unknown 48 96%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 14 28%
Student > Bachelor 11 22%
Researcher 6 12%
Professor > Associate Professor 4 8%
Student > Postgraduate 3 6%
Other 7 14%
Unknown 5 10%
Readers by discipline Count As %
Neuroscience 12 24%
Agricultural and Biological Sciences 10 20%
Medicine and Dentistry 10 20%
Biochemistry, Genetics and Molecular Biology 8 16%
Immunology and Microbiology 1 2%
Other 2 4%
Unknown 7 14%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 08 November 2015.
All research outputs
#18,430,119
of 22,832,057 outputs
Outputs from BMC Neuroscience
#882
of 1,245 outputs
Outputs of similar age
#205,462
of 285,670 outputs
Outputs of similar age from BMC Neuroscience
#29
of 44 outputs
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