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Sci Rep. 2018 Sep 13;8(1):13737. doi: 10.1038/s41598-018-31132-y.

RNA-Seq Analysis of Spinal Cord Tissues from hPFN1G118V Transgenic Mouse Model of ALS at Pre-symptomatic and End-Stages of Disease.

Author information

1
Department of Pharmacology and Toxicology, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
2
Department of Biochemistry and Molecular Genetics, University of Alabama at Birmingham, Birmingham, AL, USA.
3
Department of Biochemistry and Molecular Biology, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
4
Department of Biomedical Informatics, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
5
Department of Pharmacology and Toxicology, University of Arkansas for Medical Sciences, Little Rock, AR, USA. MKiaei@UAMS.edu.
6
Department of Geriatrics, University of Arkansas for Medical Sciences, Little Rock, AR, USA. MKiaei@UAMS.edu.
7
Department of Neurology, University of Arkansas for Medical Sciences, Little Rock, AR, USA. MKiaei@UAMS.edu.

Abstract

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that leads to the loss of motor neurons. The molecular mechanisms of motor neuron degeneration are largely unknown and there are currently no effective therapies to treat this disease. In this work, we report whole transcriptome profiling of spinal cords of mutant transgenic hPFN1G118V mice and their wildtype transgenic hPFN1WT controls at a pre-symptomatic stage and at the end-stage of disease. Analyses revealed that end-stage hPFN1G118V mice had 890 differentially expressed genes (747 up-regulated, 143 down-regulated) when compared to pre-symptomatic hPFN1G118V mice, and they had 836 differentially expressed genes (742 up-regulated, 94 down-regulated) when compared to age-matched hPFN1WT controls. Pre-symptomatic hPFN1G118V mice were not significantly different from age-matched hPFN1WT controls. Ingenuity Pathway Analysis identified inflammatory pathways significantly activated in end-stage hPFN1G118V samples, suggesting an excess of glial activation at end-stage disease, possibly due to an increase in glial composition within the spinal cord during disease progression. In conclusion, our RNA-Seq data identified molecules and pathways involved in the mechanisms of neurodegeneration that could potentially serve as therapeutic targets for ALS.

PMID:
30213953
PMCID:
PMC6137178
DOI:
10.1038/s41598-018-31132-y
[Indexed for MEDLINE]
Free PMC Article

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