Downregulation of dual-specificity phosphatase 1 (DUSP1) in post-mortem brain white matter in progressive multiple sclerosis

Dual-specificity phosphatase 1 (DUSP1) is a negative regulator of mitogen-activated protein kinase (MAPK) activity, and a player in the control of glial function. Several disease models have identified that the expression of DUSP1 is altered in tissue samples, which may contribute to disease pathogenesis. Using post-mortem brain tissue from a cohort of progressive multiple sclerosis (MS) cases, this study set out to determine if the expression of DUSP1 is altered in the brain in MS. We employed the use of a combination of PCR, western immunoblotting and immunohistochemical analysis to profile the expression of DUSP1. Data presented herein indicate that DUSP1 is significantly downregulated at gene and protein level in MS white matter tissue, when compared to samples from a non-MS control cohort. We also identify that DUSP1 is expressed on Iba1+ cells in the brain and that ITGAM (CD11b) expression is elevated in white matter in progressive MS. These findings provide evidence that DUSP1 is dysregulated centrally in CNS white matter in progressive MS.

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Publication Details

Journal
Neurological Sciences
Published
2026-03-12
DOI
https://doi.org/10.1007/s10072-026-08944-2
Primary Topic
Protein Tyrosine Phosphatases
Type
article
Field-Weighted Citation Impact
0.00

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article

Downregulation of dual-specificity phosphatase 1 (DUSP1) in post-mortem brain white matter in progressive multiple sclerosis

Hugh Kearney, Melody Cui Sun, Yvonne M. Nolan, Lisa Costelloe et al.
Neurological Sciences
Protein Tyrosine Phosphatases
article

Downregulation of dual-specificity phosphatase 1 (DUSP1) in post-mortem brain white matter in progressive multiple sclerosis

Hugh Kearney, Melody Cui Sun, Yvonne M. Nolan, Lisa Costelloe, Eric J. Downer, Thomas Reilly, Almudena Otálora-Alcaraz, Martí Oró-Nolla, Julia Anandarajah, Richard Magee
article en

Abstract

Dual-specificity phosphatase 1 (DUSP1) is a negative regulator of mitogen-activated protein kinase (MAPK) activity, and a player in the control of glial function. Several disease models have identified that the expression of DUSP1 is altered in tissue samples, which may contribute to disease pathogenesis. Using post-mortem brain tissue from a cohort of progressive multiple sclerosis (MS) cases, this study set out to determine if the expression of DUSP1 is altered in the brain in MS. We employed the use of a combination of PCR, western immunoblotting and immunohistochemical analysis to profile the expression of DUSP1. Data presented herein indicate that DUSP1 is significantly downregulated at gene and protein level in MS white matter tissue, when compared to samples from a non-MS control cohort. We also identify that DUSP1 is expressed on Iba1+ cells in the brain and that ITGAM (CD11b) expression is elevated in white matter in progressive MS. These findings provide evidence that DUSP1 is dysregulated centrally in CNS white matter in progressive MS.

Neurological SciencesVol. 47(4)
Trinity College Dublin (IE), University College Cork (IE), Beaumont Hospital (IE), St. James's Hospital (IE)
Irish Research eLibrary, Imperial College London, Trinity College Dublin
Good health and well-being
Openalex Percentile: Top 25%
Protein Tyrosine Phosphatases
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