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Filtered Cerebrospinal Fluid From Patients With Amyotrophic Lateral Sclerosis Displays an Altered Proteome and Affects Motor Phenotype in a Mouse Model.

Publication ,  Journal Article
Venkatraman, V; Filiano, AJ; Xu, L; Collins, L; Luo, E; Ripple, KM; de Castro, GC; Boua, J-VK; Marius, C; Giamberardino, C; Lad, SP ...
Published in: Cureus
December 2022

INTRODUCTION: Cerebrospinal fluid (CSF) has been implicated in amyotrophic lateral sclerosis (ALS) due to its ability to spread inflammatory proteins throughout the nervous system. We hypothesized that filtration of the CSF could remove pathogenic proteins and prevent them from altering motor phenotypes in a mouse model. METHODS: We filtered the CSF from 11 ALS patients via 100 kilodaltons (kD) molecular weight cut-off filters. We used mass spectrometry-based discovery proteomics workflows to compare protein abundances before and after filtration. To test the effects of CSF filtration on motor function, we injected groups of mice with saline, filtered ALS-CSF, or unfiltered ALS-CSF (n=12 per group) and assessed motor function via pole descent and open field tests. RESULTS: We identified proteins implicated in ALS pathogenesis and showed that these were removed in significant amounts in our workflow. Key filtered proteins included complement proteins, chitinases, serine protease inhibitors, and neuro-inflammatory proteins such as amyloid precursor protein, chromogranin A, and glial fibrillary acidic protein. Compared to the filtered ALS-CSF mice, unfiltered ALS-CSF mice took longer to descend a pole (10 days post-injection, 11.14 seconds vs 14.25 seconds, p = 0.02) and explored less on an open field (one day post-injection, 21.81 m vs 16.83 m, p = 0.0004). CONCLUSIONS: We demonstrated the ability to filter proteins from the CSF of ALS patients and identified potentially pathologic proteins that were reduced in quantity. Additionally, we demonstrated the ability of unfiltered ALS-CSF to induce motor deficits in mice on the pole descent and open field tests and showed that filtration could prevent this deficit. Given the lack of effective treatments for ALS, this could be a novel solution for patients suffering from this deadly and irreversible condition.

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Published In

Cureus

DOI

ISSN

2168-8184

Publication Date

December 2022

Volume

14

Issue

12

Start / End Page

e32980

Location

United States

Related Subject Headings

  • 42 Health sciences
  • 32 Biomedical and clinical sciences
  • 11 Medical and Health Sciences
 

Citation

APA
Chicago
ICMJE
MLA
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Venkatraman, V., Filiano, A. J., Xu, L., Collins, L., Luo, E., Ripple, K. M., … Bedlack, R. S. (2022). Filtered Cerebrospinal Fluid From Patients With Amyotrophic Lateral Sclerosis Displays an Altered Proteome and Affects Motor Phenotype in a Mouse Model. Cureus, 14(12), e32980. https://doi.org/10.7759/cureus.32980
Venkatraman, Vishal, Anthony J. Filiano, Li Xu, Leonard Collins, Emily Luo, Katelyn M. Ripple, George C. de Castro, et al. “Filtered Cerebrospinal Fluid From Patients With Amyotrophic Lateral Sclerosis Displays an Altered Proteome and Affects Motor Phenotype in a Mouse Model.Cureus 14, no. 12 (December 2022): e32980. https://doi.org/10.7759/cureus.32980.
Venkatraman, Vishal, et al. “Filtered Cerebrospinal Fluid From Patients With Amyotrophic Lateral Sclerosis Displays an Altered Proteome and Affects Motor Phenotype in a Mouse Model.Cureus, vol. 14, no. 12, Dec. 2022, p. e32980. Pubmed, doi:10.7759/cureus.32980.
Venkatraman V, Filiano AJ, Xu L, Collins L, Luo E, Ripple KM, de Castro GC, Boua J-VK, Marius C, Giamberardino C, Lad SP, Islam Williams T, Bereman MS, Bedlack RS. Filtered Cerebrospinal Fluid From Patients With Amyotrophic Lateral Sclerosis Displays an Altered Proteome and Affects Motor Phenotype in a Mouse Model. Cureus. 2022 Dec;14(12):e32980.

Published In

Cureus

DOI

ISSN

2168-8184

Publication Date

December 2022

Volume

14

Issue

12

Start / End Page

e32980

Location

United States

Related Subject Headings

  • 42 Health sciences
  • 32 Biomedical and clinical sciences
  • 11 Medical and Health Sciences