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Preliminary Analysis of Potentially Overlapping Differentially Expressed Proteins in Both the Spinal Cord and Brain of SOD1 G93A Mice

Overview
Specialty Biochemistry
Date 2024 Jul 10
PMID 38984582
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Abstract

Objective: Proteomic elucidation is an essential step in improving our understanding of the biological properties of proteins in amyotrophic lateral sclerosis (ALS).

Methods: Preliminary proteomic analysis was performed on the spinal cord and brain of SOD1 G93A (TG) and wild-type (WT) mice using isobaric tags for relative and absolute quantitation.

Results: Partial up- and downregulated proteins showing significant differences between TG and WT mice were identified, of which 105 proteins overlapped with differentially expressed proteins in both the spinal cord and brain of progression mice. Bioinformatic analyses using Gene Ontology, a cluster of orthologous groups, and Kyoto Encyclopedia of Genes and Genomes pathway revealed that the significantly up- and downregulated proteins represented multiple biological functions closely related to ALS, with 105 overlapping differentially expressed proteins in the spinal cord and brain at the progression stage of TG mice closely related to 122 pathways. Differentially expressed proteins involved in a set of molecular functions play essential roles in maintaining neural cell survival.

Conclusion: This study provides additional proteomic profiles of TG mice, including potential overlapping proteins in both the spinal cord and brain that participate in pathogenesis, as well as novel insights into the up- and downregulation of proteins involved in the pathogenesis of ALS.

References
1.
Xu R, Yuan M . Considerations on the concept, definition, and diagnosis of amyotrophic lateral sclerosis. Neural Regen Res. 2021; 16(9):1723-1729. PMC: 8328770. DOI: 10.4103/1673-5374.306065. View

2.
Ingre C, Chen L, Zhan Y, Termorshuizen J, Yin L, Fang F . Lipids, apolipoproteins, and prognosis of amyotrophic lateral sclerosis. Neurology. 2020; 94(17):e1835-e1844. PMC: 7274849. DOI: 10.1212/WNL.0000000000009322. View

3.
Cruz M . Edaravone (Radicava): A Novel Neuroprotective Agent for the Treatment of Amyotrophic Lateral Sclerosis. P T. 2018; 43(1):25-28. PMC: 5737249. View

4.
Libro R, Bramanti P, Mazzon E . The role of the Wnt canonical signaling in neurodegenerative diseases. Life Sci. 2016; 158:78-88. DOI: 10.1016/j.lfs.2016.06.024. View

5.
Rozas P, Bargsted L, Martinez F, Hetz C, Medinas D . The ER proteostasis network in ALS: Determining the differential motoneuron vulnerability. Neurosci Lett. 2016; 636:9-15. DOI: 10.1016/j.neulet.2016.04.066. View