Proteomics Analysis of Lymphoblastoid Cell Lines from Patients with Amyotrophic Lateral Sclerosis
Amyotrophic lateral sclerosis (ALS) consists of the progressive degeneration of motor neurons, caused by poorly understood mechanisms for which there is no cure. Some of the cellular perturbations associated with ALS can be detected in peripheral cells, including lymphocytes from blood. A related ce...
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MDPI AG
2023-02-01
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Online Access: | https://www.mdpi.com/1420-3049/28/5/2014 |
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author | Danielle Whitham Eugene Belenkiy Costel C. Darie Aurelian Radu |
author_facet | Danielle Whitham Eugene Belenkiy Costel C. Darie Aurelian Radu |
author_sort | Danielle Whitham |
collection | DOAJ |
description | Amyotrophic lateral sclerosis (ALS) consists of the progressive degeneration of motor neurons, caused by poorly understood mechanisms for which there is no cure. Some of the cellular perturbations associated with ALS can be detected in peripheral cells, including lymphocytes from blood. A related cell system that is very suitable for research consists of human lymphoblastoid cell lines (LCLs), which are immortalized lymphocytes. LCLs that can be easily expanded in culture and can be maintained for long periods as stable cultures. We investigated, on a small set of LCLs, if a proteomics analysis using liquid chromatography followed by tandem mass spectrometry reveals proteins that are differentially present in ALS versus healthy controls. We found that individual proteins, the cellular and molecular pathways in which these proteins participate, are detected as differentially present in the ALS samples. Some of these proteins and pathways are already known to be perturbed in ALS, while others are new and present interest for further investigations. These observations suggest that a more detailed proteomics analysis of LCLs, using a larger number of samples, represents a promising approach for investigating ALS mechanisms and to search for therapeutic agents. Proteomics data are available via ProteomeXchange with identifier PXD040240. |
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issn | 1420-3049 |
language | English |
last_indexed | 2024-03-11T07:17:53Z |
publishDate | 2023-02-01 |
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spelling | doaj.art-ac571ec412ef46e38177630e136bc4e72023-11-17T08:10:49ZengMDPI AGMolecules1420-30492023-02-01285201410.3390/molecules28052014Proteomics Analysis of Lymphoblastoid Cell Lines from Patients with Amyotrophic Lateral SclerosisDanielle Whitham0Eugene Belenkiy1Costel C. Darie2Aurelian Radu3Biochemistry & Proteomics Laboratories, Department of Chemistry & Biomolecular Science, Clarkson University, 8 Clarkson Avenue, Potsdam, NY 13699-5810, USADepartment of Cell, Developmental and Regenerative Biology, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, New York, NY 10029-6574, USABiochemistry & Proteomics Laboratories, Department of Chemistry & Biomolecular Science, Clarkson University, 8 Clarkson Avenue, Potsdam, NY 13699-5810, USADepartment of Cell, Developmental and Regenerative Biology, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, New York, NY 10029-6574, USAAmyotrophic lateral sclerosis (ALS) consists of the progressive degeneration of motor neurons, caused by poorly understood mechanisms for which there is no cure. Some of the cellular perturbations associated with ALS can be detected in peripheral cells, including lymphocytes from blood. A related cell system that is very suitable for research consists of human lymphoblastoid cell lines (LCLs), which are immortalized lymphocytes. LCLs that can be easily expanded in culture and can be maintained for long periods as stable cultures. We investigated, on a small set of LCLs, if a proteomics analysis using liquid chromatography followed by tandem mass spectrometry reveals proteins that are differentially present in ALS versus healthy controls. We found that individual proteins, the cellular and molecular pathways in which these proteins participate, are detected as differentially present in the ALS samples. Some of these proteins and pathways are already known to be perturbed in ALS, while others are new and present interest for further investigations. These observations suggest that a more detailed proteomics analysis of LCLs, using a larger number of samples, represents a promising approach for investigating ALS mechanisms and to search for therapeutic agents. Proteomics data are available via ProteomeXchange with identifier PXD040240.https://www.mdpi.com/1420-3049/28/5/2014amyotrophic lateral sclerosisproteomicsmass spectrometrybiomarkers |
spellingShingle | Danielle Whitham Eugene Belenkiy Costel C. Darie Aurelian Radu Proteomics Analysis of Lymphoblastoid Cell Lines from Patients with Amyotrophic Lateral Sclerosis Molecules amyotrophic lateral sclerosis proteomics mass spectrometry biomarkers |
title | Proteomics Analysis of Lymphoblastoid Cell Lines from Patients with Amyotrophic Lateral Sclerosis |
title_full | Proteomics Analysis of Lymphoblastoid Cell Lines from Patients with Amyotrophic Lateral Sclerosis |
title_fullStr | Proteomics Analysis of Lymphoblastoid Cell Lines from Patients with Amyotrophic Lateral Sclerosis |
title_full_unstemmed | Proteomics Analysis of Lymphoblastoid Cell Lines from Patients with Amyotrophic Lateral Sclerosis |
title_short | Proteomics Analysis of Lymphoblastoid Cell Lines from Patients with Amyotrophic Lateral Sclerosis |
title_sort | proteomics analysis of lymphoblastoid cell lines from patients with amyotrophic lateral sclerosis |
topic | amyotrophic lateral sclerosis proteomics mass spectrometry biomarkers |
url | https://www.mdpi.com/1420-3049/28/5/2014 |
work_keys_str_mv | AT daniellewhitham proteomicsanalysisoflymphoblastoidcelllinesfrompatientswithamyotrophiclateralsclerosis AT eugenebelenkiy proteomicsanalysisoflymphoblastoidcelllinesfrompatientswithamyotrophiclateralsclerosis AT costelcdarie proteomicsanalysisoflymphoblastoidcelllinesfrompatientswithamyotrophiclateralsclerosis AT aurelianradu proteomicsanalysisoflymphoblastoidcelllinesfrompatientswithamyotrophiclateralsclerosis |