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Specific Detection of Physiological S129 Phosphorylated α-Synuclein in Tissue Using Proximity Ligation Assay

BACKGROUND: Synucleinopathies are a group of neurodegenerative disorders that are pathologically characterized by intracellular aggregates called Lewy bodies. Lewy bodies are primarily composed of α-synuclein (asyn) protein, which is mostly phosphorylated at serine 129 (pS129) when aggregated and th...

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Autores principales: Arlinghaus, Ryan, Iba, Michiyo, Masliah, Eliezer, Cookson, Mark R., Landeck, Natalie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10041430/
https://www.ncbi.nlm.nih.gov/pubmed/36847016
http://dx.doi.org/10.3233/JPD-213085
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author Arlinghaus, Ryan
Iba, Michiyo
Masliah, Eliezer
Cookson, Mark R.
Landeck, Natalie
author_facet Arlinghaus, Ryan
Iba, Michiyo
Masliah, Eliezer
Cookson, Mark R.
Landeck, Natalie
author_sort Arlinghaus, Ryan
collection PubMed
description BACKGROUND: Synucleinopathies are a group of neurodegenerative disorders that are pathologically characterized by intracellular aggregates called Lewy bodies. Lewy bodies are primarily composed of α-synuclein (asyn) protein, which is mostly phosphorylated at serine 129 (pS129) when aggregated and therefore used as a marker for pathology. Currently commercial antibodies against pS129 asyn stain aggregates well but in healthy brains cross react with other proteins, thus making it difficult to specifically detect physiological pS129 asyn. OBJECTIVE: To develop a staining procedure that detects endogenous and physiological relevant pS129 asyn with high specificity and low background. METHODS: We used the fluorescent and brightfield in situ proximity ligation assay (PLA) to specifically detect pS129 asyn in cell culture, mouse, and human brain sections. RESULTS: The pS129 asyn PLA specifically stained physiological and soluble pS129 asyn in cell culture, mouse brain sections, and human brain tissue without significant cross-reactivity or background signal. However, this technique was not successful in detecting Lewy bodies in human brain tissue. CONCLUSION: We successfully developed a novel PLA method that can, in the future, be used on in vitro and in vivo samples as a tool to explore and better understand the cellular localization and function of pS129 asyn in health and disease.
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spelling pubmed-100414302023-03-28 Specific Detection of Physiological S129 Phosphorylated α-Synuclein in Tissue Using Proximity Ligation Assay Arlinghaus, Ryan Iba, Michiyo Masliah, Eliezer Cookson, Mark R. Landeck, Natalie J Parkinsons Dis Research Report BACKGROUND: Synucleinopathies are a group of neurodegenerative disorders that are pathologically characterized by intracellular aggregates called Lewy bodies. Lewy bodies are primarily composed of α-synuclein (asyn) protein, which is mostly phosphorylated at serine 129 (pS129) when aggregated and therefore used as a marker for pathology. Currently commercial antibodies against pS129 asyn stain aggregates well but in healthy brains cross react with other proteins, thus making it difficult to specifically detect physiological pS129 asyn. OBJECTIVE: To develop a staining procedure that detects endogenous and physiological relevant pS129 asyn with high specificity and low background. METHODS: We used the fluorescent and brightfield in situ proximity ligation assay (PLA) to specifically detect pS129 asyn in cell culture, mouse, and human brain sections. RESULTS: The pS129 asyn PLA specifically stained physiological and soluble pS129 asyn in cell culture, mouse brain sections, and human brain tissue without significant cross-reactivity or background signal. However, this technique was not successful in detecting Lewy bodies in human brain tissue. CONCLUSION: We successfully developed a novel PLA method that can, in the future, be used on in vitro and in vivo samples as a tool to explore and better understand the cellular localization and function of pS129 asyn in health and disease. IOS Press 2023-03-14 /pmc/articles/PMC10041430/ /pubmed/36847016 http://dx.doi.org/10.3233/JPD-213085 Text en © 2023 – The authors. Published by IOS Press https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY 4.0) License (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Report
Arlinghaus, Ryan
Iba, Michiyo
Masliah, Eliezer
Cookson, Mark R.
Landeck, Natalie
Specific Detection of Physiological S129 Phosphorylated α-Synuclein in Tissue Using Proximity Ligation Assay
title Specific Detection of Physiological S129 Phosphorylated α-Synuclein in Tissue Using Proximity Ligation Assay
title_full Specific Detection of Physiological S129 Phosphorylated α-Synuclein in Tissue Using Proximity Ligation Assay
title_fullStr Specific Detection of Physiological S129 Phosphorylated α-Synuclein in Tissue Using Proximity Ligation Assay
title_full_unstemmed Specific Detection of Physiological S129 Phosphorylated α-Synuclein in Tissue Using Proximity Ligation Assay
title_short Specific Detection of Physiological S129 Phosphorylated α-Synuclein in Tissue Using Proximity Ligation Assay
title_sort specific detection of physiological s129 phosphorylated α-synuclein in tissue using proximity ligation assay
topic Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10041430/
https://www.ncbi.nlm.nih.gov/pubmed/36847016
http://dx.doi.org/10.3233/JPD-213085
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