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Observation of α-Synuclein Preformed Fibrils Interacting with SH-SY5Y Neuroblastoma Cell Membranes Using Scanning Ion Conductance Microscopy

[Image: see text] Parkinson’s disease (PD) is the second-most prevalent neurodegenerative disorder in the U.S. α-Synuclein (α-Syn) preformed fibrils (PFFs) have been shown to propagate PD pathology in neuronal populations. However, little work has directly characterized the morphological changes on...

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Autores principales: Feng, Christina, Flores, Marisol, Dhoj, Christina, Garcia, Adaly, Belleca, Sheehan, Abbas, Dana Abou, Parres-Gold, Jacob, Anguiano, Aimee, Porter, Edith, Wang, Yixian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9782390/
https://www.ncbi.nlm.nih.gov/pubmed/36455298
http://dx.doi.org/10.1021/acschemneuro.2c00478
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author Feng, Christina
Flores, Marisol
Dhoj, Christina
Garcia, Adaly
Belleca, Sheehan
Abbas, Dana Abou
Parres-Gold, Jacob
Anguiano, Aimee
Porter, Edith
Wang, Yixian
author_facet Feng, Christina
Flores, Marisol
Dhoj, Christina
Garcia, Adaly
Belleca, Sheehan
Abbas, Dana Abou
Parres-Gold, Jacob
Anguiano, Aimee
Porter, Edith
Wang, Yixian
author_sort Feng, Christina
collection PubMed
description [Image: see text] Parkinson’s disease (PD) is the second-most prevalent neurodegenerative disorder in the U.S. α-Synuclein (α-Syn) preformed fibrils (PFFs) have been shown to propagate PD pathology in neuronal populations. However, little work has directly characterized the morphological changes on membranes associated with α-Syn PFFs at a cellular level. Scanning ion conductance microscopy (SICM) is a noninvasive in situ cell imaging technique and therefore uniquely advantageous to investigate PFF-induced membrane changes in neuroblastoma cells. The present work used SICM to monitor cytoplasmic membrane changes of SH-SY5Y neuroblastoma cells after incubation with varying concentrations of α-Syn PFFs. Cell membrane roughness significantly increased as the concentration of α-Syn PFFs increased. Noticeable protrusions that assumed a more crystalline appearance at higher α-Syn PFF concentrations were also observed. Cell viability was only slightly reduced, though statistically significantly, to about 80% but independent of the dose. These observations indicate that within the 48 h treatment period, PFFs continue to accumulate on the cell membranes, leading to membrane roughness increase without causing prominent cell death. Since PFFs did not induce major cell death, these data suggest that early interventions targeting fibrils before further aggregation may prevent the progression of neuron loss in Parkinson’s disease.
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spelling pubmed-97823902022-12-24 Observation of α-Synuclein Preformed Fibrils Interacting with SH-SY5Y Neuroblastoma Cell Membranes Using Scanning Ion Conductance Microscopy Feng, Christina Flores, Marisol Dhoj, Christina Garcia, Adaly Belleca, Sheehan Abbas, Dana Abou Parres-Gold, Jacob Anguiano, Aimee Porter, Edith Wang, Yixian ACS Chem Neurosci [Image: see text] Parkinson’s disease (PD) is the second-most prevalent neurodegenerative disorder in the U.S. α-Synuclein (α-Syn) preformed fibrils (PFFs) have been shown to propagate PD pathology in neuronal populations. However, little work has directly characterized the morphological changes on membranes associated with α-Syn PFFs at a cellular level. Scanning ion conductance microscopy (SICM) is a noninvasive in situ cell imaging technique and therefore uniquely advantageous to investigate PFF-induced membrane changes in neuroblastoma cells. The present work used SICM to monitor cytoplasmic membrane changes of SH-SY5Y neuroblastoma cells after incubation with varying concentrations of α-Syn PFFs. Cell membrane roughness significantly increased as the concentration of α-Syn PFFs increased. Noticeable protrusions that assumed a more crystalline appearance at higher α-Syn PFF concentrations were also observed. Cell viability was only slightly reduced, though statistically significantly, to about 80% but independent of the dose. These observations indicate that within the 48 h treatment period, PFFs continue to accumulate on the cell membranes, leading to membrane roughness increase without causing prominent cell death. Since PFFs did not induce major cell death, these data suggest that early interventions targeting fibrils before further aggregation may prevent the progression of neuron loss in Parkinson’s disease. American Chemical Society 2022-12-01 /pmc/articles/PMC9782390/ /pubmed/36455298 http://dx.doi.org/10.1021/acschemneuro.2c00478 Text en © 2022 American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Feng, Christina
Flores, Marisol
Dhoj, Christina
Garcia, Adaly
Belleca, Sheehan
Abbas, Dana Abou
Parres-Gold, Jacob
Anguiano, Aimee
Porter, Edith
Wang, Yixian
Observation of α-Synuclein Preformed Fibrils Interacting with SH-SY5Y Neuroblastoma Cell Membranes Using Scanning Ion Conductance Microscopy
title Observation of α-Synuclein Preformed Fibrils Interacting with SH-SY5Y Neuroblastoma Cell Membranes Using Scanning Ion Conductance Microscopy
title_full Observation of α-Synuclein Preformed Fibrils Interacting with SH-SY5Y Neuroblastoma Cell Membranes Using Scanning Ion Conductance Microscopy
title_fullStr Observation of α-Synuclein Preformed Fibrils Interacting with SH-SY5Y Neuroblastoma Cell Membranes Using Scanning Ion Conductance Microscopy
title_full_unstemmed Observation of α-Synuclein Preformed Fibrils Interacting with SH-SY5Y Neuroblastoma Cell Membranes Using Scanning Ion Conductance Microscopy
title_short Observation of α-Synuclein Preformed Fibrils Interacting with SH-SY5Y Neuroblastoma Cell Membranes Using Scanning Ion Conductance Microscopy
title_sort observation of α-synuclein preformed fibrils interacting with sh-sy5y neuroblastoma cell membranes using scanning ion conductance microscopy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9782390/
https://www.ncbi.nlm.nih.gov/pubmed/36455298
http://dx.doi.org/10.1021/acschemneuro.2c00478
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