open access publication

Article, 2024

Lipid levels correlate with neuronal and dopaminergic markers during the differentiation of SH-SY5Y cells

Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, ISSN 0925-4439, 1879-260X, Volume 1870, 6, Page 167212, 10.1016/j.bbadis.2024.167212

Contributors

Marlet, Frederik Ravnkilde 0000-0003-3781-6022 [1] Muñoz, Sonia Sanz 0000-0003-0970-3637 [1] Sotiraki, Nefeli [1] Eliasen, Jannik Nicklas 0000-0002-5407-9469 [1] Woessmann, Jakob Paul 0000-0002-2283-7237 [2] Weicher, Jan [1] Dreier, Jesper Elmsted 0000-0002-0740-1750 [1] Schoof, Erwin Marten 0000-0002-3117-7832 [2] Kohlmeier, Kristi Anne 0000-0003-0183-3816 [1] Maeda, Kenji 0000-0002-9080-5691 [3] Galvagnion, Céline 0000-0001-9753-3310 (Corresponding author) [1]

Affiliations

  1. [1] University of Copenhagen
  2. [NORA names: KU University of Copenhagen; University; Denmark; Europe, EU; Nordic; OECD];
  3. [2] Technical University of Denmark
  4. [NORA names: DTU Technical University of Denmark; University; Denmark; Europe, EU; Nordic; OECD];
  5. [3] Cell Death and Metabolism group, Center for Autophagy, Recycling and Disease, Danish Cancer Institute, Copenhagen, Denmark.
  6. [NORA names: Denmark; Europe, EU; Nordic; OECD]

Abstract

Parkinson's Disease (PD) is characterised by the loss of dopaminergic neurons and the deposition of protein inclusions called Lewy Bodies (LBs). LBs are heterogeneous structures composed of protein and lipid molecules and their main constituent is the presynaptic protein α-synuclein. SH-SY5Y cells are neuroblastoma cells commonly used to model PD because they express dopaminergic markers and α-synuclein and they can be differentiated into neuronal cells using established protocols. Despite increasing evidence pointing towards a role of lipids in PD, limited knowledge is available on the lipidome of undifferentiated and differentiated SH-SY5Y cells. Using a combination of lipidomics, proteomics, morphological and electrophysiological measurements, we identified specific lipids, including sphingolipids, whose levels are affected by the differentiation of SH-SY5Y neuroblastoma cells and found that the levels of these lipids correlate with those of neuronal and dopaminergic markers. These results provide a quantitative characterisation of the changes in lipidome associated with the differentiation of SH-SY5Y cells into more neuronal and dopaminergic-like phenotype and serve as a basis for further characterisation of lipid disruptions in association with PD and its risk factors in this dopaminergic-like neuronal cell model.

Keywords

Lewis, Lewy bodies, Parkinson, Parkinson's disease, SH-SY5Y, SH-SY5Y cells, SH-SY5Y neuroblastoma cells, a-synuclein, associated with PD, association, body, cells, changes, characterisation, combination, combination of lipidomics, constituents, deposition, differentiation, differentiation of SH-SY5Y cells, differentiation of SH-SY5Y neuroblastoma cells, disease, disruption, dopaminergic markers, dopaminergic neurons, electrophysiological measurements, evidence, factors, heterogeneous structure, inclusion, increasing evidence, knowledge, levels, lipid, lipid disruption, lipid levels, lipid molecules, lipidomics, loss, loss of dopaminergic neurons, markers, measurements, model PD, molecules, neuroblastoma, neuroblastoma cells, neuronal cells, neurons, phenotype, protein, protein inclusions, proteomics, protocol, quantitative characterisation, results, risk, risk factors, specific lipids, sphingolipids, structure

Funders

  • Lundbeck Foundation
  • Carlsberg Foundation
  • Novo Nordisk Foundation

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