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A monolayer hiPSC culture system for autophagy/mitophagy studies in human dopaminergic neurons

Stathakos, Petros; Jim�nez-Moreno, Natalia; Crompton, Lucy A.; Nistor, Paul A.; Badger, Jennifer L.; Barbuti, Peter A.; Kerrigan, Talitha L.; Randall, Andrew D.; Caldwell, Maeve A.; Lane, Jon D.

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Authors

Petros Stathakos

Natalia Jim�nez-Moreno

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Dr Lucy Crompton Lucy.Crompton@uwe.ac.uk
Senior Lecturer in Biomedical Sciences (Neuroscience)

Paul A. Nistor

Jennifer L. Badger

Peter A. Barbuti

Talitha L. Kerrigan

Andrew D. Randall

Maeve A. Caldwell

Jon D. Lane



Abstract

Macroautophagy/autophagy cytoplasmic quality control pathways are required during neural development and are critical for the maintenance of functional neuronal populations in the adult brain. Robust evidence now exists that declining neuronal autophagy pathways contribute to human neurodegenerative diseases, including Parkinson disease (PD). Reliable and relevant human neuronal model systems are therefore needed to understand the biology of disease-vulnerable neural populations, to decipher the underlying causes of neurodegenerative disease, and to develop assays to test therapeutic interventions in vitro. Human induced pluripotent stem cell (hiPSC) neural model systems can meet this demand: they provide a renewable source of material for differentiation into regional neuronal sub-types for functional assays; they can be expanded to provide a platform for screening, and they can potentially be optimized for transplantation/neurorestorative therapy. So far, however, hiPSC differentiation protocols for the generation of ventral midbrain dopaminergic neurons (mDANs)–the predominant neuronal sub-type afflicted in PD–have been somewhat restricted by poor efficiency and/or suitability for functional and/or imaging-based in vitro assays. Here, we describe a reliable, monolayer differentiation protocol for the rapid and reproducible production of high numbers of mDANs from hiPSC in a format that is amenable for autophagy/mitophagy research. We characterize these cells with respect to neuronal differentiation and macroautophagy capability and describe qualitative and quantitative assays for the study of autophagy and mitophagy in these important cells. Abbreviations: AA: ascorbic acid; ATG: autophagy-related; BDNF: brain derived neurotrophic factor; CCCP: carbonyl cyanide m-chlorophenylhydrazone; dbcAMP: dibutyryl cAMP; DAN: dopaminergic neuron; DAPI: 4ʹ,6-diamidino-2-phenylindole; DAPT: N-[N-(3,5-difluorophenacetyl)-L-alanyl]-sphenylglycine; DLG4/PSD95: discs large MAGUK scaffold protein 4; DMEM: Dulbecco’s modified eagle’s medium; EB: embryoid body; ECAR: extracellular acidification rate; EGF: epidermal growth factor; FACS: fluorescence-activated cell sorting; FCCP: arbonyl cyanide p-triflouromethoxyphenylhydrazone; FGF: fibroblast growth factor; GAPDH: glyceraldehyde-3-phosphate dehydrogenase; GDNF: glia cell derived neurotrophic factor; hiPSC: human induced pluripotent stem cell; LAMP2A: lysosomal associated membrane protein 2A; LT-R: LysoTracker Red; MAP1LC3: microtubule associated protein 1 light chain 3; mDAN: midbrain dopaminergic neuron; MEF: mouse embryonic fibroblast; MT-GR: MitoTracker Green; MT-R: MitoTracker Red; NAS2: normal SNCA2; NEM: neuroprogenitor expansion media; NR4A2/NURR1: nuclear receptor subfamily group A member 2; OA: oligomycin and antimycin A; OCR: oxygen consumption rate; PD: Parkinson disease; SHH: sonic hedgehog signaling molecule; SNCA/α-synuclein: synuclein alpha; TH: tyrosine hydroxylase; VTN: vitronectin.

Citation

Stathakos, P., Jiménez-Moreno, N., Crompton, L. A., Nistor, P. A., Badger, J. L., Barbuti, P. A., …Lane, J. D. (2021). A monolayer hiPSC culture system for autophagy/mitophagy studies in human dopaminergic neurons. Autophagy, 17(4), 855-871. https://doi.org/10.1080/15548627.2020.1739441

Journal Article Type Article
Acceptance Date Apr 1, 2020
Online Publication Date Apr 14, 2020
Publication Date Apr 3, 2021
Deposit Date Apr 21, 2022
Publicly Available Date Apr 22, 2022
Journal Autophagy
Print ISSN 1554-8627
Electronic ISSN 1554-8635
Publisher Taylor & Francis
Peer Reviewed Peer Reviewed
Volume 17
Issue 4
Pages 855-871
DOI https://doi.org/10.1080/15548627.2020.1739441
Keywords Cell Biology; Molecular Biology, stem cells, Parkinson's
Public URL https://uwe-repository.worktribe.com/output/9378308
Additional Information Peer Review Statement: The publishing and review policy for this title is described in its Aims & Scope.; Aim & Scope: http://www.tandfonline.com/action/journalInformation?show=aimsScope&journalCode=kaup20; Received: 2018-07-24; Revised: 2020-02-27; Accepted: 2020-02-28; Published: 2020-04-14

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