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Refinement of a differentiation protocol using neuroblastoma SH-SY5Y cells for use in neurotoxicology research

Simões, Rui F LU ; Ferrão, Rafaela ; Silva, Margarida R ; Pinho, Sonia L C ; Ferreira, Lino ; Oliveira, Paulo J and Cunha-Oliveira, Teresa (2021) In Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association 149. p.1-13
Abstract

Since most models used to study neuronal dysfunction display disadvantages and ethical concerns, a fast and reproducible in vitro model to study mitochondria-related neurodegeneration is required. Here, we optimized and characterized a 3-day retinoic acid-based protocol to differentiate the SH-SY5Y cell line into a neuronal-like phenotype and investigated alterations in mitochondrial physiology and distribution. Differentiation was associated with p21-linked cell cycle arrest and an increase in cell mass and area, possibly associated with the development of neurite-like extensions. Notably, increased expression of mature neuronal markers (neuronal-specific nuclear protein, microtubule-associated protein 2, βIII tubulin and enolase 2)... (More)

Since most models used to study neuronal dysfunction display disadvantages and ethical concerns, a fast and reproducible in vitro model to study mitochondria-related neurodegeneration is required. Here, we optimized and characterized a 3-day retinoic acid-based protocol to differentiate the SH-SY5Y cell line into a neuronal-like phenotype and investigated alterations in mitochondrial physiology and distribution. Differentiation was associated with p21-linked cell cycle arrest and an increase in cell mass and area, possibly associated with the development of neurite-like extensions. Notably, increased expression of mature neuronal markers (neuronal-specific nuclear protein, microtubule-associated protein 2, βIII tubulin and enolase 2) was observed in differentiated cells. Moreover, increased mitochondrial content and maximal area per cell suggests mitochondrial remodeling. To demonstrate that this model is appropriate to study mitochondrial dysfunction, cells were treated for 6 h with mitochondrial toxicants (rotenone, antimycin A, carbonyl cyanide-4-(trifluoromethoxy)phenylhydrazone (FCCP) and 6-hydroxydopamine (6-OHDA)). Differentiated cells were more susceptible to increasing concentrations of FCCP, antimycin A, and rotenone, while 6-OHDA showed a distinct dose-dependent neurotoxicity pattern. Even though differentiated cells did not exhibit a fully mature/differentiated neuronal phenotype, the protocol developed can be used to study neurotoxicity processes, mitochondrial dynamics, and bioenergetic impairment, representing an alternative to study mitochondrial impairment-related pathologies in vitro.

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author
; ; ; ; ; and
publishing date
type
Contribution to journal
publication status
published
keywords
Cell Differentiation, Cell Line, Tumor, Colorimetry, Humans, Microscopy/methods, Mitochondria/drug effects, Neuroblastoma, Neurons/drug effects, Neurotoxicity Syndromes/pathology, Rhodamines, Tretinoin/toxicity
in
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association
volume
149
article number
111967
pages
1 - 13
publisher
Elsevier
external identifiers
  • scopus:85099965849
  • pmid:33417974
ISSN
1873-6351
DOI
10.1016/j.fct.2021.111967
language
English
LU publication?
no
id
0d47fe22-dffb-473b-8124-de126ef068fc
date added to LUP
2021-09-21 19:22:25
date last changed
2024-04-06 09:10:00
@article{0d47fe22-dffb-473b-8124-de126ef068fc,
  abstract     = {{<p>Since most models used to study neuronal dysfunction display disadvantages and ethical concerns, a fast and reproducible in vitro model to study mitochondria-related neurodegeneration is required. Here, we optimized and characterized a 3-day retinoic acid-based protocol to differentiate the SH-SY5Y cell line into a neuronal-like phenotype and investigated alterations in mitochondrial physiology and distribution. Differentiation was associated with p21-linked cell cycle arrest and an increase in cell mass and area, possibly associated with the development of neurite-like extensions. Notably, increased expression of mature neuronal markers (neuronal-specific nuclear protein, microtubule-associated protein 2, βIII tubulin and enolase 2) was observed in differentiated cells. Moreover, increased mitochondrial content and maximal area per cell suggests mitochondrial remodeling. To demonstrate that this model is appropriate to study mitochondrial dysfunction, cells were treated for 6 h with mitochondrial toxicants (rotenone, antimycin A, carbonyl cyanide-4-(trifluoromethoxy)phenylhydrazone (FCCP) and 6-hydroxydopamine (6-OHDA)). Differentiated cells were more susceptible to increasing concentrations of FCCP, antimycin A, and rotenone, while 6-OHDA showed a distinct dose-dependent neurotoxicity pattern. Even though differentiated cells did not exhibit a fully mature/differentiated neuronal phenotype, the protocol developed can be used to study neurotoxicity processes, mitochondrial dynamics, and bioenergetic impairment, representing an alternative to study mitochondrial impairment-related pathologies in vitro.</p>}},
  author       = {{Simões, Rui F and Ferrão, Rafaela and Silva, Margarida R and Pinho, Sonia L C and Ferreira, Lino and Oliveira, Paulo J and Cunha-Oliveira, Teresa}},
  issn         = {{1873-6351}},
  keywords     = {{Cell Differentiation; Cell Line, Tumor; Colorimetry; Humans; Microscopy/methods; Mitochondria/drug effects; Neuroblastoma; Neurons/drug effects; Neurotoxicity Syndromes/pathology; Rhodamines; Tretinoin/toxicity}},
  language     = {{eng}},
  pages        = {{1--13}},
  publisher    = {{Elsevier}},
  series       = {{Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association}},
  title        = {{Refinement of a differentiation protocol using neuroblastoma SH-SY5Y cells for use in neurotoxicology research}},
  url          = {{http://dx.doi.org/10.1016/j.fct.2021.111967}},
  doi          = {{10.1016/j.fct.2021.111967}},
  volume       = {{149}},
  year         = {{2021}},
}