SH-SY5Y and LUHMES cells display differential sensitivity to MPP+, tunicamycin, and epoxomicin in 2D and 3D cell culture

Kristin Robin Ko, Nicky W. Tam, Alyne G. Teixeira, John P. Frampton

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11 Citations (Scopus)

Abstract

SH-SY5Y and LUHMES cell lines are widely used as model systems for studying neurotoxicity. Most of the existing data regarding the sensitivity of these cell lines to neurotoxicants have been recorded from cells growing as two-dimensional (2D) cultures on the surface of glass or plastic. With the emergence of 3D culture platforms designed to better represent native tissue, there is a growing need to compare the toxicology of neurons grown in 3D environments to those grown in 2D to better understand the impact that culture environment has on toxicant sensitivity. Here, a simple 3D culture method was used to assess the impact of growth environment on the sensitivity of SH-SY5Y cells and LUHMES cells to MPP+, tunicamycin, and epoxomicin, three neurotoxicants that have been previously used to generate experimental models for studying Parkinson's disease pathogenesis. SH-SY5Y cell viability following treatment with these three toxicants was significantly lower in 2D cultures as compared to 3D cultures. On the contrary, LUHMES cells did not show significant differences between growth conditions for any of the toxicants examined. However, LUHMES cells were more sensitive to MPP+, tunicamycin, and epoxomicin than SH-SY5Y cells. Thus, both the choice of cell line and the choice of growth environment must be considered when interpreting in vitro neurotoxicity data.

Original languageEnglish
Article numbere2942
JournalBiotechnology Progress
Volume36
Issue number2
DOIs
Publication statusPublished - Mar 1 2020

Bibliographical note

Funding Information:
The authors thank Rishima Agarwal for her assistance with culture dish preparation. KRK was supported by the Canadian Institutes of Health Research (CIHR), the Nova Scotia Health Research Foundation, and the Nova Scotia Provincial Government. NWT was supported by Faculty of Medicine, Dalhousie University and Beatrice Hunter Cancer Research Institute. AGT was supported by the Nova Scotia Provincial Government. This work was supported by the Canada Research Chairs Program, Canada Foundation for Innovation Grant Number 33533, the Natural Sciences and Engineering Research Council of Canada (NSERC) Grant Number RGPIN‐2016‐04298, and the Brain Repair Centre (Knowledge Translation Grant).

Publisher Copyright:
© 2019 American Institute of Chemical Engineers

ASJC Scopus Subject Areas

  • Biotechnology

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