4.3 Article

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

Journal

BIOTECHNOLOGY PROGRESS
Volume 36, Issue 2, Pages -

Publisher

WILEY
DOI: 10.1002/btpr.2942

Keywords

3D cell culture; matrigel; neurotoxicants; Parkinson's disease

Funding

  1. Brain Repair Centre
  2. Natural Sciences and Engineering Research Council of Canada [RGPIN-2016-04298]
  3. Canada Foundation for Innovation [33533]
  4. Canada Research Chairs
  5. Nova Scotia Provincial Government
  6. Faculty of Medicine, Dalhousie University
  7. Nova Scotia Health Research Foundation
  8. Canadian Institutes of Health Research
  9. Beatrice Hunter Cancer Research Institute

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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.

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