Abstract
The human neuroblastoma cell line, SH-SY5Y cells, is commonly used as an in vitro model for neuroscience and neurobiology research. SH-SY5Y cells were established during the 1970’s from the parental metastatic bone tumor, SK-N-SH cell line. The utilization of SH-SY5Y cells in neurobiology research is due to their resemblance to the human primary neuronal cells with several limitations, considering the cells are derived from malignant tumor cells. Since SH-SY5Y cells are widely cultured for research, several different culture media have been used to optimize the growth of the cells, including Eagle's Minimum Essential Medium (EMEM), Dulbecco’s modified Eagle’s medium (DMEM) and other recently developed culture media. The ability of SH-SY5Y cells to reach confluency in culture flasks ranges from 5 days to 15 days, depending on the culture media. Hence, the optimization of the culture media is crucial to achieve the fastest growth rate for the cells. The objective of the study is to evaluate the culture media for the proliferation of SH-SY5Y cells. We compared the growth rate of SH-SY5Y cells cultured in Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 15% heat-inactivated fetal bovine serum (hiFBS), Dulbecco’s modified Eagle’s medium: Nutrientmixture F-12 (DMEM:F12) + supplemented with 15% hiFBS and DMEM:F12 supplemented with 10% hiFBS. In DMEM:F12 supplemented with 15% hiFBS, cells grew up to 6.67E+05 cells. In DMEM:F12 supplemented with 10%hiFBS, cells grew up to 5.28E+05 cells. In DMEM supplemented with 15% hiFBS, the cells grew up to 4.76E+05 cells. There was a significant difference between culture media DMEM:F12 supplemented with 15% hiFBS as compared to DMEM:F12 supplemented with 10%hiFBS and DMEM supplemented with 15% hiFBS (p<0.05) following 24h incubation. However, there is no significant difference between DMEM:F12 supplemented with 10%hiFBS as compared to DMEM supplemented with 15% hiFBS (p>0.05).
References
Arora, M. (2013). Cell culture media: A review. Mater methods, 3, 175.
https://doi.org/10.13070/mm.en.3.175
Bak, L. K., Iversen, P., Sørensen, M., Keiding, S., Vilstrup, H., Ott, P., Waagepetersen, H. S., & Schousboe, A. (2009). Metabolic fate of isoleucine in a rat model of hepatic encephalopathy and in cultured neural cells exposed to ammonia. Met Brain Dis, 24(1), 135-145.
https://doi.org/10.1007/s11011-008-9123-4
Chen, J., & Herrup, K. (2012). Glutamine acts as a neuroprotectant against DNA damage, beta-amyloid and H2O2-induced stress. PLoS One, 7(3), e33177.
https://doi.org/10.1371/journal.pone.0033177
Dwane, S., Durack, E., & Kiely, P. A. (2013). Optimising parameters for the differentiation of SH-SY5Y cells to study cell adhesion and cell migration. BMC Res Notes, 6, 366.
https://doi.org/10.1186/1756-0500-6-366
Fang, C. Y., Wu, C. C., Fang, C. L., Chen, W. Y., & Chen, C. L. (2017). Long-term growth comparison studies of FBS and FBS alternatives in six head and neck cell lines. PLoS One, 12(6), e0178960.
https://doi.org/10.1371/journal.pone.0178960
Forster, J. I., Koglsberger, S., Trefois, C., Boyd, O., Baumuratov, A. S., Buck, L., Balling, R., & Antony, P. M. (2016). Characterization of differentiated SH-SY5Y as neuronal screening model reveals increased oxidative vulnerability. J Biomol Screen, 21(5), 496-509.
https://doi.org/10.1177/1087057115625190
Gürdal, M., Barut Selver, Ö., Baysal, K., & Durak, İ. (2018). Comparison of culture media indicates a role for autologous serum in enhancing phenotypic preservation of rabbit limbal stem cells in explant culture. Cytotechnology, 70(2), 687-700.
https://doi.org/10.1007/s10616-017-0171-7
Hattangady, N. G., & Rajadhyaksha, M. S. (2009). A brief review of in vitro models of diabetic neuropathy. Int J Diabetes Dev Ctries, 29(4), 143-149.
https://doi.org/10.4103/0973-3930.57344
Kovalevich, J., & Langford, D. (2013). Considerations for the use of SH-SY5Y neuroblastoma cells in neurobiology. Neuronal cell culture (pp. 9-21): Springer.
https://doi.org/10.1007/978-1-62703-640-5_2
Popova, D., Karlsson, J., & Jacobsson, S. O. P. (2017). Comparison of neurons derived from mouse p19, rat pc12 and human SH-SY5Y cells in the assessment of chemical- and toxin-induced neurotoxicity. BMC Pharmacol Toxicol, 18(1), 42.
https://doi.org/10.1186/s40360-017-0151-8
Sakagami, H., Suzuki, R., Shirataki, Y., Iwama, S., Nakagawa, M., Suzuki, H., Tanaka, K., Tamura, N., & Takeshima, H. (2017). Re-evaluation of culture condition of pc12 and SH-SY5Y cells based on growth rate and amino acid consumption. In Vivo, 31(6), 1089-1095.
https://doi.org/10.21873/invivo.11174
Shipley, M. M., Mangold, C. A., & Szpara, M. L. (2016). Differentiation of the SH-SY5Y human neuroblastoma cell line. J Vis Exp(108), 53193.
Smerker, H. (2014). Weaning and adaptation of SH-SY5Y cells to low glucose media for manganese exposure studies. 2014 NCUR.
Xicoy, H., Wieringa, B., & Martens, G. J. (2017). The SH-SY5Y cell line in Parkinson's disease research: A systematic review. Mol Neurodegener, 12(1), 10.
This work is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License.
Copyright (c) 2018 Array