Journals / Celal Bayar Üniversitesi Fen Bilimleri Dergisi / 2018 / Cilt: 14 - Sayı: 1

Development of a Direct Trypan Blue Exclusion Method to Detect Cell Viability of Adherent Cells into ELISA Plates

Pages
99–104
Publication Date
2022-10-12
DOI
—
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⚡ TL;DR(Too Long; Didn't Read)

This modified protocol was validated by testing the effect of dimethylsulfoxide-a cytotoxic agent-on cells, and expectedly found that cell viability reduced with higher concentrations of dimethylsulfoxide suggesting that in situ detection of cell viability by trypan blue can be a useful tool for preliminary detection of cells cultured on ELISA plates before performing automatized experiments with such flow cytometer and/or microplate reader.

📌 3 Key Takeaways

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Objective & Hypothesis:Cell viability detection is important in cell culture applications including measurement of cell proliferation i.e for understanding cytotoxic effects of compounds on cells.
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Key Findings & Data:Thus, further fluorescence assays can include less concentrations rather than experiencing all used along 96- well plates.
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Conclusion & Impact:This modified protocol was validated by testing the effect of dimethylsulfoxide-a cytotoxic agent-on cells, and expectedly found that cell viability reduced with higher concentrations of dimethylsulfoxide suggesting that in situ detection of cell viability by trypan blue can be a useful tool for preliminary detection of cells cultured on ELISA plates before performing automatized experiments with such flow cytometer and/or microplate reader.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Cell viability detection is important in cell culture applications including measurement of cell proliferation i.e for understanding cytotoxic effects of compounds on cells. There are some cell viability methods based on fluorescence or non-fluorescence detection. More simplified evaluation for cell viability, such as trypan blue staining, can be preferred before performing fluorescence assays. This appears advantageous when to have a large number of cell samples in ELISA plates after treatments with different concentrations of drug candidates. Thus, further fluorescence assays can include less concentrations rather than experiencing all used along 96- well plates. For this, trypan blue exclusion method is an option. Traditionally, treated cells are harvested by centrifugation and incubated with trypan blue within tubes followed by transferring the mixture into a hemacytometer with two chambers and assessed under the microscope. Nevertheless, using a hemacytometer limits practicability of this method when analyzing various cell samples into 96-well plates at the same time. This study was aimed to adapt trypan blue method to in situ staining of adherent cells cultured on ELISA plates. For this, cells were fixed with different fixatives after trypan blue incubation to maintain cells in impenetrable meshwork, and paraformaldehyde was the most effective fixative. This modified protocol was validated by testing the effect of dimethylsulfoxide-a cytotoxic agent-on cells, and expectedly found that cell viability reduced with higher concentrations of dimethylsulfoxide suggesting that in situ detection of cell viability by trypan blue can be a useful tool for preliminary detection of cells cultured on ELISA plates before performing automatized experiments with such flow cytometer and/or microplate reader.

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Cite This Article

UZUNER, S. Ç. (2022). Development of a Direct Trypan Blue Exclusion Method to Detect Cell Viability of Adherent Cells into ELISA Plates. Celal Bayar Üniversitesi Fen Bilimleri Dergisi, Cilt: 14 - Sayı: 1, 99–104. https://ajindex.com/articles/472260

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References (1)

  1. Tapani, E., et al., Toxicity of ethanol in low concentrations - Experimental evaluation in cell culture. Acta Radiologica, 1996. 37(6): p. 923-926. 21. Yuan, C., et al., Dimethyl Sulfoxide Damages Mitochondrial Integrity and Membrane Potential in Cultured Astrocytes. Plos One, 2014. 9(9). 20. Jamalzadeh, L., et al., Cytotoxic Effects of Some Common Organic Solvents on MCF-7, RAW-264.7 and Human Umbilical Vein Endothelial Cells. The Avicenna Journal of Medical Biotechnology, 2016. 4(1): p. 10-33453. 19. Qi, W., D. Ding, and R.J. Salvi, Cytotoxic effects of dimethyl sulphoxide (DMSO) on cochlear organotypic cultures. Hear Research, 2008. 236(1-2): p. 52-60. 18. Da Violante, G., et al., Evaluation of the cytotoxicity effect of dimethyl sulfoxide (DMSO) on Caco2/TC7 colon tumor cell cultures. Biological and Pharmaceutical Bulletin, 2002. 25(12): p. 1600-163. 17. Bekircan, O., B. Kahveci, and M. Kucuk, Synthesis and anticancer evaluation of some new unsymmetrical 3,5-diaryl- 4H-1,2,4-triazole derivatives. Turkish Journal of Chemistry, 2006. 30(1): p. 29-40. 16. Amer, S., N. El-Wakiel, and H. Ei-Ghamry, Synthesis, spectral, antitumor and antimicrobial studies on Cu(II) complexes of purine and triazole Schiff base derivatives. Journal of Molecular Structure, 2013. 1049: p. 326-335. 15. Thavarajah, R., et al., Chemical and physical basics of routine formaldehyde fixation. Journal of Oral and Maxillofacial Pathology, 2012. 16(3): p. 400-405. 14. Wang, H., et al., Different fixative methods influence histological morphology and TUNEL staining in mouse testes. Reproductive Toxicology, 2016. 60: p. 53-61. 13. Kading, R., M. Crabtree, and B. Miller, Inactivation of infectious virus and serological detection of virus antigen in Rift Valley fever virus-exposed mosquitoes fixed with paraformaldehyde. Journal of Virological Methods, 2013. 189(1): p. 184-188. 12. Schnell, U., et al., Immunolabeling artifacts and the need for live- cell imaging. Nature Methods, 2012. 9(2): p. 152-158. 11. Mihara, K., T. Nakayama, and H. Saitoh, A Convenient Technique to Fix Suspension Cells on a Coverslip for Microscopy. Current Protocols in Cell Biology, 2015. 68: p. 4 30 1-10. 10. Perry, S.W., L.G. Epstein, and H.A. Gelbard, In situ Trypan Blue staining of monolayer cell cultures for permanent fixation and mounting. Biotechniques, 1997. 22(6): p. 1020-&. 9. Tanaka, K.A.K., et al., Membrane molecules mobile even after chemical fixation. Nature Methods, 2010. 7(11): p. 865-866. 8. Strobe