The Unreliability of MTT Assay in the Cytotoxic Test of Primary Cultured Glioblastoma Cells.
- Author:
Hwa Yeon JO
1
;
Yona KIM
;
Hyung Woo PARK
;
Hyo Eun MOON
;
Seongtae BAE
;
Jinwook KIM
;
Dong Gyu KIM
;
Sun Ha PAEK
Author Information
- Publication Type:Original Article
- Keywords: primary cell; ethanol; Tetrazolium salts; non-specific intracellular reduction
- MeSH: Apoptosis Regulatory Proteins; Blotting, Western; Ethanol; Glioblastoma*; Membranes; NAD; Tetrazolium Salts
- From:Experimental Neurobiology 2015;24(3):235-245
- CountryRepublic of Korea
- Language:English
- Abstract: MTT assay is commonly used to assess the cellular cytotoxicity caused by anticancer drugs in glioblastomas. However, there have been some reports insisting that MTT assay exhibited non-specific intracellular reduction of tetrazolium which led to underestimated results of cytotoxicity. Here, we examine whether or not MTT assay can lead to incorrect information regarding alcohol-induced cytotoxicity on immortalized and primary glioblastoma cells. MTT assay was applied to assess the ethanol-induced cytotoxicity at various ethanol concentrations. The cellular cytotoxicity induced by different doses of ethanol was analyzed and compared through several cytotoxic assays. Ethanol-induced cytotoxicity observed through MTT assay on both cell types was shown to be ethanol dose-dependent below a 3% concentration. However, the cytotoxicity was shown to be markedly underestimated only in primary cells at a 5% concentration. RT-PCR and Western Blot showed increased expressions of pro-apoptotic proteins and decreased expressions of anti-apoptotic proteins in an ethanol dose-dependent manner in both cell types. Furthermore, we present a possible mechanism for the unreliable result of MTT assay. A high concentration of ethanol induces more severe membrane damage and increased intracellular concentration of NADH in primary cells which enhances the nonspecific reduction of tetrazolium salt. Together, our findings demonstrate that the cytotoxicity on primary cells could inaccurately be assessed when detected through MTT assay. Therefore, a careful interpretation is needed when one would analyze the cytotoxic results of MTT assay, and it is suggested that other assays must be accompanied to produce more reliable and accurate cytotoxic results on primary glioblastoma cells.
