Combining three in vitro assays for detecting early signs of UVB cytotoxicity in cultured human skin fibroblasts

Abstract

The aim of this study was to determine the most sensitive approach for detecting the early signs of UVB-induced cellular damage using human skin fibroblasts. UVB-induced cell damage was assessed immediately and 24 h post irradiation using 3 in vitro colorimetric assays: neutral red (NR); 5-(3-carboxymethoxyphenyl)-2-(4.5-dimethylthiazolyl)-3-(4-sulphonyl) MTS; and (iii) LDH enzyme release. A good correlation was observed immediately post exposure between the MTS and NR in measuring damage levels, but was lost 24 h post exposure. This loss of correlation was the result of delayed expression of lysosomal damage and led to investigating cell membrane damage using LDH cell leakage assay. LDH levels observed immediately post UVB irradiation indicated significant LDH release at exposure doses of 2.2 and 2.8 J/cm 2 , while LDH release reported 24 h post exposure was recorded for doses as low as 0.70 J/cm 2 . The data reported in this paper indicated that cell viability and damage were significantly affected in a dose dependent manner as a result of exposure doses. The assays used displayed different sensitivities in detecting damage with the earliest signs of cellular UVB damage best-measured 24 h following exposure using the LDH assay. Furthermore UVB contributed to denaturing the cellular LDH released during irradiation. Therefore the use of LDH cytotoxicity based assays with UVB exposure must be considered with extreme care.

Surface water toxicity assessment by ecotoxicological andin vitrotoxicologocical assays

“…Human-derived cell use assisted in eliminating uncertainties in data extrapolation (animals to humans) and the use of animals in testing [8]. Furthermore, the techniques used are rapid and reproducible as they generate accurate toxicity profiles within hours of conducting the assays.…”

“…Furthermore the samples were tested looking at cell death as an end point using human-derived cell cultures that represents potential target organs (skin, lung and liver) in the human body. These cells by virtue of their location, numbers and ease of growth in culture could be used as possible indicators of cellular damage caused by contaminant exposure [8].…”

Toxicity of volatile organic compounds (VOCs) mixtures using human derived cells

“…The cell culture selection was based on potential targets of exposure in humans (mainly lung and liver). The selected cells by virtue of their location, numbers and ease of growth in culture could be used as possible indicators of cellular damage caused by multiple contaminant exposure in vitro [6]. Furthermore, the techniques used are rapid, reproducible and generate accurate individual and mixtures toxicity profiles within hours of conducting a full set of assays.…”