Premium
Tracking Live‐Cell Response to Hexavalent Chromium Toxicity by using Scanning Electrochemical Microscopy
Author(s) -
Henderson Jeffrey D.,
Filice Fraser P.,
Li Michelle S. M.,
Ding Zhifeng
Publication year - 2017
Publication title -
chemelectrochem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.182
H-Index - 59
ISSN - 2196-0216
DOI - 10.1002/celc.201600783
Subject(s) - scanning electrochemical microscopy , hexavalent chromium , membrane permeability , biophysics , membrane , chemistry , permeability (electromagnetism) , viability assay , cell membrane , incubation , homeostasis , cytotoxicity , toxicity , chromium , cell , electrochemistry , biochemistry , in vitro , microbiology and biotechnology , biology , electrode , organic chemistry
The effects of exposure to toxic heavy metals, such as chromium, are of interest in scientific research, owing to its association with oxidative stress, cytotoxicity, and carcinogenicity. This study aims to explore the effects of Cr (VI) on live cell responses. Herein, scanning electrochemical microscopy (SECM) is employed by using depth scan imaging and feedback mode to monitor the membrane permeability of single live human bladder cancer (T24) cells following 1 h incubations with Cr (VI) stimuli. By using membrane‐permeable and impermeable redox mediators, ferrocenemethanol and ferrocenecarboxylic acid, respectively, SECM depth scans yield both electrochemical and topographic information. This provides insights into the relative changes in membrane homeostasis with increased exposure to Cr (VI). Here, SECM has shown great power in determining membrane response to Cr (VI) exposure. Dependent on the level of exposure, transition between three distinct trends was observed. At low incubation concentrations of Cr (VI), the cell membrane permeability coefficients were relatively unaffected. With moderate increases in Cr (VI) concentrations, membrane permeability coefficients of the incubated cells were observed to decrease. Finally, with the higher incubation concentrations, membrane permeability coefficients were found to increase toward values similar to control cells. The Cr (VI) toxicity was further investigated by means of a MTT cell viability study, which exhibited a similar decreasing trend to the cell membrane permeability. These findings further demonstrate the strength of SECM as a bioanalytical technique for monitoring cellular homeostasis.