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Preventive effects of a water‐soluble derivative of chroman moiety of vitamin E on lipid hydroperoxide‐induced cell injuries and DNA cleavages through repressions of oxidative stress in the cytoplasm of human keratinocytes
Author(s) -
Huang Zhe,
Senoh Yuichiro,
Katoh Shinya,
Miwa Nobuhiko
Publication year - 2004
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.20081
Subject(s) - hacat , cytoplasm , cytotoxicity , oxidative stress , reactive oxygen species , intracellular , vitamin e , biochemistry , chemistry , antioxidant , cell , human skin , dna damage , microbiology and biotechnology , dna , biology , in vitro , genetics
ChrCrx (6‐hydroxy‐2, 5, 7, 8‐tetramethyl‐chroman‐2‐carboxylic acid) is a water‐soluble analog in which 4′, 8′, 12′‐trimethyltridecyl chain is deleted from an alpha‐tocopherol molecule known as a hydrophobic antioxidant. Cell viability of human skin epidermal keratinocytes HaCaT was lowered by treatment with tert ‐butylhydroperoxide ( t ‐BuOOH) of 50 μM for 48 h, designated as a subacute cytotoxicity, which was prevented by previous administration with ChrCrx in a dose‐dependent manner as estimated by mitochondrial function‐based WST‐1 assay and cell morphological microscopy. In contrast an acute cytotoxicity due to treatment with t ‐BuOOH as dense as 200 μM for a period as short as 2 h could be also prevented with ChrCrx that was administered before and after, but was eliminated during, treatment with t ‐BuOOH. In contrast α‐tocopherol was not cytoprotective against t ‐BuOOH. DNA strand cleavages were induced with t ‐BuOOH in the keratinocytes, and could be prevented by ChrCrx more effectively than α‐tocopherol as assayed by TUNEL stain. The intracellular reactive oxygen species (ROS) was accumulated in a manner dependent on periods of t ‐BuOOH treatment in the cytoplasm more abundantly rather than the nucleus of keratinocytes, and was markedly diminished by ChrCrx as shown by fluorography using the redox indicator dye. Thus t ‐BuOOH‐induced cell injuries and DNA cleavages of the keratinocytes can be prevented at least in part through efficient diminishment of ROS generated in the cytoplasm, to which the preferred distribution of ChrCrx may be advantageous over to the nucleus or membrane owing to its molecular hydrophilicity relative to α‐tocopherol. © 2004 Wiley‐Liss, Inc.