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Chemical hormesis in cell growth: a molecular target at the cell surface
Author(s) -
Morré D. James
Publication year - 2000
Publication title -
journal of applied toxicology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.784
H-Index - 87
eISSN - 1099-1263
pISSN - 0260-437X
DOI - 10.1002/(sici)1099-1263(200003/04)20:2<157::aid-jat648>3.0.co;2-9
Subject(s) - hormesis , nox , cell , cell division , chemistry , cell growth , microbiology and biotechnology , biochemistry , biophysics , biology , oxidative stress , organic chemistry , combustion
A multifunctional ubiquinol (NADH) oxidase with protein disulfide–thiol interchange activity of the cell surface, abbreviated as NOX, is described as a molecular target for chemical hormesis of cell growth. The activity of the NOX correlates with rate of cell enlargement, which helps to determine how rapidly cells will divide. When NOX activity is inhibited, cells fail to enlarge following division and the result is a population of small cells unable to reach the minimum size required for them to divide again. In plants, cells fail to enlarge when NOX activity is inhibited. When NOX activity is stimulated or constitutively activated, as in cancer, cells enlarge more rapidly and the rate of cell division also is enhanced. Both cell growth and NOX activity are sometimes stimulated by low concentrations of normally inhibitory molecules. These properties define chemical hormesis, making the NOX molecule a molecular target to explain hormetic growth responses and to utilize hormetic principles to increase, for example, crop yields with plants. The NOX activity at the cell surface oscillates with a temperature‐compensated 24‐min ultradian (<24 h) periodicity. The indicated function of the NOX protein as a time‐keeping mechanism adds to its potential importance as a molecular target for chemical hormesis. Copyright © 2000 John Wiley & Sons, Ltd.