Document Detail

Chemical hormesis in cell growth: a molecular target at the cell surface.
MedLine Citation:
PMID:  10715615     Owner:  NLM     Status:  MEDLINE    
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.
D J Morré
Related Documents :
9501025 - Control of cell division in the root epidermis of arabidopsis thaliana.
2842315 - Cell division control in escherichia coli k-12: some properties of the ftsz84 mutation ...
7275175 - Asymmetric division of lymphoid cells of the thymus of embryonic guinea-pigs. a cell ki...
19704565 - Skp2a protein, an f-box that regulates cell division, is degraded via the ubiquitin pat...
24110255 - Retinal ganglion cells electrophysiology: the effect of cell morphology on impulse wave...
21273685 - Effects of ethylene glycol ethers on cell viability in the human neuroblastoma sh-sy5y ...
Publication Detail:
Type:  Journal Article; Review    
Journal Detail:
Title:  Journal of applied toxicology : JAT     Volume:  20     ISSN:  0260-437X     ISO Abbreviation:  J Appl Toxicol     Publication Date:    2000 Mar-Apr
Date Detail:
Created Date:  2000-04-21     Completed Date:  2000-04-21     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  8109495     Medline TA:  J Appl Toxicol     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  157-63     Citation Subset:  IM    
Copyright Information:
Copyright 2000 John Wiley & Sons, Ltd.
Department of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, IN 47907-1333, USA.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Adaptation, Physiological / drug effects,  physiology*
Cell Division / physiology
Cell Membrane / drug effects,  enzymology
Cells, Cultured / drug effects,  enzymology
Crops, Agricultural
Dose-Response Relationship, Drug
Enzyme Inhibitors / pharmacology
Multienzyme Complexes / antagonists & inhibitors,  metabolism*
NADH, NADPH Oxidoreductases / antagonists & inhibitors,  metabolism*
Plants / drug effects,  growth & development
Xenobiotics / adverse effects
Reg. No./Substance:
0/Enzyme Inhibitors; 0/Multienzyme Complexes; 0/Xenobiotics; EC 1.6.-/NADH oxidase; EC 1.6.-/NADH, NADPH Oxidoreductases

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Environmental law applications of hormesis concepts: risk assessment and cost-benefit implications.
Next Document:  The relevance of the rat lung response to particle overload for human risk assessment: a workshop co...