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Lens epithelial cell apoptosis and intracellular Ca(2+) increase in the presence of xanthurenic acid
BACKGROUND: Xanthurenic acid is an endogenous product of tryptophan degradation by indoleamine 2,3-dioxygenase (IDO). We have previously reported that IDO is present in mammalian lenses, and xanthurenic acid is accumulated in the lenses with aging. Here, we studied the involvement of xanthurenic aci...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2002
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC103667/ https://www.ncbi.nlm.nih.gov/pubmed/11934353 http://dx.doi.org/10.1186/1471-2415-2-1 |
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author | Malina, Halina Richter, Christoph Frueh, Beatrice Hess, Otto M |
author_facet | Malina, Halina Richter, Christoph Frueh, Beatrice Hess, Otto M |
author_sort | Malina, Halina |
collection | PubMed |
description | BACKGROUND: Xanthurenic acid is an endogenous product of tryptophan degradation by indoleamine 2,3-dioxygenase (IDO). We have previously reported that IDO is present in mammalian lenses, and xanthurenic acid is accumulated in the lenses with aging. Here, we studied the involvement of xanthurenic acid in the human lens epithelial cell physiology. METHODS: Human lens epithelial cells primary cultures were used. Control cells, and cells in the presence of xanthurenic acid grow in the dark. Western blot analysis and immunofluorescence studies were performed. RESULTS: In the presence of xanthurenic acid human lens epithelial cells undergo apoptosis-like cell death. In the control cells gelsolin stained the perinuclear region, whereas in the presence of 10 μM xanthurenic acid gelsolin is translocated to the cytoskeleton, but does not lead to cytoskeleton breakdown. In the same condition caspase-3 activation, and DNA fragmentation was observed. At low (5 to 10 μM) of xanthurenic acid concentration, the elongation of the cytoskeleton was associated with migration of mitochondria and cytochrome c release. At higher concentrations xanthurenic acid (20 μM and 40 μM) damaged mitochondria were observed in the perinuclear region, and nuclear DNA cleavage was observed. We observed an induction of calpain Lp 82 and an increase of free Ca(2+) in the cells in a xanthurenic acid concentration-dependent manner. CONCLUSIONS: The results show that xanthurenic acid accumulation in human lens epithelial cells disturbs the normal cell physiology and leads to a cascade of pathological events. Xanthurenic acid induces calpain Lp82 and caspases in the cells growing in the dark and can be involved in senile cataract development. |
format | Text |
id | pubmed-103667 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2002 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-1036672002-05-02 Lens epithelial cell apoptosis and intracellular Ca(2+) increase in the presence of xanthurenic acid Malina, Halina Richter, Christoph Frueh, Beatrice Hess, Otto M BMC Ophthalmol Research Article BACKGROUND: Xanthurenic acid is an endogenous product of tryptophan degradation by indoleamine 2,3-dioxygenase (IDO). We have previously reported that IDO is present in mammalian lenses, and xanthurenic acid is accumulated in the lenses with aging. Here, we studied the involvement of xanthurenic acid in the human lens epithelial cell physiology. METHODS: Human lens epithelial cells primary cultures were used. Control cells, and cells in the presence of xanthurenic acid grow in the dark. Western blot analysis and immunofluorescence studies were performed. RESULTS: In the presence of xanthurenic acid human lens epithelial cells undergo apoptosis-like cell death. In the control cells gelsolin stained the perinuclear region, whereas in the presence of 10 μM xanthurenic acid gelsolin is translocated to the cytoskeleton, but does not lead to cytoskeleton breakdown. In the same condition caspase-3 activation, and DNA fragmentation was observed. At low (5 to 10 μM) of xanthurenic acid concentration, the elongation of the cytoskeleton was associated with migration of mitochondria and cytochrome c release. At higher concentrations xanthurenic acid (20 μM and 40 μM) damaged mitochondria were observed in the perinuclear region, and nuclear DNA cleavage was observed. We observed an induction of calpain Lp 82 and an increase of free Ca(2+) in the cells in a xanthurenic acid concentration-dependent manner. CONCLUSIONS: The results show that xanthurenic acid accumulation in human lens epithelial cells disturbs the normal cell physiology and leads to a cascade of pathological events. Xanthurenic acid induces calpain Lp82 and caspases in the cells growing in the dark and can be involved in senile cataract development. BioMed Central 2002-04-05 /pmc/articles/PMC103667/ /pubmed/11934353 http://dx.doi.org/10.1186/1471-2415-2-1 Text en Copyright © 2002 Malina et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL. |
spellingShingle | Research Article Malina, Halina Richter, Christoph Frueh, Beatrice Hess, Otto M Lens epithelial cell apoptosis and intracellular Ca(2+) increase in the presence of xanthurenic acid |
title | Lens epithelial cell apoptosis and intracellular Ca(2+) increase in the presence of xanthurenic acid |
title_full | Lens epithelial cell apoptosis and intracellular Ca(2+) increase in the presence of xanthurenic acid |
title_fullStr | Lens epithelial cell apoptosis and intracellular Ca(2+) increase in the presence of xanthurenic acid |
title_full_unstemmed | Lens epithelial cell apoptosis and intracellular Ca(2+) increase in the presence of xanthurenic acid |
title_short | Lens epithelial cell apoptosis and intracellular Ca(2+) increase in the presence of xanthurenic acid |
title_sort | lens epithelial cell apoptosis and intracellular ca(2+) increase in the presence of xanthurenic acid |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC103667/ https://www.ncbi.nlm.nih.gov/pubmed/11934353 http://dx.doi.org/10.1186/1471-2415-2-1 |
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