PloS one, 2013-04, Vol.8 (4), p.e59749-e59749
2013
Details
- Autor(en) / Beteiligte
- Titel
- Expression of tryptophan 2,3-dioxygenase and production of kynurenine pathway metabolites in triple transgenic mice and human Alzheimer's disease brain
- Ist Teil von
- PloS one, 2013-04, Vol.8 (4), p.e59749-e59749
- Ort / Verlag
- United States: Public Library of Science
- Erscheinungsjahr
- 2013
- Link zum Volltext
- Quelle
- MEDLINE
- Beschreibungen/Notizen
- To assess the role of the kynurenine pathway in the pathology of Alzheimer's disease (AD), the expression and localization of key components of the kynurenine pathway including the key regulatory enzyme tryptophan 2,3 dioxygenase (TDO), and the metabolites tryptophan, kynurenine, kynurenic acid, quinolinic acid and picolinic acid were assessed in different brain regions of triple transgenic AD mice. The expression and cell distribution of TDO and quinolinic acid, and their co-localization with neurofibrillary tangles and senile β amyloid deposition were also determined in hippocampal sections from human AD brains. The expression of TDO mRNA was significantly increased in the cerebellum of AD mouse brain. Immunohistochemistry demonstrated that the density of TDO immuno-positive cells was significantly higher in the AD mice. The production of the excitotoxin quinolinic acid strongly increased in the hippocampus in a progressive and age-dependent manner in AD mice. Significantly higher TDO and indoleamine 2,3 dioxygenase 1 immunoreactivity was observed in the hippocampus of AD patients. Furthermore, TDO co-localizes with quinolinic acid, neurofibrillary tangles-tau and amyloid deposits in the hippocampus of AD. These results show that the kynurenine pathway is over-activated in AD mice. This is the first report demonstrating that TDO is highly expressed in the brains of AD mice and in AD patients, suggesting that TDO-mediated activation of the kynurenine pathway could be involved in neurofibrillary tangles formation and associated with senile plaque. Our study adds to the evidence that the kynurenine pathway may play important roles in the neurodegenerative processes of AD.
- Sprache
- Englisch
- Identifikatoren
- ISSN: 1932-6203eISSN: 1932-6203DOI: 10.1371/journal.pone.0059749Titel-ID: cdi_plos_journals_1335054153
- Format
- –
- Schlagworte
- 3-Hydroxyanthranilate 3,4-Dioxygenase - genetics, 3-Hydroxyanthranilate 3,4-Dioxygenase - metabolism, Acids, Advertising executives, Age, Aged, Aged, 80 and over, Agriculture, Alzheimer Disease - enzymology, Alzheimer's disease, Alzheimers disease, Amyloid, Animals, Biology, Brain, Brain research, CA1 Region, Hippocampal - enzymology, CA3 Region, Hippocampal - enzymology, Carboxy-Lyases - genetics, Carboxy-Lyases - metabolism, Case-Control Studies, Cerebellum, Cerebellum - enzymology, Cerebral Cortex - enzymology, Discipline, Enzymes, Gene Expression, Genetic engineering, Hippocampus, Humans, Immunohistochemistry, Indoleamine-Pyrrole 2,3,-Dioxygenase - genetics, Indoleamine-Pyrrole 2,3,-Dioxygenase - metabolism, Kynurenic acid, Kynurenine - metabolism, Localization, Medical research, Medicine, Medicine, Experimental, Metabolic Networks and Pathways, Metabolism, Metabolites, Mice, Mice, 129 Strain, Mice, Inbred C57BL, Mice, Transgenic, Middle Aged, mRNA, Muridae, Neurodegeneration, Neurodegenerative diseases, Neurofibrillary tangles, Organ Specificity, Pathology, Patients, Pentosyltransferases - genetics, Pentosyltransferases - metabolism, Pharmaceutical sciences, Pharmacology, Picolinic acid, Quinolinic acid, Real-Time Polymerase Chain Reaction, RNA, RNA, Messenger - genetics, RNA, Messenger - metabolism, Rodents, Senile plaques, Tau protein, Transgenic mice, Tryptophan, Tryptophan - metabolism, Tryptophan 2,3-dioxygenase, Tryptophan Oxygenase - genetics, Tryptophan Oxygenase - metabolism