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Role for Glyoxalase I in Alzheimer's Disease
by
Münch, Gerald
, Hoerndli, Frederic
, Kuhla, Björn
, Rogaev, Evgeny I.
, Chen, Feng
, Tsolaki, Magdalini
, Götz, Jürgen
, Baulieu, Etienne-Emile
, Wollmer, M. Axel
, Papassotiropoulos, Andreas
in
Alzheimer Disease - enzymology
/ Alzheimer Disease - metabolism
/ Alzheimer's disease
/ Alzheimers disease
/ Amino Acid Substitution
/ Amino acids
/ Animal diseases
/ Animal models
/ Animals
/ Antibodies
/ Biological Sciences
/ Brain
/ Brain - enzymology
/ Brain - metabolism
/ Dementia
/ Dementia disorders
/ Detoxification
/ Diabetes
/ Gene expression
/ Gene Expression Profiling
/ Genes
/ Humans
/ Immunohistochemistry
/ Lactoylglutathione Lyase - genetics
/ Lactoylglutathione Lyase - metabolism
/ Mice
/ Mice, Transgenic
/ Nervous system diseases
/ Neurons
/ Oligonucleotide Array Sequence Analysis
/ Oligonucleotide probes
/ Polymorphism, Single Nucleotide
/ Ribonucleic acid
/ RNA
/ RNA, Messenger - metabolism
/ T tests
/ Transgenic animals
/ Up-Regulation
2004
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Role for Glyoxalase I in Alzheimer's Disease
by
Münch, Gerald
, Hoerndli, Frederic
, Kuhla, Björn
, Rogaev, Evgeny I.
, Chen, Feng
, Tsolaki, Magdalini
, Götz, Jürgen
, Baulieu, Etienne-Emile
, Wollmer, M. Axel
, Papassotiropoulos, Andreas
in
Alzheimer Disease - enzymology
/ Alzheimer Disease - metabolism
/ Alzheimer's disease
/ Alzheimers disease
/ Amino Acid Substitution
/ Amino acids
/ Animal diseases
/ Animal models
/ Animals
/ Antibodies
/ Biological Sciences
/ Brain
/ Brain - enzymology
/ Brain - metabolism
/ Dementia
/ Dementia disorders
/ Detoxification
/ Diabetes
/ Gene expression
/ Gene Expression Profiling
/ Genes
/ Humans
/ Immunohistochemistry
/ Lactoylglutathione Lyase - genetics
/ Lactoylglutathione Lyase - metabolism
/ Mice
/ Mice, Transgenic
/ Nervous system diseases
/ Neurons
/ Oligonucleotide Array Sequence Analysis
/ Oligonucleotide probes
/ Polymorphism, Single Nucleotide
/ Ribonucleic acid
/ RNA
/ RNA, Messenger - metabolism
/ T tests
/ Transgenic animals
/ Up-Regulation
2004
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Role for Glyoxalase I in Alzheimer's Disease
by
Münch, Gerald
, Hoerndli, Frederic
, Kuhla, Björn
, Rogaev, Evgeny I.
, Chen, Feng
, Tsolaki, Magdalini
, Götz, Jürgen
, Baulieu, Etienne-Emile
, Wollmer, M. Axel
, Papassotiropoulos, Andreas
in
Alzheimer Disease - enzymology
/ Alzheimer Disease - metabolism
/ Alzheimer's disease
/ Alzheimers disease
/ Amino Acid Substitution
/ Amino acids
/ Animal diseases
/ Animal models
/ Animals
/ Antibodies
/ Biological Sciences
/ Brain
/ Brain - enzymology
/ Brain - metabolism
/ Dementia
/ Dementia disorders
/ Detoxification
/ Diabetes
/ Gene expression
/ Gene Expression Profiling
/ Genes
/ Humans
/ Immunohistochemistry
/ Lactoylglutathione Lyase - genetics
/ Lactoylglutathione Lyase - metabolism
/ Mice
/ Mice, Transgenic
/ Nervous system diseases
/ Neurons
/ Oligonucleotide Array Sequence Analysis
/ Oligonucleotide probes
/ Polymorphism, Single Nucleotide
/ Ribonucleic acid
/ RNA
/ RNA, Messenger - metabolism
/ T tests
/ Transgenic animals
/ Up-Regulation
2004
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Journal Article
Role for Glyoxalase I in Alzheimer's Disease
2004
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Overview
P301L mutant tau transgenic mice develop neurofibrillary tangles, a histopathologic hallmark of Alzheimer's disease and frontotemporal dementia (FTDP-17). To identify differentially expressed genes and to gain insight into pathogenic mechanisms, we performed a stringent analysis of the microarray dataset obtained with RNA from whole brains of P301L mutant mice and identified a single up-regulated gene, glyoxalase I. This enzyme plays a critical role in the detoxification of dicarbonyl compounds and thereby reduces the formation of advanced glycation end products. In situ hybridization analysis revealed expression of glyoxalase I in all brain areas analyzed, both in transgenic and control mice. However, levels of glyoxalase I protein were significantly elevated in P301L brains, as shown by Western blot analysis and immunohistochemistry. Moreover, a glyoxalase I-specific antiserum revealed many intensely stained flame-shaped neurons in Alzheimer's disease brain compared with brains from nondemented controls. In addition, we examined a single nucleotide polymorphism predicting a nonconservative amino acid substitution at position 111 (E111A) in ethnically independent populations. We identified significant and consistent deviations from Hardy-Weinberg equilibrium, which points to the presence of selection forces. The E111A single nucleotide polymorphism was not associated with the risk for Alzheimer's disease in the overall population. Together, our data demonstrate the potential of transcriptomics applied to animal models of human diseases. They suggest a previously unidentified role for glyoxalase I in neurodegenerative disease.
Publisher
National Academy of Sciences,National Acad Sciences
Subject
Alzheimer Disease - enzymology
/ Alzheimer Disease - metabolism
/ Animals
/ Brain
/ Dementia
/ Diabetes
/ Genes
/ Humans
/ Lactoylglutathione Lyase - genetics
/ Lactoylglutathione Lyase - metabolism
/ Mice
/ Neurons
/ Oligonucleotide Array Sequence Analysis
/ Polymorphism, Single Nucleotide
/ RNA
/ T tests
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