TY - JOUR
T1 - Widespread nitration of pathological inclusions in neurodegenerative synucleinopathies
AU - Duda, John E.
AU - Giasson, Benoit I.
AU - Chen, Qiping
AU - Gur, Tamar L.
AU - Hurtig, Howard I.
AU - Stern, Matthew B.
AU - Gollomp, Steven M.
AU - Ischiropoulos, Harry
AU - Lee, Virginia M.Y.
AU - Trojanowski, John Q.
N1 - Funding Information:
Supported by grants from the National Institutes of Health and by a Pioneer Award from the Alzheimer's Association. B. I. G. is the recipient of a fellowship from the Human Frontier Science Program Organization.
PY - 2000
Y1 - 2000
N2 - Reactive nitrogen species may play a mechanistic role in neurodegenerative diseases by posttranslationally altering normal brain proteins. In support of this hypothesis, we demonstrate that an anti-3-nitrotyrosine polyclonal antibody stains all of the major hallmark lesions of synucleinopathies including Lewy bodies, Lewy neurites and neuraxonal spheroids in dementia with Lewy bodies, the Lewy body variant of Alzheimer's disease, and neurodegeneration with brain iron accumulation type 1, as well as glial and neuronal cytoplasmic inclusions in multiple system atrophy. This antibody predominantly recognized nitrated α-synuclein when compared to other in vitro nitrated constituents of these pathological lesions, such as neurofilament subunits and microtubules. Collectively, these findings imply that α-synuclein is nitrated in pathological lesions. The widespread presence of nitrated α-synuclein in diverse intracellular inclusions suggests that oxidation/nitration is involved in the onset and/or progression of neurodegenerative diseases.
AB - Reactive nitrogen species may play a mechanistic role in neurodegenerative diseases by posttranslationally altering normal brain proteins. In support of this hypothesis, we demonstrate that an anti-3-nitrotyrosine polyclonal antibody stains all of the major hallmark lesions of synucleinopathies including Lewy bodies, Lewy neurites and neuraxonal spheroids in dementia with Lewy bodies, the Lewy body variant of Alzheimer's disease, and neurodegeneration with brain iron accumulation type 1, as well as glial and neuronal cytoplasmic inclusions in multiple system atrophy. This antibody predominantly recognized nitrated α-synuclein when compared to other in vitro nitrated constituents of these pathological lesions, such as neurofilament subunits and microtubules. Collectively, these findings imply that α-synuclein is nitrated in pathological lesions. The widespread presence of nitrated α-synuclein in diverse intracellular inclusions suggests that oxidation/nitration is involved in the onset and/or progression of neurodegenerative diseases.
UR - https://www.scopus.com/pages/publications/0033678217
U2 - 10.1016/S0002-9440(10)64781-5
DO - 10.1016/S0002-9440(10)64781-5
M3 - Article
C2 - 11073803
AN - SCOPUS:0033678217
SN - 0002-9440
VL - 157
SP - 1439
EP - 1445
JO - American Journal of Pathology
JF - American Journal of Pathology
IS - 5
ER -