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NEDD8 protein is involved in ubiquitinated inclusion bodies
The Journal of pathology, 2003-02, Vol.199 (2), p.259-266
Dil Kuazi, Afroz
Kito, Katsumi
Abe, Yasuhito
Shin, Ryong-Woon
Kamitani, Tetsu
Ueda, Norifumi
2003
Volltextzugriff (PDF)
Details
Autor(en) / Beteiligte
Dil Kuazi, Afroz
Kito, Katsumi
Abe, Yasuhito
Shin, Ryong-Woon
Kamitani, Tetsu
Ueda, Norifumi
Titel
NEDD8 protein is involved in ubiquitinated inclusion bodies
Ist Teil von
The Journal of pathology, 2003-02, Vol.199 (2), p.259-266
Ort / Verlag
Chichester, UK: John Wiley & Sons, Ltd
Erscheinungsjahr
2003
Quelle
MEDLINE
Beschreibungen/Notizen
Proteolysis by the ubiquitin–proteasome system is considered to play a pathological role in several degenerative diseases that involve ubiquitinated inclusion bodies. In recent years, several ubiquitin‐like proteins have been isolated, but it is uncertain whether their roles are associated with protein degradation through the ubiquitin–proteasome system. NEDD8 (neural precursor cell‐expressed and developmentally down‐regulated gene), which consists of 81 amino acid residues, possesses the highest sequence similarity to ubiquitin. Recent studies have indicated that NEDD8 is covalently ligated to cullin family proteins, which are components of certain ubiquitin E3 ligases, by a pathway analogous to that of ubiquitin. Thus, by focusing on the structural and functional association between NEDD8 and ubiquitin, it would be of interest to know whether the NEDD8 system is involved in pathological disorders of the ubiquitin–proteasome system. This study has examined the immunohistochemical distribution of NEDD8 protein by using a highly purified antibody in normal tissues and in tissues known to contain ubiquitinated inclusions. NEDD8 protein expression was widely observed in most types of tissues. Furthermore, accumulation of the NEDD8 protein was commonly observed in ubiquitinated inclusion bodies, including Lewy bodies in Parkinson's disease, Mallory bodies in alcoholic liver disease, and Rosenthal fibres in astrocytoma. Two of ten cases of neurofibrillary tangles and senile plaques from patients with Alzheimer's disease showed intense staining for NEDD8 as well as for ubiquitin. These findings suggest the possibility that the NEDD8 system is involved in the metabolism of these inclusion bodies via the ubiquitin–proteasome system. Copyright © 2003 John Wiley & Sons, Ltd.
Sprache
Englisch
Identifikatoren
ISSN: 0022-3417
eISSN: 1096-9896
DOI: 10.1002/path.1283
Titel-ID: cdi_crossref_primary_10_1002_path_1283
Format
–
Schlagworte
Alzheimer Disease - pathology
,
Antibodies - analysis
,
Antibody Specificity - immunology
,
Biological and medical sciences
,
Blotting, Western - methods
,
Cell Line
,
Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
,
Gastroenterology. Liver. Pancreas. Abdomen
,
Gene Expression
,
Humans
,
Immunohistochemistry - methods
,
inclusion bodies
,
Inclusion Bodies - metabolism
,
Inclusion Bodies - pathology
,
Lewy Bodies - metabolism
,
Lewy body
,
Liver Diseases, Alcoholic - pathology
,
Liver. Biliary tract. Portal circulation. Exocrine pancreas
,
Mallory body
,
Medical sciences
,
NEDD8
,
NEDD8 Protein
,
neurofibrillary tangle
,
Neurofibrillary Tangles - metabolism
,
Neurology
,
Other diseases. Semiology
,
Parkinson Disease - pathology
,
Recombinant Proteins - metabolism
,
Rosenthal fibre
,
senile plaque
,
ubiquitin
,
Ubiquitin - metabolism
,
Ubiquitins - immunology
,
Ubiquitins - metabolism
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