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Protein Carbonylation-Dependent Photoreceptor Cell Death Induced by N-Methyl-N-nitrosourea in Mice.
- Source :
-
Advances in experimental medicine and biology [Adv Exp Med Biol] 2018; Vol. 1074, pp. 297-302. - Publication Year :
- 2018
-
Abstract
- Retinal degenerative diseases, such as retinitis pigmentosa, are characterized by night blindness and peripheral vision loss caused by the slowly progressive loss of photoreceptor cells. A comprehensive molecular mechanism of the photoreceptor cell death remains unclear. We previously reported that heat shock protein 70 (HSP70), which has a protective effect on neuronal cells, was cleaved by a calcium-dependent protease, calpain, in N-methyl-N-nitrosourea (MNU)-treated mice retina. Carbonylated HSP70 is much more vulnerable than noncarbonylated HSP70 to calpain cleavage. However, it was not known whether protein carbonylation occurs in MNU-treated mice retina. In this study, we clearly show protein carbonylation-dependent photoreceptor cell death induced by MNU in mice. Therefore, protein carbonylation and subsequent calpain-dependent cleavage of HSP70 are key events in MNU-mediated photoreceptor cell death. Our data provide a comprehensive molecular mechanism of the photoreceptor cell death.
- Subjects :
- Aldehydes metabolism
Animals
Calpain metabolism
Cell Death drug effects
Disease Models, Animal
Injections, Intraperitoneal
Male
Methylnitrosourea administration & dosage
Mice
Mice, Inbred C57BL
Models, Molecular
Oxidative Stress
Retina metabolism
Retinal Degeneration metabolism
Retinal Degeneration pathology
Retinitis Pigmentosa metabolism
Eye Proteins metabolism
HSP70 Heat-Shock Proteins metabolism
Methylnitrosourea toxicity
Protein Carbonylation drug effects
Retina drug effects
Retinal Degeneration chemically induced
Subjects
Details
- Language :
- English
- ISSN :
- 0065-2598
- Volume :
- 1074
- Database :
- MEDLINE
- Journal :
- Advances in experimental medicine and biology
- Publication Type :
- Academic Journal
- Accession number :
- 29721956
- Full Text :
- https://doi.org/10.1007/978-3-319-75402-4_36