期刊
ARCHIVES OF TOXICOLOGY
卷 91, 期 9, 页码 3065-3078出版社
SPRINGER HEIDELBERG
DOI: 10.1007/s00204-017-1936-7
关键词
Lysosomes; Cathepsins; Apoptosis; Manganese; Glia; Parkinsonism
类别
资金
- Consejo Nacional de Investigaciones Cientificas y Tecnicas [CONICET PIP 0356, 0771]
- CONICET scholarships
Manganese (Mn) is an essential trace metal which plays a critical role in brain physiology by acting as a cofactor for several enzymes. However, upon overexposure, Mn preferentially accumulates within the basal ganglia leading to the development of a Parkinsonism known as Manganism. Data from our group have proved that Mn induces oxidative stress-mediated apoptosis in astrocytoma C6 cells. In the present study we described how cathepsins impact on different steps of each apoptotic cascade. Evidence obtained demonstrated that Mn generates lysosomal membrane permeabilization (LMP) and cathepsin release. Both cathepsins B (Ca-074 Me) and D (Pepstatin A) inhibitors as well as Bafilomycin A1 prevented caspases-3, -7, -8 and -9 activation, FasL upregulation, Bid cleavage, Delta phi m disruption and cytochrome c release. Results from in vivo studies showed that intrastriatal Mn injection increased cathepsin D levels from corpus striatum and substantia nigra pars compacta. Our results point to LMP and lysosomal cathepsins as key mediators in the apoptotic process triggered by Mn. These findings highlight the relevance of targeting the lysosomal pathway for Manganism therapy.
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