Data di Pubblicazione:
2001
Citazione:
Huntingtin’s neuroprotective activity occurs via inhibition of pro-caspase 9 processing / D. Rigamonti, S. Sipione, D. Goffredo, C. Zuccato, E. Fossale, E. Cattaneo. - In: THE JOURNAL OF BIOLOGICAL CHEMISTRY. - ISSN 0021-9258. - 276:18(2001), pp. 14545-14548. [10.1074/jbc.C100044200]
Abstract:
Huntington's Disease is an inherited neurodegenerative disease that affects the medium spiny neurons in the striatum. The disease is caused by the expansion of a polyglutamine sequence in the N terminus of Huntingtin (Htt), a widely expressed protein. Recently, we have found that Htt is an antiapoptotic protein in striatal cells and acts by preventing caspase-3 activity. Here we report that Htt overexpression in other CNS-derived cells can protect them from more than 20 days exposure to fatal stimuli. In particular, we found that cytochrome c continues to be released from mitochondria into the cytosol of cells that overexpress normal Htt. However, procaspase-9 is not processed, indicating that wild-type Htt (wtHtt) acts downstream of cytochrome c release. These data show that Htt inhibits neuronal cell death by interfering with the activity of the apoptosome complex.
Tipologia IRIS:
01 - Articolo su periodico
Elenco autori:
D. Rigamonti, S. Sipione, D. Goffredo, C. Zuccato, E. Fossale, E. Cattaneo
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