The neuroprotective effects of virally-derived caspase inhibitors p35 and crmA following a necrotic insult
Neuronal excitotoxicity causes energetic impairment and the ensuing cell death has historically been regarded as necrotic. Recent findings, however, indicate that apoptosis may participate in excitotoxicity. Here we examined the neuroprotective mechanisms of the well-characterized viral caspase inhi...
Main Authors: | , |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2003-10-01
|
Series: | Neurobiology of Disease |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S0969996103000834 |
id |
doaj-540aebc0713746509951a39b7f3778c3 |
---|---|
record_format |
Article |
spelling |
doaj-540aebc0713746509951a39b7f3778c32021-03-20T04:48:33ZengElsevierNeurobiology of Disease1095-953X2003-10-0114119The neuroprotective effects of virally-derived caspase inhibitors p35 and crmA following a necrotic insultMadhuri Roy0Robert M Sapolsky1Department of Biological Sciences, Stanford University, Stanford, CA 94305-5020, USADepartment of Biological Sciences, Stanford University, Stanford, CA 94305-5020, USANeuronal excitotoxicity causes energetic impairment and the ensuing cell death has historically been regarded as necrotic. Recent findings, however, indicate that apoptosis may participate in excitotoxicity. Here we examined the neuroprotective mechanisms of the well-characterized viral caspase inhibitors, p35 and crmA, following domoic acid-induced excitotoxicity in hippocampal neurons. We show that though p35 and crmA rescued neurons from toxicity, they did so under conditions of negligible caspase activation and morphological apoptosis. Thus, we characterized the novel neuroprotective effects of p35 and crmA and found that they attenuated the drop in the mitochondrial potential and blunted the decline in ATP levels. These data, to our knowledge, are the first detailed descriptions of the cell death mechanisms following domoic acid treatment of neurons. Moreover, in demonstrating the previously unexplored modulation of these processes, these data underline the capacity for classically “anti-apoptotic” proteins to alter other branches of cell death processes.http://www.sciencedirect.com/science/article/pii/S0969996103000834HippocampusApoptosisDomoic acidcrmAp35Caspase |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Madhuri Roy Robert M Sapolsky |
spellingShingle |
Madhuri Roy Robert M Sapolsky The neuroprotective effects of virally-derived caspase inhibitors p35 and crmA following a necrotic insult Neurobiology of Disease Hippocampus Apoptosis Domoic acid crmA p35 Caspase |
author_facet |
Madhuri Roy Robert M Sapolsky |
author_sort |
Madhuri Roy |
title |
The neuroprotective effects of virally-derived caspase inhibitors p35 and crmA following a necrotic insult |
title_short |
The neuroprotective effects of virally-derived caspase inhibitors p35 and crmA following a necrotic insult |
title_full |
The neuroprotective effects of virally-derived caspase inhibitors p35 and crmA following a necrotic insult |
title_fullStr |
The neuroprotective effects of virally-derived caspase inhibitors p35 and crmA following a necrotic insult |
title_full_unstemmed |
The neuroprotective effects of virally-derived caspase inhibitors p35 and crmA following a necrotic insult |
title_sort |
neuroprotective effects of virally-derived caspase inhibitors p35 and crma following a necrotic insult |
publisher |
Elsevier |
series |
Neurobiology of Disease |
issn |
1095-953X |
publishDate |
2003-10-01 |
description |
Neuronal excitotoxicity causes energetic impairment and the ensuing cell death has historically been regarded as necrotic. Recent findings, however, indicate that apoptosis may participate in excitotoxicity. Here we examined the neuroprotective mechanisms of the well-characterized viral caspase inhibitors, p35 and crmA, following domoic acid-induced excitotoxicity in hippocampal neurons. We show that though p35 and crmA rescued neurons from toxicity, they did so under conditions of negligible caspase activation and morphological apoptosis. Thus, we characterized the novel neuroprotective effects of p35 and crmA and found that they attenuated the drop in the mitochondrial potential and blunted the decline in ATP levels. These data, to our knowledge, are the first detailed descriptions of the cell death mechanisms following domoic acid treatment of neurons. Moreover, in demonstrating the previously unexplored modulation of these processes, these data underline the capacity for classically “anti-apoptotic” proteins to alter other branches of cell death processes. |
topic |
Hippocampus Apoptosis Domoic acid crmA p35 Caspase |
url |
http://www.sciencedirect.com/science/article/pii/S0969996103000834 |
work_keys_str_mv |
AT madhuriroy theneuroprotectiveeffectsofvirallyderivedcaspaseinhibitorsp35andcrmafollowinganecroticinsult AT robertmsapolsky theneuroprotectiveeffectsofvirallyderivedcaspaseinhibitorsp35andcrmafollowinganecroticinsult AT madhuriroy neuroprotectiveeffectsofvirallyderivedcaspaseinhibitorsp35andcrmafollowinganecroticinsult AT robertmsapolsky neuroprotectiveeffectsofvirallyderivedcaspaseinhibitorsp35andcrmafollowinganecroticinsult |
_version_ |
1724212119620026368 |