Calpain cleavage and inactivation of the sodium calcium exchanger-3 occur downstream of Aβ in Alzheimer's disease
Calpain cleavage and inactivation of the sodium calcium exchanger-3 occur downstream of Aβ in Alzheimer's disease
Alzheimer's disease (AD) is a neurodegenerative disorder characterized by pathological deposits of β-amyloid (Aβ) in senile plaques, intracellular neurofibrillary tangles (NFTs) comprising hyperphosphorylated aggregated tau, synaptic dysfunction and neuronal death. Substantial evidence indicates that disrupted neuronal calcium homeostasis is an early event in AD that could mediate synaptic dysfunction and neuronal toxicity. Sodium calcium exchangers (NCXs) play important roles in regulating intracellular calcium, and accumulating data suggests that reduced NCX function, following aberrant proteolytic cleavage of these exchangers, may contribute to neurodegeneration. Here, we show that elevated calpain, but not caspase-3, activity is a prominent feature of AD brain. In addition, we observe increased calpain-mediated cleavage of NCX3, but not a related family member NCX1, in AD brain relative to unaffected tissue and that from other neurodegenerative conditions. Moreover, the extent of NCX3 proteolysis correlated significantly with amounts of Aβ1-42. We also show that exposure of primary cortical neurons to oligomeric Aβ1-42 results in calpain-dependent cleavage of NCX3, and we demonstrate that loss of NCX3 function is associated with Aβ toxicity. Our findings suggest that Aβ mediates calpain cleavage of NCX3 in AD brain and therefore that reduced NCX3 activity could contribute to the sustained increases in intraneuronal calcium concentrations that are associated with synaptic and neuronal dysfunction in AD.
49-59
Atherton, Joe
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Kurbatskaya, Ksenia
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Bondulich, Marie
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Croft, Cara L.
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Garwood, Claire J.
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Chhabra, Resham
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Wray, Selina
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Jeromin, Andreas
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Hanger, Diane P.
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Noble, Wendy
e53fafef-a7f4-4b9c-982f-65ef7f00c35f
February 2014
Atherton, Joe
0317fd5f-260c-42ed-ab8e-4f910dcc13af
Kurbatskaya, Ksenia
11d25414-e10d-413a-aaf3-fb6b6c2cf890
Bondulich, Marie
06fc8188-8e41-485d-8808-b70cc61c1e18
Croft, Cara L.
c557d59a-042a-43a4-b0a5-cc501677ec4d
Garwood, Claire J.
ca6fa497-3fc9-452c-9efe-a04fd9c3f2a0
Chhabra, Resham
fd88d22f-8aa3-410b-ba40-b445be812e86
Wray, Selina
2352de05-d45d-49e0-a735-3dbfc540f16a
Jeromin, Andreas
cbcadb50-e689-48b5-89bc-20a9a5e4f40e
Hanger, Diane P.
7f1b5bc4-2410-4239-b6ac-8988f65d2973
Noble, Wendy
e53fafef-a7f4-4b9c-982f-65ef7f00c35f
Atherton, Joe, Kurbatskaya, Ksenia, Bondulich, Marie, Croft, Cara L., Garwood, Claire J., Chhabra, Resham, Wray, Selina, Jeromin, Andreas, Hanger, Diane P. and Noble, Wendy
(2014)
Calpain cleavage and inactivation of the sodium calcium exchanger-3 occur downstream of Aβ in Alzheimer's disease.
Aging Cell, 13 (1), .
(doi:10.1111/acel.12148).
Abstract
Alzheimer's disease (AD) is a neurodegenerative disorder characterized by pathological deposits of β-amyloid (Aβ) in senile plaques, intracellular neurofibrillary tangles (NFTs) comprising hyperphosphorylated aggregated tau, synaptic dysfunction and neuronal death. Substantial evidence indicates that disrupted neuronal calcium homeostasis is an early event in AD that could mediate synaptic dysfunction and neuronal toxicity. Sodium calcium exchangers (NCXs) play important roles in regulating intracellular calcium, and accumulating data suggests that reduced NCX function, following aberrant proteolytic cleavage of these exchangers, may contribute to neurodegeneration. Here, we show that elevated calpain, but not caspase-3, activity is a prominent feature of AD brain. In addition, we observe increased calpain-mediated cleavage of NCX3, but not a related family member NCX1, in AD brain relative to unaffected tissue and that from other neurodegenerative conditions. Moreover, the extent of NCX3 proteolysis correlated significantly with amounts of Aβ1-42. We also show that exposure of primary cortical neurons to oligomeric Aβ1-42 results in calpain-dependent cleavage of NCX3, and we demonstrate that loss of NCX3 function is associated with Aβ toxicity. Our findings suggest that Aβ mediates calpain cleavage of NCX3 in AD brain and therefore that reduced NCX3 activity could contribute to the sustained increases in intraneuronal calcium concentrations that are associated with synaptic and neuronal dysfunction in AD.
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Accepted/In Press date: 28 July 2013
e-pub ahead of print date: 6 August 2013
Published date: February 2014
Identifiers
Local EPrints ID: 420387
URI: http://eprints.soton.ac.uk/id/eprint/420387
ISSN: 1474-9718
PURE UUID: ed35b757-0fab-4b6d-8537-7629e96b209f
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Date deposited: 04 May 2018 16:30
Last modified: 16 Mar 2024 04:29
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Contributors
Author:
Joe Atherton
Author:
Marie Bondulich
Author:
Cara L. Croft
Author:
Claire J. Garwood
Author:
Resham Chhabra
Author:
Selina Wray
Author:
Andreas Jeromin
Author:
Diane P. Hanger
Author:
Wendy Noble
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