Cdk5: Multitasking between physiological and pathological conditions

Detalhes bibliográficos
Autor(a) principal: Lopes, João P.
Data de Publicação: 2011
Outros Autores: Agostinho, Paula
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/21827
https://doi.org/10.1016/j.pneurobio.2011.03.006,
Resumo: Cyclin-dependent kinase 5 (Cdk5) is a peculiar proline-directed serine/threonine kinase. Unlike the other members of the Cdk family, Cdk5 is not directly involved in cell cycle regulation, being normally associated with neuronal processes such as migration, cortical layering and synaptic plasticity. This kinase is present mainly in post-mitotic neurons and its activity is tightly regulated by the interaction with the specific activators, p35 and p39. Despite its pivotal role in CNS development, Cdk5 dysregulation has been implicated in different pathologies, such as Alzheimer's disease (AD), amyotrophic lateral sclerosis (ALS), Parkinson's disease (PD) and, most recently, prion-related encephalopathies (PRE). In these neurodegenerative conditions, Cdk5 overactivation and relocalization occurs upon association with p25, a truncated form of the normal activator p35. This activator switching will cause a shift in the phosphorylative pattern of Cdk5, with an alteration both in targets and activity, ultimately leading to neuronal demise. In AD and PRE, two disorders that share clinical and neuropathological features, Cdk5 dysregulation is a linking event between the major neuropathological markers: amyloid plaques, tau hyperphosphorylation and synaptic and neuronal loss. Moreover, this kinase was shown to be involved in abortive cell cycle re-entry, a feature recently proposed as a possible step in the neuronal apoptosis mechanism of several neurological diseases. This review focuses on the role of Cdk5 in neurons, namely in the regulation of cytoskeletal dynamics, synaptic function and cell survival, both in physiological and in pathological conditions, highlighting the relevance of Cdk5 in the main mechanisms of neurodegeneration in Alzheimer's disease and other brain pathologies.
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spelling Cdk5: Multitasking between physiological and pathological conditionsCdk5Alzheimer's diseaseSynaptic dysfunctionCell cycleNeurodegenerationCyclin-dependent kinase 5 (Cdk5) is a peculiar proline-directed serine/threonine kinase. Unlike the other members of the Cdk family, Cdk5 is not directly involved in cell cycle regulation, being normally associated with neuronal processes such as migration, cortical layering and synaptic plasticity. This kinase is present mainly in post-mitotic neurons and its activity is tightly regulated by the interaction with the specific activators, p35 and p39. Despite its pivotal role in CNS development, Cdk5 dysregulation has been implicated in different pathologies, such as Alzheimer's disease (AD), amyotrophic lateral sclerosis (ALS), Parkinson's disease (PD) and, most recently, prion-related encephalopathies (PRE). In these neurodegenerative conditions, Cdk5 overactivation and relocalization occurs upon association with p25, a truncated form of the normal activator p35. This activator switching will cause a shift in the phosphorylative pattern of Cdk5, with an alteration both in targets and activity, ultimately leading to neuronal demise. In AD and PRE, two disorders that share clinical and neuropathological features, Cdk5 dysregulation is a linking event between the major neuropathological markers: amyloid plaques, tau hyperphosphorylation and synaptic and neuronal loss. Moreover, this kinase was shown to be involved in abortive cell cycle re-entry, a feature recently proposed as a possible step in the neuronal apoptosis mechanism of several neurological diseases. This review focuses on the role of Cdk5 in neurons, namely in the regulation of cytoskeletal dynamics, synaptic function and cell survival, both in physiological and in pathological conditions, highlighting the relevance of Cdk5 in the main mechanisms of neurodegeneration in Alzheimer's disease and other brain pathologies.Elsevier2011-06info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/21827http://hdl.handle.net/10316/21827https://doi.org/10.1016/j.pneurobio.2011.03.006,engLOPES, João P.; AGOSTINHO, Paula - Cdk5: Multitasking between physiological and pathological conditions. "Progress in Neurobiology". ISSN 0301-0082. 94:1 (2011) 49–630301-0082http://www.sciencedirect.com/science/journal/03010082Lopes, João P.Agostinho, Paulainfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2020-05-29T09:42:25Zoai:estudogeral.uc.pt:10316/21827Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:53:34.661613Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Cdk5: Multitasking between physiological and pathological conditions
title Cdk5: Multitasking between physiological and pathological conditions
spellingShingle Cdk5: Multitasking between physiological and pathological conditions
Lopes, João P.
Cdk5
Alzheimer's disease
Synaptic dysfunction
Cell cycle
Neurodegeneration
title_short Cdk5: Multitasking between physiological and pathological conditions
title_full Cdk5: Multitasking between physiological and pathological conditions
title_fullStr Cdk5: Multitasking between physiological and pathological conditions
title_full_unstemmed Cdk5: Multitasking between physiological and pathological conditions
title_sort Cdk5: Multitasking between physiological and pathological conditions
author Lopes, João P.
author_facet Lopes, João P.
Agostinho, Paula
author_role author
author2 Agostinho, Paula
author2_role author
dc.contributor.author.fl_str_mv Lopes, João P.
Agostinho, Paula
dc.subject.por.fl_str_mv Cdk5
Alzheimer's disease
Synaptic dysfunction
Cell cycle
Neurodegeneration
topic Cdk5
Alzheimer's disease
Synaptic dysfunction
Cell cycle
Neurodegeneration
description Cyclin-dependent kinase 5 (Cdk5) is a peculiar proline-directed serine/threonine kinase. Unlike the other members of the Cdk family, Cdk5 is not directly involved in cell cycle regulation, being normally associated with neuronal processes such as migration, cortical layering and synaptic plasticity. This kinase is present mainly in post-mitotic neurons and its activity is tightly regulated by the interaction with the specific activators, p35 and p39. Despite its pivotal role in CNS development, Cdk5 dysregulation has been implicated in different pathologies, such as Alzheimer's disease (AD), amyotrophic lateral sclerosis (ALS), Parkinson's disease (PD) and, most recently, prion-related encephalopathies (PRE). In these neurodegenerative conditions, Cdk5 overactivation and relocalization occurs upon association with p25, a truncated form of the normal activator p35. This activator switching will cause a shift in the phosphorylative pattern of Cdk5, with an alteration both in targets and activity, ultimately leading to neuronal demise. In AD and PRE, two disorders that share clinical and neuropathological features, Cdk5 dysregulation is a linking event between the major neuropathological markers: amyloid plaques, tau hyperphosphorylation and synaptic and neuronal loss. Moreover, this kinase was shown to be involved in abortive cell cycle re-entry, a feature recently proposed as a possible step in the neuronal apoptosis mechanism of several neurological diseases. This review focuses on the role of Cdk5 in neurons, namely in the regulation of cytoskeletal dynamics, synaptic function and cell survival, both in physiological and in pathological conditions, highlighting the relevance of Cdk5 in the main mechanisms of neurodegeneration in Alzheimer's disease and other brain pathologies.
publishDate 2011
dc.date.none.fl_str_mv 2011-06
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/21827
http://hdl.handle.net/10316/21827
https://doi.org/10.1016/j.pneurobio.2011.03.006,
url http://hdl.handle.net/10316/21827
https://doi.org/10.1016/j.pneurobio.2011.03.006,
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv LOPES, João P.; AGOSTINHO, Paula - Cdk5: Multitasking between physiological and pathological conditions. "Progress in Neurobiology". ISSN 0301-0082. 94:1 (2011) 49–63
0301-0082
http://www.sciencedirect.com/science/journal/03010082
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv Elsevier
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