Role of alpha 7 Nicotinic Acetylcholine Receptor in Calcium Signaling Induced by Prion Protein Interaction with Stress-inducible Protein 1


Autoria(s): BERALDO, Flavio H.; ARANTES, Camila P.; SANTOS, Tiago G.; QUEIROZ, Nicolle G. T.; YOUNG, Kirk; RYLETT, R. Jane; MARKUS, Regina P.; PRADO, Marco A. M.; MARTINS, Vilma R.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2010

Resumo

The prion protein (PrP(C)) is a conserved glycosylphosphatidyl-inositol-anchored cell surface protein expressed by neurons and other cells. Stress-inducible protein 1 (STI1) binds PrP(C) extracellularly, and this activated signaling complex promotes neuronal differentiation and neuroprotection via the extracellular signal-regulated kinase 1 and 2 (ERK1/2) and cAMP-dependent protein kinase 1 (PKA) pathways. However, the mechanism by which the PrPC-STI1 interaction transduces extracellular signals to the intracellular environment is unknown. We found that in hippocampal neurons, STI1-PrP(C) engagement induces an increase in intracellular Ca(2+) levels. This effect was not detected in PrP(C)-null neurons or wild-type neurons treated with an STI1 mutant unable to bind PrP(C). Using a best candidate approach to test for potential channels involved in Ca(2+) influx evoked by STI1-PrP(C), we found that alpha-bungarotoxin, a specific inhibitor for alpha 7 nicotinic acetylcholine receptor (alpha 7nAChR), was able to block PrP(C)-STI1-mediated signaling, neuroprotection, and neuritogenesis. Importantly, when alpha 7nAChR was transfected into HEK 293 cells, it formed a functional complex with PrP(C) and allowed reconstitution of signaling by PrP(C)-STI1 interaction. These results indicate that STI1 can interact with the PrP(C).alpha 7nAChR complex to promote signaling and provide a novel potential target for modulation of the effects of prion protein in neurodegenerative diseases.

FAPESP Fundacao de Amparo a Pesquisa do Estado de Sao Paulo[03-13189-2]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Programa Institutos Nacionais de Ciencia e Tecnologia (INCT), do Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

PrioNet-Canada

PrioNet-Canada

Canadian Institutes for Health Research

Canadian Institutes of Health Research (CIHR)

Department of Foreign Affairs and International Trade-Canada

Department of Foreign Affairs and International Trade-Canada

Identificador

JOURNAL OF BIOLOGICAL CHEMISTRY, v.285, n.47, p.36542-36550, 2010

0021-9258

http://producao.usp.br/handle/BDPI/27428

10.1074/jbc.M110.157263

http://dx.doi.org/10.1074/jbc.M110.157263

Idioma(s)

eng

Publicador

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC

Relação

Journal of Biological Chemistry

Direitos

restrictedAccess

Copyright AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC

Palavras-Chave #CELLULAR PRION #ALZHEIMERS-DISEASE #MOUSE MODEL #TRANSGENIC MICE #BETA OLIGOMERS #AMYLOID-BETA #CROSS-TALK #NEUROPROTECTION #EXPRESSION #LAMININ #Biochemistry & Molecular Biology
Tipo

article

original article

publishedVersion