Alpha7 Nicotinic Acetylcholine Receptor Expression and Activity During Neuronal Differentiation of PC12 Pheochromocytoma Cells


Autoria(s): NERY, Arthur A.; RESENDE, Rodrigo R.; MARTINS, Antonio H.; TRUJILLO, Cleber A.; ETEROVIC, Vesna A.; ULRICH, Henning
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2010

Resumo

Nicotinic acetylcholine receptors (nAChR) exert pivotal roles in synaptic transmission, neuroprotection and differentiation. Particularly, homomeric alpha 7 receptors participate in neurite outgrowth, presynaptic control of neurotransmitter release and Ca(2+) influx. However, the study of recombinant alpha 7 nAChRs in transfected cell lines is difficult due to low expression of functional receptor channels. We show that PC12 pheochromocytoma cells induced to differentiation into neurons are an adequate model for studying differential nAChR gene expression and receptor activity. Whole-cell current recording indicated that receptor responses increased during the course of differentiation. Transcription of mRNAs coding for alpha 3, alpha 5, alpha 7, beta 2 and beta 4 subunits was present during the course of differentiation, while mRNAs coding for alpha 2, alpha 4 and beta 3 subunits were not expressed in PC12 cells. alpha 7 subunit expression was highest following 1 day of induction to differentiation. Activity of alpha 7 nAChRs, however, was most elevated on day 2 as revealed by inhibition experiments in the presence of 10 nM methyllycaconitine, rapid current decay and receptor responsiveness to the alpha 7 agonist choline. Increased alpha 7 receptor activity was noted when PC12 were induced to differentiation in the presence of choline, confirming that chronic agonist treatment augments nAChR activity. In summary, PC12 cells are an adequate model to study the role and pharmacological properties of this receptor during neuronal differentiation.

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

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)[2006/61285-9]

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) Brazil

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

NIH

NIH[UPR-PRAABREP20RR016470]

NIH[G12RR03035-24]

NIH

FAPEMIG

Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG)

Identificador

JOURNAL OF MOLECULAR NEUROSCIENCE, v.41, n.3, p.329-339, 2010

0895-8696

http://producao.usp.br/handle/BDPI/30974

10.1007/s12031-010-9369-2

http://dx.doi.org/10.1007/s12031-010-9369-2

Idioma(s)

eng

Publicador

HUMANA PRESS INC

Relação

Journal of Molecular Neuroscience

Direitos

restrictedAccess

Copyright HUMANA PRESS INC

Palavras-Chave #Nicotinic acetylcholine receptors #PC12 pheochromocytoma cells #Alpha7 subtypes #Whole-cell recording #Nicotinic receptor expression during differentiation #NERVE GROWTH-FACTOR #EMBRYONAL CARCINOMA-CELLS #NEURITE OUTGROWTH #UP-REGULATION #CYCLIC-AMP #FUNCTIONAL-PROPERTIES #MECHANISM #MODULATION #EXPOSURE #CALCIUM #Biochemistry & Molecular Biology #Neurosciences
Tipo

article

original article

publishedVersion