Kinin-B2 Receptor Activity Determines the Differentiation Fate of Neural Stem Cells


Autoria(s): Trujillo, Cleber Augusto; Negraes, Priscilla Davidson; Gomes, Telma Tiemi Schwindt Diniz; Gomes, Claudiana Lameu; Carromeu, Cassiano; Muotri, Alysson R.; Pesquero, Joao B.; Cerqueira, Debora M.; Pillat, Micheli Mainardi; Souza, Hellio Danny Nobrega de; Turaca, Lauro T.; Abreu, Jose G.; Ulrich, Henning
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

31/10/2013

31/10/2013

2012

Resumo

Bradykinin is not only important for inflammation and blood pressure regulation, but also involved in neuromodulation and neuroprotection. Here we describe novel functions for bradykinin and the kinin-B2 receptor (B2BkR) in differentiation of neural stem cells. In the presence of the B2BkR antagonist HOE-140 during rat neurosphere differentiation, neuron-specific beta 3-tubulin and enolase expression was reduced together with an increase in glial protein expression, indicating that bradykinin- induced receptor activity contributes to neurogenesis. In agreement, HOE-140 affected in the same way expression levels of neural markers during neural differentiation of murine P19 and human iPS cells. Kinin-B1 receptor agonists and antagonists did not affect expression levels of neural markers, suggesting that bradykinin-mediated effects are exclusively mediated via B2BkR. Neurogenesis was augmented by bradykinin in the middle and late stages of the differentiation process. Chronic treatment with HOE-140 diminished eNOS and nNOS as well as M1-M4 muscarinic receptor expression and also affected purinergic receptor expression and activity. Neurogenesis, gliogenesis, and neural migration were altered during differentiation of neurospheres isolated from B2BkR knock-out mice. Whole mount in situ hybridization revealed the presence of B2BkR mRNA throughout the nervous system in mouse embryos, and less beta 3-tubulin and more glial proteins were expressed in developing and adult B2BkR knock-out mice brains. As a underlying transcriptional mechanism for neural fate determination, HOE-140 induced up-regulation of Notch1 and Stat3 gene expression. Because pharmacological treatments did not affect cell viability and proliferation, we conclude that bradykinin-induced signaling provides a switch for neural fate determination and specification of neurotransmitter receptor expression.

National Institutes of Health

National Institutes of Health [1-DP2-OD006495-01]

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

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

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Provost's Office for Research of the University of Sao Paulo Programa de Incentivo a Pesquisa [2011.1.9333.1.3]

Provosts Office for Research of the University of Sao Paulo Programa de Incentivo a Pesquisa

NAPNA-USP, Brazil

NAPNAUSP, Brazil

International Rett Syndrome Foundation [2517]

International Rett Syndrome Foundation

Emerald Foundation

Emerald Foundation

California Institute for Regenerative Medicine Grant

California Institute for Regenerative Medicine Grant [TR2-01814]

Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)

Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico

Identificador

JOURNAL OF BIOLOGICAL CHEMISTRY, BETHESDA, v. 287, n. 53, p. 44046-44061, DEC 28, 2012

0021-9258

http://www.producao.usp.br/handle/BDPI/37090

10.1074/jbc.M112.407197

http://dx.doi.org/10.1074/jbc.M112.407197

Idioma(s)

eng

Publicador

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC

BETHESDA

Relação

Journal of Biological Chemistry

Direitos

closedAccess

Copyright AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC

Palavras-Chave #EMBRYONAL CARCINOMA-CELLS #NITRIC-OXIDE #ADULT NEUROGENESIS #PROGENITOR CELLS #NEURONAL DIFFERENTIATION #INHIBITING APOPTOSIS #SUBVENTRICULAR ZONE #ALZHEIMERS-DISEASE #ISCHEMIC-STROKE #NERVOUS-SYSTEM #BIOCHEMISTRY & MOLECULAR BIOLOGY
Tipo

article

original article

publishedVersion