Enhanced Neural Progenitor/Stem Cells Self-Renewal via the Interaction of Stress-Inducible Protein 1 with the Prion Protein


Autoria(s): SANTOS, Tiago G.; SILVA, Iara R.; COSTA-SILVA, Bruno; LEPIQUE, Ana Paula; MARTINS, Vilma R.; LOPES, Marilene H.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2011

Resumo

Prion protein (PrPC), when associated with the secreted form of the stress-inducible protein 1 (STI1), plays an important role in neural survival, neuritogenesis, and memory formation. However, the role of the PrP(C)-STI1 complex in the physiology of neural progenitor/stem cells is unknown. In this article, we observed that neurospheres cultured from fetal forebrain of wild-type (Prnp(+/+)) and PrP(C)-null (Prnp(0/0)) mice were maintained for several passages without the loss of self-renewal or multipotentiality, as assessed by their continued capacity to generate neurons, astrocytes, and oligodendrocytes. The homogeneous expression and colocalization of STI1 and PrP(C) suggest that they may associate and function as a complex in neurosphere-derived stem cells. The formation of neurospheres from Prnp(0/0) mice was reduced significantly when compared with their wild-type counterparts. In addition, blockade of secreted STI1, and its cell surface ligand, PrP(C), with specific antibodies, impaired Prnp(+/+) neurosphere formation without further impairing the formation of Prnp(0/0) neurospheres. Alternatively, neurosphere formation was enhanced by recombinant STI1 application in cells expressing PrP(C) but not in cells from Prnp(0/0) mice. The STI1-PrP(C) interaction was able to stimulate cell proliferation in the neurosphere-forming assay, while no effect on cell survival or the expression of neural markers was observed. These data suggest that the STI1-PrP(C) complex may play a critical role in neural progenitor/stem cells self-renewal via the modulation of cell proliferation, leading to the control of the stemness capacity of these cells during nervous system development. STEM CELLS 2011;29:1126-1136

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)[07/08410-2]

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

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)[09/14027-2]

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

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

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

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

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Identificador

STEM CELLS, v.29, n.7, p.1126-1136, 2011

1066-5099

http://producao.usp.br/handle/BDPI/28298

10.1002/stem.664

http://dx.doi.org/10.1002/stem.664

Idioma(s)

eng

Publicador

WILEY-BLACKWELL

Relação

Stem Cells

Direitos

restrictedAccess

Copyright WILEY-BLACKWELL

Palavras-Chave #Prion protein #Stress inducible protein 1 #Neurospheres #Self-renewal #Proliferation #EMBRYONIC STEM-CELLS #NICOTINIC ACETYLCHOLINE-RECEPTOR #FOCAL CEREBRAL-ISCHEMIA #CELLULAR PRION #DEVELOPMENTAL EXPRESSION #LAMININ RECEPTOR #NEURONAL DIFFERENTIATION #MEDIATED APOPTOSIS #NEURITE OUTGROWTH #PRECURSOR CELLS #Cell & Tissue Engineering #Biotechnology & Applied Microbiology #Oncology #Cell Biology #Hematology
Tipo

article

original article

publishedVersion