Extrinsic Purinergic Regulation of Neural Stem/Progenitor Cells: Implications for CNS Development and Repair


Autoria(s): Ulrich, Henning; Abbracchio, Maria P.; Burnstock, Geoffrey
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

29/10/2013

29/10/2013

02/08/2013

Resumo

There has been tremendous progress in understanding neural stem cell (NSC) biology, with genetic and cell biological methods identifying sequential gene expression and molecular interactions guiding NSC specification into distinct neuronal and glial populations during development. Data has emerged on the possible exploitation of NSC-based strategies to repair adult diseased brain. However, despite increased information on lineage specific transcription factors, cell-cycle regulators and epigenetic factors involved in the fate and plasticity of NSCs, understanding of extracellular cues driving the behavior of embryonic and adult NSCs is still very limited. Knowledge of factors regulating brain development is crucial in understanding the pathogenetic mechanisms of brain dysfunction. Since injury-activated repair mechanisms in adult brain often recapitulate ontogenetic events, the identification of these players will also reveal novel regenerative strategies. Here, we highlight the purinergic system as a key emerging player in the endogenous control of NSCs. Purinergic signalling molecules (ATP, UTP and adenosine) act with growth factors in regulating the synchronized proliferation, migration, differentiation and death of NSCs during brain and spinal cord development. At early stages of development, transient and time-specific release of ATP is critical for initiating eye formation; once anatomical CNS structures are defined, purinergic molecules participate in calcium-dependent neuron-glia communication controlling NSC behaviour. When development is complete, some purinergic mechanisms are silenced, but can be re-activated in adult brain after injury, suggesting a role in regeneration and self-repair. Targeting the purinergic system to develop new strategies for neurodevelopmental disorders and neurodegenerative diseases will be also discussed.

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

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

CNPq (Conselho Nacional de Desenvolvimento Cientifico), Brazil

CNPq (Conselho Nacional de Desenvolvimento Cientifico), Brazil

Italian Ministero dell'Universita e della Ricerca (MIUR

Italian Ministero dellUniversita e della Ricerca (MIUR

PRIN-/COFIN program Project) [2006059022, 2008XFMEA3]

PRIN/COFIN program Project)

Fondazione Italiana Sclerosi Multipla (FISM)

Fondazione Italiana Sclerosi Multipla (FISM) [COD. 2010/R/2]

Identificador

STEM CELL REVIEWS AND REPORTS, TOTOWA, v. 8, n. 3, pp. 755-767, SEP, 2012

1550-8943

http://www.producao.usp.br/handle/BDPI/36217

10.1007/s12015-012-9372-9

http://dx.doi.org/10.1007/s12015-012-9372-9

Idioma(s)

eng

Publicador

HUMANA PRESS INC

TOTOWA

Relação

STEM CELL REVIEWS AND REPORTS

Direitos

closedAccess

Copyright HUMANA PRESS INC

Palavras-Chave #ATP #BRAIN INJURY #EYE #PURINERGIC #REGENERATION #NEURAL STEM CELL #TRANSCRIPTION FACTOR #RADIAL GLIAL-CELLS #EMBRYONAL CARCINOMA-CELLS #CENTRAL-NERVOUS-SYSTEM #STEM-CELLS #NEURONAL DIFFERENTIATION #PROGENITOR CELLS #OLFACTORY EPITHELIUM #RECEPTOR EXPRESSION #INDUCED PROLIFERATION #DEVELOPING NEOCORTEX #CELL & TISSUE ENGINEERING #CELL BIOLOGY #MEDICINE, RESEARCH & EXPERIMENTAL
Tipo

article

original article

publishedVersion