期刊
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE
卷 23, 期 5, 页码 413-424出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijdevneu.2005.04.001
关键词
TGF-beta 1; neuron-glia interaction; astrocyte; development; central nervous system; Smads
Transforming growth factor betas (TGF-beta s) are known as multifunctional growth factors, which participate in the regulation of key events of development, disease and tissue repair. In central nervous system (CNS), TGF-beta 1 has been widely recognized as an injury-related cytokine, specially associated with astrocyte scar formation in response to brain injury. TGF-beta s family is represented by three isoforms: TGF-beta 1, -beta 2 and -beta 3, all produced by both glial and neuronal cells. They are involved in essential tissue functions, including cell-cycle control, regulation of early development and differentiation, neuron survival and astrocyte differentiation. TGF-beta signaling is mediated mainly by two serine threonine kinase receptors, TGFRI and TGFRII, which activate Smad 2/3 and Smad 4 transcription factors. Phosphorylation and activation of these protein is followed by formation of Smad 2/3-4 complex, which translocates to the nucleus regulating transcriptional responses to TGF-beta. Very few data are available concerning the intracellular pathway required for the effect of TGF-beta in brain cells. Recently, emerging data on TGF-beta 1 and its signaling molecules have been suggesting that besides its role in brain injury, TGF-beta 1 might be a crucial regulator of CNS development. In this review, we will focus on TGF-beta s members, specially TGF-beta 1, in neuron and astrocyte development. We will discuss some advances concerning the emerging scenario of TGF-beta 1 and its signaling pathways as putative modulators of astrocyte biology and their implications as a novel mediator of cellular interactions in the CNS. (c) 2005 ISDN. Published by Elsevier Ltd. All rights reserved.
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