Literature DB >> 16035109

Expression of the transcription factor Pax 6 in the adult rat dentate gyrus.

Juan Nacher1, Emilio Varea, Jose M Blasco-Ibañez, Esther Castillo-Gomez, Carlos Crespo, Francisco J Martinez-Guijarro, Bruce S McEwen.   

Abstract

The transcription factor Pax 6 is expressed in precursor cells during embryonic CNS development, and it plays an important role in the regulation of cell proliferation and neuronal fate determination. Pax 6-expressing cells are also present in the adult hippocampal dentate gyrus and subventricular zone/rostral migratory stream, regions in which neuronal precursors exist during adult life. In the adult dentate gyrus, precursor cells are located in the innermost portion of the granule cell layer, and Pax 6-expressing nuclei are most abundant in this region. To examine the putative role of Pax 6 in adult hippocampal neurogenesis, we have studied the proliferative activity, distribution, and phenotype of Pax 6-expressing cells by using immunohistochemistry. Our results indicate that Pax 6 is intensely expressed in proliferating precursors of the adult dentate gyrus. Pax 6 is also expressed in nonproliferating cells, which may correspond to resting progenitor cells and to granule neurons in their very early developmental stages, because this transcription factor is strongly down-regulated during granule neuron differentiation. However, a small subpopulation of hilar mature neurons and certain astrocytes of the adult hippocampus also express Pax 6. Although the precise roles of this transcription factor in the adult brain remain to be determined, our findings support the idea that its function in the control of cell proliferation and neuronal fate determination during embryogenesis is also operative in the adult hippocampus. However, the expression of Pax 6 in astrocytes and certain mature neurons may indicate the existence of other roles for this transcription factor in this telencephalic region. (c) 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 16035109     DOI: 10.1002/jnr.20596

Source DB:  PubMed          Journal:  J Neurosci Res        ISSN: 0360-4012            Impact factor:   4.164


  24 in total

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