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Transforming growth factor-beta1 is a negative modulator of adult neurogenesis
Wachs, Frank-Peter, Winner, Beate
, Couillard-Despres, Sebastien, Schiller, Thorsten, Aigner, Robert, Winkler, Jürgen, Bogdahn, Ulrich und Aigner, Ludwig
(2006)
Transforming growth factor-beta1 is a negative modulator of adult neurogenesis.
Journal of neuropathology and experimental neurology 65 (4), S. 358-370.
Veröffentlichungsdatum dieses Volltextes: 05 Aug 2009 13:26
Artikel
DOI zum Zitieren dieses Dokuments: 10.5283/epub.1236
Zusammenfassung
Transforming growth factor (TGF)-beta 1 has multiple functions in the adult central nervous system (CNS). It modulates inflammatory responses in the CNS and controls proliferation of microglia and astrocytes. In the diseased brain, TGF-beta 1 expression is upregulated and, depending on the cellular context, its activity can be beneficial or detrimental regarding regeneration. We focus on the role ...
Transforming growth factor (TGF)-beta 1 has multiple functions in the adult central nervous system (CNS). It modulates inflammatory responses in the CNS and controls proliferation of microglia and astrocytes. In the diseased brain, TGF-beta 1 expression is upregulated and, depending on the cellular context, its activity can be beneficial or detrimental regarding regeneration. We focus on the role of TGF-beta 1 in adult neural stem cell biology and neurogenesis. In adult neural stem and progenitor cell cultures and after intracerebroventricular infusion, TGF-beta 1 induced a long-lasting inhibition of neural stem and progenitor cell proliferation and a reduction in neurogenesis. In vitro, although TGF-beta 1 specifically arrested neural stem and progenitor cells in the G0/1 phase of the cell cycle, it did not affect the self-renewal capacity and the differentiation fate of these cells. Also, in vivo, TGF-beta 1 did not influence the differentiation fate of newly generated cells as shown by bromo-deoxyuridine incorporation experiments. Based on these data, we suggest that TGF-beta 1 is an important signaling molecule involved in the control of neural stem and progenitor cell proliferation in the CNS. This might have potential implications for neurogenesis in a variety of TGF-beta 1-associated CNS diseases and pathologic conditions.
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| Dokumentenart | Artikel | ||||||
| Titel eines Journals oder einer Zeitschrift | Journal of neuropathology and experimental neurology | ||||||
| Verlag: | OXFORD UNIV PRESS INC | ||||||
|---|---|---|---|---|---|---|---|
| Ort der Veröffentlichung: | CARY | ||||||
| Band: | 65 | ||||||
| Nummer des Zeitschriftenheftes oder des Kapitels: | 4 | ||||||
| Seitenbereich: | S. 358-370 | ||||||
| Datum | April 2006 | ||||||
| Institutionen | Medizin > Lehrstuhl für Neurologie | ||||||
| Identifikationsnummer |
| ||||||
| Stichwörter / Keywords | GROWTH-FACTOR-BETA; NEURAL STEM-CELLS; HEMATOPOIETIC STEM/PROGENITOR CELLS; MIDDLE CEREBRAL-ARTERY; CENTRAL-NERVOUS-SYSTEM; TGF-BETA; TRANSFORMING GROWTH-FACTOR-BETA-1; ALZHEIMERS-DISEASE; HUNTINGTONS-DISEASE; TRANSGENIC MICE; brain repair; cell fate; differentiation; doublecortin; neurodegenerative diseases | ||||||
| Dewey-Dezimal-Klassifikation | 600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin | ||||||
| Status | Veröffentlicht | ||||||
| Begutachtet | Ja, diese Version wurde begutachtet | ||||||
| An der Universität Regensburg entstanden | Ja | ||||||
| Dokumenten-ID | 1236 |
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