Direkt zum Inhalt

Wachs, Frank-Peter ; Winner, Beate ; Couillard-Despres, Sebastien ; Schiller, Thorsten ; Aigner, Robert ; Winkler, Jürgen ; Bogdahn, Ulrich ; Aigner, Ludwig

Transforming growth factor-beta1 is a negative modulator of adult neurogenesis

Artikel

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.

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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Details

DokumentenartArtikel
Titel eines Journals oder einer ZeitschriftJournal of neuropathology and experimental neurology
VerlagOXFORD UNIV PRESS INC
Ort der VeröffentlichungCARY
Band65
Nummer des Zeitschriftenheftes oder des Kapitels4
SeitenbereichS. 358-370
DatumApril 2006
Veröffentlichungsdatum05 Aug 2009 13:26
InstitutionenMedizin > Lehrstuhl für Neurologie
Identifikationsnummer
WertTyp
10.1097/01.jnen.0000218444.53405.f0DOI
16691117PubMed-ID
Stichwörter / KeywordsGROWTH-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-Klassifikation600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin
StatusVeröffentlicht
BegutachtetJa, diese Version wurde begutachtet
An der Universität Regensburg entstandenJa
Dokumenten-ID1236

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