Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8264213 | Experimental Gerontology | 2014 | 6 Pages |
Abstract
We recently reported that young (3 to 4Â months old) mice lacking Exon 1 of the Smad7 gene (S7ÎEx1 mice) show enhanced proliferation of neural stem and progenitor cells (NPCs) in the hippocampal dentate gyrus (DG) and in the subventricular zone (SVZ) of the lateral ventricles. It remained unclear, however, whether this phenotype would persist along aging, the latter typically being associated with a profound decrease in neurogenesis. Analysis of NPCs' proliferation based on the cell cycle marker PCNA in 12Â month-old S7ÎEx1 mice revealed a reversal of the phenotype. Hence, in contrast to their younger counterparts, 12Â month-old S7ÎEx1 mice had a reduced number of proliferating cells, compared to wildtype (WT) mice. At the same time, the survival of newly generated cells was enhanced in the aged transgenic animals. 12Â month-old S7ÎEx1 mice further displayed a reduced level of neurogenesis based on the numbers of cells expressing doublecortin (DCX), a marker for newborn neurons. The reduced neurogenesis in aged S7ÎEx1 mice was not due to a stem cell depletion, which might have occurred as a consequence of hyperproliferation in the young mice, since the number of Nestin and Sox2 positive cells was similar in WT and S7ÎEx1 mice. Instead, Nestin positive cells in the DG as well as primary neurosphere cultures derived from 12Â month-old S7ÎEx1 mice had a reduced capability to proliferate. However, after passaging, when released from their age- and niche-associated proliferative block, neurospheres from aged S7ÎEx1 mice regained the hyperproliferative property. Further, pSmad2 antibody staining intensity was elevated in the DG and SVZ of 12-month old transgenic compared to WT mice, indicating increased intracellular TGF-beta signaling in the aged S7ÎEx1 mice. In summary, this points toward differential effects of S7ÎEx1 on neurogenesis: (i) a hyperproliferation in young animals caused by a cell autonomous mechanism, and (ii) a TGF-beta dependent modulation of neurogenesis in aged S7ÎEx1 animals that abrogates the cell-intrinsic hyperproliferative properties and results in reduced proliferation, increased stem cell quiescence, and enhanced survival of newly generated cells.
Related Topics
Life Sciences
Biochemistry, Genetics and Molecular Biology
Ageing
Authors
Julia Marschallinger, Monika Krampert, Sebastien Couillard-Despres, Rainer Heuchel, Ulrich Bogdahn, Ludwig Aigner,