MicroRNAs and Aging
To understand the regulation of microRNAs during aging, next-generation sequencing is applied. These microRNAs are part of a network that is centered on the antagonistic actions of MYC and TP53 and is conserved in mammals and humans. Some of these microRNAs, like miR-15a and the miR cluster 17~92 are specifically expressed and regulated in the neuronal stem cells in vivo. We will now proceed with functional tests of the activity of these genes.
Aging of Neuronal Stem Cells
As a consequence of aging, the neuronal stem cells of N. furzeri greatly reduce their proliferative capacity. Using next-generation sequencing, we identified novel genes that are expressed in the neuronal stem cells and are regulated similarly in N. furzeri and humans. In addition, we revealed that brain aging is associated to prominent epigenetic remodeling and activation of the polycomb complex. Our research will then focus on in vivo manipulation of gene expression to investigate how these genes regulate neuronal stem cell function.
Effects of Mild Stress (Hormesis)
It is known that low-dosage stressors can induce positive effects on cellular function by inducing a protective response. Using N. furzeri, we are currently investigating how mild stress can contrast the effects of aging and promote longevity.
|Alessandro Cellerino||+49 3641 656441||alessandro.cellerinoleibniz-flide||Associated Group Leader|
|Mario Baumgart||+49 3641 656441||mario.baumgartleibniz-flide||Postdoc|
|Chiara Giannuzzi||+49 3641 656301||chiara.giannuzzileibniz-flide||Doctoral Candidate (external)|
|Sabine Matz||+49 3641 656301||sabine.matzleibniz-flide||Technical Assistant|
|Özge Candemir||---||oezge.candemirleibniz-flide||Master Student|
* incomplete due to Data protection