TY - JOUR
T1 - High Fat Diet Multigenerationally Affects Hippocampal Neural Stem Cell Proliferation via Epigenetic Mechanisms
AU - Natale, Francesca
AU - Spinelli, Matteo
AU - Barbati, Saviana Antonella
AU - Leone, Lucia
AU - Fusco, Salvatore
AU - Grassi, Claudio
PY - 2022
Y1 - 2022
N2 - Early-life metabolic stress has been demonstrated to affect brain development, persistently
influence brain plasticity and to exert multigenerational effects on cognitive functions. However,
the impact of an ancestor’s diet on the adult neurogenesis of their descendants has not yet been
investigated. Here, we studied the effects of maternal high fat diet (HFD) on hippocampal adult
neurogenesis and the proliferation of neural stem and progenitor cells (NSPCs) derived from the
hippocampus of both the second and the third generations of progeny (F2HFD and F3HFD). Maternal
HFD caused a multigenerational depletion of neurogenic niche in F2HFD and F3HFD mice. Moreover,
NSPCs derived from HFD descendants showed altered expression of genes regulating stem cell
proliferation and neurodifferentiation (i.e., Hes1, NeuroD1, Bdnf). Finally, ancestor HFD-related
hyper-activation of both STAT3 and STAT5 induced enhancement of their binding on the regulatory
sequences of Gfap gene and an epigenetic switch from permissive to repressive chromatin on the
promoter of the NeuroD1 gene. Collectively, our data indicate that maternal HFD multigenerationally
affects hippocampal adult neurogenesis via an epigenetic derangement of pro-neurogenic gene
expression in NSPCs
AB - Early-life metabolic stress has been demonstrated to affect brain development, persistently
influence brain plasticity and to exert multigenerational effects on cognitive functions. However,
the impact of an ancestor’s diet on the adult neurogenesis of their descendants has not yet been
investigated. Here, we studied the effects of maternal high fat diet (HFD) on hippocampal adult
neurogenesis and the proliferation of neural stem and progenitor cells (NSPCs) derived from the
hippocampus of both the second and the third generations of progeny (F2HFD and F3HFD). Maternal
HFD caused a multigenerational depletion of neurogenic niche in F2HFD and F3HFD mice. Moreover,
NSPCs derived from HFD descendants showed altered expression of genes regulating stem cell
proliferation and neurodifferentiation (i.e., Hes1, NeuroD1, Bdnf). Finally, ancestor HFD-related
hyper-activation of both STAT3 and STAT5 induced enhancement of their binding on the regulatory
sequences of Gfap gene and an epigenetic switch from permissive to repressive chromatin on the
promoter of the NeuroD1 gene. Collectively, our data indicate that maternal HFD multigenerationally
affects hippocampal adult neurogenesis via an epigenetic derangement of pro-neurogenic gene
expression in NSPCs
KW - epigenetics
KW - hippocampal adult neurogenesis
KW - maternal HFD
KW - neural stemand progenitor cells
KW - epigenetics
KW - hippocampal adult neurogenesis
KW - maternal HFD
KW - neural stemand progenitor cells
UR - http://hdl.handle.net/10807/214468
U2 - 10.3390/cells11172661
DO - 10.3390/cells11172661
M3 - Article
SN - 2073-4409
VL - 11
SP - N/A-N/A
JO - Cells
JF - Cells
ER -