Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Glycogen synthase kinase-3 (GSK-3), a multifunctional serine-threonine kinase, is an important regulator in numerous signaling pathways and processes including adult brain neurogenesis. GSK-3 (mal)functioning was implicated in many diseases, in particular neurological and behavioral disorders. We investigated the impact of altered levels of the GSK-3β isoform on hippocampal size, number of doublecortin-positive cells, and hippocampal-dependent behaviors. Both GSK-3β transgenic mice (GSK-3β[S9A] mice) and GSK-3β neuron-specific knockout (GSK-3β(n-/-)) mice, showed reduced size of the dentate gyrus (DG) and were impaired in three hippocampal-dependent, species-typical behavioral tasks: digging, marble burying and nest building. We further demonstrate that the number of differentiating, doublecortin-positive new neurons is reduced in GSK-3β[S9A] mice, but not in GSK-3β(n-/-) mice. We conclude that GSK-3β activity must be critically controlled to allow wild type-like volume of the dentate gyrus and for normal execution of hippocampal-dependent, species-typical behavior.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.bbr.2013.03.045DOI Listing

Publication Analysis

Top Keywords

dentate gyrus
12
glycogen synthase
8
size dentate
8
species-typical behavioral
8
behavioral tasks
8
gsk-3β[s9a] mice
8
gsk-3βn-/- mice
8
hippocampal-dependent species-typical
8
mice
6
synthase kinase-3beta
4

Similar Publications

Alcohol use disorder (AUD) is characterized by pathological motivation to consume alcohol and cognitive inflexibility, leading to excessive alcohol seeking and use. In this study, we investigated the molecular correlates of impaired extinction of alcohol seeking during forced abstinence using a mouse model of AUD in the automated IntelliCage social system. This model distinguished AUD-prone and AUD-resistant animals based on the presence of ≥2 or <2 criteria of AUD, respectively.

View Article and Find Full Text PDF

The plasma membrane acts as a capacitor that plays a critical role in neuronal excitability and signal propagation. Neuronal capacitance is proportional to the area of the cell membrane, thus is often used as a measure of cell size that is assumed to be relatively stable. Recent work proposes that the capacitance of dentate granule cells and cortical pyramidal cells changes across the light-dark cycle in a manner that alters synaptic integration.

View Article and Find Full Text PDF

Advances in intravital imaging of adult neurogenesis in mice.

Stem Cell Reports

September 2025

Laboratory of Neural Plasticity, Faculties of Medicine and Science, Brain Research Institute, University of Zurich, 8057 Zurich, Switzerland. Electronic address:

The lifelong addition of stem-cell-derived neurons into distinct areas of the mammalian brain, such as the olfactory bulb and hippocampal dentate gyrus, provides structural and functional plasticity to neural circuits. To understand the dynamic processes underlying adult neurogenesis, from dividing stem/progenitor cells to integrating neurons, and to probe how new neurons shape brain function, intravital imaging turned out to be a powerful tool. Here, we review recent advances in the field of adult neurogenesis achieved by using in vivo imaging approaches in mice and discuss future directions of imaging-based experiments that will further our understanding of adult neurogenesis.

View Article and Find Full Text PDF

Background: Staphylococcus epidermidis (SE) is a predominant hospital-acquired bacterium leading to late-onset sepsis in preterm infants. Recent findings have suggested that postnatal S. epidermidis infection is associated with short-term neurodevelopmental consequences.

View Article and Find Full Text PDF

Background And Purpose: The pathological role of the bile acid receptor TGR5/GPBA in Alzheimer's disease (AD) is not fully understood. We investigated the pharmacological effects and mechanisms of TGR5 in AD model mice.

Experimental Approach: TGR5 expression was assessed in AD mice using immunofluorescence and immunoblotting.

View Article and Find Full Text PDF