Limited effects of an eIF2αS51A allele on neurological impairments in the 5xFAD mouse model of Alzheimer's disease.

Alzheimer's disease (AD) has been associated with increased phosphorylation of the translation initiation factor 2α (eIF2α) at serine 51. Increased phosphorylation of eIF2α alters translational control and may thereby have adverse effects on synaptic plasticity, learning, and memory. To analyze if increased levels of p-eIF2α indeed promote AD-related neurocognitive impairments, we crossed 5xFAD transgenic mice with an eIF2α(S51A) knock-in line that expresses the nonphosphorylatable eIF2α variant eIF2α(S51A). Behavioral assessment of the resulting mice revealed motor and cognitive deficits in 5xFAD mice that were, with the possible exception of locomotor hyperactivity, not restored by the eIF2α(S51A) allele. Telemetric intracranial EEG recordings revealed no measurable effects of the eIF2α(S51A) allele on 5xFAD-associated epileptic activity. Microarray-based transcriptome analyses showed clear transcriptional alterations in 5xFAD hippocampus that were not corrected by the eIF2α(S51A) allele. In contrast to prior studies, our immunoblot analyses did not reveal increased levels of p-eIF2α in the hippocampus of 5xFAD mice, suggesting that elevated p-eIF2α levels are not a universal feature of AD models. Collectively, our data indicate that 5xFAD-related pathologies do not necessarily require hyperphosphorylation of eIF2α to emerge; they also show that heterozygosity for the nonphosphorylatable eIF2α(S51A) allele has limited effects on 5xFAD-related disease manifestations.

Propagation of spontaneous slow-wave activity across columns and layers of the adult rat barrel cortex in vivo.

During slow-wave sleep, neocortical networks exhibit self-organized activity switching between periods of concurrent spiking (up-states) and periods of network silence (down-states), a phenomenon also occurring under the effects of different anesthetics and in in vitro brain slice preparations. Although this type of ongoing activity has been implicated into important functions such as memory consolidation and learning, the manner in which it propagates across different cortical modules (i.e., columns and layers) has not been fully characterized. In the present study, we investigated this issue by measuring spontaneous activity at large scale in the adult rat barrel cortex under urethane anesthesia by means of voltage-sensitive dye imaging and 128-channel probe recordings. Up to 74 neurons located in all layers of up to four functionally identified barrel-related columns were recorded simultaneously. The spontaneous activity propagated isotropically across the cortical surface with a median speed of ~35 µm/ms. A concomitant radial spread of activation was present from deep to superficial cortical layers. Thus, spontaneous activity occurred rather globally in the barrel cortex, with ≥50 % of the up-states presenting spikes in ≥3 columns and layers. Temporally precise spike sequences, which occurred repeatedly (although sporadically) within the up-states, were typically led by putative excitatory neurons in the infragranular cortical layers. In summary, our data provide for the first time an overall view of the spontaneous slow-wave activity within the barrel cortex circuit, characterizing its propagation across columns and layers at high spatio-temporal resolution.