The interplay of environmental and genetic factors in the developmental organization of the hippocampus has not been fully elucidated. The neuropeptide corticotropin-releasing factor (CRF) is released from hippocampal interneurons by environmental signals, including stress, to increase synaptic efficacy. In the early postnatal hippocampus, we have previously characterized a transient population of CRF-expressing Cajal-Retzius-like cells. Here we queried whether this stress-activated neuromodulator influences connectivity in the developing hippocampal network. Using mice deficient in the principal hippocampal CRF receptor [CRF 1(؊͞؊)] and organotypic cultures grown in the presence of synthetic CRF, or CRF receptor antagonists, we found robust effects of CRF on dendritic differentiation in hippocampal neurons. In CRF 1(؊͞؊) mice, the dendritic trees of hippocampal principal cells were exuberant, an effect that was induced in normal hippocampi in vitro by the presence of CRF 1 antagonists. In both cases, total dendritic length and dendritic branching were significantly increased. In contrast, exogenous synthetic CRF blunted the dendritic growth in hippocampal organotypic cultures. Taken together, these findings suggest that endogenous CRF, if released excessively by previous early postnatal stress, might influence neuronal connectivity and thus function of the immature hippocampus.corticotropin-releasing hormone ͉ stress ͉ corticotropin-releasing factor receptor ͉ neuropeptide ͉ Cajal-Retzius cells T he developmental organization of the hippocampal network is a complex process, requiring the interplay of genetic and environmental factors. Establishment of basic hippocampal connectivity is governed by genetically determined mechanisms, including the coordinated activation of transcription factors (1-3), and the expression of both local and more generally acting guidance molecules (4-6). Once the basic elements are in place, refinement of connectivity is achieved through environmental stimuli that influence neuronal activity (7-9). Among the elements that contribute to developmental organization of the hippocampus are the Cajal-Retzius (CR) cells (10, 11). CR cells, found in hippocampal marginal zones, release reelin, an extracellular matrix protein required for layer formation and positioning of cortical neurons (12, 13). Because lack of reelin causes perturbation of cortical lamination (14), control of neuronal positioning has been considered the major function of CR cells. However, recent results suggest additional roles for CR cells that are independent of reelin (15-18).We have previously characterized a subset of CR cells that do not express reelin but release the neuropeptide corticotropinreleasing factor (CRF).ʈ CRF functions primarily as a regulator of the neuroendocrine stress response (19,20) but is also widely expressed within the central nervous system, where it acts as a neuromodulator (21)(22)(23)(24) 5-dimethyl-N,N-dipropyl-pyrazolo[2,3-a]pyrimidin-7-amine, previously R121919} were 0.1 or 1 M (for G...

Elderly adults may master challenging cognitive demands by additionally recruiting the cross-hemispheric counterparts of otherwise unilaterally engaged brain regions, a strategy that seems to be at odds with the notion of lateralized functions in cerebral cortex. We wondered whether bilateral activation might be a general coping strategy that is independent of age, task content and brain region. While using functional magnetic resonance imaging (fMRI), we pushed young and old subjects to their working memory (WM) capacity limits in verbal, spatial, and object domains. Then, we compared the fMRI signal reflecting WM maintenance between hemispheric counterparts of various task-relevant cerebral regions that are known to exhibit lateralization. Whereas language-related areas kept their lateralized activation pattern independent of age in difficult tasks, we observed bilaterality in dorsolateral and anterior prefrontal cortex across WM domains and age groups. In summary, the additional recruitment of cross-hemispheric counterparts seems to be an age-independent domain-general strategy to master cognitive challenges. This phenomenon is largely confined to prefrontal cortex, which is arguably less specialized and more flexible than other parts of the brain. working memory | subjective task difficulty | lateralization | prefrontal cortex | cognitive aging

While C9orf72 repeat expansions usually present with frontotemporal dementia (FTD) and/or amyotrophic lateral sclerosis (ALS), an increasing number of reports suggests that the primary phenotype of C9orf72 patients may also include movement disorders. We here provide the first systematic clinical characterisation of C9orf72-associated parkinsonism. We report a C9orf72 expansion carrier presenting with a clinical syndrome of progressive supranuclear palsy (PSP), pronounced mesencephalic atrophy on MRI and PSP-characteristic electrooculography findings. Moreover, we systematically review all previous reports on C9orf72 patients with parkinsonian features. Review of 28 reports revealed 45 C9orf72-positive patients with hypokinesia, rigidity and/or resting tremor. C9orf72-associated parkinsonism predominantly consisted in a hypokinetic-rigid syndrome without resting tremor (61%), with both asymmetric (59%) and symmetric (41%) distributions. Additional features included upper motor neuron signs (60%), lower motor neuron signs (36%), cognitive dysfunction (85%), behaviour and/or personality change (55%) and psychiatric symptoms (29%). Vertical supranuclear gaze palsy was reported in three further cases and cerebellar dysfunction in four cases. Family history frequently yielded evidence of ALS (31%) and FTD (21%). Atypical parkinsonism is a recurrent phenotypic manifestation of C9orf72 expansions. It occurs as part of a broad spectrum of C9orf72-related multi-system neurodegeneration, which can include basal ganglia, mesencephalic and cerebellar dysfunction. C9orf72 genotyping should be considered in those patients with atypical parkinsonism who present with a family history of ALS or FTD, upper or lower motor neuron signs and/or cognitive dysfunction with pronounced frontotemporal impairment.

Humans derive causality judgments reliably from highly abstract stimuli, such as moving discs that bump into each other [1]. This fascinating visual capability emerges gradually during human development [2], perhaps as consequence of sensorimotor experience [3]. Human functional imaging studies suggest an involvement of the "action observation network" in the processing of such stimuli [4, 5]. In addition, theoretical studies suggest a link between the computational mechanisms of action and causality perception [6, 7], consistent with the fact that both functions require an analysis of sequences of spatiotemporal relationships between interacting stimulus elements. Single-cell correlates of the perception of causality are completely unknown. In order to find such neural correlates, we investigated the responses of "mirror neurons" in macaque premotor area F5 [8, 9]. These neurons respond during the observation as well as during the execution of actions and show interesting invariances, e.g., with respect to the stimulus view [10], occlusions [11], or whether an action is really executed or suppressed [12]. We investigated the spatiotemporal properties of the visual responses of mirror neurons to naturalistic hand action stimuli and to abstract stimuli, which specified the same causal relationships. We found a high degree of generalization between these two stimulus classes. In addition, many features that strongly reduced the similarity of the response patterns coincided with the ones that also destroy the perception of causality in humans. This implies an overlap of neural structures involved in the processing of actions and the visual perception of causality at the single-cell level.

No abstract

Prolonged seizures, e.g., induced by fever, experienced early in life are considered a precipitating injury for the subsequent development of temporal lobe epilepsy. During in vitro epileptiform activity, spreading depressions (SDs) have often been observed. However, their contribution to changes in the properties of juvenile neuronal tissue is unknown. We therefore used the juvenile hippocampal slice culture preparation (JHSC) maintained in normoxia (20% O(2)-5% CO(2)-75% N(2)) to assess the effect of repetitive SD-like events (SDLEs) on fast field potentials and cell damage. Repetitive SDLEs in the CA1 region could be induced in about two-thirds of the investigated JHSCs (n = 61) by repetitive electrical stimulation with 2-200 pulses. SDLEs were characterized by a transient large negative field potential shift accompanied by intracellular depolarization, ionic redistribution, slow propagation (assessed by intrinsic optical signals) and glutamate receptor antagonist sensitivity. The term "SDLE" was used because evoked fast field potentials were only incompletely suppressed and superimposed discharges occurred. With 20 +/- 1 repetitive SDLEs (interval of 10-15 min, n = 7 JHSCs), the events got longer, their amplitude of the first peak declined, while threshold for induction became reduced. Evoked fast field potentials deteriorated and cell damage (assessed by propidium iodide fluorescence) occurred, predominantly in regions CA1 and CA3. As revealed by measurements of tissue partial oxygen pressure during SDLEs repetitive transient anoxia accompanying SDLE might be critical for the observed cell damage. These results, limited so far to the slice culture preparation, suggest SDs to be harmful events in juvenile neuronal tissue in contrast to what is known about their effect on adult neuronal tissue.

No abstract

No abstract