359 results match your criteria: "CNRS UPR 3212 & University of Strasbourg[Affiliation]"

In the neocortex, higher-order areas are essential to integrate sensory-motor information and have expanded in size during evolution. How higher-order areas are specified, however, remains largely unknown. Here, we show that the migration and distribution of early-born neurons, the Cajal-Retzius cells (CRs), controls the size of higher-order areas in the mouse somatosensory, auditory, and visual cortex.

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In the dorsal horn of the spinal cord (DH), noradrenaline (NA) is released by axons originating from the locus coeruleus and induces spinal analgesia, the mechanisms of which are poorly understood. Here, the effects of NA on synaptic transmission in the deep laminae (III-V) of the DH were characterized. It was shown that exogenously applied, as well as endogenously released, NA facilitated inhibitory [γ-aminobutyric acid (GABA)ergic and glycinergic] synaptic transmission in laminae III-IV of the DH by activating α1-, α2- and β-adrenoceptors (ARs).

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Oligophrenin-1 Connects Exocytotic Fusion to Compensatory Endocytosis in Neuroendocrine Cells.

J Neurosci

August 2015

Institut des Neurosciences Cellulaires et Intégratives, Centre National de la Recherche Scientifique, UPR 3212, and Université de Strasbourg, 67084 Strasbourg, France, and

Oligophrenin-1 (OPHN1) is a protein with multiple domains including a Rho family GTPase-activating (Rho-GAP) domain, and a Bin-Amphiphysin-Rvs (BAR) domain. Involved in X-linked intellectual disability, OPHN1 has been reported to control several synaptic functions, including synaptic plasticity, synaptic vesicle trafficking, and endocytosis. In neuroendocrine cells, hormones and neuropeptides stored in large dense core vesicles (secretory granules) are released through calcium-regulated exocytosis, a process that is tightly coupled to compensatory endocytosis, allowing secretory granule recycling.

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In prion diseases, synapse dysfunction, axon retraction and loss of neuronal polarity precede neuronal death. The mechanisms driving such polarization defects, however, remain unclear. Here, we examined the contribution of RhoA-associated coiled-coil containing kinases (ROCK), key players in neuritogenesis, to prion diseases.

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Post-illumination pupil response after blue light: Reliability of optimized melanopsin-based phototransduction assessment.

Exp Eye Res

October 2015

Netherlands Institute for Neuroscience, Dept. Sleep and Cognition, Amsterdam, The Netherlands; Depts. of Integrative Neurophysiology and Medical Psychology, Center for Neurogenomics and Cognitive Research (CNCR), Neuroscience Campus Amsterdam, VU University and Medical Center, Amsterdam, The Netherlands.

Melanopsin-containing retinal ganglion cells have recently been shown highly relevant to the non-image forming effects of light, through their direct projections on brain circuits that regulate alertness, mood and circadian rhythms. A quantitative assessment of functionality of the melanopsin-signaling pathway could be highly relevant in order to mechanistically understand individual differences in the effects of light on these regulatory systems. We here propose and validate a reliable quantification of the melanopsin-dependent Post-Illumination Pupil Response (PIPR) after blue light, and evaluated its sensitivity to dark adaptation, time of day, body posture, and light exposure history.

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When food availability is restricted, animals adjust their behavior according to the timing of food access. Most rodents, such as rats and mice, and a wide number of other animals express before timed food access a bout of activity, defined as food-anticipatory activity (FAA). One notable exception amongst rodents is the Syrian hamster, a photoperiodic species that is not prone to express FAA.

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[A circannual clock wakes up hibernating mammals].

Med Sci (Paris)

April 2015

Institut des neurosciences cellulaires et intégratives, UPR CNRS 3212, 5, rue Blaise Pascal, 67084 Strasbourg, France.

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The RhoGEF DOCK10 is essential for dendritic spine morphogenesis.

Mol Biol Cell

June 2015

Centre de Recherche en Biochimie Macromoléculaire, CNRS-UMR 5237, Université de Montpellier, 34293 Montpellier, France

By regulating actin cytoskeleton dynamics, Rho GTPases and their activators RhoGEFs are implicated in various aspects of neuronal differentiation, including dendritogenesis and synaptogenesis. Purkinje cells (PCs) of the cerebellum, by developing spectacular dendrites covered with spines, represent an attractive model system in which to decipher the molecular signaling underlying these processes. To identify novel regulators of dendritic spine morphogenesis among members of the poorly characterized DOCK family of RhoGEFs, we performed gene expression profiling of fluorescence-activated cell sorting (FACS)-purified murine PCs at various stages of their postnatal differentiation.

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Internalization of staphylococcal leukotoxins that bind and divert the C5a receptor is required for intracellular Ca(2+) mobilization by human neutrophils.

Cell Microbiol

August 2015

Fédération de Médecine Translationnelle de Strasbourg, EA7290 Virulence Bactérienne Précoce, Institut de Bactériologie et Hôpitaux Universitaires de Strasbourg, Université de Strasbourg, Strasbourg, France.

A growing number of receptors, often associated with the innate immune response, are being identified as targets for bacterial toxins of the beta-stranded pore-forming family. These findings raise the new question of whether the receptors are activated or merely used as docking points facilitating the formation of a pore. To elucidate whether the Staphylococcus aureus Panton-Valentine leukocidin and the leukotoxin HlgC/HlgB act through the C5a receptor (C5aR) as agonists, antagonists or differ from the C5a complement-derived peptide, their activity is explored on C5aR-expressing cells.

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Bedtime-related jerks in the upper limbs associated with restless arms syndrome.

Neurology

March 2015

From the Sleep Disorders Center (E.R., U.K.-H., N.C., M.B., P.B.), FMTS, Hôpital Civil, University of Strasbourg; Institute for Cellular and Integrative Neurosciences (E.R., U.K.-H., M.B., P.B.), CNRS-UPR 3212, Strasbourg; and the Center for Movement Disorders (C.T.), Hôpital de Hautepierre, University of Strasbourg, France.

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ADP ribosylation factor 6 (ARF6) promotes acrosomal exocytosis by modulating lipid turnover and Rab3A activation.

J Biol Chem

April 2015

From the Instituto de Histología y Embriología, CONICET, Facultad de Ciencias Médicas, CC56, Universidad Nacional de Cuyo, 5500 Mendoza, Argentina and

Regulated secretion is a central issue for the specific function of many cells; for instance, mammalian sperm acrosomal exocytosis is essential for egg fertilization. ARF6 (ADP-ribosylation factor 6) is a small GTPase implicated in exocytosis, but its downstream effectors remain elusive in this process. We combined biochemical, functional, and microscopy-based methods to show that ARF6 is present in human sperm, localizes to the acrosomal region, and is required for calcium and diacylglycerol-induced exocytosis.

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Precise patterns of connectivity are established by different types of afferents on a given target neuron, leading to well-defined and non-overlapping synaptic territories. What regulates the specific characteristics of each type of synapse, in terms of number, morphology, and subcellular localization, remains to be understood. Here, we show that the signaling pathway formed by the secreted complement C1Q-related protein C1QL1 and its receptor, the adhesion-GPCR brain angiogenesis inhibitor 3 (BAI3), controls the stereotyped pattern of connectivity established by excitatory afferents on cerebellar Purkinje cells.

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Cardioinhibition can be the unique manifestation of epilepsy-like syncope.

J Clin Neurophysiol

February 2015

*Department of Neurology, Sleep and Electrophysiology Clinic, Hôpital Civil, Fédération de Médecine Translationnelle de Strasbourg (FMTS), University of Strasbourg, Strasbourg, France; †Institute for Cellular and Integrative Neurosciences, CNRS UPR 3212, Strasbourg, France; ‡Epilepsy Center, Clinique Sainte Barbe, Strasbourg, France; and §Department of Cardiology, Rhythmology Center, Hôpital Civil, University of Strasbourg, Strasbourg, France.

Article Synopsis
  • A case study is presented of a pacemaker patient who experienced a complete atrioventricular block during a video-polysomnography, coinciding with an electrical seizure, despite showing no symptoms.
  • The patient had a history of recurrent syncope previously attributed to convulsive vasovagal syncope connected to heart issues.
  • This raises crucial awareness among physicians that cardiac-related syncope can mimic epilepsy, challenging the traditional understanding of epilepsy-like syncope.
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Fluorescent knock-in mice to decipher the physiopathological role of G protein-coupled receptors.

Front Pharmacol

January 2015

CNRS, Institut des Neurosciences Cellulaires et Intégratives, UPR 3212 Strasbourg, France.

G protein-coupled receptors (GPCRs) modulate most physiological functions but are also critically involved in numerous pathological states. Approximately a third of marketed drugs target GPCRs, which places this family of receptors in the main arena of pharmacological pre-clinical and clinical research. The complexity of GPCR function demands comprehensive appraisal in native environment to collect in-depth knowledge of receptor physiopathological roles and assess the potential of therapeutic molecules.

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Circadian clocks in rat skin and dermal fibroblasts: differential effects of aging, temperature and melatonin.

Cell Mol Life Sci

June 2015

Department of Neurobiology of Rhythms, Institute of Cellular and Integrative Neurosciences, UPR 3212 CNRS, Université de Strasbourg, 5 rue Blaise Pascal, 67084, Strasbourg, France.

As a peripheral tissue localized at the interface between internal and external environments, skin performs functions which are critical for the preservation of body homeostasis, in coordination with environmental changes. Some of these functions undergo daily variations, such as temperature or water loss, suggesting the presence of time-keeping mechanisms. Rhythmic functions are controlled by a network of circadian oscillators present virtually in every cell and coordinated by the central clock located in the suprachiasmatic nuclei.

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Calcium dynamics in astrocyte processes during neurovascular coupling.

Nat Neurosci

February 2015

1] Institut National de la Santé et de la Recherche Médicale (INSERM), U1128, Paris, France. [2] Laboratory of Neurophysiology and New Microscopies, Université Paris Descartes, Paris, France.

Enhanced neuronal activity in the brain triggers a local increase in blood flow, termed functional hyperemia, via several mechanisms, including calcium (Ca(2+)) signaling in astrocytes. However, recent in vivo studies have questioned the role of astrocytes in functional hyperemia because of the slow and sparse dynamics of their somatic Ca(2+) signals and the absence of glutamate metabotropic receptor 5 in adults. Here, we reexamined their role in neurovascular coupling by selectively expressing a genetically encoded Ca(2+) sensor in astrocytes of the olfactory bulb.

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Study Objectives: Sleep neurobiology studies use nocturnal species, mainly rats and mice. However, because their daily sleep/wake organization is inverted as compared to humans, a diurnal model for sleep studies is needed. To fill this gap, we phenotyped sleep and waking in Arvicanthis ansorgei, a diurnal rodent widely used for the study of circadian rhythms.

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The internal time-giver role of melatonin. A key for our health.

Rev Neurol (Paris)

November 2014

UPR 3212, CNRS-university of Strasbourg, institute for cellular and integrative neurosciences, 5, rue Blaise-Pascal, 67084 Strasbourg, France. Electronic address:

Daily rhythms in physiological and behavioural processes are controlled by a network of circadian clocks. In mammals, at the top of the network is a master clock located in the suprachiasmatic nuclei (SCN) of the hypothalamus. The nocturnal synthesis and release of melatonin by the pineal gland are tightly controlled by the SCN clock.

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Two ground burrowing crickets are described from the oceanic island of Mauritius (South Western Indian Ocean): Gialaia (Eugialaia) strasbergi n. sp. belongs to a subgenus that was only known from Papua-New Guinea, and Taciturna baiderae n.

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Circadian insights into dopamine mechanisms.

Neuroscience

December 2014

Institute of Cellular and Integrative Neurosciences, CNRS UPR-3212, University of Strasbourg, 5 rue Blaise Pascal, 67084 Strasbourg cedex, France.

Almost every physiological or behavioral process in mammals follows rhythmic patterns, which depend mainly on a master circadian clock located in the hypothalamic suprachiasmatic nucleus (SCN). The dopaminergic (DAergic) system in the brain is principally implicated in motor functions, motivation and drug intake. Interestingly, DA-related parameters and behaviors linked to the motivational and arousal states, show daily rhythms that could be regulated by the SCN or by extra-SCN circadian oscillator(s) modulating DAergic systems.

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Daily regulation of body temperature rhythm in the camel (Camelus dromedarius) exposed to experimental desert conditions.

Physiol Rep

September 2014

Department of Neurobiology of Rhythms, CNRS UPR 3212, Institute for Cellular and Integrative Neurosciences, University of Strasbourg, Strasbourg, France.

In the present work, we have studied daily rhythmicity of body temperature (Tb) in Arabian camels challenged with daily heat, combined or not with dehydration. We confirm that Arabian camels use heterothermy to reduce heat gain coupled with evaporative heat loss during the day. Here, we also demonstrate that this mechanism is more complex than previously reported, because it is characterized by a daily alternation (probably of circadian origin) of two periods of poikilothermy and homeothermy.

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Cholesterol in brain disease: sometimes determinant and frequently implicated.

EMBO Rep

October 2014

Centro Biología Molecular 'Severo Ochoa' CSIC-UAM, Madrid, Spain

Cholesterol is essential for neuronal physiology, both during development and in the adult life: as a major component of cell membranes and precursor of steroid hormones, it contributes to the regulation of ion permeability, cell shape, cell-cell interaction, and transmembrane signaling. Consistently, hereditary diseases with mutations in cholesterol-related genes result in impaired brain function during early life. In addition, defects in brain cholesterol metabolism may contribute to neurological syndromes, such as Alzheimer's disease (AD), Huntington's disease (HD), and Parkinson's disease (PD), and even to the cognitive deficits typical of the old age.

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Activity-dependent gating of calcium spikes by A-type K+ channels controls climbing fiber signaling in Purkinje cell dendrites.

Neuron

October 2014

Inhibitory Transmission Team, IBENS, CNRS UMR UMR8197, INSERM U1024, Ecole Normale Supérieure, 75005 Paris, France. Electronic address:

In cerebellar Purkinje cell dendrites, heterosynaptic calcium signaling induced by the proximal climbing fiber (CF) input controls plasticity at distal parallel fiber (PF) synapses. The substrate and regulation of this long-range dendritic calcium signaling are poorly understood. Using high-speed calcium imaging, we examine the role of active dendritic conductances.

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Cerebellum involvement in cortical sensorimotor circuits for the control of voluntary movements.

Nat Neurosci

September 2014

1] Institut de Biologie de l'Ecole Normale Supérieure, Paris, France. [2] Centre National de la Recherche Scientifique (CNRS) UMR8197, Paris, France. [3] Institut National de la Santé et de la Recherche Médicale (INSERM) U1024, Paris, France. [4].

Sensorimotor integration is crucial to perception and motor control. How and where this process takes place in the brain is still largely unknown. Here we analyze the cerebellar contribution to sensorimotor integration in the whisker system of mice.

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Semaphorin 3A (Sema3A) is a secreted protein involved in axon path-finding during nervous system development. Calcium signaling plays an important role during axonal growth in response to different guidance cues; however it remains unclear whether this is also the case for Sema3A. In this study we used intracellular calcium imaging to figure out whether Sema3A-induced growth cone collapse is a Ca2+ dependent process.

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