Human Neural Stem Cell Systems

Building and functioning of the human brain requires the precise orchestration and execution of myriad molecular and cellular processes, across a multitude of cell types and over an extended period of time. Neural Stem Cells (NSCs) represent the heart of these processes, since they increase the pool of neural progenitors and are the founders of all the neural progeny which will constitute the adult human brain

Molecular and cellular logic of cerebral cortex development, evolution, and disease

Editorial on the Research Topic Molecular and cellular logic of cerebral cortex development, evolution, and diseas

Induced pluripotent stem cell lines from Huntington's disease mice undergo neuronal differentiation while showing alterations in the lysosomal pathway

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Designing Mobile Applications for Emergency Response: Citizens Acting as Human Sensors

When an emergency occurs, citizens can be a helpful support for the operation centers involved in the response activities. As witnesses to a crisis, they initially can share updated and detailed information about what is going on. Moreover, thanks to the current technological evolution people are able to quickly and easily gather rich information and transmit it through different communication channels. Indeed, modern mobile devices embed several sensors such as GPS receivers, Wi-Fi, accelerometers or cameras that can transform users into well-equipped human sensors. For these reasons, emergency organizations and small and medium enterprises have demonstrated a growing interest in developing smart applications for reporting any exceptional circumstances. In this paper, we present a practical study about this kind of applications for identifying both limitations and common features.This work is supported by the project emerCien grant funded by the Spanish Ministry of Economy and Competitivity (TIN2012-09687)

Human Neural Stem Cell Systems to Explore Pathogen-Related Neurodevelopmental and Neurodegenerative Disorders

Building and functioning of the human brain requires the precise orchestration and execution of myriad molecular and cellular processes, across a multitude of cell types and over an extended period of time. Dysregulation of these processes affects structure and function of the brain and can lead to neurodevelopmental, neurological, or psychiatric disorders. Multiple environmental stimuli affect neural stem cells (NSCs) at several levels, thus impairing the normal human neurodevelopmental program. In this review article, we will delineate the main mechanisms of infection adopted by several neurotropic pathogens, and the selective NSC vulnerability. In particular, TORCH agents, i.e., Toxoplasma gondii, others (including Zika virus and Coxsackie virus), Rubella virus, Cytomegalovirus, and Herpes simplex virus, will be considered for their devastating effects on NSC self-renewal with the consequent neural progenitor depletion, the cellular substrate of microcephaly. Moreover, new evidence suggests that some of these agents may also affect the NSC progeny, producing long-term effects in the neuronal lineage. This is evident in the paradigmatic example of the neurodegeneration occurring in Alzheimer's disease

evaluating the performance of a rotary vane expander for small scale organic rankine cycles using cfd tools

Abstract This work proposes a focus on the simulation of a rotative volumetric expander via a CFD code. A customized application of OpenFOAMOR has been developed to handle the particular motion of the calculation grid. In particular, a prescribed shape of the stator has been defined in order to adapt the motion of the vanes along the whole cycle. The model uses a mesh to mesh interpolation technique, switching from a calculation grid to the new one on the basis of dynamic mesh quality considerations. This particular approach allows to account for the presence of leakages occurring between the stator and vane tips and also occurring at the top and bottom of the vanes. The fluid considered is the refrigerant R245fa, whose particular properties have been determined resorting to the NIST database. Experimental data, measured at different conditions of mass flow and fluid temperature, are compared to calculation results. Moreover, the CFD analysis has allowed the estimation of the influence of the leakage mass flow occurring at the tip of the vanes on the overall machine performances

A specific box switches the cell fate determining activity of XOTX2 and XOTX5b in the Xenopus retina

<p>Abstract</p> <p>Background</p> <p><it>Otx </it>genes, orthologues of the <it>Drosophila orthodenticle </it>gene (<it>otd</it>), play crucial roles in vertebrate brain development. In the <it>Xenopus </it>eye, <it>Xotx2 </it>and <it>Xotx5b </it>promote bipolar and photoreceptor cell fates, respectively. The molecular basis of their differential action is not completely understood, though the carboxyl termini of the two proteins seem to be crucial. To define the molecular domains that make the action of these proteins so different, and to determine whether their retinal abilities are shared by <it>Drosophila </it>OTD, we performed an <it>in vivo </it>molecular dissection of their activity by transfecting retinal progenitors with several wild-type, deletion and chimeric constructs of <it>Xotx2</it>, <it>Xotx5b </it>and <it>otd</it>.</p> <p>Results</p> <p>We identified a small 8–10 amino acid divergent region, directly downstream of the homeodomain, that is crucial for the respective activities of XOTX2 and XOTX5b. In lipofection experiments, the exchange of this 'specificity box' completely switches the retinal activity of XOTX5b into that of XOTX2 and <it>vice versa</it>. Moreover, the insertion of this box into <it>Drosophila </it>OTD, which has no effect on retinal cell fate, endows it with the specific activity of either XOTX protein. Significantly, in cell transfection experiments, the diverse ability of XOTX2 and XOTX5b to synergize with NRL, a cofactor essential for vertebrate rod development, to transactivate the rhodopsin promoter is also switched depending on the box. We also show by GST-pull down that XOTX2 and XOTX5b differentially interact with NRL, though this property is not strictly dependent on the box.</p> <p>Conclusion</p> <p>Our data provide molecular evidence on how closely related homeodomain gene products can differentiate their functions to regulate distinct cell fates. A small 'specificity box' is both necessary and sufficient to confer on XOTX2 and XOTX5b their distinct activities in the developing frog retina and to convert the neutral orthologous OTD protein of <it>Drosophila </it>into a positive and specific XOTX-like retinal regulator. Relatively little is known of what gives developmental specificity to homeodomain regulators. We propose that this box is a major domain of XOTX proteins that provides them with the appropriate developmental specificity in retinal histogenesis.</p

Neuropotent self-renewing neural stem (NS) cells derived from mouse induced pluripotent stem (iPS) cells

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Human Pluripotent Stem Cell Differentiation into Authentic Striatal Projection Neurons

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Is it possible to assess the best mitral valve repair in the individual patient? Preliminary results of a finite element study from magnetic resonance imaging data

ObjectivesFinite element modeling was adopted to quantitatively compare, for the first time and on a patient-specific basis, the biomechanical effects of a broad spectrum of different neochordal implantation techniques for the repair of isolated posterior mitral leaflet prolapse.MethodsCardiac magnetic resonance images were acquired from 4 patients undergoing surgery. A patient-specific 3-dimensional model of the mitral apparatus and the motion of the annulus and papillary muscles were reconstructed. The location and extent of the prolapsing region were confirmed by intraoperative findings, and the mechanical properties of the mitral leaflets, chordae tendineae and expanded polytetrafluoroethylene neochordae were included. Mitral systolic biomechanics was simulated under preoperative conditions and after 5 different neochordal procedures: single neochorda, double neochorda, standard neochordal loop with 3 neochordae of the same length and 2 premeasured loops with 1 common neochordal loop and 3 different branched neochordae arising from it, alternatively one third and two thirds of the entire length.ResultsThe best repair in terms of biomechanics was achieved with a specific neochordal technique in the single patient, according to the location of the prolapsing region. However, all techniques achieved a slight reduction in papillary muscle forces and tension relief in intact native chordae proximal to the prolapsing region. Multiple neochordae implantation improved the repositioning of the prolapsing region below the annular plane and better redistributed mechanical stresses on the leaflet.ConclusionsAlthough applied on a small cohort of patients, systematic biomechanical differences were noticed between neochordal techniques, potentially affecting their short- to long-term clinical outcomes. This study opens the way to patient-specific optimization of neochordal techniques