Pulsars with NenuFAR: Backend and pipelines

Context. NenuFAR (New extension in Nançay upgrading LOFAR) is a new radio telescope developed and built on the site of the Nançay Radio Observatory. It is designed to observe the largely unexplored frequency window from 10 to 85 MHz, offering a high sensitivity across its full bandwidth. NenuFAR has started its “early science” operation in July 2019, with 58% of its final collecting area. Aims. Pulsars are one of the major phenomena utilized in the scientific exploitation of this frequency range and represent an important challenge in terms of instrumentation. Designing instrumentation at these frequencies is complicated by the need to compensate for the effects of both the interstellar medium and the ionosphere on the observed signal. We have designed a dedicated backend and developed a complete pulsar observation and data analysis pipeline, which we describe in detail in the present paper, together with first science results illustrating the diversity of the pulsar observing modes. Methods. Our real-time pipeline LUPPI (Low frequency Ultimate Pulsar Processing Instrumentation) is able to cope with a high data rate and provide real-time coherent de-dispersion down to the lowest frequencies reached by NenuFAR (10 MHz). The full backend functionality is described, as the available pulsar observing modes (folded, single-pulse, waveform, and dynamic spectrum). Results. We also present some of the early science results of NenuFAR on pulsars: the detection of 12 millisecond pulsars (eight of which are detected for the first time below 100 MHz); a high-frequency resolution mapping of the PSR B1919+21 emission profile and a detailed observation of single-pulse substructures from PSR B0809+74 down to 16 MHz; the high rate of giant-pulse emission from the Crab pulsar detected at 68.7 MHz (43 events per minute); and the illustration of the very good timing performance of the instrumentation, which allows us to study dispersion measure variations in great detail

TSP-1 Secreted by Bone Marrow Stromal Cells Contributes to Retinal Ganglion Cell Neurite Outgrowth and Survival

BACKGROUND: Bone marrow stromal cells (BMSCs) are pluripotent and thereby a potential candidate for cell replacement therapy for central nervous system degenerative disorders and traumatic injury. However, the mechanism of their differentiation and effect on neural tissues has not been fully elucidated. This study evaluates the effect of BMSCs on neural cell growth and survival in a retinal ganglion cell (RGCs) model by assessing the effect of changes in the expression of a BMSC-secreted protein, thrombospondin-1 (TSP-1), as a putative mechanistic agent acting on RGCs. METHODS AND FINDINGS: The effect of co-culturing BMSCs and RGCs in vitro was evaluated by measuring the following parameters: neurite outgrowth, RGC survival, BMSC neural-like differentiation, and the effect of TSP-1 on both cell lines under basal secretion conditions and when TSP-1 expression was inhibited. Our data show that BMSCs improved RGC survival and neurite outgrowth. Synaptophysin, MAP-2, and TGF-beta expression are up-regulated in RGCs co-cultured with BMSCs. Interestingly, the BMSCs progressively displayed neural-like morphology over the seven-day study period. Restriction display polymerase chain reaction (RD-PCR) was performed to screen for differentially expressed genes in BMSCs cultured alone or co-cultured with RGCs. TSP-1, a multifactorial extracellular matrix protein, is critically important in the formation of neural connections during development, so its function in our co-culture model was investigated by small interfering RNA (siRNA) transfection. When TSP-1 expression was decreased with siRNA silencing, BMSCs had no impact on RGC survival, but reduced neurite outgrowth and decreased expression of synaptophysin, MAP-2 and TGF-beta in RGCs. Furthermore, the number of BMSCs with neural-like characteristics was significantly decreased by more than two-fold using siRNA silencing. CONCLUSIONS: Our data suggest that the TSP-1 signaling pathway might have an important role in neural-like differentiation in BMSCs and neurite outgrowth in RGCs. This study provides new insights into the potential reparative mechanisms of neural cell repair

Neuroimmune crosstalk in the central nervous system and its significance for neurological diseases

The central nervous system (CNS) is now known to actively communicate with the immune system to control immune responses both centrally and peripherally. Within the CNS, while studies on glial cells, especially microglia, have highlighted the importance of this cell type in innate immune responses of the CNS, the immune regulatory functions of other cell types, especially neurons, are largely unknown. How neuroimmune cross-talk is homeostatically maintained in neurodevelopment and adult plasticity is even more elusive. Inspiringly, accumulating evidence suggests that neurons may also actively participate in immune responses by controlling glial cells and infiltrated T cells. The potential clinical application of this knowledge warrants a deeper understanding of the mutual interactions between neurons and other types of cells during neurological and immunological processes within the CNS, which will help advance diagnosis, prevention, and intervention of various neurological diseases. The aim of this review is to address the immune function of both glial cells and neurons, and the roles they play in regulating inflammatory processes and maintaining homeostasis of the CNS.Peer reviewe

Etat des lieux de l’emploi, du maintien dans l’emploi et de la formation des personnes handicapées à La Réunion

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Elucidating links between the mechanical performance of flax fibres and their structural defects

Single flax fibres develop morphological deformations, called kink-bands, which are considered to be areas of weakness. The correlation between the occurrence of kink-bands, fibre extraction method and fibre mechanical properties still needs to be clarified. To this end, an extensive multi-scale statistical study was conducted on 96 elementary fibres extracted from four distinct batches processed with different scutching and combing conditions. First, kink-bands were observed and quantified through polarized light microscopy (PLM), scanning electron microscopy (SEM) and synchrotron X-ray microtomography. PLM quantification demonstrated that uncombed fibres have more cortical residues and larger surface kink-bands with many small internal porosities. Then, the mechanical characteristics of each PLM-quantified single fibre were measured by tensile tests. A larger number of kink-bands was observed for the most intensively combed batch, 18.2 kink-bands/mm, as well as a surprisingly low average kink-band area, of the order of 158 µm² per kink-band. In addition, the same batch had a higher tensile strength and modulus than the other three batches with a negative Pearson correlation of -0.69 and -0.63 with the proportion of defects, respectively. Finally, 74% of the fibres in this intensively combed batch, had a ‘Type I’ linear elastic behaviour, highlighting a significant change of behaviour in comparison to the uncombed batch, attributed to local reorientation and pre-stretching. We demonstrated that changes in kink-bands structure are principally responsible for these evolutions; due to both new distribution of pores in kink-bands regions and reduction in kink-band size induced by local cellulose realignment.The authors gratefully thank the ANR (Agence Nationale de la Recherche) for funding the FLOEME project (ANR-21-CE10-0008 – FLOEME) and Synchrotron SOLEIL for the ANATOMIX beamline time (proposal n° 20211421). ANATOMIX is an Equipment of Excellence (EQUIPEX) funded by the Investments for the Future program of the French National Research Agency (ANR), project NanoimagesX, grant no. ANR-11-EQPX-0031

Candidate genes of the transcellular and paracellular calcium absorption pathways in the small intestine of laying hens

International audienceTo meet the high calcium (Ca) demand during eggshell biomineralization (2 g of Ca per egg), laying hens develop specific metabolic regulations to maintain Ca homeostasis. The intake of Ca, its solubilization, and absorption capacity are enhanced at sexual maturity (SM). A better knowledge of the intestinal Ca transporters involved in their variations at this stage could indicate new nutritional strategies to enhance Ca digestive utilization. Transcellular Ca absorption pathway and its major player calbindin-D 28 K (CALB1) mediate a saturable transport, which has been extensively described in this model. Conversely, a contribution by the paracellular pathway involving non-saturable Ca transport through intercellular tight junction has also been suggested. The aim of the present study was to identify candidate genes of these two pathways and their patterns of expression, in immature pullets (12, 15, and 17 wk old) and mature laying hens (23 wk old) in the duodenum, jejunum, and ileum. Using RT-qPCR, this study identifies 3 new candidate genes for transcellular, and 9 for paracellular Ca transport. A total of 5 candidates of the transcellular pathway, transient receptor potential cation channels subfamily C member 1 (TRPC1) and M member 7 (TRPM7); CALB1 and ATPase plasma membrane Ca2+ transporting 1 (ATP2B1) and ATPase plasma membrane Ca2+ transporting 2 (ATP2B2) were enhanced with age or after SM in the duodenum, the jejunum or all 3 segments. A total of 4 candidates of the paracellular pathway Claudin 2 (CLDN2) and tight junction proteins 1, 2, and 3 (TJP1, TJP2 and TJP3) increased in the small intestine after SM. Additionally, CALB1, ATP2B2, and CLDN2 were overexpressed in the duodenum or the jejunum or both segments after SM. The enhanced expression of candidate genes of the paracellular Ca pathway after SM, supports that the non-saturable transport could be a mechanism of great importance when high concentrations of soluble Ca are observed in the intestinal content during eggshell formation. Both pathways may work cooperatively in the duodenum and jejunum, the main sites of Ca absorption in laying hens

Neural progenitor cells regulate microglia functions and activity

We found mouse neural progenitor cells (NPCs) to have a secretory protein profile distinct from other brain cells and to modulate microglial activation, proliferation and phagocytosis. NPC-derived vascular endothelial growth factor was necessary and sufficient to exert at least some of these effects in mice. Thus, neural precursor cells may not only be shaped by microglia, but also regulate microglia functions and activity