Publications by authors named "A Nicot"

Amphiphysin 2 (BIN1) is a membrane and actin remodeling protein mutated in congenital and adult centronuclear myopathies. Here, we report an unexpected function of this N-BAR domain protein BIN1 in filopodia formation. We demonstrated that BIN1 expression is necessary and sufficient to induce filopodia formation.

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Article Synopsis
  • A pilot study investigated the gut and oral microbiota in multiple sclerosis (MS) patients and found significant bacterial alterations compared to healthy volunteers (HV).
  • The analysis revealed decreased diversity and specific bacteria depletion in MS patients, along with enrichment of inflammation-associated bacteria and altered microbial pathways.
  • A distinctive oral metabolite signature was identified in MS patients, which has high specificity for discriminating them from HV and patients with rheumatoid arthritis, suggesting the potential for future research on oral microbiota in autoimmune diseases.
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Mutations allowing pathogens to escape host immunity promote the spread of infectious diseases in heterogeneous host populations and can lead to major epidemics. Understanding the conditions that slow down this evolution is key for the development of durable control strategies against pathogens. Here, we use theory and experiments to compare the efficacy of three strategies for the deployment of resistance: (i) a strategy where the host population contains two single-resistant genotypes, (ii) a strategy where the host carries a double-resistant genotype, (iii) a strategy where the host population is a mix of a single-resistant genotype and a double-resistant genotype.

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In neurons, fast axonal transport (FAT) of vesicles occurs over long distances and requires constant and local energy supply for molecular motors in the form of adenosine triphosphate (ATP). FAT is independent of mitochondrial metabolism. Indeed, the glycolytic machinery is present on vesicles and locally produces ATP, as well as nicotinamide adenine dinucleotide bonded with hydrogen (NADH) and pyruvate, using glucose as a substrate.

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Cocaine predictive cues and contexts exert powerful control over behaviour and can incite cocaine seeking and taking. This type of conditioned behaviour is encoded within striatal circuits, and these circuits and behaviours are, in part, regulated by opioid peptides and receptors expressed in striatal medium spiny neurons. We previously showed that augmenting levels of the opioid peptide enkephalin in the striatum facilitates acquisition of cocaine conditioned place preference (CPP), while opioid receptor antagonists attenuate expression of cocaine CPP.

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