Publications by authors named "J F Prost"

Cell adhesion proteins typically form stable clusters that anchor the cell membrane to its environment. Several works have suggested that cell membrane protein clusters can emerge from a local feedback between the membrane curvature and the density of proteins. Here, we investigate the effect of such a curvature-sensing mechanism in the context of cell adhesion proteins.

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Article Synopsis
  • The current standard for preventing rejection in vascularized composite allotransplantation (VCA) uses systemic immunosuppression, which poses significant side effects, leading to interest in local immunosuppression methods.
  • Researchers investigated a local drug delivery system for tacrolimus (TGMS-TAC) to reduce toxicity and enhance graft survival, showing promising results in a porcine model, although some rejection signs were noted.
  • Results indicated that while systemic immune responses remained stable, local tissue analysis revealed infiltration of immune cells and involvement of neutrophil extracellular traps (NETs) in the rejection process, highlighting the need for better understanding of VCA graft rejection mechanisms.
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Cell adhesion receptors are transmembrane proteins that bind cells to their environment. These proteins typically cluster into disk-shaped or linear structures. Here, we show that such clustering patterns spontaneously emerge when the receptor senses the membrane deformation gradient, for example, by reaching a lower-energy conformation when the membrane is tilted relative to the underlying binding substrate.

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We compare three different setups for measuring cell-cell adhesion. We show that the measured strength depends on the type of setup that is used. For identical cells different assays measure different detachment forces.

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Mucopolysaccharidoses (MPS) screening is tedious and still performed by analysis of total glycosaminoglycans (GAG) using 1,9-dimethylmethylene blue (DMB) photometric assay, although false positive and negative tests have been reported. Analysis of differentiated GAGs have been pursued classically by gel electrophoresis or more recently by quantitative LC-MS assays. Secondary elevations of GAGs have been reported in urinary tract infections (UTI).

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