Publications by authors named "Marie-Amelie De Menorval"

Article Synopsis
  • Changes in certain proteins called cytokines play a big role in sickle-cell disease (SCD), especially when patients have painful episodes or when they have reactions after blood transfusions.
  • The study looked at 36 SCD patients with severe symptoms and 31 with fewer symptoms to see how these cytokines were linked to delayed blood transfusion reactions.
  • The results showed that some cytokines were higher in SCD patients compared to healthy people, and specific changes in these proteins were linked to the beginning of reactions after blood transfusions.
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Human adipose mesenchymal stem cells (haMSCs) are multipotent adult stem cells of great interest in regenerative medicine or oncology. They present spontaneous calcium oscillations related to cell cycle progression or differentiation but the correlation between these events is still unclear. Indeed, it is difficult to mimic haMSCs spontaneous calcium oscillations with chemical means.

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Article Synopsis
  • Sickle cell disease (SCD) patients often receive blood transfusions to help with severe pain caused by blocked blood flow, but the quality of stored blood can change over time.
  • Researchers tested how the condition of SCD patients affected the blood cells in transfusions and found that older blood cells did not work as well when mixed with patient plasma.
  • The study suggests that fresher blood may be better for SCD patients because older blood can become less effective and fresh or cryopreserved blood works similarly well in helping patients.
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Mesenchymal stem cells (MSCs) are multipotent nonhematopoietic cells with the ability to differentiate into various specific cell types, thus holding great promise for regenerative medicine. Early clinical trials have proven that MSC-based therapy is safe, with possible efficacy in various diseased states. Moreover, genetic modification of MSCs to improve their function can be safely achieved using electrogene transfer.

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Dimethyl sulfoxide (DMSO) has been known to enhance cell membrane permeability of drugs or DNA. Molecular dynamics (MD) simulations with single-component lipid bilayers predicted the existence of three regimes of action of DMSO: membrane loosening, pore formation and bilayer collapse. We show here that these modes of action are also reproduced in the presence of cholesterol in the bilayer, and we provide a description at the atomic detail of the DMSO-mediated process of pore formation in cholesterol-containing lipid membranes.

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