Publications by authors named "M J Jimenez Arjona"

Here, we present a protocol for using Myotally, a user-friendly software for fast, automated quantification of muscle fiber size, number, and central nucleation from immunofluorescent stains of mouse skeletal muscle cross-sections. We describe steps for installing the software, preparing compatible images, finding the file path, and selecting key parameters like image quality and size limits. We also detail optional features, such as measuring mean fluorescence.

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As cells organize spatially or divide, they translocate many micron-scale organelles in their cytoplasm. These include endomembrane vesicles, nuclei, microtubule asters, mitotic spindles, or chromosomes. Organelle motion is powered by cytoskeleton forces but is opposed by viscoelastic forces imparted by the surrounding crowded cytoplasm medium.

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Article Synopsis
  • Aging slows down the activation and increases the death of skeletal muscle stem cells (MuSCs), which leads to poor muscle repair.
  • Researchers used a multiomics approach, single-cell analysis, and functional tests to compare MuSCs from young and old mice, revealing that glutathione (GSH) metabolism is disrupted in older cells.
  • They discovered that older MuSCs form two distinct groups based on their GSH functionality and identified a mechanism involving NRF2 and NF-κB that maintains this division, suggesting that manipulating GSH levels could help reverse aging effects in MuSCs.
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The formation of ultrathin films of Rh-based porous metal-organic polyhedra (Rh-MOPs) by the Langmuir-Blodgett method has been explored. Homogeneous and dense monolayer films were formed at the air-water interface either using two different coordinatively alkyl-functionalized Rh-MOPs (HRhMOP(diz) and HRhMOP(oiz)) or by incorporation of aliphatic chains to the axial sites of dirhodium paddlewheels of another Rh-MOP (OHRhMOP) at the air-liquid interface. All these Rh-MOP monolayers were successively deposited onto different substrates in order to obtain multilayer films with controllable thicknesses.

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Current advances in materials science have demonstrated that extracellular mechanical cues can define cell function and cell fate. However, a fundamental understanding of the manner in which intracellular mechanical cues affect cell mechanics remains elusive. How intracellular mechanical hindrance, reinforcement, and supports interfere with the cell cycle and promote cell death is described here.

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