Publications by authors named "L E Martinez de Villarreal"

MFN1 (mitofusin 1) and MFN2 are key players in mitochondrial fusion, endoplasmic reticulum (ER)-mitochondria juxtaposition, and macroautophagy/autophagy. However, the mechanisms by which these proteins participate in these processes are poorly understood. Here, we studied the interactomes of these two proteins by using CRISPR-Cas9 technology to insert an HA-tag at the C terminus of MFN1 and MFN2, and thus generating HeLa cell lines that endogenously expressed MFN1-HA or MFN2-HA.

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Porcine circovirus type 2 (PCV2) is a highly damaging pathogen for pig farming, causing significant economic losses. Despite the availability of vaccines based on different technologies, the virus steadily infects the world's pig population. In this context, virus-like particles (VLPs) constitute appealing alternatives for vaccine development as they lack the viral genome but present intact external surfaces.

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Histone H1 is involved in the regulation of chromatin structure. Human somatic cells express up to seven subtypes. The variability in the proportions of somatic H1s (H1 complement) is one piece of evidence supporting their functional specificity.

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Article Synopsis
  • Diabetes mellitus increases the risk of cardiovascular disease and is a leading cause of death among patients, impacting cardiac cell mechanics and stiffness.
  • The study investigates how Type 1 Diabetes Mellitus (T1DM) alters costameric proteins in heart cells and affects their cellular mechanics using advanced imaging techniques.
  • Findings reveal that diabetic cardiomyocytes exhibit higher stiffness compared to normal cells, suggesting that changes in cellular communication may contribute to diabetic cardiomyopathy and affect heart function.
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Background: Yerba mate (YM, Ilex paraguariensis) consumption beneficially affects the bones. However, whether YM components exert their effect on bone cells directly remains elusive.

Methods: We evaluated how main YM components affect osteoblastic (MC3T3-E1) and osteocytic (MLO-Y4) cells in vitro when administered separately or in an aqueous extract.

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