Víctor Hugo Sánchez-Vázquez

ORCID: 0000-0001-5715-2599
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About
Contact & Profiles
Research Areas
  • Calcium signaling and nucleotide metabolism
  • Mitochondrial Function and Pathology
  • Ion Channels and Receptors
  • Ion channel regulation and function
  • Neurobiology and Insect Physiology Research
  • Neuroscience and Neural Engineering
  • Metabolism, Diabetes, and Cancer
  • Cellular transport and secretion
  • Connexins and lens biology
  • ATP Synthase and ATPases Research
  • Metabolism and Genetic Disorders

Thomas Jefferson University
2025

Center for Research and Advanced Studies of the National Polytechnic Institute
2014-2022

Universidad de las Américas
2022

Cells utilize protein disaggregases to avoid abnormal aggregation that causes many diseases. Among these, caseinolytic peptidase B homolog (CLPB) is localized in the mitochondrial intermembrane space and linked human disease. Upon CLPB loss, MICU1 MICU2, regulators of calcium uniporter complex (mtCU), OPA1, a main mediator fusion, become insoluble but functional outcome remains unclear. In this work we demonstrate required maintain signalling fusion dynamics. loss results altered mtCU...

10.1038/s41467-025-57641-9 article EN cc-by-nc-nd Nature Communications 2025-03-21

The overexpression of the Orai1 channel inhibits SOCE when using Ca2+ readdition protocol. However, we found that HeLa cells overexpressing displayed enhanced entry and a limited ER depletion in response to combination ATP thapsigargin (TG) presence external Ca2+. As these effects require an agonist TG, decided study whether phosphorylation S27/S30 residues had any role two different mutants: Orai1-S27/30A (O1-AA, phosphorylation-resistant) Orai1-S27/30D (O1-DD, phosphomimetic). Both O1-wt...

10.3390/cells11132037 article EN cc-by Cells 2022-06-27
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