Your browser doesn't support javascript.
loading
The phenol red compound: A potential artifact in pharmacological induction of ferroptosis.
Vera, Matías; Barahona, María José; Nova-Lamperti, Estefanía; Nualart, Francisco; Ferrada, Luciano.
Afiliación
  • Vera M; Center for Advanced Microscopy CMA BIO BIO, Faculty of Biological Sciences, University of Concepción, Concepción, Chile; Laboratory of Neurobiology and Stem Cells, NeuroCellT, Department of Cellular Biology, Faculty of Biological Sciences, University of Concepción, Concepción, Chile.
  • Barahona MJ; Laboratory of Neurobiology and Stem Cells, NeuroCellT, Department of Cellular Biology, Faculty of Biological Sciences, University of Concepción, Concepción, Chile; Laboratory of Physiology of Appetite, FIDELA, Faculty of Medicine and Science, Universidad San Sebastián, Concepción Campus, Concepción,
  • Nova-Lamperti E; Molecular and Translational Immunology Laboratory, Clinical Biochemistry and Immunology Department, Pharmacy Faculty, Universidad de Concepción, Concepción, Chile.
  • Nualart F; Center for Advanced Microscopy CMA BIO BIO, Faculty of Biological Sciences, University of Concepción, Concepción, Chile; Laboratory of Neurobiology and Stem Cells, NeuroCellT, Department of Cellular Biology, Faculty of Biological Sciences, University of Concepción, Concepción, Chile.
  • Ferrada L; Center for Advanced Microscopy CMA BIO BIO, Faculty of Biological Sciences, University of Concepción, Concepción, Chile. Electronic address: luferrada@udec.cl.
Free Radic Biol Med ; 222: 397-402, 2024 Sep.
Article en En | MEDLINE | ID: mdl-38944214
ABSTRACT
Phenol red (PR) is a commonly used compound in culture media as a pH indicator. However, it is unknown whether this compound can interfere with the pharmacological induction of ferroptosis. Here, using high-content live-cell imaging death analysis, we determined that the presence of PR in the culture medium preconditioned normal and tumor cells to ferroptosis induced by system xc- inhibition mediated by imidazole ketone erastin (IKE) or GPX4 blockade in response to RSL-3, but had no significant effects against treatment with the endoperoxide FINO2. Mechanistically, we revealed that PR decreases the levels of the antiferroptotic genes Slc7a11, Slc3a2, and Gpx4, while promoting the overexpression de Acls4, a key inducer of ferroptosis. Additionally, through superresolution analysis, we determined that the presence of PR mislocalizes the system xc- from the plasma membrane. Thus, our results show that the presence of PR in the culture medium can be a problematic artifact for the accurate interpretation of cell sensitivity to IKE or RSL-3-mediated ferroptosis induction.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fenolsulfonftaleína / Ferroptosis / Fosfolípido Hidroperóxido Glutatión Peroxidasa Límite: Animals / Humans Idioma: En Revista: Free Radic Biol Med / Free radic. biol. med / Free radical biology and medicine Asunto de la revista: BIOQUIMICA / MEDICINA Año: 2024 Tipo del documento: Article País de afiliación: Chile

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fenolsulfonftaleína / Ferroptosis / Fosfolípido Hidroperóxido Glutatión Peroxidasa Límite: Animals / Humans Idioma: En Revista: Free Radic Biol Med / Free radic. biol. med / Free radical biology and medicine Asunto de la revista: BIOQUIMICA / MEDICINA Año: 2024 Tipo del documento: Article País de afiliación: Chile