TY - JOUR
T1 - The phenol red compound: A potential artifact in pharmacological induction of ferroptosis
AU - Vera, Matías
AU - Barahona Figueroa, María José
AU - Nova-Lamperti, Estefanía
AU - Nualart, Francisco
AU - Ferrada, Luciano
N1 - Publisher Copyright:
© 2024
PY - 2024/9
Y1 - 2024/9
N2 - 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.
AB - 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.
KW - ACSL4
KW - Ferroptosis
KW - GPX4
KW - IKE
KW - Phenol red
KW - RSL-3
KW - System x
KW - System xc−
UR - http://www.scopus.com/inward/record.url?scp=85197073064&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/177e2d03-6d6a-3787-826b-67277963735b/
U2 - 10.1016/j.freeradbiomed.2024.06.023
DO - 10.1016/j.freeradbiomed.2024.06.023
M3 - Article
SN - 0891-5849
VL - 222
SP - 397
EP - 402
JO - Free Radical Biology and Medicine
JF - Free Radical Biology and Medicine
ER -