The phenol red compound: A potential artifact in pharmacological induction of ferroptosis

IF 7.1 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Free Radical Biology and Medicine Pub Date : 2024-06-27 DOI:10.1016/j.freeradbiomed.2024.06.023
Matías Vera , María José Barahona , Estefanía Nova-Lamperti , Francisco Nualart , Luciano Ferrada
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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.

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酚红化合物:药理诱导铁变态反应的潜在假象。
酚红(PR)是培养基中常用的一种化合物,可作为 pH 指示剂。然而,这种化合物是否会干扰药理诱导的铁变态反应还不得而知。在这里,我们利用高含量活细胞成像死亡分析法确定,培养基中含有酚红可预处理正常细胞和肿瘤细胞在咪唑酮erastin(IKE)介导的系统xc-抑制或RSL-3作用下的GPX4阻断诱导的铁蜕变,但对内过氧化物FINO2的处理无明显影响。从机理上讲,我们发现 PR 会降低抗铁锈色素沉着基因 Slc7a11、Slc3a2 和 Gpx4 的水平,同时促进铁锈色素沉着的关键诱导因子 Acls4 的过度表达。此外,通过超分辨率分析,我们确定 PR 的存在会使 xc- 系统从质膜错位。因此,我们的研究结果表明,培养液中 PR 的存在可能会成为一个有问题的假象,不利于准确解释细胞对 IKE 或 RSL-3 介导的铁突变诱导的敏感性。
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来源期刊
Free Radical Biology and Medicine
Free Radical Biology and Medicine 医学-内分泌学与代谢
CiteScore
14.00
自引率
4.10%
发文量
850
审稿时长
22 days
期刊介绍: Free Radical Biology and Medicine is a leading journal in the field of redox biology, which is the study of the role of reactive oxygen species (ROS) and other oxidizing agents in biological systems. The journal serves as a premier forum for publishing innovative and groundbreaking research that explores the redox biology of health and disease, covering a wide range of topics and disciplines. Free Radical Biology and Medicine also commissions Special Issues that highlight recent advances in both basic and clinical research, with a particular emphasis on the mechanisms underlying altered metabolism and redox signaling. These Special Issues aim to provide a focused platform for the latest research in the field, fostering collaboration and knowledge exchange among researchers and clinicians.
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