Caution for the routine use of phenol red - It is more than just a pH indicator.
Cell culture
HL-60 cells
Myeloperoxidase
Oxidative stress
Phenol red
Journal
Chemico-biological interactions
ISSN: 1872-7786
Titre abrégé: Chem Biol Interact
Pays: Ireland
ID NLM: 0227276
Informations de publication
Date de publication:
01 Sep 2019
01 Sep 2019
Historique:
received:
07
05
2019
revised:
18
06
2019
accepted:
05
07
2019
pubmed:
10
7
2019
medline:
10
9
2019
entrez:
10
7
2019
Statut:
ppublish
Résumé
Phenol red (PR) is the standard pH indicator in various cell and tissue culture media, as it provides a quick check for the health of the culture. PR has also been used in multiple protocols to detect cellular hydrogen peroxide as well as peroxidase activity from human peroxidase enzymes. The majority of promyelocytic leukemia cell lines (e.g. HL-60 cells) express myeloperoxidase (MPO), which may react with PR, especially as the latter is present in cell culture media at sufficient concentrations (~15 μM) to partake in redox reactions. Moreover, phenolic molecules are often efficient donor substrates for peroxidase enzymes. In this study, we hypothesized that MPO metabolism of PR via MPO-expressing HL-60 cells could result in PR metabolite(s) that could modulate cell viability. We used purified human MPO for UV-visible spectrophotometry, electron paramagnetic resonance (EPR) and LC-MS analyses to investigate PR peroxidation. 2-chloro-5,5-dimethyl-1,3-cyclohexanedione (monochloro-dimedone, MCD) was used to assess the effect of PR on MPO-catalyzed chlorination activity, and we assessed PR uptake by HL-60 cells using LC-MS analysis. Lastly, we investigated the impact of PR metabolism by intracellular MPO on cell viability (ATP, using CellTiter-Glo
Identifiants
pubmed: 31288001
pii: S0009-2797(19)30781-1
doi: 10.1016/j.cbi.2019.108739
pii:
doi:
Substances chimiques
Hydrogen Peroxide
BBX060AN9V
Peroxidase
EC 1.11.1.7
Phenolsulfonphthalein
I6G9Y0J1OJ
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
108739Informations de copyright
Copyright © 2019 Elsevier B.V. All rights reserved.