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Production of Peroxymonocarbonate by Steady-State Micromolar H 2 O 2 and Activated Macrophages in the Presence of CO 2 /HCO 3 - Evidenced by Boronate Probes.

Authors :
Linares E
Severino D
Truzzi DR
Rios N
Radi R
Augusto O
Source :
Chemical research in toxicology [Chem Res Toxicol] 2024 Jul 15; Vol. 37 (7), pp. 1129-1138. Date of Electronic Publication: 2024 Jun 25.
Publication Year :
2024

Abstract

Peroxymonocarbonate (HCO <subscript>4</subscript> <superscript>-</superscript> /HOOCO <subscript>2</subscript> <superscript>-</superscript> ) is produced by the reversible reaction of CO <subscript>2</subscript> /HCO <subscript>3</subscript> <superscript>-</superscript> with H <subscript>2</subscript> O <subscript>2</subscript> ( K = 0.33 M <superscript>-1</superscript> , pH 7.0). Although produced in low yields at physiological pHs and H <subscript>2</subscript> O <subscript>2</subscript> and CO <subscript>2</subscript> /HCO <subscript>3</subscript> <superscript>-</superscript> concentrations, HCO <subscript>4</subscript> <superscript>-</superscript> oxidizes most nucleophiles with rate constants 10 to 100 times higher than those of H <subscript>2</subscript> O <subscript>2</subscript> . Boronate probes are known examples because HCO <subscript>4</subscript> <superscript>-</superscript> reacts with coumarin-7-boronic acid pinacolate ester (CBE) with a rate constant that is approximately 100 times higher than that of H <subscript>2</subscript> O <subscript>2</subscript> and the same holds for fluorescein-boronate (Fl-B) as reported here. Therefore, we tested whether boronate probes could provide evidence for HCO <subscript>4</subscript> <superscript>-</superscript> formation under biologically relevant conditions. Glucose/glucose oxidase/catalase were adjusted to produce low steady-state H <subscript>2</subscript> O <subscript>2</subscript> concentrations (2-18 μM) in Pi buffer at pH 7.4 and 37 °C. Then, CBE (100 μM) was added and fluorescence increase was monitored with time. The results showed that each steady-state H <subscript>2</subscript> O <subscript>2</subscript> concentration reacted more rapidly (∼30%) in the presence of CO <subscript>2</subscript> /HCO <subscript>3</subscript> <superscript>-</superscript> (25 mM) than in its absence, and the data permitted the calculation of consistent rate constants. Also, RAW 264.7 macrophages were activated with phorbol 12-myristate 13-acetate (PMA) (1 μg/mL) at pH 7.4 and 37 °C to produce a time-dependent H <subscript>2</subscript> O <subscript>2</subscript> concentration (8.0 ± 2.5 μM after 60 min). The media contained 0, 21.6, or 42.2 mM HCO <subscript>3</subscript> <superscript>-</superscript> equilibrated with 0, 5, or 10% CO <subscript>2</subscript> , respectively. In the presence of CBE or Fl-B (30 μM), a time-dependent increase in the fluorescence of the bulk solution was observed, which was higher in the presence of CO <subscript>2</subscript> /HCO <subscript>3</subscript> <superscript>-</superscript> in a concentration-dependent manner. The Fl-B samples were also examined by fluorescence microscopy. Our results demonstrated that mammalian cells produce HCO <subscript>4</subscript> <superscript>-</superscript> and boronate probes can evidence and distinguish it from H <subscript>2</subscript> O <subscript>2</subscript> under biologically relevant concentrations of H <subscript>2</subscript> O <subscript>2</subscript> and CO <subscript>2</subscript> /HCO <subscript>3</subscript> <superscript>-</superscript> .

Details

Language :
English
ISSN :
1520-5010
Volume :
37
Issue :
7
Database :
MEDLINE
Journal :
Chemical research in toxicology
Publication Type :
Academic Journal
Accession number :
38916595
Full Text :
https://doi.org/10.1021/acs.chemrestox.4c00059