The Quantum Biology of Reactive Oxygen Species Partitioning Impacts Cellular Bioenergetics

Quantum biology is the study of quantum effects on biochemical mechanisms and biological function. We show that the biological production of reactive oxygen species (ROS) in live cells can be influenced by coherent electron spin dynamics, providing a new example of quantum biology in cellular regulation. ROS partitioning appears to be mediated during the activation of molecular oxygen (O2) by reduced flavoenzymes, forming spin-correlated radical pairs (RPs). We find that oscillating magnetic fields at Zeeman resonance alter relative yields of cellular superoxide (O2•−) and hydrogen peroxide (H2O2) ROS products, indicating coherent singlet-triplet mixing at the point of ROS formation. Furthermore, the orientation-dependence of magnetic stimulation, which leads to specific changes in ROS levels, increases either mitochondrial respiration and glycolysis rates. Our results reveal quantum effects in live cell cultures that bridge atomic and cellular levels by connecting ROS partitioning to cellular bioenergetics.

is formed from the singlet RP state. A subsequent second electron transfer releases hydrogen peroxide (H 2 O 2 ). Besides kinetic requirements 22 , the coherent evolution between the singlet and triplet states of FADH • :O 2 •− RP determines the amount of the products for the two reaction channels. We hypothesize that RP spin dynamics can be altered by external static and oscillating magnetic fields 23 , which change singlet-triplet intersystem crossing (ISC) rates, and thus affect the outcome of cellular ROS product ratios.
To test the RPM hypothesis for ROS-related quantum biology, we developed low-frequency, low-field instrumentation for product-yield detected magnetic resonance (PYDMR) 21 . In the present PYDMR study, primary human umbilical vein endothelial cells (HUVECs) were exposed to either 50 μ T static magnetic fields (SMF) in control samples, or to 50 μ T SMFs combined with 1.4 MHz, 20 μ T rms RF magnetic fields at Zeeman resonance in experimental samples. The RF orientation was applied in parallel or perpendicular angles with respect to the SMF. Intracellular O 2 •− and extracellular H 2 O 2 were measured by selective assays in HUVEC cultures. Figure 2 exhibits the changes observed in the ROS product distributions measured for parallel and perpendicular RF orientations. In the perpendicular orientation, we measured a 36% ± 4 reduction of O 2 •− (p < 0.002) and a 21% ± 5 reduction of H 2 O 2 (p < 0.02). For the parallel orientation, we measured a 10% ± 2 (p < 0.002) reduction of O 2 •− and an 8% ± 8 increase oaf H 2 O 2 (p < 0.02). Changes in ROS products in cell cultures between SMF ± RF are indicative of a resonance effect on singlet-triplet intersystem crossing (or quantum coherences) at the point of ROS formation 21 .
Singlet-triplet product yields were modeled by numerical simulations of a triplet-born one-proton radical-pair reaction with static and RF magnetic fields at Zeeman resonance 7 , Fig. 3. The numerical results predict an orientation-dependent increase in singlet product yield (H 2 O 2 ) and decrease in triplet product yield (O 2 •− ) when the resonant RF field is added to the static field. These simulations are in agreement with perpendicular experimental results (Fig. 2) and are consistent with our previous cellular results with hyperfine resonance effects 21 . The theoretical model of a one-proton RP does not account for changes in ROS yields (O 2 •− and H 2 O 2 ) in the parallel orientation, which suggests either limitations of the simplified model in the complex cellular environment or anisotropic hyperfine resonances near the Zeeman resonance.
To understand the potential effects of ROS signaling on cellular bioenergetics, we measured the oxygen consumption rate (OCR) and extracellular acidification rate (ECAR) with a Seahorse XF Analyzer, Fig. 4. OCR indicates the mitochondrial respiration rate and ECAR is predominately a measure of lactic acid formed during glycolytic energy metabolism 24,25 . Figure 4 illustrates experiments in HUVECs that show RF orientation dependence of OCR and ECAR bioenergetic measurements, which appear to result from changes in ROS partitioning. Zeeman resonance at perpendicular excitation did not affect OCR levels ( Fig. 4A) but increased ECAR by 100% ± 13 (Fig. 4C). Zeeman resonance at parallel excitation had an opposite effect, where OCR increased by 54% ± 4 ( Fig. 4B) while ECAR remained unchanged (Fig. 4D). Altered OCR and ECAR values indicate phenotypic changes in HUVECs bioenergetic pathways, demonstrating spin biochemistry intervention of ROS signaling by RF magnetic fields at Zeeman resonance.
The orientation effects that lead to specific ROS product distributions are in agreement with the simple RPM model for the perpendicular orientation, which predicts an increase in singlet yields with a concomitant decrease in triplet yields, Fig. 3. The overall reduction in measured ROS products at perpendicular excitation suggests a possible ROS signaling link to increased glycolytic activity 26,27 . The decrease in steady-state ROS levels with enhanced glycolytic activity might be due to scavenging of ROS by pyruvate 28 . The differential effect on ROS product yields at parallel excitation indicate a signaling channel of increased mitochondrial respiration. Our experiments did not explore the downstream targets of the ROS signaling pathways that lead to regulation of glycolysis and respiration. We suggest that ROS signaling channels are likely to involve the activation of bioenergetic regulation proteins 26,29,30 , eliciting a type of hormesis response 31 or a Warburg effect 27 .
Magnetic stimulation of ROS partitioning in live cells reveals hallmarks of quantum coherence, manifested by changes in cellular ROS product distributions. Changes in ROS product partitioning, in turn, altered cellular bioenergetics by increasing either mitochondrial respiration or glycolysis. ROS formation is inextricably linked to bioenergetics by normal cellular metabolism, connecting persistent quantum effects in ROS oxidative signaling to cellular bioenergetics. Because of the importance of ROS in human health and disease 32 , this research is likely to have significance for several areas in bio-medical research. Our results provide fundamental insights into the role of the RPM in ROS redox biology and cellular bioenergetics, revealing a new example of quantum biology.  and 50 μT magnetic field). The data is presented as a product yield ratio percentage with ± RF in the static field. RF magnetic fields in perpendicular orientation decreased both O 2 •− and H 2 O 2 levels by 36% ± 4% (p < 0.002) and 21% ± 5% (p < 0.02), respectively, relative to controls. In parallel orientation, H 2 O 2 levels increased by 8% ± 8% (p < 0.02), whereas O 2 •− decreased by 10% ± 2% (p < 0.002), relative to controls. The amount of ROS produced were normalized to protein concentrations and represent the average of 3 independent experiments. lial growth medium (Promocell GmbH, Heidelberg, Germany) supplemented with 2% fetal calf serum (FCS), 0.004 ml/ml endothelial cell growth supplement/heparin, 0.1 ng/ml epidermal growth factor (EGF), 1 ng/ml basic fibroblast growth factor, and 1 mg/ml hydrocortisone at 37 °C with 5% CO 2 . The cells were cultured in a 75-cm 2 flask to expand cell number. After reaching confluence, the cells were seeded in (a) 6-well culture plates at a density of 3.5× 10 3 cells/cm 2 for ROS experiments; (b) and in mini plates at 3,500 cells per well for Seahorse XFp Analyzer (Agilent Technologies, Santa Clara, CA).

ROS Measurements. Cellular H 2 O 2 production was measured with the horseradish peroxidase-linked
Amplex Ultra Red (HRP-AUR) fluorometric assay (Invitrogen). After cells were seeded, they were exposed to SMF ± RF magnetic fields for the duration of the experiment, by use of the PYDMR apparatus we previously described 21 . At day 3, medium was aspirated and cells were washed with Hank's Buffer (HB) with 100 μ M diethylenetriaminepentaacetic acid (DTPA) and incubated for 1 h with HB containing 10 μ M AUR and 0.2 units/ ml HRP. Resorufin fluorescence was collected on a Gemini fluorescence microplate reader (Molecular Devices, Sunnyvale, CA).
To measure intracellular production of O 2 •− , HUVECs were incubated for 30 min at 37 °C in HB containing 50 μ M dihydroethidium (DHE) at day 3. Cells were washed twice in HB with 100 μ M DTPA and harvested in 300 μ L of methanol. The samples were spun down for 15 min at 12,000 rpm at 4 °C, the supernatant was collected and dried for 5-6 hrs at 37 °C and stored at − 20 °C for 7-10 days before high-performance liquid chromatography (HPLC) analysis. An Agilent 1100 series HPLC with a G1321A fluorescence detector was used for DHE product Oligomycin was added at 21 min to inhibit ATP synthesis, the proton ionophore FCCP was added at 41 min to assess the maximum possible oxygen consumption, and antimycin A was added at 61 min to inhibit electron flow through complex III. The static magnetic field was 50 μ T and the RF was 1.4 MHz at Zeeman resonance. The RF was oriented perpendicular (A and C) or parallel (B and D) to the static field. Perpendicular RF excitation did not affect the oxygen consumption rate (OCR) (Panel A), whereas extracellular acidification rate (ECAR) was increased by 100 ± 13 (p < 0.001, Panel C). Parallel RF excitation lead to increased OCR by 54 ± 4 (p < 0.001, Panel B), while ECAR remained unchanged (Panel D). These are results of 3 independent representative experiments and data were normalized to total cellular protein.
Scientific RepoRts | 6:38543 | DOI: 10.1038/srep38543 separation. Analytes were separated using a C-18 reverse-phase column (Nucleosil 250 to 4.5 mm) as previously described 33 . The total fluorescence intensity of the 2-hydroxyethidium peak were averaged for all wells and then averaged for three separate experiments.
Protein content, HPLC analysis, and resorufin fluorescence were measured at the same termination points. H 2 O 2 and O 2 •− measurements were normalized to total protein concentration (BCA, Pierce). H 2 O 2 calibration curves with HRP-AUR under the same RF magnetic field strengths showed no differences compared to SMF controls, demonstrating that RF fields do not interact with the H 2 O 2 detection assay.

Cellular
Bioenergetics. An XFp Analyzer from Seahorse Bioscience was used for the bioenergetic measurements. HUVECs were seeded at 4,000 cells per well in XFp miniplates and exposed to RF magnetic fields for 2 days. The MitoStress Test Assay was performed as described previously 24,25 . The XFp Analyzer measured mitochondrial respiration and glycolysis in vitro 34,35 in the same samples. Mitochondrial respiration was determined by the oxygen consumption rate (OCR) in cell culture. Glycolysis was assessed by the extracellular acidification rate (ECAR). To estimate the proportion of the OCR coupled to ATP synthesis, oligomycin (1 μ g/ml) was injected at 21 minutes into all samples to inhibit the ATP synthase. Typically, the OCR rate decreases in response to oligomycin by the extent to which the cells are using mitochondria to generate ATP. The remaining OCR can be ascribed to both proton leak across the mitochondrial membrane and oxygen consumption by processes other than reduction at cytochrome c oxidase. To determine the maximal OCR that the cells can sustain, the proton ionophore (uncoupler) FCCP (1 μ M) was injected at 41 minutes. Lastly, antimycin A (10 μ M) is injected at 61 minutes to inhibit electron flux through Complex III, which suppresses OCR dramatically. What remains is the OCR that is attributable to O 2 consumption due to the formation of mitochondrial ROS and non-mitochondrial sources.