Article | Open | Published:

HIF-1α regulates COXIV subunits, a potential mechanism of self-protective response to microwave induced mitochondrial damages in neurons

Abstract

Anxiety and speculation about potential health hazards of microwaves exposure are spreading in the past decades. Hypoxia-inducible factor-1α (HIF-1α), which can be activated by reactive oxygen species (ROS), played pivotal roles in protective responses against microwave in neuron-like cells. In this study, we established 30 mW/cm2 microwave exposed animal model, which could result in revisable injuries of neuronal mitochondria, including ultrastructure and functions, such as ROS generation and cytochrome c oxidase (COX) activity. We found that the ratio of COXIV-1/COXIV-2, two isoforms of COXIV, decreased at 1 d and increased from 3 d to 14 d. Similar expression changes of HIF-1α suggested that COXIV-1 and COXIV-2 might be regulated by HIF-1α. In neuron-like cells, 30 mW/cm2 microwave down-regulated COX activity from 30 min to 6 h, and then started to recover. And, both HIF-1α transcriptional activity and COXIV-1/COXIV-2 ratio were up-regulated at 6 h and 9 h after exposure. Moreover, HIF-1α inhibition down-regulated COXIV-1 expression, promoted ROS generation, impaired mitochondrial membrane potentials (MMP), as well as abolished microwave induced ATP production. In conclusion, microwave induced mitochondrial ROS production activated HIF-1α and regulated COXIV-1 expression to restore mitochondria functions. Therefore, HIF-1α might be a potential target to impair microwave induced injuries.

Introduction

Mitochondria play pivotal roles in maintaining energy metabolism, and mitochondrial dysfunctions are always associated with neurological damages, including non-infectious stimuli induced injuries1,2,3. Studies from our group and others demonstrated that microwave exposure, a type of electromagnetic radiation, could induce mitochondrial function disorder and mitochondrial structural injuries4,5,6,7. Interestingly, hypoxia-inducible factor-1α (HIF-1α), a key physiological sensor of oxygen level in most mammalian cells, was up-regulated in PC12 derived neuron-like cells after 30 mW/cm2 microwave exposure. Importantly, increased HIF-1α expression initiated the protective responses against microwave5. Under condition of non-infectious stimuli, such as hypoxia, ionizing and electromagnetic radiation, HIF-1α always acts as the master switch between acute response and adaptive response8,9,10. Recently, studies highlighted that mitochondrial disorder, such as increased ROS production, could directly or indirectly activate HIF-1α signaling in mammalian cells11,12. Importantly, numerous HIF-1α target genes, including pyruvate dehydrogenase kinase 1, BNIP3, lactate dehydrogenase A and complex IV, are critical in maintaining mitochondrial functions and energy metabolism13,14.

Cytochrome c oxidase (COX) subunits, complex IV in the mitochondrial respiratory chain, are located in the inner mitochondrial membrane and play pivotal roles in oxidative phosphorylation and ATP production15. COXIV, an important regulatory subunit of COX, could allosterically inhibit COX activity at high ATP/ADP ratios, through binding to ATP16. COXIV have two isoforms, COXIV-1 and COXIV-2. It has been reported that HIF-1α regulates COXIV subunit expression by activating transcription of the genes encoding COXIV-2 and LON, which is a mitochondrial protease for COXIV-1 degradation. Moreover, mammalian cells could optimize the efficiency of respiration, via altering COX subunit composition, to adapt hypoxia environment17. However, whether HIF-1α regulated COXIV subunits to protect neurons from microwave induced damages are still unknown.

In this study, we detected the HIF-1α, COXIV-1 and COXIV-2 protein expression both in the rat hippocampus and PC12 derived neuron-like cells. Moreover, we investigated the roles of HIF-1α in regulating COXIV subunits and in protecting mitochondrial functions in neuron-like cells in vitro.

Materials and Methods

Animals and microwave exposure

All the animal protocols were approved by the Animal Care and Use Committee at Beijing Institute of Radiation Medicine. And, all methods were performed in accordance with the relevant guidelines and regulations. Seventy-two male Wistar rats (203.7 g ± 8.87 g) were randomly divided into two groups: microwave exposure (MW) group and sham exposure (SH) group.

Pulsed microwaves at S-band with the frequency of 2.856 GHz, was generated by a klystron amplifier (model JD 2000) (Vacuum electronics research institute, Beijing, China). Microwave energy was transmitted by rectangular waveguide and A16-dB standard-gain horn antenna to an electromagnetic shield chamber (7 m × 6.5 m × 4 m). And, the diagonal of the antenna was 33 cm. To minimize reflections, interior walls of the chamber were covered with 500 mm and 300 mm pyramidal microwave absorber. The exposure table was 1.4 m below the lower edge of horn antenna, and the center of the table was just under middle of horn antenna. The animals were placed in a plastic cage inside a Plexiglas cylinder, which has a rotational symmetry around the center and contains twenty radial boxes for placing the rats. Microwave from the horn antenna irradiates animals from up to down (Supplementary Fig. 1). The peak power density was 200 W/cm2 in this study. And, the microwave pulse was delivered at 300 pps, with a pulse width of 500 ns. The GX12M30A power heads were fixed at one port of the circulator (plexiglas cylinder), and connected to GX12M1CHP power meter (Guanghua microelectronics instruments, Hefei, China) via waveguide antenna. The average power density was calculated to be 30 mW/cm2. And, the rats were exposed to microwave for at 30 mW/cm2 for 15 min18,19,20. During microwave exigposure, no significant environmental temperature elevation was detected. Moreover, the body temperature before and after exposure was measured by infrared imager (ThermaVision A40, FLIR systems, Wilsonville, OR, USA), and no obvious elevation was observed. For SH group, animals were processed in parallel to that in MW group, but without microwave exposure.


Cell culture and microwave exposure

Rat pheochromocytoma (PC12) cells, a neuron precursor cell line, were cultured in Dulbecco’s Modified Eagle Medium (DMEM) (Gibco, Grand Island, NY) supplemented with 10% horse serum (Gibco) and 5% fetal bovine serum (FBS, Kang Yuan Biology, Tianjin, China). Neuron-like cells were induced by 5 ng/mL nerve growth factor (NGF, Sigma, St. Louis, MO) as described previously5. For exposure, neuron-like cells in 6-well plate were plated at the exposure table, and the average power density was monitored by GX12M30A power heads and GX12M1CHP power meter as described above. The cells in MW group were exposed to 30 mW/cm² microwaves for 6 min. Cells in SH group were treated as the MW group, but without microwave exposure.


Transmission Electron Microscopy (TEM)

At 6 h, 7 d and 14 d after 30 mW/cm2 microwave exposure, hippocampus were dissected from the CA3 region under anatomical microscope. Then, the samples were fixed in 2.5% glutaraldehyde, sequentially processed with 1% osmium tetroxide, graded ethyl alcohols, and embedded in EPON618. Samples cut into ultrathin (70 nm) sections, and were stained with the heavy metals, uranyl acetate, and lead citrate for contrast. After drying, the ultrastructure of mitochondria was observed by TEM (HITACHI Ltd, Tokyo, Japan).


Mitochondrial function assay

COX activity

At 6 h, 1 d, 3 d, 7 d, 14 d and 28 d after 30 mW/cm2 microwave exposure, rat hippocampus were collected, and then mitochondria were isolated by using Mitochondrial Isolation Kit (GENMED Scientifics INC., South San Francisco, CA). Mitochondria suspensions were collected. Then, COX activity was quantified by using COX Assay Kit (GENMED Scientifics INC., South San Francisco, CA) according to the manufacture’s instruction, and normalized by protein concentration.

ATP content

PC12 derived neuron-like cells were treated by the inhibitors of HIF-1α (Bisphenol A) at 1 h before microwave exposure. At 9 h after exposure, cells were collected and schizolysed, and then the supernatant were collected. The ATP content was measured by using a Firefly Luciferase-based ATP Kit (Beyotime, Nanjing, China) as described previously5, and normalized by protein content.

Mitochondrial Membrane Potentials (MMP)

At 9 h after microwave exposure, inhibitors treated neuron-like cells and control cells were used for detecting MMP by using a JC-1 MMP Assay Kit (Beyotime, Nanjing, China). Briefly, cells in 6-well plates were washed with PBS and incubated with JC-1 staining solution at 37 °C for 20 min. After rinsed twice with JC-1 staining buffer, the MMPs were monitored by fluorescent microscope (Olympus, Tokyo, Japan) and were quantified by flow cytometry (BD Bioscience, San Jose, CA). And, relative MMP were calculated.

Intracellular ROS Production

At 9 h after microwave exposure, inhibitors treated neuron-like cells and control cells were collected and incubated with 2′,7′-dichlorofluorescein diacetate (DCFH-DA) (Beyotime, Nanjing, China) at 37 °C for 20 min. Then, fluorescent DCF were measured by flow cytometry to evaluate the ROS level using. Moreover, at appointed time points after exposure, the hippocampal mitochondria were isolated to detect the ROS content using ROS Detection Kit (GENMED Scientifics INC., South San Francisco, CA). And, ROS content was normalized by mitochondrial concentration.


Immunohistochemistry

Rat brains were removed at 6 h, 3 d, 7 d, 14 d and 28 d after microwave exposure, and were fixed in 10% buffered formalin solution, embedded in paraffin and cut at 3 μm thick in the coronal plane. The HIF-1α protein was detected by immunohistochemistry using rabbit anti-rat HIF-1α polyclonal antibody (Bioworld Technology, MN). And, HIF-1α expression was observed blindly under a light microscope (Leica, Wetzlar, Germany). The HIF-1α expressed cells were filled with brown and yellow granules. Ten random visions were selected, and the rate of HIF-1α expressed cells to total cells was calculated.


Immunofluorescence staining

At 9 h after microwave exposure, neuron-like cells were labeled with rabbit anti-rat HIF-1α polyclonal antibody overnight at 4 °C, and then incubated with FITC conjugated goat anti-rabbit IgG secondary antibody (ZSGB-BIO, Beijing, China) for 1 h at room temperature. The HIF-1α expression was observed by fluorescent microscope after DAPI staining.


HIF-1α inhibition

To investigate the roles of HIF-1α in the protective responses against microwave, we blocked HIF-1α protein expression by adding HIF-1α inhibitor Bisphenol A (400 μM) to neuron-like cells at 1 h before exposure. And, at 9 h after exposure, the HIF-1α, COXIV-1 and COXIV-2 expression, mitochondrial functions, such as ATP, MMP and ROS, were evaluated.


Western blot

Total protein and nuclear protein (Nuclear Protein Extraction kit, BestBio, Shanghai, China) were extracted from rat hippocampus, neuron-like cells, Bisphenol A treated neuron-like cells at appointed time points after microwave exposure. Protein expression was detected by rabbit anti-rat HIF-1α antibody (Bioworld Technology, MN), mouse anti-rat COXIV-1 antibody (Thermo Fisher Scientific, Rockford, IL), goat anti-rat COXIV-2 antibody (Santa Cruz Biotechnology, Dallas, TX), rabbit anti-Lamin B1 antibody (Bioworld Technology, MN) and anti-glycolytic glyceraldehyde-3-phosphate dehydrogenase (GAPDH) antibody (KangChen Biology, Nanjing, China). The protein expression was normalized by GAPDH or Lamin B.


Real-time reverse transcript polymerase chain reaction (RT-PCR)

Total RNA was isolated from hippocampus after microwave exposure. Then, the complementary DNA (cDNA) was synthesized by using RevertAid First Strand cDNA Synthesis Kit (Thermo Scientific, Wilmington, DE). The mRNA expression of HIF-1α was measured by real-time RT-PCR using Power SYBR@ Green PCR Master Mix (Thermo Fisher Scientific, Wilmington, DE), and normalized by the expression of GAPDH. The specific primers were shown as followed, HIF-1α forward, 5′- tctagtgaacaggatggaatggag-3′ and reverse, 5′- tcgtaactggtcagctgtggtaa-3′; GAPDH forward, 5′- ggcacagtcaaggctgagaatg-3′ and reverse 5′- atggtggtgaagacgccagta-3′.


Statistical analysis

Data were presented as mean ± s.e.m. and statistically analyzed by using GraphPad Prism software version 5 (GraphPad software, San Diego, CA). One-way ANOVA followed by Bonferroni post hoc tests were performed to analyze multiple groups. Longitudinal data were analyzed by using a two-way repeated measure ANOVA followed by Bonferroni post hoc tests for all the data of over time course. Differences were considered significant at two sided p < 0.05.

Results

Microwave damages ultrastructure of mitochondria, increases ROS production and impairs COX activity in rat hippocampus

We have previously reported that 30 mW/cm2 microwave induced rat hippocampal injuries18,21,22,23. Mitochondria are the pivotal organelle to maintain energy metabolism. Therefore, we observed the ultrastructure of mitochondria in rat hippocampus after microwave exposure. In SH group, round or oval mitochondria were well-distributed in size and shape, with clear boundary and intact mitochondrial cristae. After microwave exposure, slight disorder of mitochondrial cristae could be observed at 6 h, while aggravated injuries, such as swelling, cavitation, and broken or disappeared mitochondrial cristae were observed at 7 d. Interestingly, mitochondria started to recover at 14 d after exposure and showed alleviated injuries (Fig. 1A).

Figure 1
figure1

Mitochondrial ultrastructure, reactive oxygen species generation, activity of cytochrome c oxidase (COX), and dynamic expression of COXIV subunits in rat hippocampal tissues after microwave exposure. Seventy-two rats were exposed to 30 mW/cm2 microwave for 15 min. (A) Ultrastructure of mitochondria in hippocampus. After exposure, 5 rats from each group were euthanized and the hippocampus were isolated at appointed time points. The ultrastructure of mitochondria was observed by transmission electron microscopy after staining with heavy metals. And, the representative images were shown. (B) Mitochondrial ROS Production. Mitochondria were isolated from hippocampus. The ROS content in mitochondrial suspension was detected via calculating the conversion from DCFH-DA to DCF, and normalized by mitochondrial concentration. The relative ROS production to that in SH group was presented. (C) COX activity. The COX activity in mitochondrial suspension was quantified by using COX assay kit. (DF) Dynamic expression of COXIV subunits. After microwave exposure, hippocampus was isolated. The COXIV-1 and COXIV-2 protein expression was analyzed by western-blotting. The representative images were shown in D, and quantitative analysis was presented in E and F. Moreover, the ratio of COXIV-1 to COXIV-2 was also presented in G. Data were shown as mean ± s.e.m. **p < 0.01, ***p < 0.001 vs corresponding group.

Mitochondrial respiratory chain plays critical roles in mitochondrial respiration and energy metabolism. We showed that intracellular ROS was up-regulated significantly from 6 h to 3 d after 30 mW/cm2 microwave exposure (Fig. 1B). Meanwhile, microwave significantly reduced the activity of COX at 1 d and 3 d, while increased the activity at 14 d and 28 d after exposure (Fig. 1C). These results indicated that microwave could regulate the efficiency of mitochondrial respiratory chain.

COXIV contains two different isoforms: COXIV-1 and COXIV-2, and the balance between COXIV-1 and COXIV-2 plays important roles in maintaining oxidation phosphorylation. We showed that microwave increased COXIV-1 protein at 7 d and 14 d, while up-regulated COXIV-2 expression at 1 d after exposure. Moreover, the ratio of COXIV-1/2 decreased at 1 d and increased from 3 d to 14 d (Fig. 1D–G). These results suggested that COXIV-1 and COXIV-2 participated in the mitochondrial injuries and recovery after microwave exposure.

Microwave induces dynamic expression of HIF-1α in rat hippocampus

Our previous work has demonstrated that HIF-1α could protect neuron-like cells from microwave-induced mitochondrial disorder. In this study, we showed that HIF-1α protein expression was up-regulated in rat hippocampus from 6 h to 14 d after microwave exposure (Fig. 2A,B). Similar HIF-1α mRNA expression was detected in microwave exposed rat hippocampus (Fig. 2C). Moreover, nuclear HIF-1α level was increased both at 6 h and 1 d after microwave exposure (Fig. 2D). These results suggested that HIF-1α could activate its transcriptional activities to protected neurons from microwave induced mitochondrial injuries.

Figure 2
figure2

Dynamic expression of hypoxia-inducible factor-1α (HIF-1α) in rat hippocampal tissues after microwave exposure. (A,B) HIF-1α protein expression. Rat brains were removed after microwave exposure at various time points, and the HIF-1α protein expression in situ was detected by using immunohistochemistry. The representative images were shown in A, and the statistical analysis were presented in B. (C) HIF-1α mRNA expression. Hippocampus was isolated from microwave exposed rats. Then, the total RNA was extracted and cDNA was synthesized. HIF-1α mRNA expression was detected by real-time reverse transcript polymerase chain reaction, and normalized by GAPDH expression. (D) Nuclear HIF-1α protein. The nuclear protein from rat hippocampus was prepared, and the HIF-1α protein expression was analyzed by western-blotting and normalized by Lamin B. Data were shown as mean ± s.e.m. ***p < 0.001 compared to the corresponding group.

Microwave regulates COXIV-1 and COXIV-2 expression, and COX activity in neuron-like cells

To investigate the mechanisms under HIF-1α mediated protective responses, we established an in vitro model in PC12-derived neuron-like cells. In this model, COXIV-1 was up-regulated from 30 min to 9 h and down-regulated at 12 h after exposure, while COXIV-2 was up-regulated at 30 min after exposure (Fig. 3A,B). Moreover, the ratio of COXIV-1/2 decreased at 30 min, and increased from 3 h to 9 h after exposure (Fig. 3C). Meanwhile, COX activity significantly decreased from 30 min to 9 h, and then restored to normal level at 12 h after exposure (Fig. 3D). These results suggested that increasing COXIV1/2 might drive the recovery of mitochondrial functions.

Figure 3
figure3

COXIV-1 and COXIV-2 expression, and COX activity in PC12 cell derived neuron-like cells. Neuron-like cells were induced from rat pheochromocytoma (PC12) cells, by 5 ng/mL nerve growth factor. Then, neuron-like cells were exposed to 30 mW/cm² microwaves for 6 min. Cells were harvested at various time points after exposure. Protein expression of COXIV-1 (A) and COXIV-2 (B) were analyzed by western-blotting. And, the ratio of COXIV-1 to COXIV-2 was presented in (C). Moreover, The COX activity was detected by COX assay kit and normalized by protein concentration (D). Data were shown as mean ± s.e.m. *p < 0.05, **p < 0.01 compared to corresponding group.

Microwave exposure up-regulates the transcription activity of HIF-1α in neuron-like cells

Then, we showed that microwave induced HIF-1α expression from 9 h to 24 h after microwave exposure (Fig. 4A). Further analysis suggested that microwave increased the level of nuclear HIF-1α, especially at 6 h and 9 h after exposure, indicating activation of HIF-1α mediated transcription (Fig. 4B). The increase of nuclear HIF-1α level was also confirmed by immunofluorescence. These results suggested that microwave could increase HIF-1α expression and enhance its transcriptional activity.

Figure 4
figure4

Microwave exposure promotes HIF-1α nuclear translocation in neuron-like cells. Neuron-like cells were exposed to 30 mW/cm2 microwave. After exposure, the total HIF-1α protein expression was detected by western-blotting, and normalized by GAPDH (A). Moreover, nuclear protein was also extracted. Then, nuclear HIF-1α level was detected by western-blotting, and normalized by Lamin B (B). Immunofluorescence staining was conducted to show the expression and distribution of HIF-1α. The representative images were captured under fluorescent microscope (C). Data were shown as mean ± s.e.m. *p < 0.05, **p < 0.01 vs corresponding group.

HIF-1α regulates COXIV-1 and COXIV-2 expression to protect mitochondrial functions after microwave

HIF-1α protein was inhibited after treated with Bisphenol A, at 9 h after microwave exposure (Fig. 5A,B). HIF-1α inhibition reduced COXIV-1 protein, but had no obvious effects on COXIV-2. Moreover, the ratio of COXIV-1 to COXIV-2 was down-regulated after inhibiting HIF-1α (Fig. 5A,C–E). These results suggested that COXIV-1 expression was regulated by HIF-1α in neuron-like cells.

Figure 5
figure5

HIF-1α inhibition abolishes the up-regulation of COXIV-1 after microwave exposure and impairs mitochondrial functions in neuron-like cells. Neuron-like cells were treated with 400 μM Bisphenol A at 1 h before microwave exposure. At 9 h after exposure, cells were collected. The protein expression of HIF-1α, COXIV-1 and COXIV-2 were detected by western-blotting (A). And, the quantitative analysis were presented in (B), (C) and (D), respectively. The ratio of COXIV-1 to COXIV-2 was also calculated (E). To evaluate the mitochondrial functions, the ATP content (F), the mitochondrial membrane potentials (MMP) (G), and mitochondrial ROS (H) was analyzed by commercial kit. Data were shown as mean ± s.e.m. *p < 0.05, **p < 0.01, ***p < 0.001 compared to corresponding group.

Then, we analyzed mitochondrial functions, such as ATP level and MMP. Microwave elevated ATP level at 9 h after microwave exposure, suggesting recovery mechanism has been initiated. However, HIF-1α inhibition not only reduced ATP production in sham-exposed cells, but also abolished microwave induced up-regulation of ATP (Fig. 5F). Moreover, HIF-1α inhibitor also down-regulated MMP (Fig. 5G). Dysfunction of mitochondrial respiratory chain could produce ROS to damage structures and functions of corresponding tissues and organs. We found HIF-1α inhibition could increase ROS level, in both sham- and microwave-exposed cells (Fig. 5H). Therefore, our results indicated that HIF-1α played pivotal roles in protecting mitochondrial functions after microwave exposure, via regulating COXIV-1 expression and COX activity.

Discussion

The anxiety and speculation about potential health hazards caused by microwave radiation, nonionizing electromagnetic radiation ranging from 300 MHz to 300 GHz, has been growing fast in recent years24. Our group and others have been focusing on the biological effects of microwave exposure and its mechanisms5,18,21,22,23,25,26,27,28. Our previous work revealed the pivotal roles of HIF-1α in the self-protective response to 30 mW/cm2 microwave in neuron-like cells. Mitochondria are the major sites of ROS production, which could cause oxidative damages. Importantly, HIF-1α mediated self-protection could be activated by increased ROS11,12,29,30. In this study, we investigated the mechanisms under HIF-1α mediated protective responses against microwave. We showed that HIF-1α could be activated both in rat hippocampus and neuron-like cells. And, HIF-1α inhibition could down-regulate the ATP production and decrease MMP of mitochondria, while increase intercellular ROS level.

Under hypoxia or other non-infectious stimuli conditions, mitochondrial ROS can prevent the hydroxylation of HIF-1α and stabilize HIF-1α. Then, stabilized HIF-1α proteins translocate to the nucleus and dimerize with HIF-1β subunit to form heterodimeric protein and activate transcription of numerous target genes, such as pyruvate dehydrogenase kinase 1, BNIP3, lactate dehydrogenase A and complex IV, miRNAs, and so on8,10,31,32. In this study, we demonstrated that microwave could up-regulated nuclear HIF-1α level, suggesting the activation of HIF-1α mediated transcription. We speculated that the activation of HIF-1α might be one of the mechanisms to promote recovery of COX activity in rat hippocampus after microwave exposure.

COXIV is a regulatory subunit for COX activity, and interacts with COXI and COXII15. In complex IV, COXIV binds ATP and acts as a sensitive master switch, which can result in allosteric inhibition of COX activity under high ATP/ADP ratio16. It has been reported that two isoforms of COXIV, COXIV-1 and COXIV-2 were O2 regulated in mammalian cells. In hypoxic mammalian cells, up-regulated HIF-1α can activate transcription of COXIV-2 and LON genes, encoding a protease for COXIV-1 degradation17. In this study, we found that dynamic expression of COXIV-1 and COXIV-2 protein could be observed after microwave exposure. Briefly, an obvious down-regulation of the COXIV-1/COXIV-2 ratio was detected at the early stage, and then rapidly restored. And, a significant increase could be induced at the later stage, in accordance with the HIF-1α expression. These results suggested that HIF-1α modulated COX activity through regulating the expression of COXIV-1 and COXIV-2. Previous studies have demonstrated that the switch from COXIV-1 to COXIV-2 represents an adaptive response that optimizes COX activity, O2 consumption, and ROS generation, which can reduce the oxidative damages of mitochondria under hypoxic conditions. Therefore, up-regulation of COXIV-2 at the early stage after exposure was a potential mechanism to protect neurons from mitochondrial oxidative damages.

In conclusion, microwave exposure promoted ROS production in mitochondria, which could dynamically regulate HIF-1α expression both in rat hippocampus and PC12 derived neuron-like cells. Then, HIF-1α regulated COXIV-1 and COXIV-2 expression to protect mitochondria from microwave induced injuries, including oxidative damages. The ratio of COXIV-1 to COXIV-2 were dynamically changed in animal model, which indicated that different mechanisms were involved in HIF-1α mediated protective responses at different stages after microwave exposure. Combining with previous reports13,14,17,33, we speculated that at early stage after microwave exposure, increased HIF-1α protein could switch the COXIV proteins from COXIV-1 to COXIV-2, which could optimize the efficiency of mitochondrial respiratory chain. At the later stage, increased HIF-1α participated in the up-regulation of COXIV-1 to enhance oxidative phosphorylation in mitochondria.

Additional information

Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  1. 1.

    Acsadi, G. et al. Mitochondrial dysfunction in a neural cell model of spinal muscular atrophy. Journal of Neuroscience Research 87, 2748–2756 (2009).

  2. 2.

    Srivastava, S. et al. Microwave irradiation decreases ATP, increases free [Mg(2)(+)], and alters in vivo intracellular reactions in rat brain. Journal of Neurochemistry 123, 668–675 (2012).

  3. 3.

    McElroy, G. S. & Chandel, N. S. Mitochondria control acute and chronic responses to hypoxia. Experimental Cell Research 356, 217–222 (2017).

  4. 4.

    Wang, C. et al. Electromagnetic pulse reduces free radical generation in rat liver mitochondria in vitro. Free Radical Research 47, 276–282 (2013).

  5. 5.

    Zhao, L. et al. Upregulation of HIF-1alpha via activation of ERK and PI3K pathway mediated protective response to microwave-induced mitochondrial injury in neuron-like cells. Molecular Neurobiology 50, 1024–1034 (2014).

  6. 6.

    Zuo, H. et al. Neural cell apoptosis induced by microwave exposure through mitochondria-dependent caspase-3 pathway. International Journal of Medical Sciences 11, 426–435 (2014).

  7. 7.

    Esmekaya, M. A. et al. Mitochondrial hyperpolarization and cytochrome-c release in microwave-exposed MCF-7 cells. General Physiology and Biophysics 36, 211–218 (2017).

  8. 8.

    Ball, K. A., Nelson, A. W., Foster, D. G. & Poyton, R. O. Nitric oxide produced by cytochrome c oxidase helps stabilize HIF-1alpha in hypoxic mammalian cells. Biochemical and Biophysical Research Communications 420, 727–732 (2012).

  9. 9.

    Selfridge, A. C. et al. Hypercapnia Suppresses the HIF-dependent Adaptive Response to Hypoxia. Journal of Biological Chemistry 291, 11800–11808 (2016).

  10. 10.

    Sutendra, G. et al. Mitochondrial activation by inhibition of PDKII suppresses HIF1a signaling and angiogenesis in cancer. Oncogene 32, 1638–1650 (2013).

  11. 11.

    Dirnagl, U. & Meisel, A. Endogenous neuroprotection: mitochondria as gateways to cerebral preconditioning? Neuropharmacology 55, 334–344 (2008).

  12. 12.

    Movafagh, S., Crook, S. & Vo, K. Regulation of hypoxia-inducible factor-1a by reactive oxygen species: new developments in an old debate. Journal of Cellular Biochemistry 116, 696–703 (2015).

  13. 13.

    Semenza, G. L. Oxygen-dependent regulation of mitochondrial respiration by hypoxia-inducible factor 1. Biochemical Journal 405, 1–9 (2007).

  14. 14.

    Semenza, G. L. Hypoxia-inducible factor 1: regulator of mitochondrial metabolism and mediator of ischemic preconditioning. Biochimica et Biophysica Acta (BBA) - Reviews on Cancer 1813, 1263–1268 (2011).

  15. 15.

    Tsukihara, T. et al. The whole structure of the 13-subunit oxidized cytochrome c oxidase at 2.8 A. Science 272, 1136–1144 (1996).

  16. 16.

    Napiwotzki, J. & Kadenbach, B. Extramitochondrial ATP/ADP-ratios regulate cytochrome c oxidase activity via binding to the cytosolic domain of subunit IV. Biological Chemistry 379, 335–339 (1998).

  17. 17.

    Fukuda, R. et al. HIF-1 regulates cytochrome oxidase subunits to optimize efficiency of respiration in hypoxic cells. Cell 129, 111–122 (2007).

  18. 18.

    Wang, H. et al. Impairment of long-term potentiation induction is essential for the disruption of spatial memory after microwave exposure. International Journal of Radiation Biology 89, 1100–1107 (2013).

  19. 19.

    Zhao, L. et al. Microwave-induced Apoptosis and Cytotoxicity of NK Cells through ERK1/2 Signaling. Biomedical and Environmental Sciences 30, 323–332 (2017).

  20. 20.

    Hu, S. et al. Neuroprotective effects of dietary supplement Kang-fu-ling against high-power microwave through antioxidant action. Food & function 5, 2243–2251 (2014).

  21. 21.

    Xiong, L. et al. Microwave exposure impairs synaptic plasticity in the rat hippocampus and PC12 cells through over-activation of the NMDA receptor signaling pathway. Biomedical and Environmental Sciences 28, 13–24 (2015).

  22. 22.

    Liu, Y. Q. et al. Dynamic Expression of Hyperpolarization-activated Cyclic Nucleotide-gated Cation Channel 4 Involved in Microwave Induced Pacemaker Cell Injuries. Biomedical and Environmental Sciences 28, 823–828 (2015).

  23. 23.

    Zhao, L. et al. Relationship between cognition function and hippocampus structure after long-term microwave exposure. Biomedical and Environmental Sciences 25, 182–188 (2012).

  24. 24.

    Kocaman, A. et al. Genotoxic and carcinogenic effects of non-ionizing electromagnetic fields. Environmental research 163, 71–79 (2018).

  25. 25.

    Zhao, L. et al. MicroRNAs: Novel Mechanism Involved in the Pathogenesis of Microwave Exposure on Rats’ Hippocampus. Journal of molecular neuroscience: MN 53, 222–230 (2014).

  26. 26.

    Zuo, H. et al. RKIP Regulates Neural Cell Apoptosis Induced by Exposure to Microwave Radiation Partly Through the MEK/ERK/CREB Pathway. Molecular Neurobiology 51, 1520–1529 (2015).

  27. 27.

    Terzi, M., Ozberk, B., Deniz, O. G. & Kaplan, S. The role of electromagnetic fields in neurological disorders. Journal of chemical neuroanatomy 75, 77–84 (2016).

  28. 28.

    Kaplan, S. et al. Electromagnetic field and brain development. Journal of chemical neuroanatomy 75, 52–61 (2016).

  29. 29.

    Dirnagl, U., Becker, K. & Meisel, A. Preconditioning and tolerance against cerebral ischaemia: from experimental strategies to clinical use. Lancet Neurology 8, 398–412 (2009).

  30. 30.

    Correia, S. C. et al. Mitochondrial preconditioning: a potential neuroprotective strategy. Frontiers in Aging Neuroscience 2, (2010).

  31. 31.

    Singh, N., Sharma, G. & Mishra, V. Hypoxia inducible factor-1: its potential role in cerebral ischemia. Cellular and Molecular Neurobiology 32, 491–507 (2012).

  32. 32.

    Rey, S., Luo, W., Shimoda, L. A. & Semenza, G. L. Metabolic reprogramming by HIF-1 promotes the survival of bone marrow-derived angiogenic cells in ischemic tissue. Blood 117, 4988–4998 (2011).

  33. 33.

    Ngo, J. K., Pomatto, L. C. & Davies, K. J. Upregulation of the mitochondrial Lon Protease allows adaptation to acute oxidative stress but dysregulation is associated with chronic stress, disease, and aging. Redox biology 1, 258–264 (2013).

Download references

Acknowledgements

This work was supported by the National Natural Science Foundation of China (No. 81372926).

Author information

L.Z. and R.P. conceived and designed the experiments L.Z., Y.H., J.Z., H.W. (Hui Wang), H.W. (Haoyu Wang) and H.Z. performed the experiments L.Z., B.Y. and L.W. analyzed the data; J.D. and X.X. contributed reagents/materials/analysis tools L.Z., Y.H. and R.P. wrote the manuscript.

Competing Interests

The authors declare no competing interests.

Correspondence to Li Zhao or Rui-Yun Peng.

Electronic supplementary material

  1. Supplementary Figure 1 Schematic diagram of experimental setup for microwave exposure

Rights and permissions

Creative Commons BY

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.