Skip to main content
Download PDF

Mitochondrial dysfunction and mitophagy activation in blood mononuclear cells of fibromyalgia patients: implications in the pathogenesis of the disease

Arthritis Research & Therapy volume 12, Article number: R17 (2010) Cite this article

Abstract

Introduction

Fibromyalgia is a chronic pain syndrome with unknown etiology. Recent studies have shown some evidence demonstrating that oxidative stress may have a role in the pathophysiology of fibromyalgia. However, it is still not clear whether oxidative stress is the cause or the effect of the abnormalities documented in fibromyalgia. Furthermore, the role of mitochondria in the redox imbalance reported in fibromyalgia also is controversial. We undertook this study to investigate the role of mitochondrial dysfunction, oxidative stress, and mitophagy in fibromyalgia.

Methods

We studied 20 patients (2 male, 18 female patients) from the database of the Sevillian Fibromyalgia Association and 10 healthy controls. We evaluated mitochondrial function in blood mononuclear cells from fibromyalgia patients measuring, coenzyme Q10 levels with high-performance liquid chromatography (HPLC), and mitochondrial membrane potential with flow cytometry. Oxidative stress was determined by measuring mitochondrial superoxide production with MitoSOX™ and lipid peroxidation in blood mononuclear cells and plasma from fibromyalgia patients. Autophagy activation was evaluated by quantifying the fluorescence intensity of LysoTracker™ Red staining of blood mononuclear cells. Mitophagy was confirmed by measuring citrate synthase activity and electron microscopy examination of blood mononuclear cells.

Results

We found reduced levels of coenzyme Q10, decreased mitochondrial membrane potential, increased levels of mitochondrial superoxide in blood mononuclear cells, and increased levels of lipid peroxidation in both blood mononuclear cells and plasma from fibromyalgia patients. Mitochondrial dysfunction was also associated with increased expression of autophagic genes and the elimination of dysfunctional mitochondria with mitophagy.

Conclusions

These findings may support the role of oxidative stress and mitophagy in the pathophysiology of fibromyalgia.

Introduction

Fibromyalgia (FM) is a common chronic pain syndrome accompanied by other symptoms such as fatigue, headache, sleep disturbances, and depression. It is diagnosed according to the classification criteria established by the American College of Rheumatology (ACR) [1]. Despite being a common disorder that affects at least 5 million individuals in the United States [2], its pathogenic mechanism remains elusive. Recently oxidative stress markers were proposed as a relevant event in the pathogenesis of this disorder [3, 4].

Previously, we detected decreased coenzyme Q10 (CoQ10) levels and increased reactive oxygen species (ROS) production in blood mononuclear cells of FM patients, providing direct evidence of increased oxidative stress at the cellular level [5]. CoQ10 plays a crucial role in cellular metabolism, acting as an electron carrier between complexes I and II and complex III of the mitochondrial respiratory chain. CoQ10 also has been reported to play an important role in the regulation of uncoupling proteins, mitochondrial permeability transition pore, β-oxidation of fatty acids, and the nucleotide-biosynthesis pathway [6]. Moreover, CoQ10 levels have been suggested to be useful as a mitochondrial-dysfunction marker [7]. CoQ10 deficiency induces decreased activities of complex II + III, complex III and complex IV, reduced expression of mitochondrial proteins involved in oxidative phosphorylation, decreased mitochondrial membrane potential, increased production of reactive oxygen species (ROS), activation of mitochondrial permeability transition (MPT), mitophagy of dysfunctional mitochondria, and reduced growth rates [8, 9].

The purpose of the present work was to assess the mitochondrial dysfunction in blood mononuclear cells of FM patients and to elucidate whether mitochondrial disturbance was involved in the pathophysiology of oxidative stress present in FM.

Materials and methods

Patients and controls

The study was performed with the informed consent of all participants and the approval of the local ethical committee. We studied 20 patients (two male and 18 female patients) recruited from the database of the Sevillian Fibromyalgia Association (AFIBROSE) and 10 healthy controls (two male and eight female patients). The diagnosis of FM was established by an experienced rheumatologist according to ACR criteria [1]. All patients and controls had not taken any drug or vitamin/nutritional supplement during a 15-day period before the collection of the blood samples.

Blood mononuclear cells cultures

Peripheral blood mononuclear cells (BMCs) were purified from heparinized blood with isopycnic centrifugation by using Histopaque-1119 and Histopaque-1077 (Sigma Chemical Co., St. Louis, MO, USA). BMCs were cultured at 37°C in a 5% CO2 atmosphere in RPMI-1640 medium supplemented with L-glutamine, an antibiotic/antimycotic solution (Sigma Chemical Co.), and 10% fetal bovine serum.

Measurement of CoQ10levels

CoQ10 contents in BMCs were analysed with HPLC (Beckman Coulter, Brea, CA, USA; 166-126 HPLC) with ultraviolet detection (275 nm), according to the method of Montero and colleagues

Mitochondrial membrane potential (ΔΨm)

BMCs were cultured in six-well plates (35-mm diameter well) until confluence. Mitotracker Red CMXRos (Invitrogen/Molecular Probes, Eugene, OR, USA) 100 nmol/L was added and incubated for 30 min. Then cells were washed and analyzed with flow cytometry.

Mitochondrial ROS production

Mitochondrial ROS generation in BMCs was assessed with MitoSOX™ (Invitrogen/Molecular Probes, Eugene, OR, USA) incubated with 1 μmol/L MitoSox for 30 min at 37°C and washed twice with PBS. Cells were analyzed with flow cytometry. To assay ROS production with antioxidants, mononuclear cells were incubated 24 h with 10 μmol/L CoQ10, 30 μmol/L α-tocopherol (α-toc), and 10 mmol/L N-acetylcisteine (N-Acet; Sigma Chemical Co.).

Lipid peroxidation

TBARS (thiobarbituric acid reactive substances) levels in plasma were determined by a method based on the reaction with thiobarbituric acid at 90-100°C. Lipid peroxidation in cells was determined by analyzing the accumulation of lipoperoxides with a commercial kit from Cayman Chemical (Ann Arbor, Michigan, USA). TBARS are expressed in terms of malondialdehyde (MDA) levels. In these assays, an MDA standard is used to construct a standard curve against which unknown samples can be plotted.

Loading of Lysotracker Red

BMCs were cultured in RPMI-1640 medium. LysoTracker™ red (Invitrogen/Molecular Probes) (100 nmol/L), a cell-permeant fluorophore that typically concentrate in acidic vacuoles, was added to isolated BMCs from control and FM patients. After 30 min, cells were washed, and the red fluorescence of LysoTracker was quantified with flow cytometry.

Real-time PCR

The expression of both MAP-LC3 and BECLIN 1 genes in BMCs was analyzed with SYBR Green quantitative PCR by using mRNA extracts and primers. Real-time BECLIN 1 primers 5'-GGA TGG ATG TGG AGA AAG GCA AG-3' (forward primer) and 5'-TGA GGA CAC CCA AGC AAG ACC-3' (reverse primer) amplify a sequence of 152 nucleotides. Human MAP-LC3 primers 5'-GCC TTC TTC CTG CTG GTG AAC-3' (forward primer) and 5'-AGC CGT CCT CGT CTT TCT CC-3' (reverse primer) amplify a sequence of 91 nucleotides. Actin was used as a housekeeping control gene.

Measurement of citrate synthase activity

The specific activity of citrate synthase in whole-cell extracts prepared from BMCs was measured at 412 nm minus 360 nm (13.6 mmol/L/cm) by using 5,5-dithio-bis(2-nitrobenzoic acid) to detect free sulfhydryl groups in coenzyme A, as described previously [11].

Electron microscopy

BMCs were fixed for 15 min with 2% glutaraldehyde in culture medium and then for 30 min in 2% glutaraldehyde-0.1 mol/L NaCacodylate/HCl, pH 7.4. Samples were processed as described previously [9]. Observations were performed on a Philips CM-10 transmission electron microscope.

Statistical analysis

All results are expressed as mean ± SD, unless stated otherwise. The unpaired Student's t test was used to evaluate the significance of differences between groups. Statistical analyses included Pearson's correlations between CoQ10 levels and autophagic gene expression levels. The P values less than 0.05 were considered significant.

Results

Mitochondrial dysfunction in FM

The mean age of patients was 50.8 ± 8.6 years for the FM group and 49.1 ± 9.8 years for the control group. The mean duration of symptoms in the FM group was 13.65 ± 9.19 years. The mean tender points in the FM group were 14.9 ± 3.1 points. The most prominent features of these FM patients were pain and stiffness. They were sedentary people. Routine laboratory tests yielded normal results for glucose, urea, uric acid, total protein, creatinine, aspartate aminotransferase, alanine aminotransferase, cholesterol, and triglycerides (data not shown).

CoQ10 levels, determined in BMCs isolated from 20 FM patients, were found to be about 40% lower than those in control cells (Figure 1a). To examine further the mitochondrial dysfunction in BMCs from FM patients, we determined the mitochondrial membrane potential (ΔΨm) with flow cytometry. Mitochondrial membrane potential was significantly reduced by about 36% in BMCs from FM patients (Figure 1b).

Figure 1
figure 1

Coenzyme Q 10 levels and mitochondrial membrane potential (ΔΨm) in blood mononuclear cells (BMCs) from fibromyalgia (FM) patients and healthy control subjects. (a) CoQ10 levels were measured with high-performance liquid chromatography, as described in Materials and Methods. Data represent the mean ± SD of three separate experiments. (b) Mitochondrial membrane potential was analyzed in BMCs from control subjects and FM patients with flow cytometry, as described in Materials and Methods. Data represent the mean ± SD of three separate experiments. *P < 0.001 between controls and FM patients.

Full size image

Oxidative stress in FM

Oxidative stress has been proposed as a relevant event in the pathogenesis of FM [3, 12]. In a previous work, we showed the presence of high levels of ROS production in the BMCs of FM patients [5]. To assess the mitochondrial origin of ROS production, BMCs from FM patients and controls were exposed to MitoSOX™, a red mitochondrial superoxide indicator. Quantification of ROS production with flow-cytometry analysis demonstrated a significant increase in ROS production in mitochondria of BMCs from FM patients with respect to control (Figure 2a). Additionally, we determined lipid peroxidation as a marker of oxidative stress-induced membrane damage by mitochondrial ROS in BMCs and plasma from FM patients. On average, FM patients showed a higher level of lipid peroxidation in both cells and plasma with respect to control subjects (Figure 2b and 2c).

Figure 2
figure 2

Reactive oxygen species (ROS) production and lipid peroxidation in fibromyalgia (FM) patients. (a) ROS production was analyzed in BMCs from control subjects and FM patients with flow cytometry, as described in Materials and Methods. Lipid peroxidation (MDA levels) in blood mononuclear cells (BMCs) (b) and plasma (c) from control subjects and FM patients were determined as described in Materials and Methods. Data represent the mean ± SD of three separate experiments. *P < 0.001 between controls and FM patients.

Full size image

Further to examine the role of ROS generation in FM, BMCs of one representative patient were incubated with three antioxidants, CoQ10, α-toc, and N-Acet, and mitochondrial ROS production was examined (Figure 3). Only lipophilic antioxidants, CoQ10 and α-toc, significantly attenuated ROS production.

Figure 3
figure 3

Effect of antioxidants on reactive oxygen species (ROS) generation. Blood mononuclear cells (BMCs) of representative fibromyalgia (FM) patients were treated with 10 μmol/L CoQ10, 30 μmol/L α-tocopherol (α-toc), and 10 μmol/L N-acetylcysteine (N-Acet) for 24 h. Data represent the mean ± SD of three separate experiments. *P < 0.001 between controls and FM patients; **P < 0.005 between the absence or presence of CoQ10 and α-toc treatment.

Full size image

Autophagy in BMC from FM patients

Recently, it was demonstrated that CoQ10-deficient fibroblasts exhibit increased levels of lysosomal markers (β-galactosidase, cathepsin, LC3, and Lyso Tracker) and enhanced expression of autophagic genes at both transcriptional and translational levels, indicating the presence of autophagy [9]. To verify that CoQ10 deficiency also induces activation of autophagy in BMCs from FM patients, we first quantified levels of acidic vacuoles in BMCs by using Lysotracker fluorescence and flow-cytometry analysis. Acidic vacuoles were significantly increased in patient BMCs with respect to controls (Figure 4a). To elucidate whether autophagy in CoQ10-deficient BMCs could be mitigated by restoring mitochondrial functionality by CoQ10 supplementation, we cultured both control and patient BMCs in the presence of CoQ10 (100 μmol/L) for 24 hours and analyzed them by Lysotracker fluorescence. As is shown in Figure 4b, CoQ10 supplementation drastically reduced the intensity of Lysotracker fluorescence, indicating a reduction in lysosomal activity after CoQ10 treatment.

Figure 4
figure 4

Autophagic markers in blood mononuclear cells (BMCs) from fibromyalgia (FM) patients. (a) Quantification of acidic vacuoles in control and patient BMCs by LysoTracker fluorescence and flow-cytometry analysis. (b) Reduction of LysoTracker fluorescence in BMCs from FM patients under CoQ10 supplementation (100 μmol/L) for 24 h. Data represent the mean ± SD of three separate experiments. *P < 0.001 between controls and FM patients.

Full size image

In addition, we analyzed the expression of genes involved in autophagic processes, such as BECLIN 1 and MAP-LC3. Figure 5a and 5b show that autophagic genes were overexpressed in BMCs of five of the eight patients tested as compared with controls. FM patients with increased expression of autophagic genes were those with a most pronounced CoQ10 deficiency (P3, P5, P6, P7, P8). A negative correlation was seen between the expression of autophagic genes and CoQ10 levels (r = -0.80, P < 0.01 for BECLIN 1, and r = -0.76, P < 0.001 for MAP-LC3) (Figure 5c).

Figure 5
figure 5

Autophagic genes expression. Expression levels of BECLIN 1 (a) and MAP-LC3 (b) transcripts in blood mononuclear cells (BMCs) from control and fibromyalgia (FM) patients were assessed with real-time polymerase chain reaction (PCR), as described in Materials and Methods. Data represent the mean ± SD of three separate experiments. *P < 0.001 between controls and FM patients. (c) Correlation of CoQ10 levels and BECLIN 1 and MAP-LC3 expression levels in BMCs from FM patients.

Full size image

To determine whether autophagy was specific for mitochondria, we first examined mitochondrial mass in BMCs derived from FM patients. BMC extracts were prepared from control and FM patients and analyzed for citrate synthase activity. Citrate synthase is a mitochondrial matrix protein whose activity has been shown to correlate well with mitochondrial mass [13]. Figure 6a shows a statistically significant decrease in citrate synthase activity in BMCs from FM patients compared with controls. The reproducible reduction in citrate synthase activity indicates a decrease in mitochondrial mass and suggests selective degradation of mitochondria. To confirm the presence of mitochondrial degradation or mitophagy in BMCs, we then performed electron microscopy on control and patient BMCs (Figure 6b and 6c. Figure 6c clearly shows the presence of autophagosomes in BMCs from a representative FM patient (P6), indicating extensive autophagy of mitochondria. In early autophagosomes, it can clearly be observed that mitochondria are being degraded.

Figure 6
figure 6

Mitophagy in fibromylagia (FM) patients. (a) Decreased mitochondrial mass in blood mononuclear cells (BMCs) from FM patients. Citrate synthase specific activity in BMCs from control and FM patients was performed, as described in Materials and Methods. Data represent the mean ± SD of three separate experiments. *P < 0.001 between control and FM patients. (b) Ultrastructure of BMCs from FM patients. The control BMCs show mitochondria with a typical ultrastructure. Autophagosomes with mitochondria (arrows) were present in BMCs from a representative FM patient (P6); Bar = 1 μm.

Full size image

Discussion

Mitochondria generate energy primarily in the form of the electrochemical proton gradient, which fuels ATP production, ion transport, and metabolism. Mitochondria are also the major source of ROS. Both complexes I and III, along with CoQ10, leak electrons to oxygen [14–17]. CoQ10deficiency has been associated with a variety of human disorders, some of them caused by a direct defect of CoQ10 biosynthesis genes or as a secondary consequence of other diseases [18, 19]. Recent findings show that CoQ10 deficiency alters mitochondrial function and mitochondrial respiratory complex organization, leading to increased ROS generation, activation of MPT, and increased autophagy of dysfunctional mitochondria by mitophagy [8, 9]. In the present study, we found that CoQ10-deficient BMCs in FM patients showed high levels of ROS production in mitochondria and increased levels of lipid peroxidation in both cells and plasma. In this respect, high levels of lipid peroxidation and protein carbonyls [20, 21] and disturbances in the homeostasis of platelet ATP have been observed in FM patients [22]. The fact that CoQ10 and α-toc, two lipophilic antioxidants, significantly reduced mitochondrial ROS production, also suggests that ROS are produced in the lipophilic environment of mitochondrial membranes and that CoQ10 deficiency may be involved in oxidative stress in FM.

If oxidative damage plays a role in FM through the activation of MPT and mitophagy, then therapeutic strategies that reduce ROS may ameliorate the pathologic process. What is the relation between oxidative stress and FM symptoms? Recent studies showed that oxidative stress can cause peripheral and central sensitization and alter nociception [23], resulting in hyperalgesia mediated by both local and spinal oxidant mechanisms. Furthermore, oxidative stress is increased in patients with chronic-fatigue syndrome [24, 25]. Superoxide plays a major role in the development of pain through direct peripheral sensitization, the release of various cytokines (for example, TNF-α, IL-1β, and IL-6), the formation of peroxynitrite (ONOO-), and PARP activation [23]. In addition, studies on depression, a typical symptom in FM patients, have elucidated the possible link between depression and lipid peroxidation [26]. Lipid peroxidation may play an important role in depression, and the peroxidation-reducing effect of different selective serotonin reuptake inhibitors in major depression was demonstrated by Bilici and associates [27].

In addition, and supporting the role of mitochondrial dysfunction, BMCs of FM patients showed a decrease of 36% of mitochondrial membrane potential (ΔΨm), possibly reflecting a reduced electron flow and proton pumping caused by CoQ deficiency. Interestingly, a positive correlation between the content of CoQ10 in BMCs and skeletal muscle [28, 29] was demonstrated; therefore, CoQ10 deficiency and mitochondrial dysfunction can also be present in other cells and tissues in FM patients. Furthermore, changes in the morphology and number of mitochondria have been shown in skeletal muscle from FM patients [30–32], suggesting the role of mitochondrial dysfunction in this disorder. CoQ deficiency, mitochondrial dysfunction, and cell bioenergetics alteration could also explain the low muscular and aerobic capacity observed in some groups of FM patients [33, 34].

It has been proposed that ROS damage can induce MPT by opening of permeability transition pores in the mitochondrial inner membrane [35–37]. This, in turn, leads to a simultaneous collapse of mitochondrial membrane potential and the elimination of dysfunctional mitochondria by mitophagy. Our results support this hypothesis, showing the presence of mitophagy in BMCs of FM patients. Autophagy is a regulated lysosomal pathway involved in the degradation and recycling of cytoplasmic materials [38–42]. During autophagy, cytoplasmic materials are sequestered into double-membraned vesicles, 'autophagosomes', which then fuse with lysosomes to form autolysosomes, in which degradation of cellular structures occurs. Many cellular stresses can cause induction of autophagy, such as endoplasmic reticulum stress, mitochondrial dysfunction, or oxidative stress [42–44]. 'Mitophagy' was coined to describe the selective removal of mitochondria by autophagy during development and under pathologic conditions [36, 45]. In our work, biochemical analysis of citrate synthase indicated a depletion of mitochondrial mass, suggesting selective mitochondrial degradation by mitophagy in BMCs from FM patients. These results were confirmed with electron microscopy that clearly shows autophagosomes where mitochondria are being degraded. Autophagy can be beneficial for the cells by eliminating dysfunctional mitochondria, but massive autophagy can promote cell injury [41] and may contribute to the pathophysiology of FM.

Conclusions

Our study supports the hypothesis that CoQ10 deficiency, oxidative stress, and extensive mitophagy can contribute to cell-bioenergetics imbalance, compromising cell functionality. Abnormal BMC performance can promote oxidative stress and may contribute to altered nociception in FM.

Abbreviations

α-toc:

α-tocopherol

BMCs:

blood mononuclear cells

CoQ10:

coenzyme Q10

FM:

fibromyalgia

MPT:

mitochondrial permeability transition

ROS:

reactive oxygen species

TBARS:

thiobarbituric acid reactive substances.

References

  1. Wolfe F, Smythe HA, Yunus MB, Bennett RM, Bombardier C, Goldenberg DL, Tugwell P, Campbell SM, Abeles M, Clark P, Fam AG, Farber SJ, Fiechtner JJ, Franklin CM, Gatter RA, Hamaty D, Lessard J, Lichtbroun AS, Masi AT, Mccain GA, Reynolds WJ, Romano TJ, Russell IJ, Sheon RP: The American College of Rheumatology 1990 criteria for the classification of fibromyalgia: report of the Multicenter Criteria Committee. Arthritis Rheum. 1990, 33: 160-172.

    Article  CAS  PubMed  Google Scholar 

  2. Lawrence RC, Felson DT, Helmick CG, Arnold LM, Choi H, Deyo RA, Gabriel S, Hirsch R, Hochberg MC, Hunder GG, Jordan JM, Katz JN, Kremers HM, Wolfe F: Estimates of the prevalence of arthritis and other rheumatic conditions in the United States, Part II. Arthritis Rheum. 2008, 58: 26-35.

    Article  PubMed Central  PubMed  Google Scholar 

  3. Ozgocmen S, Ozyurt H, Sogut S, Akyol O: Current concepts in the pathophysiology of fibromyalgia: the potential role of oxidative stress and nitric oxide. Rheumatol Int. 2006, 26: 585-597.

    Article  CAS  PubMed  Google Scholar 

  4. Pieczenik SR, Neustadt J: Mitochondrial dysfunction and molecular pathways of disease. Exp Mol Pathol. 2007, 83: 84-92.

    Article  CAS  PubMed  Google Scholar 

  5. Cordero MD, Moreno-Fernandez AM, deMiguel M, Bonal P, Campa F, Jimenez-Jimenez LM, Ruiz-Losada A, Sanchez-Dominguez B, Sanchez Alcazar JA, Salviati L, Navas P: Coenzyme Q10 distribution in blood is altered in patients with fibromyalgia. Clin Biochem. 2009, 42: 732-735.

    Article  CAS  PubMed  Google Scholar 

  6. Turunen M, Olsson J, Dallner G: Metabolism and function of coenzyme Q. Biochim Biophys Acta. 2004, 1660: 171-199.

    Article  CAS  PubMed  Google Scholar 

  7. Haas RH, Parikh S, Falk MJ, Saneto RP, Wolf NI, Darin N, Wong LJ, Cohen BH, Naviaux RK: The in-depth evaluation of suspected mitochondrial disease. Mol Genet Metab. 2008, 94: 16-37.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  8. Quinzii CM, Lopez LC, Von-Moltke J, Naini A, Krishna S, Schuelke M, Salviati L, Navas P, Dimauro S, Hirano M: Respiratory chain dysfunction and oxidative stress correlate with severity of primary CoQ10 deficiency. FASEB J. 2008, 22: 1874-1885.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  9. Rodriguez-Hernandez A, Cordero MD, Salviati L, Artuch R, Pineda M, Briones P, Gomez Izquierdo L, Cotan D, Navas P, Sanchez-Alcazar JA: Coenzyme Q deficiency triggers mitochondria degradation by mitophagy. Autophagy. 2009, 5: 19-32.

    Article  CAS  PubMed  Google Scholar 

  10. Montero R, Sanchez-Alcazar JA, Briones P, Hernandez AR, Cordero MD, Trevisson E, Salviati L, Pineda M, Garcia-Cazorla A, Navas P, Artuch R: Analysis of coenzyme Q10 in muscle and fibroblasts for the diagnosis of CoQ10 deficiency syndromes. Clin Biochem. 2008, 41: 697-700.

    Article  CAS  PubMed  Google Scholar 

  11. Trounce IA, Kim YL, Jun AS, Wallace DC: Assessment of mitochondrial oxidative phosphorylation in patient muscle biopsies, lymphoblasts, and transmitochondrial cell lines. Methods Enzymol. 1996, 264: 484-509.

    Article  CAS  PubMed  Google Scholar 

  12. Bagis S, Tamer L, Sahin G, Bilgin R, Guler H, Ercan B, Erdogan C: Free radicals and antioxidants in primary fibromyalgia: an oxidative stress disorder?. Rheumatol Int. 2005, 25: 188-190.

    Article  CAS  PubMed  Google Scholar 

  13. Garrabou G, Soriano A, Lopez S, Guallar JP, Giralt M, Villarroya F, Martinez JA, Casademont J, Cardellach F, Mensa J, Miro O: Reversible inhibition of mitochondrial protein synthesis during linezolid-related hyperlactatemia. Antimicrob Agents Chemother. 2007, 51: 962-967.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  14. Addabbo F, Montagnani M, Goligorsky MS: Mitochondria and reactive oxygen species. Hypertension. 2009, 53: 885-892.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  15. Kowaltowski AJ, de Souza-Pinto NC, Castilho RF, Vercesi AE: Mitochondria and reactive oxygen species. Free Radic Biol Med. 2009, 47: 333-343.

    Article  CAS  PubMed  Google Scholar 

  16. Lambert AJ, Brand MD: Reactive oxygen species production by mitochondria. Methods Mol Biol. 2009, 554: 165-181.

    Article  CAS  PubMed  Google Scholar 

  17. Murphy MP: How mitochondria produce reactive oxygen species. Biochem J. 2009, 417: 1-13.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  18. DiMauro S: Mitochondrial myopathies. Curr Opin Rheumatol. 2006, 18: 636-641.

    Article  CAS  PubMed  Google Scholar 

  19. Quinzii CM, DiMauro S, Hirano M: Human coenzyme Q10 deficiency. Neurochem Res. 2007, 32: 723-727.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  20. Hein G, Franke S: Are advanced glycation end-product-modified proteins of pathogenetic importance in fibromyalgia?. Rheumatology (Oxford). 2002, 41: 1163-1167.

    Article  CAS  Google Scholar 

  21. Ozgocmen S, Ozyurt H, Sogut S, Akyol O, Ardicoglu O, Yildizhan H: Antioxidant status, lipid peroxidation and nitric oxide in fibromyalgia: etiologic and therapeutic concerns. Rheumatol Int. 2006, 26: 598-603.

    Article  CAS  PubMed  Google Scholar 

  22. Bazzichi L, Giannaccini G, Betti L, Fabbrini L, Schmid L, Palego L, Giacomelli C, Rossi A, Giusti L, De Feo F, Giuliano T, Mascia G, Bombardieri S, Lucacchini A: ATP, calcium and magnesium levels in platelets of patients with primary fibromyalgia. Clin Biochem. 2008, 41: 1084-1090.

    Article  CAS  PubMed  Google Scholar 

  23. Wang ZQ, Porreca F, Cuzzocrea S, Galen K, Lightfoot R, Masini E, Muscoli C, Mollace V, Ndengele M, Ischiropoulos H, Salvemini D: A newly identified role for superoxide in inflammatory pain. J Pharmacol Exp Ther. 2004, 309: 869-878.

    Article  CAS  PubMed  Google Scholar 

  24. Manuel y Keenoy B, Moorkens G, Vertommen J, De Leeuw I: Antioxidant status and lipoprotein peroxidation in chronic fatigue syndrome. Life Sci. 2001, 68: 2037-2049.

    Article  CAS  PubMed  Google Scholar 

  25. Vecchiet J, Cipollone F, Falasca K, Mezzetti A, Pizzigallo E, Bucciarelli T, De Laurentis S, Affaitati G, De Cesare D, Giamberardino MA: Relationship between musculoskeletal symptoms and blood markers of oxidative stress in patients with chronic fatigue syndrome. Neurosci Lett. 2003, 335: 151-154.

    Article  CAS  PubMed  Google Scholar 

  26. Evans PH: Free radicals in brain metabolism and pathology. Br Med Bull. 1993, 49: 577-587.

    CAS  PubMed  Google Scholar 

  27. Bilici M, Efe H, Koroglu MA, Uydu HA, Bekaroglu M, Deger O: Antioxidative enzyme activities and lipid peroxidation in major depression: alterations by antidepressant treatments. J Affect Disord. 2001, 64: 43-51.

    Article  CAS  PubMed  Google Scholar 

  28. Duncan AJ, Heales SJ, Mills K, Eaton S, Land JM, Hargreaves IP: Determination of coenzyme Q10 status in blood mononuclear cells, skeletal muscle, and plasma by HPLC with di-propoxy-coenzyme Q10 as an internal standard. Clin Chem. 2005, 51: 2380-2382.

    Article  CAS  PubMed  Google Scholar 

  29. Land JM, Heales SJ, Duncan AJ, Hargreaves IP: Some observations upon biochemical causes of ataxia and a new disease entity ubiquinone, CoQ10 deficiency. Neurochem Res. 2007, 32: 837-843.

    Article  CAS  PubMed  Google Scholar 

  30. Park JH, Niermann KJ, Olsen N: Evidence for metabolic abnormalities in the muscles of patients with fibromyalgia. Curr Rheumatol Rep. 2000, 2: 131-140.

    Article  CAS  PubMed  Google Scholar 

  31. Sprott H, Salemi S, Gay RE, Bradley LA, Alarcon GS, Oh SJ, Michel BA, Gay S: Increased DNA fragmentation and ultrastructural changes in fibromyalgic muscle fibres. Ann Rheum Dis. 2004, 63: 245-251.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  32. Yunus MB, Kalyan-Raman UP, Kalyan-Raman K: Primary fibromyalgia syndrome and myofascial pain syndrome: clinical features and muscle pathology. Arch Phys Med Rehabil. 1988, 69: 451-454.

    CAS  PubMed  Google Scholar 

  33. Bennett RM, Clark SR, Goldberg L, Nelson D, Bonafede RP, Porter J, Specht D: Aerobic fitness in patients with fibrositis: a controlled study of respiratory gas exchange and 133xenon clearance from exercising muscle. Arthritis Rheum. 1989, 32: 454-460.

    Article  CAS  PubMed  Google Scholar 

  34. Jacobsen S, Danneskiold-Samsoe B: Dynamic muscular endurance in primary fibromyalgia compared with chronic myofascial pain syndrome. Arch Phys Med Rehabil. 1992, 73: 170-173.

    CAS  PubMed  Google Scholar 

  35. Kim I, Rodriguez-Enriquez S, Lemasters JJ: Selective degradation of mitochondria by mitophagy. Arch Biochem Biophys. 2007, 462: 245-253.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  36. Lemasters JJ: Selective mitochondrial autophagy, or mitophagy, as a targeted defense against oxidative stress, mitochondrial dysfunction, and aging. Rejuvenation Res. 2005, 8: 3-5.

    Article  CAS  PubMed  Google Scholar 

  37. Rodriguez-Enriquez S, Kim I, Currin RT, Lemasters JJ: Tracker dyes to probe mitochondrial autophagy (mitophagy) in rat hepatocytes. Autophagy. 2006, 2: 39-46.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  38. Baehrecke EH: Autophagy: dual roles in life and death?. Nat Rev Mol Cell Biol. 2005, 6: 505-510.

    Article  CAS  PubMed  Google Scholar 

  39. Codogno P, Meijer AJ: Autophagy and signaling: their role in cell survival and cell death. Cell Death Differ. 2005, 12 (suppl 2): 1509-1518.

    Article  CAS  PubMed  Google Scholar 

  40. Gozuacik D, Kimchi A: Autophagy as a cell death and tumor suppressor mechanism. Oncogene. 2004, 23: 2891-2906.

    Article  CAS  PubMed  Google Scholar 

  41. Levine B, Yuan J: Autophagy in cell death: an innocent convict?. J Clin Invest. 2005, 115: 2679-2688.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  42. Marino G, Lopez-Otin C: Autophagy: molecular mechanisms, physiological functions and relevance in human pathology. Cell Mol Life Sci. 2004, 61: 1439-1454.

    Article  CAS  PubMed  Google Scholar 

  43. Matsui Y, Takagi H, Qu X, Abdellatif M, Sakoda H, Asano T, Levine B, Sadoshima J: Distinct roles of autophagy in the heart during ischemia and reperfusion: roles of AMP-activated protein kinase and Beclin 1 in mediating autophagy. Circ Res. 2007, 100: 914-922.

    Article  CAS  PubMed  Google Scholar 

  44. Scherz-Shouval R, Shvets E, Fass E, Shorer H, Gil L, Elazar Z: Reactive oxygen species are essential for autophagy and specifically regulate the activity of Atg4. EMBO J. 2007, 26: 1749-1760.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  45. Tolkovsky AM: Mitophagy. Biochim Biophys Acta. 2009, 1793: 1508-1515.

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

This work was supported by grants FIS PI080500 and FIS EC08/00076, Ministerio de Sanidad, Spain. The authors dedicate this manuscript to FM patients and AFIBROSE (Asociación de Fibromialgia de Sevilla) for their unconditional help.

Author information

Author notes

    Authors and Affiliations

    1. Centro Andaluz de Biología del Desarrollo (CABD), Universidad Pablo de Olavide-CSIC, Ctra. de Utrera, km. 1, ISCIII, Sevilla, 41013, Spain

      Mario D Cordero, Juan Garrido Maraver, David Cotán, Plácido Navas & José A Sánchez Alcázar

    2. Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Universidad Pablo de Olavide-CSIC, Ctra. de Utrera, km. 1, ISCIII, Sevilla, 41013, Spain

      Mario D Cordero, Juan Garrido Maraver, David Cotán, Plácido Navas & José A Sánchez Alcázar

    3. Dpto. Citología e Histología Normal y Patológica, Facultad de Medicina, Universidad de Sevilla, Avda. Dr. Fedriani s/n, Sevilla, 41009, Spain

      Mario D Cordero, Manuel De Miguel, Ana M Moreno Fernández & Inés M Carmona López

    4. Departamento de Anatomía Patológica, Hospital Virgen del Rocío, Sevilla, 41013, Spain

      Lourdes Gómez Izquierdo

    5. Dpto. de Medicina, Facultad de Medicina, Universidad de Sevilla, Avda. Dr. Fedriani s/n, Sevilla, 41009, Spain

      Pablo Bonal & Francisco Campa

    6. Distrito Sanitario Sevilla Sur., Facultad de Odontología, Universidad de Sevilla, Campus de los Perdigones, C/Avicena s/n, Sevilla, 41009, Spain

      Francisco Campa

    7. Departamento de Periodontología, Facultad de Odontología, Universidad de Sevilla, Campus de los Perdigones, C/Avicena s/n, Sevilla, 41009, Spain

      Pedro Bullon

    Authors
    1. Mario D Cordero
      View author publications

      You can also search for this author in PubMed Google Scholar

    2. Manuel De Miguel
      View author publications

      You can also search for this author in PubMed Google Scholar

    3. Ana M Moreno Fernández
      View author publications

      You can also search for this author in PubMed Google Scholar

    4. Inés M Carmona López
      View author publications

      You can also search for this author in PubMed Google Scholar

    5. Juan Garrido Maraver
      View author publications

      You can also search for this author in PubMed Google Scholar

    6. David Cotán
      View author publications

      You can also search for this author in PubMed Google Scholar

    7. Lourdes Gómez Izquierdo
      View author publications

      You can also search for this author in PubMed Google Scholar

    8. Pablo Bonal
      View author publications

      You can also search for this author in PubMed Google Scholar

    9. Francisco Campa
      View author publications

      You can also search for this author in PubMed Google Scholar

    10. Pedro Bullon
      View author publications

      You can also search for this author in PubMed Google Scholar

    11. Plácido Navas
      View author publications

      You can also search for this author in PubMed Google Scholar

    12. José A Sánchez Alcázar
      View author publications

      You can also search for this author in PubMed Google Scholar

    Corresponding author

    Correspondence to José A Sánchez Alcázar.

    Additional information

    Competing interests

    The authors declare that they have no competing interests.

    Authors' contributions

    MDC, MDM, AMNF, IMCL, and JGM carried out the biochemical studies. DC and LGI carried out the electron microscopy studies. PB and FC participated in the design of the study and performed the statistical analysis. PB, PN, and JASA conceived of the study, participated in its design and coordination, and helped to draft the manuscript. All authors read and approved the final manuscript.

    Mario D Cordero, Manuel De Miguel contributed equally to this work.

    Authors’ original submitted files for images

    Rights and permissions

    Reprints and Permissions

    About this article

    Cite this article

    Cordero, M.D., De Miguel, M., Moreno Fernández, A.M. et al. Mitochondrial dysfunction and mitophagy activation in blood mononuclear cells of fibromyalgia patients: implications in the pathogenesis of the disease. Arthritis Res Ther 12, R17 (2010). https://doi.org/10.1186/ar2918

    Download citation

    • Received:

    • Revised:

    • Accepted:

    • Published:

    • DOI: https://doi.org/10.1186/ar2918

    Keywords

    Arthritis Research & Therapy

    ISSN: 1478-6362

    Contact us