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Open Access Research article

The effect of oxygen tension on calcium homeostasis in bovine articular chondrocytes

Rachel White and John S Gibson*

Author Affiliations

Department of Veterinary Medicine, University of Cambridge, Madingley Road, Cambridge, CB3 OES, UK

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Journal of Orthopaedic Surgery and Research 2010, 5:27  doi:10.1186/1749-799X-5-27


The electronic version of this article is the complete one and can be found online at: http://www.josr-online.com/content/5/1/27


Received:21 September 2009
Accepted:26 April 2010
Published:26 April 2010

© 2010 White and Gibson; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

Articular chondrocytes normally experience a lower O2 tension compared to that seen by many other tissues. This level may fall further in joint disease. Ionic homeostasis is essential for chondrocyte function but, at least in the case of H+ ions, it is sensitive to changes in O2 levels. Ca2+ homeostasis is also critical but the effect of changes in O2 tension has not been investigated on this parameter. Here we define the effect of hypoxia on Ca2+ homeostasis in bovine articular chondrocytes.

Methods

Chondrocytes from articular cartilage slices were isolated enzymatically using collagenase. Cytoplasmic Ca2+ levels ([Ca2+]i) were followed fluorimetrically using Fura-2 to determine the effect of changes in O2 tension. The effects of ion substitution (replacing extracellular Na+ with NMDG+ and chelating Ca2+ with EGTA) were tested. Levels of reactive oxygen species (ROS) and the mitochondrial membrane potential were measured and correlated with [Ca2+]i.

Results

A reduction in O2 tension from 20% to 1% for 16-18 h caused [Ca2+]i to approximately double, reaching 105 ± 23 nM (p < 0.001). Ion substitutions indicated that Na+/Ca2+ exchange activity was not inhibited at low O2 levels. At 1% O2, ROS levels fell and mitochondria depolarised. Restoring ROS levels (with an oxidant H2O2, a non-specific ROS generator Co2+ or the mitochondrial complex II inhibitor antimycin A) concomitantly reduced [Ca2+]i.

Conclusions

O2 tension exerts a significant effect on [Ca2+]i. The proposed mechanism involves ROS from mitochondria. Findings emphasise the importance of using realistic O2 tensions when studying the physiology and pathology of articular cartilage and the potential interactions between O2, ROS and Ca2+.

Background

Due to the avascularity of its matrix, articular cartilage is hypoxic compared to other tissue types [1]. O2 tension is uncertain, but most cells probably experience 5-7% O2 [2]. Perhaps as a consequence, articular chondrocytes have few mitochondria and metabolism is largely anaerobic. Notwithstanding, chondrocytes consume O2 and are adversely affected if maintained in an anoxic environment [3,4]. Lowered O2 levels can occur in vivo in various disease conditions [2].

It is becoming increasingly evident that O2 tension is a critical parameter in modulating chondrocyte function [5]. At low O2 tension, glycolysis is inhibited, glucose uptake is reduced, and ATP and lactic acid production fall, the apparently paradoxical "negative Pasteur effect" [3]. Other responses include changes in production of growth factors, proinflammatory mediators and matrix components [5]. In other tissues, change in O2 tension is an important signal leading to modulation of ionic permeability and alteration of ionic homeostasis, thereby impacting upon cell function [6]. Similarly, pH homeostasis in articular chondrocytes is perturbed by alteration in O2 levels [7,8]. When O2 is reduced from 20% to 1%, the main H+ efflux pathway, the Na+/H+ exchanger [9], is inhibited leading to acidification of the cells. A reduction in reactive oxygen species (ROS) acting, via alterations in protein phosphorylation, appears to constitute the link between hypoxia and reduction in NHE activity [7].

Intracellular Ca2+ levels are also critical [10]. Changes in Ca2+ will affect matrix synthesis, as well as other functions. Low O2 tension has been shown previously to cause a rise in Ca2+ in cultured embryonal chick chondrocytes, acting to slow ageing processes [11]. An interaction between O2 and Ca2+ is therefore anticipated in articular chondrocytes but has not been described hitherto. Our overall aim therefore was to elucidate whether Ca2+ levels are sensitive to O2. Because reduction in O2 tension from 20% to 1% has been shown to have important effects on pH homeostasis, we concentrated on these values for this study. Cytoplasmic Ca2+ levels, ROS and the mitochondrial membrane pd were measured fluorimetrically. Results show that Ca2+ levels are increased during hypoxia, with a transduction path involving mitochondrial depolarization and ROS.

Methods

Chondrocytes

Bovine feet from animals aged between 18 and 36 months were obtained following abattoir slaughter. Full depth hyaline cartilage shavings from the proximal metacarpophalangeal joint were taken at ambient O2 tension, then placed in DMEM containing penicillin (100 IU.ml-1), streptomycin (0.1 μg.ml-1) and fungizone (2.5 μg.ml-1) and incubated at 37°C, 5% CO2 for 16-18 h at 20% or 1% O2 whilst matrix was digested with 0.1% (w/v) collagenase type I. Isolated chondrocytes were resuspended in saline (at the required O2 tension) at a final dilution of 106 cells.ml-1. Cell viability was determined by the Trypan Blue exclusion test, at >95%. See [12] for further details.

Solutions and chemicals

Standard saline comprised (in mM): NaCl (145), KCl (5), CaCl2 (2), MgSO4 (1), D+ glucose (10) and 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES, 10), pH 7.40 at 37°C. To investigate Ca2+-free conditions, CaCl2 was omitted and the Ca2+ chelator EGTA (1 mM) added; for Na+-free saline, NMDG+ replaced Na+ - cells were prepared in standard saline and only exposed to these solutions for a few minutes. Stock solutions of digitonin, antimycin A and the fluorophores Fura-2, DCF-DA and JC-1 were dissolved in DMSO; CoCl2 and H2O2 were dissolved in water. Fluorophores were obtained from Calbiochem (Fura-2-AM) or Molecular Probes, Invitrogen, UK; other chemicals from Sigma-Aldrich, UK.

Maintenance of O2 tension

During longer term incubations (>3 hours), cells were maintained at the correct O2 tension in a variable O2/CO2 incubator (Galaxy R, RS Biotech, Irvine, UK). For shorter term incubations, cells were placed in Eschweiler tonometers (Kiel, Germany) and flushed with appropriate gas mixtures using a Wösthoff gas mixing pump (Bochum, Germany). Similarly, solutions were pre-equilibrated to the required O2 tension in Eschweiler tonometers before being applied to cells.

Measurement of Ca2+

Cytoplasmic Ca2+ levels ([Ca2+]i) were measured using Fura-2 (see [12]). Cells were loaded with 5 μM fura-2-AM for 30 min at room temperature followed by 15 min at 37°C. Fluorescence was measured in a thermostatically regulated fluorimeter (F-2000 Fluorescence Spectrophotometer, Hitachi). Fura-2 was alternately excited at 340 nm and 380 nm, with emission intensity was measured at 510 nm. In most cases, the 340:380 nm fluorescence ratio (R) was converted to Ca2+ values, as described previously [12]. When reagents were added to alter ROS levels, however, Ca2+ levels are presented as raw R values. In these cases, exact [Ca2+]i could not be calculated because, after digitonin treatment, on exposure to the high concentrations of the reagents found extracellularly, Fura-2 was partially quenched.

Measurement of reactive oxygen species (ROS)

Chondrocytes were loaded with DCF-DA (10 μM) at 37°C for 45 min [7]. In the presence of ROS, DCF is converted to dichlorofluorescin, resulting in a change in fluorescence. DCF was excited at 488 nm and emission intensity measured at 530 nm.

Measurement of the mitochondrial pd

Chondrocytes were loaded with 5 μM JC-1 for 20 min at 37°C [8]. JC-1 was then excited at 490 nm and the emission intensity monitored at 525 nm (green) and 590 nm (red). The dye is sequestered inside mitochondria at negative pds. Membrane depolarization is indicated by a shift in the emission fluorescence from red to green, as dye is released into the cytosol and the formation of red fluorescent J-aggregates causing a fall in the red/green fluorescence intensity ratio.

Statistics

Student's paired or Independent t-test were used to determine statistical significance (p < 0.05) between results. Data are given as means ± S.E.M. for n replicates, where each replicate indicates a separate individual animal.

Results

Effect of hypoxia on Ca2+ homeostasis

Previously published reports on the effects of hypoxia on pH homeostasis in equine articular chondrocytes demonstrated effects within 3 hours when O2 was reduced from 20% to 1% [7]. Evidence for a similar effect was therefore tested on Ca2+ levels. Bovine articular chondrocytes were isolated at 20% O2 and the effect of maintaining O2 at this level was then compared with that of reducing it to 1% O2. At 3 hours, [Ca2+]i was 60 ± 10 nM at 20% O2 compared with 62 ± 10 nM at 1% O2 (means ± S.E.M., n = 12; N.S. values at 1% cf 20%). At both O2 tensions, therefore, steady state cytoplasmic Ca levels ([Ca2+]i) remained steady at about 60 nM. We went on to study the effects of longer term hypoxia. Chondrocytes were both digested from their matrix and then maintained for 16-18 hours at either 20% or 1% O2 levels before measuring steady state Ca2+ levels at the same O2 tension. At hypoxic levels, 1% O2, a significant elevation in steady state [Ca2+]i was observed (Figures 1 and 2), with levels approximately doubling from 55 ± 4 nM at 20% O2 to 105 ± 23 nM at 1% (n = 12; p < 0.001). Thus, like pH, steady state Ca2+ levels in articular chondrocytes are sensitive to changes in O2 albeit with a slower time course.

thumbnailFigure 1. Effect of hypoxia and extracellular Ca2+ on cytoplasmic Ca2+ levels in bovine articular chondroytes. Chondrocytes were isolated with collagenase at either 20% or 1% O2 and maintained at these O2 tensions throughout (16-18 hours). Cytoplasmic Ca2+ levels ([Ca2+]i) were then measured with Fura-2 in the presence (2 mM Ca2+) or absence (Ca2+-free plus 1 mM EGTA) extracellular Ca2+. Histograms represent means ± S.E.M., n = 9. * p < 0.02 ** p < 0.006.

thumbnailFigure 2. Effect of hypoxia and extracellular Na+ on cytoplasmic Ca2+ levels in bovine articular chondroytes. Methods as legend to Figure 1, except that during measurement of [Ca2+]I, chondrocytes were suspended in the presence (145 mM) or absence (Na+ replaced with NMDG+) of extracellular Na+. Histograms represent means ± S.E.M., n = 9. * p < 0.05 ** p < 0.02.

Hypoxia, Ca2+ and ion substitutions

Ion substitution experiments were carried out to determine the source of the extra Ca2+. Chondrocytes were again isolated, and then maintained for 16-18 hours, at either 20% or 1% O2 in standard Ca2+- and Na+- containing saline. Ca2+ levels were then measured in this standard saline and also following transfer to Ca2+-free or Na+-free saline (Figures 1 and 2). In Ca2+-free conditions (Figure 1), Ca2+ was decreased at both 20% and 1% O2. Notwithstanding, [Ca2+]i remained higher at 1% O2 compared to 20% O2. In Na+-free saline, [Ca2+]i was elevated at both O2 tensions (Figure 2), but again remained higher at 1% O2 compared to 20% O2. In fact, the difference in Ca2+ comparing cells maintained at 20% and 1% O2 was greater in Na+-free conditions.

Interaction of reactive oxygen species and Ca2+ homeostasis

Levels of reactive oxygen species (ROS) in equine articular chondrocytes decrease when O2 tension is reduced from 20% to 1% [7]. This finding was confirmed in the present work for bovine chondrocytes held at different O2 levels for 16-18 hours. ROS levels at 1% fell to 60 ± 6% (mean ± S.E.M., n = 3) of the value at 20% O2. Three different protocols were carried out to elevate ROS levels: treatment with the oxidant H2O2 (100 μM), the non-specific ROS generator Co2+ (100 μM) or the mitochondrial complex III inhibitor antimycin A (50 μM). In each case, ROS levels recorded in treated cells incubated at 1% O2 were restored to those observed at 20%, (eg for Co2+ levels reached 96 ± 8% values at 20%, N.S.). Using Fura-2 340 nm:380 nm emission ratio (R) as a measure of [Ca2+]i, in cells incubated at 1% but treated to raise ROS levels, it was found that R decreased by a similar amount, reaching values similar to those observed at 20%. For example, R at 1% following addition of H2O2 fell from 1.41 ± 0.001 to 1.06 ± 0.001 (n = 15). For all three protocols, therefore, at 1% O2 when ROS levels were restored, so was [Ca2+]i.

Hypoxia and mitochondria

The effect of changes in O2 and treatment with antimycin A on mitochondrial pd was then investigated. Chondrocytes were isolated at 20% O2 and then incubated at either 20% O2 or 1% O2 for 16-18 hours prior to loading with JC-1. They were also treated with antimycin A (50 μM) at both O2 tensions (Figure 3). It can be seen that the red/green ratio was reduced at 1% O2 indicative of mitochondrial depolarization. Antimycin A, a complex III inhibitor, also caused mitochondrial depolarization at 20% O2 but not in cells held at 1% O2.

thumbnailFigure 3. Effect of hypoxia and antimycin A on mitochondrial membrane pd of bovine articular chondrocytes. Chondrocytes were isolated as in Figure 1, being maintained at 20% or 1% O2 throughout. They were loaded with JC-1 to measure mitochondrial pd (as the red/green ratio - see Methods) in the presence or absence of antimycin A (50 μM). Histograms represent means ± SEM n = 9-11. ** p < 0.004 # < 0.002.

Discussion

The effect of O2 tension on steady state Ca2+

The present findings are the first to demonstrate an effect of changes in O2 tension on Ca2+ homeostasis in articular chondrocytes. We show here that Ca2+ homeostasis is maintained in response to shorter term (3 hours) reduction in O2 tension from 20% to 1%. Longer exposure to 1% O2, however, caused significant elevation in [Ca2+]i with levels approximately doubling, sufficient to perturb cell function. These effects were associated with both mitochondrial depolarization and a fall in levels of reactive oxygen species (ROS).

Source of Ca2+

Rise in [Ca2+]i can occur through increased entry or decreased removal across the plasma membrane or from intracellular stores. It is not easy to distinguish unequivocally between these possibilities. Despite a decrease in [Ca2+]i in Ca2+-free saline, however, hypoxic chondrocytes still showed higher Ca2+ compared to those at 20% O2. Thus even if increased influx across the plasma membrane was involved, other mechanisms were still able to elevate Ca2+ during hypoxia. Substitution of extracellular Na+ increased [Ca2+]i and exacerbated the difference at the two O2 tensions. This finding is consistent with elevated activity of NCE at low O2, perhaps in an attempt to reduce Ca2+ to levels found at 20% O2. Since NCE activity requires a functional ATP-driven Na+/K+ pump, it is unlikely that ATP was limiting (as shown previously [7]). In addition, because inhibition of the mitochondrial electron transport chain with antimycin A reduces [Ca2+]i, any Ca2+ release from mitrochondrial stores following their hypoxia-induced depolarization, would likely to be insufficient on its own to raise [Ca2+]i. In this context, it is important to note that mitochondria in articular chondrocytes occupy a relatively small volume (1-2% cytoplasm) [13] compared to that seen in other tissues (typically 15-20%, eg liver). There is also some reduction in mitochondrial volume with depth and age [14,15]. They may also lack a functional electron transport chain [16], relying on glycolysis for metabolic energy [3]. Taken together, these findings are consistent with hypoxic release of Ca2+ into the cytoplasm from intracellular non-mitochondrial stores, probably endoplasmic reticulum.

Oxygen and chondrocyte function

As noted above, it is unlikely that articular chondrocytes require O2 for energy, at least directly. Nevertheless, O2 tension is a critical parameter in modulating chondrocyte function. Changes in O2 level affect ATP production [3], growth factors [17], proinflammatory mediators [18] and matrix components [19]. Dedifferentiation of chondrocytes occurs when they are maintained at abnormally high O2. This includes restoration of the ability to carry out oxidative phosphorylation [20]. Standard chondrocyte markers, such as collagen type II and aggrecan, are affected [19]. In effect, low O2 tensions (c.5%), which are normal for articular cartilage but hypoxic for other cell types, promote a chondrocyte phenotype [21-23]. In addition, however, a pathological role for O2 has also received considerable attention. Thus abnormally high or low O2 levels with concomitant alterations in levels of ROS, may be important in disease states such as osteoarthritis [24-26]. O2 also affects acid-base balance in articular chondrocytes [7,8]. The present findings extend the action of O2 to include modulation of an additional important ion, ie Ca2+, with low O2 causing intracellular [Ca2+] to rise. The O2 tension at which perturbation of Ca2+ requires further definition, it being particularly important to study the likely physiological levels of between 10% and 1%.

Calcium and chondrocyte function

Intracellular Ca2+ in chondrocytes, as in other cell types, also has numerous physiological and probably pathological roles [27]. Of particular relevance to chondrocytes is the observation that perturbation of normal Ca2+ levels reduces matrix synthesis [10]. It also affects both chondrocyte differentiation [28] and ageing [11]. Ca2+ signalling has been implicated in a range of other chondrocyte functions including mechanotransduction [29-32], volume regulation [33-39] and response to electrical stimulation [40]. It may therefore play a critical role in how joint loading and unloading promotes cartilage health. Intracellular Ca2+ elevations, for example, induce chondrogenesis via a calcineurin/NF-AT pathway [41]. Extracellular levels of Ca2+ are also important in the longer term, when they too may be involved in alteration of matrix production including proteoglycan synthesis and expression of collagen [42-44] - extracellular Ca2+ receptors are present. Ca2+ is also implicated in the action of proinflammatory cytokines such as IL-1 and, again therefore, has received attention in the context of joint disease such as osteoarthritis [45].

Crosstalk between oxygen, reactive oxygen species and Ca2+

The elevation of intracellular Ca2+ at low O2 reported here was associated with a fall in ROS and also mitochondrial depolarization. In most cell types, though probably not articular chondrocytes, mitochondria are critical for oxdative phosphorylation and hence central to energy production. They are also involved in Ca2+ regulation, acting as a sink of, or sometimes a source for, cytoplasmic Ca2+ - Ca2+ being released via the mitochondrial permeability transition pore (PTP) [46-48]. ROS are generated during mitochondrial respiration [49,50], as well as at other cellular sites. ROS, of course, can be harmful but have also been implicated in intracellular signalling, regulating redox sensitive enzymes and also ion channels. By these means, ROS may modulate intracellular Ca2+, eg acting via modulation of ryanodine receptors, IP3 receptors, Ca2+ pumps and NCE [51-53]. Ca2+ uptake by mitochondria may itself alter ROS generation - both reduction of ROS (through dissipation of the negative mitochondrial pd) or their elevation have been reported [54,55]. To a certain extent, the direction of change depends on tissue type and respiratory rate. Another obvious signal is represented by hypoxia-inducible factor (HIF). Stabilization of HIF1α occurs during hypoxia (eg [6,56,57]) and may affect [Ca2+]i through effects calcium channel gene expression and activity [58,59]. There is thus considerable scope for cross-talk between O2, ROS and Ca2+, together with the role of mitochondria [51,53,55] but the exact coupling in chondrocytes awaits description.

Reactive oxygen species, mitochondria and regulation of Ca2+

We show here that a fall in ROS during hypoxia correlated with elevation of Ca2+, whilst restoration of ROS levels to those seen at 20% by three disparate reagents (H2O2, Co2+ or antimycin A) all resulted in decreased Ca2+. Hypoxia also induced depolarization of mitochondria, indicative of a reduction in electron flow through the mitochondrial electron transport chain, and hence ROS production. Addition of antimycin A also blocks electron transport to the terminal complexes, acting at the Qi site of complex III to increase ROS output [8], as also observed in the present work. It is thus likely that reduced production of ROS from mitochondria is involved in the rise in Ca2+, as proposed for O2-induced changes in NHE activity and intracellular pH [8]. In the case of H+, however, perturbed homeostasis on change in O2 tension is observed rapidly, within a few minutes [60]. Effects on Ca2+ appear to occur over a much longer time course, despite sharing sensitivity to ROS levels. The reason for this is not immediately apparent. It may be that Ca2+ homeostasis, as a more critical modulator of chondrocyte function, is better protected than pH. Alternatively, it may be that the mechanism involves genomic effects, such as though involving HIF. In addition, a link between Ca2+ and pH in chondrocytes has been shown previously, with alkalinisation causing a rise in Ca2+ [61]. Since chondrocytes acidify in response to low O2, however, rather than increasing their pH, the hypoxia-induced rise in Ca2+ cannot be secondary to changes in pH.

Conclusion

O2 tension exerts a significant effect on cytoplasmic Ca2+ levels of articular chondrocytes, with the proposed mechanism involving ROS from mitochondria. Results emphasise the importance of O2 to chondrocyte function and that of using realistic O2 tensions when studying the pathophysiology of articular cartilage.

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

RW helped plan the experiments, carried them, analysed the data and helped write the manuscript; JSG planned the experiments, analysed data and prepared the manuscript.

All authors have read and approved the final manuscript.

Acknowledgements

This work was supported by the BBSRC, UK.

References

  1. Silver IA: Measurement of pH and ionic composition of pericellular sites.

    Phil Trans Roy Soc B 1975, 271:261-272. Publisher Full Text OpenURL

  2. Zhou S, Chiu Z, Urban JPG: Factors affecting the oxygen concentration gradient from the synovial surface of articular cartilage to the cartilage-bone interface: a modelling study.

    Arthritis Rheum 2004, 50:3915-3924. PubMed Abstract | Publisher Full Text OpenURL

  3. Lee RB, Urban JPG: Evidence for a negative Pasteur effect in articular cartilage.

    Biochem J 1997, 321:95-102. PubMed Abstract | PubMed Central Full Text OpenURL

  4. Grimshaw MJ, Mason RM: Bovine articular chondrocyte function in vitro depends upon oxygen tension.

    Osteoarthritis Cartil 2000, 8:386-392. Publisher Full Text OpenURL

  5. Gibson JS, Milner PI, White R, Fairfax TPA, Wilkins RJ: Oxygen and reactive oxygen species in articular cartilage: modulators of ionic homeostasis.

    Pflug Archiv 2008, 455:563-573. Publisher Full Text OpenURL

  6. Chandel NS, Schumacker PT: Cellular oxygen sensing by mitochondria: old questions, new insight.

    J Appl Physiol 2000, 88:1880-1889. PubMed Abstract | Publisher Full Text OpenURL

  7. Milner PI, Fairfax TPA, Browning JA, Wilkins RJ, Gibson JS: The effect of O2 tension on pH homeostasis in equine articular chondrocytes.

    Arthritis Rheum 2006, 54:3523-3532. PubMed Abstract | Publisher Full Text OpenURL

  8. Milner PI, Wilkins RJ, Gibson JS: The role of mitochondrial reactive oxygen species in pH regulation in articular chondrocytes.

    Osteoarthritis Cart 2007, 15:735-742. Publisher Full Text OpenURL

  9. Tattersall AL, Meredith D, Furla P, Shen M-R, Ellory JC, Wilkins RJ: Molecular and functional identification of the Na+/H+ exchange isoforms NHE1 and NHE3 in isolated bovine articular chondrocytes.

    Cell Physiol Biochem 2003, 13:215-222. PubMed Abstract | Publisher Full Text OpenURL

  10. Wilkins RJ, Browning JA, Ellory JC: Surviving in a matrix: membrane transport in articular chondrocytes.

    J Membrane Biol 2000, 177:95-108. Publisher Full Text OpenURL

  11. Nevo Z, Beit-Or A, Eilam Y: Slowing down aging of cultured embryonal chick chondrocytes by maintenance under lowered oxygen tension.

    Mech Ageing Develop 1988, 45:157-165. Publisher Full Text OpenURL

  12. Sanchez JC, Wilkins RJ: Mechanisms involved in the increase in intracellular calcium following hypotonic shock in bovine articular chondrocytes.

    Gen Physiol Biophys 2003, 22:487-500. PubMed Abstract | Publisher Full Text OpenURL

  13. Brighton CT, Kitajima T, Hunt RM: Zonal analysis of cytoplasmic components of articular cartilage chondrocytes.

    Arthritis Rheum 1984, 27:1290-1299. PubMed Abstract | Publisher Full Text OpenURL

  14. Stockwell RA: Morphometry of cytoplasmic components of mammalian articular chondrocytes and corneal keratocytes: species and zonal variations of mitochondria in relation to nutrition.

    J Anat 1991, 175:251-261. PubMed Abstract | PubMed Central Full Text OpenURL

  15. Martin JA, Buckwalter JA: The role of chondrocyte senescence in the pathogenesis of osteoarthritis and in limiting cartilage repair.

    J Bone Joint Surg 2003, 85A:106-110. OpenURL

  16. Mignotte F, Champagne A-M, Froger-Gaillard B, Benel L, Gueride M, Adolphe M, Mounolou JC: Mitochondrial biogenesis in rabbit articular chondrocytes transferred to culture.

    Biol Cell 1991, 71:67-72. PubMed Abstract | Publisher Full Text OpenURL

  17. Etherington PJ, Winlove P, Taylor P, Paleolog E, Miotla JM: VEGF release is associated with reduced oxygen tensions in experimental inflammatory arthritis.

    Clin Exp Rheumatol 2002, 20:799-805. PubMed Abstract OpenURL

  18. Cernanec J, Guilak F, Weinberg JB, Pisetsky DS, Fermor B: Influence of hypoxia and reoxygenation on cytokine-induced production of proinflammatory mediators in articular cartilage.

    Arthritis Rheum 2002, 46:968-975. PubMed Abstract | Publisher Full Text OpenURL

  19. Murphy CL, Polak JM: Control of human articular chondrocyte differentiation by reduced oxygen tension.

    J Cell Physiol 2004, 199:451-459. PubMed Abstract | Publisher Full Text OpenURL

  20. Marcus RE, Srivastava VML: Effect of low oxygen tension on glucose-metabolising enzymes in cultured articular chondrocytes.

    Proc Soc Exp Biol Med 1973, 143:488-491. PubMed Abstract OpenURL

  21. Murphy CL, Sambanis A: Effect of oxygen tension on chondrocyte extracellular matrix accumulation.

    Conn Tissue Res 2001, 42:87-96. Publisher Full Text OpenURL

  22. Wang DW, Fermor B, Gimble JM, Awad HA, Guilak F: Influence of oxygen on the proliferation and metabolism of adipose-derived adult stem cells.

    J Cell Physiol 2005, 204:184-191. PubMed Abstract | Publisher Full Text OpenURL

  23. Betre H, Ong SR, Guilak F, Chilkoti A, Fermor B, Setton LA: Chondrocyte differentiation of human adipose-derived adult stem cells in elastin-like polypeptide.

    Biomaterials 2006, 27:91-99. PubMed Abstract | Publisher Full Text OpenURL

  24. Henroitin YE, Bruckner P, Pujol JP: The role of reactive oxygen species in homeostasis and degradation of cartilage.

    Osteoarthritis Cart 2003, 11:747-755. Publisher Full Text OpenURL

  25. Hitchon CA, El-Gabalawy HS: Oxidation in rheumatoid arthritis.

    Arthritis Res Ther 2004, 6:265-278. PubMed Abstract | BioMed Central Full Text | PubMed Central Full Text OpenURL

  26. Henroitin YE, Kurz B, Aigner T: Oxygen and reactive oxygen species in cartilage degradation: friends or foes?

    Osteoarthritis Cart 2005, 13:643-654. Publisher Full Text OpenURL

  27. Berridge MJ, Bootman MD, Lipp P: Calcium - a life and death signal.

    Nature 1998, 395:645-648. PubMed Abstract | Publisher Full Text OpenURL

  28. Matta C, Fodor J, Szijgyarto Z, Juhász T, Gergely P, Csernoch L, Zákány R: Cytosolic free Ca2+ concentration exhibits a characteristic temporal pattern during in vitro cartilage differentiation: a possible role of calcineurin in Ca-signalling of chondrogenic cells.

    Cell Calcium 2008, 44:310-323. PubMed Abstract | Publisher Full Text OpenURL

  29. Yellowley CE, Jacobs CR, Li Z, Zhou Z, J DH: Effects of fluid flow on intracellular calcium in bovine articular chondrocytes.

    Am J Physiol 1997, 273:C30-C36. PubMed Abstract | Publisher Full Text OpenURL

  30. Guilak F, Zell RA, Erickson GR, Grande DA, Rubin CT, McLeod KJ, Donahue HJ: Mechanically induced calcium waves in articular chondrocytes are inhibited by gadolinium and amiloride.

    J Orthop Res 1999, 17:421-429. PubMed Abstract | Publisher Full Text OpenURL

  31. Ushida T, Murata T, Mizuno S, Tateishi T: Transients of intracellular calcium ion concentrations of cultured bovine chondrocytes loaded with intermittent hydrostatic pressure.

    Mol Cell Biol 1997, 8:S405. OpenURL

  32. Browning JA, Saunders K, Urban JPG, Wilkins RJ: The influence and interactions of hydrostatic pressure and osmotic pressure on the intracellular milieu of chondrocytes.

    Biorheology 2004, 41:299-308. PubMed Abstract | Publisher Full Text OpenURL

  33. Erickson GR, Alexopoulos LG, Guilak F: Hyper-osmotic stress induces volume change and calcium transients in chondrocytes by transmembrane, phospholipid, and G-protein pathways.

    J Biomech 2001, 34:1527-1535. PubMed Abstract | Publisher Full Text OpenURL

  34. Erickson GR, Northrup DL, Guilak F: Hypo-osmotic stress induces calcium-dependent actin reorganisation in articular chondrocytes.

    Osteoarthritis Cart 2003, 11:187-197. Publisher Full Text OpenURL

  35. Yellowley CE, Hancox JC, Donahue HJ: Cell swelling activation of membrane currents, Ca2+ transients and regulatory volume decrease in bovine articular chondrocytes.

    J Bone Mineral Res 2001, 16:S254. OpenURL

  36. Wilkins RJ, Davies ME, Muzyamba MC, Gibson JS: Homeostasis of intracellular Ca2+ in equine chondrocytes: response to hypotonic shock.

    Equine Vet J 2003, 35:439-443. PubMed Abstract | Publisher Full Text OpenURL

  37. Kerrigan MJP, Hall AC: The role of [Ca2+]i in mediating regulatory volume decrease in isolated bovine articular chondrocytes.

    J Physiol 2000, 527P:42P. OpenURL

  38. Kerrigan MJP, Hall AC: Control of chondrocyte regulatory volume decrease (RVD) by [Ca2+]i and cell shape.

    Osteoarthritis Cart 2008, 16:312-322. Publisher Full Text OpenURL

  39. Phan MN, Leddy HA, Votta BJ, Kumar S, Levy DS, Lipshutz DB, Lee SH, Liedtke W, Guilak F: Functional characterisation of TRPV4 as an osmotically sensitive ion channel in porcine articular chondrocytes.

    Arthritis Rheum 2009, 60:3028-3037. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  40. Xu J, Wang W, Clark CC, Brighton CT: Signal transduction in electrically stimulated articular chondrocytes involves translocation of extracellular calcium through voltage-gated channels.

    Osteoarthritis Cart 2009, 17:397-405. Publisher Full Text OpenURL

  41. Tomita M, Reinhold MI, Molkentin JD, Naski MC: Calcineurin and NFAT4 induce chondrogenesis.

    J Biol Chem 2002, 277:42214-42218. PubMed Abstract | Publisher Full Text OpenURL

  42. Shulman HJ, Opler A: The stimulatory effect of calcium on the synthesis of cartilage proteoglycan.

    Biochem Biophy Res Comm 1974, 59:914-919. Publisher Full Text OpenURL

  43. Benya PD, Shaffer JD: Dedifferentiated chondrocytes reexpress the differentiated collagen phenotype when cultured in agarose gels.

    Cell 1982, 30:215-224. PubMed Abstract | Publisher Full Text OpenURL

  44. Urban JP, Hall AC, Gehl KA: Regulation of matrix synthesis rates by the ionic and osmotic environment of articular chondrocytes.

    J Cell Physiol 1993, 154:262-270. PubMed Abstract | Publisher Full Text OpenURL

  45. Pritchard S, Guilak F: Effects of interleukin-1 on calcium signalling and the increase of filamentous actin in isolated and in situ chondrocytes.

    Arthritis Rheum 2006, 54:2164-2174. PubMed Abstract | Publisher Full Text OpenURL

  46. Herrington J, Park YB, Babcock DF, Hille B: Dominant role of mitochondria in clearance of large Ca2+ loads from rat adrenal chromaffin cells.

    Neuron 1996, 16:219-228. PubMed Abstract | Publisher Full Text OpenURL

  47. Eager KR, Roden LD, Dulhunty AF: Actions of sulfhydryl reagents on single ryanodine receptor Ca2+-release channels from sheep myocardium.

    Am J Physiol 1997, 272:C1908-C1918. PubMed Abstract | Publisher Full Text OpenURL

  48. Boitier E, Rea R, Duchen MR: Mitochondria exert a negative feedback on the propagation of intracellular Ca2+ waves in rat cortical astrocytes.

    J Cell Biol 1999, 145:795-808. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  49. Kowaltowski AJ, Naia-da-Silva ES, Castilho RF, Vercesi AE: Ca2+-stimulated mitochondrial reactive oxygen species generation and permeabiliy transition are inhibited by dibucaine or Mg2+.

    Arch Biochem Biophys 1998, 359:77-81. PubMed Abstract | Publisher Full Text OpenURL

  50. Maciel EN, Vercesi AE, Castilho RF: Oxidative stress in Ca2+-induced membrane permeability transition in brain mitochondria.

    J Neurochemistry 2001, 79:1237-1245. Publisher Full Text OpenURL

  51. Yan Y, Wei CL, Zhang WR, Cheng HP, Liu J: Cross-talk between calcium and reactive oxygen species signaling.

    Acta Pharmacol Sin 2006, 27:821-826. PubMed Abstract | Publisher Full Text OpenURL

  52. Zima AV, Blatter LA: Redox regulation of cardiac calcium channels and transporters.

    Cardiovascular Res 2006, 71:310-321. Publisher Full Text OpenURL

  53. Camello-Almarez C, Gomez-Pinilla PJ, Pozo MJ, Camello PJ: Mitochondrial reactive oxygen species and Ca2+ signaling.

    Am J Cell Physiol 2006, 291:C1082-C1088. Publisher Full Text OpenURL

  54. Starkov AA, Chinopoulos C, Fiskum G: Mitochondrial calcium and oxidative stress as mediators of ischemic brain injury.

    Cell Calcium 2004, 36:257-264. PubMed Abstract | Publisher Full Text OpenURL

  55. Feissner RF, Skalska J, Gaum WE, Sheu S-S: Crosstalk signaling between mitochondrial Ca2+ and ROS.

    Frontiers Bioscience 2009, 14:1197-1218. Publisher Full Text OpenURL

  56. Wang GL, Semenza GL: Oxygen sensing and response to hypoxia by mammalian cells.

    Redox Report 1996, 2:89-96. OpenURL

  57. Fahling M: Cellular oxygen sensing, signalling and how to survive translational arrest in hypoxia.

    Acta Physiol 2009, 195:205-230. Publisher Full Text OpenURL

  58. Del Toro R, Levitsky KL, Lopez-Barneo J, Chiara MD: Induction of T-type calcium channel gene expression by chronic hypoxia.

    J Biol Chem 2003, 278:22316-22324. PubMed Abstract | Publisher Full Text OpenURL

  59. Wang J, Weigand L, Lu W, Sylvester JT, Semenza GL, Shimoda LA: Hypoxia inducible factor 1 mediates hypoxia-induced TRPC expression and elevated intracellular Ca2+ in pulmonary arterial smooth muscle cells.

    Circulation Res 2006, 98:1528-1537. PubMed Abstract | Publisher Full Text OpenURL

  60. Gibson JS, McCartney D, Sumpter J, Fairfax TP, Milner PI, Edwards HL, Wilkins RJ: Rapid effects of hypoxia on H+ homeostasis in articular chondrocytes.

    Pflug Archiv 2009, 458:1085-1092. Publisher Full Text OpenURL

  61. Browning JA, Wilkins RJ: The effect of intracellular alkalinisation on intracellular Ca2+ homeostasis in a human chondrocyte cell line.

    Eur J Physiol 2002, 444:744-751. Publisher Full Text OpenURL