Introduction
Rheumatoid arthritis (RA) is a common inflammatory joint disease with a prevalence of 0.5 to 1% [
1]. RA is more common in women than in men, and the peak incidence in women coincides with the time of menopause [
2]. There is evidence that the female sex hormone estrogen can influence both the incidence and the progression of RA. Exposure to oral contraceptives has been shown to reduce the risk of developing RA [
3], and disease activity often decreases during pregnancy [
4], when levels of female sex hormones are elevated. Recently, we reported beneficial effects of hormone replacement therapy in women with postmenopausal RA. Patients treated with hormone replacement therapy displayed increased bone mineral density (BMD), better clinical outcome, decreased erythrocyte sedimentation rate and elevated levels of serum hemoglobin as well as retarded progression of joint erosion [
5].
RA is characterized by different skeletal manifestations including periarticular osteoporosis, bone erosions and generalized osteoporosis. The frequency of generalized osteoporosis in postmenopausal RA has been shown to be almost 50% [
6,
7], and these patients are at high risk for fractures. The bone loss in postmenopausal RA is believed to be caused by the combined effects of estrogen deficiency [
8] and the inflammatory disease [
9]. The relative importance of each of these two factors is not yet known.
Collagen-induced arthritis (CIA) is a well established murine model for human RA [
10]. It has been shown that treatment with physiological doses of estradiol suppresses the disease progression in this model [
11], whereas loss of endogenous estrogen by ovariectomy (OVX) leads to a more severe disease. OVX of mice leads to significant bone loss and is used as a model of postmenopausal osteopenia [
12]. It has been demonstrated that OVX enhances the severity of arthritis and bone loss in CIA in rats, whereas exposure to estrogen suppresses it [
13].
The aim of this study was to establish a murine model for studies of osteoporosis in postmenopausal RA, and to evaluate the relative importance and possible different mechanisms of estrogen deficiency versus joint inflammation for the induction of bone loss.
Materials and methods
Mice
The ethical committee for animal experiments at the University of Göteborg approved this study. Female DBA/1 mice (Taconic M&B A/S, Ry, Denmark) were kept, 5 to 10 animals to a cage, under standard environmental conditions and were fed with standard laboratory chow and tap water ad libitum.
Castration
OVX or sham operation was performed at 10 weeks of age. Ovaries were removed by using a midline incision of the skin, and flank incisions of the peritoneum. The skin incision was closed with metallic clips. Sham-operated animals had their ovaries exposed but not removed. Surgery was performed under Ketalar® (Pfizer AB, Täby, Sweden) and Domitor® (Orion Pharma, Espoo, Finland) anesthesia.
Induction and evaluation of arthritis
Nine days after surgery the mice were immunized with 100 μg of chicken type II collagen (CII; Sigma, St Louis, MO) dissolved in 0.1M acetic acid and emulsified with an equal volume of incomplete Freund's adjuvant (Sigma) supplemented with 0.5 mg/ml Mycobacterium tuberculosis (Sigma). A total volume of 100 μl was injected intradermally at the base of the tail (50 μl on each side). After 21 days mice received a booster injection in the same way using CII emulsified in incomplete Freund's adjuvant.
The animals were observed twice weekly for frequency and severity of arthritis. Severity was graded as described previously [
14], scoring 1 to 3 in each paw (maximum of 12 points per mouse) as follows: 1, swelling or erythema in one joint; 2, swelling or erythema in two joints; 3, severe swelling of the entire paw or ankylosis.
Tissue collection and histological examination
At 45 days after immunization mice were anaesthetized with Ketalar®/Domitor®, bled, and killed by cervical dislocation. Sera were individually stored at -20°C until use. Paws and femurs were collected.
Paws were placed in 4% paraformaldehyde dissolved in water, decalcified, and embedded in paraffin. Sections were stained with eosin/hematoxylin and encoded before examination. In each animal the front and back of all four paws were graded separately on a scale 0 to 4 and divided by 2, with a maximum of 16 points per mouse, as follows: 1, synovial hypertrophy; 2, pannus, erosions of cartilage; 3, erosions of bone; 4, complete ankylosis.
Bone mineral density
One femur was subjected to a peripheral quantitative computed tomography (pQCT) scan with a Stratec pQCT XCT Research M, software version 5.4 B (Norland, Fort Atkinson, WI) at a resolution of 70 μm, as described previously [
15]. Trabecular BMD was determined with a metaphyseal scan at a point 3% of the length of the femur from the growth plate. The inner 45% of the area was defined as the trabecular bone compartment. Cortical BMD was determined with a mid-diaphyseal scan, which contains only cortical bone.
Serological markers of bone and cartilage remodeling
As a marker of bone resorption, serum levels of fragments of type I collagen were assessed using a RatLaps ELISA kit (Nordic Bioscience Diagnostics A/S, Herlev, Denmark). Serum levels of osteocalcin, a marker of bone formation, were determined with a Mouse Osteocalcin IRMA kit (Immutopics, Inc., San Clemente, CA).
As a marker of cartilage destruction, serum levels of COMP (cartilage oligomeric matrix protein) were determined with an Animal COMP® ELISA kit (provided by AnaMar Medical AB, Uppsala, Sweden).
Quantification of serum IgG and CII-specific antibodies
Serum levels of IgG were measured by single radial immunodiffusion as described previously [
16]. By use of a previously described ELISA, serum levels of anti-CII antibodies were determined [
17].
Interleukin-6 bioassay
A bioassay [
18] with cell line B13.29, subclone B9 (which is dependent on interleukin (IL)-6 for growth), was used to measure levels of IL-6 in serum. B9 cells were seeded with 5,000 cells per well into flat-bottomed 96-well plates (Nunc, Roskilde, Denmark) and cultured in Iscove's medium (Sigma) enriched with 50 μg/ml gentamicin (Sigma), 4 mM L-glutamine (Sigma), 50 μM mercaptoethanol (Sigma) and 10% fetal calf serum (Biological Ind., Beit Haemek, Israel). Sera were diluted 1:50 and added in triplicates. After 68 hours of culture, 1 μCi of
3H-thymidine (Amersham Pharmacia Biotech, Uppsala, Sweden) was added; the cells were harvested 4 hours later. Recombinant mouse IL-6 (National Institute for Biological Standards and Control, Potters Bar, Hertfordshire, UK) was used as a standard.
Analysis of bone marrow cells
One femur was flushed with 2 ml of phosphate-buffered saline through the bone cavity to harvest bone marrow cells. After centrifugation at 515 g for 5 min, the pellet was resuspended in Tris-buffered 0.83% NH4Cl solution, pH 7.29, for 5 min to lyse erythrocytes, and then washed in phosphate-buffered saline. The cells were kept in complete Iscove's medium (described above) until use. Leukocytes were counted with an automated cell counter (Sysmex, Kobe, Japan).
The cells were stained with anti-CD45R/B220 conjugated with fluorescein isothiocyanate (clone RA3-6B2; BD) for B-lymphocytes and anti-CD3-conjugated with phycoerythrin (PE) (clone 145-2C11; BD), anti-CD4-biotin (clone RM4-5; BD), anti-CD8-biotin (clone 53-6.7; BD), anti-CD69-PE (clone H1.2F3; BD) and anti-CD25-PE (clone 7D4; BD) for T-lymphocytes. Cells were then subjected to fluorescence-activated cell sorting (FACS) analysis with FACSCalibur (BD Pharmingen, Franklin Lakes, NJ) and analyzed with Paint-A-Gate software (BD). Results are expressed as the numbers of positively stained cells per femur.
Statistical analysis
For statistical evaluation the non-parametric Kruskal–Wallis test followed by a post hoc test was used between all four groups. A Mann–Whitney test was used when two groups were compared. P < 0.05 was considered statistically significant.
Discussion
Osteoporosis is one of the major problems in postmenopausal RA [
7,
19] and is a factor contributing to increased risk for fractures [
20]. The mechanisms and relative importance of estrogen deficiency versus inflammation for the bone loss in postmenopausal RA are not fully understood. Our study is the first to demonstrate equal contributions of estrogen deficiency and polyarthritis to bone loss in a model of human postmenopausal RA. In addition, serum markers of bone and cartilage turnover and FACS analysis of bone marrow leukocyte phenotypes indicate different mechanisms for the development of osteoporosis.
OVX of the DBA/1 mice several weeks before the development of arthritis enabled separate and concurrent analyses of the effects of estrogen deficiency and the inflammatory disease on bone loss. Our results show that the loss of endogenous estrogen and the ongoing arthritic disease cause a similar degree of trabecular bone loss (22% and 26%, respectively) and clearly have an additive effect, because ovariectomized mice with arthritis lost 58% of trabecular BMD. Interestingly, arthritis also induced a significant decrease in cortical BMD, whereas OVX, irrespective of inflammatory status, did not affect this parameter.
It has previously been demonstrated in CIA in rats that OVX enhances the severity of arthritis and bone loss, whereas exposure to estrogen suppresses it [
13]. A more detailed comparison between the previous study and ours is not possible because we ovariectomized the mice 2 weeks before initial immunization (that is, 5 weeks before the development of arthritis) to achieve an established postmenopausal state, whereas Yamasaki and colleagues ovariectomized the rats 1 week after sensitization.
Systemic inflammation, impaired physical activity, low body mass and treatment with corticosteroids are some important factors associated with the development of osteoporosis in RA. The pathophysiological mechanisms of bone loss in arthritis have been shown to be mediated through the activation of osteoclasts by the macrophage-derived proinflammatory cytokines tumor necrosis factor-α and IL-1, and by the production of RANKL by activated T-lymphocytes and fibroblasts. Garnero and colleagues [
21] found increased serum levels of markers of bone resorption in patients with erosive RA, and decreased markers of bone formation. The discrepancy between bone formation and bone resorption results in the enhanced bone loss in arthritis.
We showed that there was strongly increased bone resorption measured by RatLaps in the arthritic mice but not in ovariectomized mice. This was expected, as we sought to study changes in established menopause, and not the rapid phase of bone loss that follows OVX. In contrast to what Garnero and colleagues found in RA patients, we failed to demonstrate decreased serum levels of osteocalcin associated with arthritis. In accord with our results, Nishida and colleagues [
22] have previously suggested that reduced bone formation might not be a substantial contributor to bone loss in DBA/1 mice, so this difference might be species dependent.
The exact mechanism whereby OVX induces bone loss in mice is not yet known. Several mechanisms are involved, and recent studies have shown that OVX of mice was associated with an increase in the number of activated, tumor necrosis factor-producing, bone marrow T lymphocytes stimulating monocytes to differentiate into osteoclasts [
12,
23,
24]. We did not show an increase in bone marrow T lymphocytes. The explanation for this discrepancy could be either that we used CD3 as a marker for T cells, whereas others have used anti-CD90 (which is also expressed on natural killer cells, monocytes and dendritic cells), or the very late time point (8 weeks after OVX) that we used for analysis of the bone marrow. Indeed, the finding that RatLaps, a serum marker of bone resorption, was unaltered whereas osteocalcin, a serum marker of bone formation, was increased in ovariectomized mice indicates that the period of OVX-induced increased activation of osteoclasts had already ended at this late time point. As has been shown previously, the number of B lymphocytes in bone marrow was increased after OVX [
25] and decreased in the arthritic mice [
26]. As increased B lymphopoiesis has been shown to be associated with bone loss [
27], our data suggest separate mechanisms for the bone loss found in estrogen deficiency and in arthritis.
COMP is an extracellular matrix protein initially found in cartilage but recently also shown to be secreted by synovial fibroblasts. Serum levels of COMP are used as a marker of cartilage destruction and have previously been evaluated in CIA in rats [
28,
29]. We found increased serum COMP levels in all arthritic mice, irrespective of the estrogen level, indicating a lack of cartilage protection by endogenous ovarian hormones.
Taken together, although the analyses in this study were all performed on day 45, the differences in serum levels of RatLaps, osteocalcin, COMP and frequencies and phenotypes of bone marrow lymphocytes between mice subjected to OVX and CIA suggest the possibility of different mechanisms for the development of osteoporosis in estrogen deficiency and arthritic disease.
The female sex hormone estradiol not only preserves bone but also has a clear anti-arthritic effect both in human RA [
4,
5] as well as in rat [
13] and murine [
11,
30] CIA. Clinically, the arthritic ovariectomized mice developed a more severe disease than the sham-operated mice. However, at termination of the experiment all mice, irrespective of hormonal status, had developed severe arthritic disease, with histological destruction score, pro-inflammatory cytokines and CII antibodies at similar levels.
Acknowledgements
We thank Berit Eriksson, Anette Hansevi and Maud Petersson for excellent technical assistance. This study was supported by grants from the Göteborg Medical Society, King Gustav V's 80 years' foundation, the Sahlgrenska Foundation, the Novo Nordic Foundation, the Börje Dahlin foundation, the Association against Rheumatism, Reumaforskningsfond Margareta, the Medical Faculty of Göteborg University (ALF) and the Swedish Research Council.
Competing interests
The author(s) declare that they have no competing interests.
Authors' contributions
HC and CO participated in study design, interpretation of data and manuscript preparation. UI aided with analysis of data and statistical analysis. ME and MV aided with acquisition of data. The study was performed mainly by CJ. All authors read and approved the final manuscript.