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DNAX adaptor protein 12 (DAP12) is a trans-membrane adaptor molecule that transduces activating signals in NK and myeloid cells. Absence of functional Dap12 results in osteoclast defects and bone abnormalities. Because DAP12 has no extracelluar binding domains, it must pair with cell surface receptors for signal transduction. There are at least 15 known DAP12-associating cell surface receptors with distinct temporal and cell type–specific expression patterns. Our aim was to determine which receptors may be important in DAP12-associated bone pathologies. Here, we identify myeloid DAP12-associating lectin (MDL)-1 receptor (also known as CLEC5A) as a key regulator of synovial injury and bone erosion during autoimmune joint inflammation. Activation of MDL-1 leads to enhanced recruitment of inflammatory macrophages and neutrophils to the joint and promotes bone erosion. Functional blockade of MDL-1 receptor via Mdl1 deletion or treatment with MDL-1-Ig fusion protein reduces the clinical signs of autoimmune joint inflammation. These findings suggest that MDL-1 receptor may be a therapeutic target for treatment of immune-mediated skeletal disorders.
The balance between osteoblast and osteoclast activation and function is critical for bone homeostasis. Osteoblasts, which are cells of mesenchymal origin, secrete bone-matrix proteins to promote mineralization; whereas macrophages, neutrophils, and osteoclasts, which are derived from a common hematopoietic precursor, are key contributors to the pathogenesis in bone resorptive disorders such as rheumatoid arthritis (RA). During autoimmune joint disease the excessive influx of inflammatory macrophages and granulocytes leads to an increased development and activation of osteoclasts. The inflammatory response promotes tissue injury and osteoclast activation, which leads to detrimental cartilage and bone loss. The primary signals for this process are induced in the presence of M-CSF by receptor activator of NF-κB ligand (RANKL), which in turn activates the TRAF6, c-Fos, and the NFATc1 pathway (Ishida et al., 2002; Takayanagi, 2002, 2005a). Additional co-stimulatory signals derived from immunoreceptor tyrosine-based activation motif (ITAM)–containing molecules are also essential for osteoclastogenesis (Koga et al., 2004). DNAX adaptor protein 12 (DAP12) is a trans-membrane adaptor molecule that transduces activating signals via ITAM for a range of cell surface receptors on NK cells, granulocytes, and macrophages (Lanier et al., 1998; Kaifu et al., 2003). There are many known DAP12 pairing partners, including myeloid DAP12-associating lectin-1 (MDL-1), which has been shown to regulate myeloid cell–associated inflammatory responses (Bakker et al., 1999; Aoki et al., 2004; Chen et al., 2008). MDL-1—a C-type lectin domain family 5, member A (CLEC5A)—is highly expressed on TNF-activated macrophages (Bakker et al., 1999). Cross-linking cell surface MDL-1 receptors induces DAP12-ITAM–dependent calcium mobilization (Bakker et al., 1999) and activation of the Syk and phospholipase Cγ signaling pathways (Lanier et al., 1998; Mao et al., 2006). The ITAM-dependent calcium signaling pathway is a critical “co-stimulatory” signal for RANKL-dependent regulation of bone remodeling and homeostasis (Takayanagi, 2005a).
Although MDL-1 expression is up-regulated in activated myeloid cells, it is not known whether this receptor plays any role in autoimmune inflammation. Given the fact that MDL-1’s pairing partner, DAP12, has a role in osteoclast formation and bone remodeling (Humphrey et al., 2004, 2006; Kaifu et al., 2003), we tested whether MDL-1 activation could affect autoimmune arthritis. In this study, we demonstrate that MDL-1 is expressed on inflammatory macrophages and neutrophils, as well as bone marrow–derived osteoclast precursors. Activation of the MDL-1 receptor during joint inflammation enhances myeloid cell infiltration and promotes IL-1, IL-6, IL-17A, and TNF expression, resulting in severe cartilage damage and bone erosion. In contrast, neutralization of MDL-1 function down-regulates TRAP, cathepsin K, and MMP9 expression, subsequently preserving bone mineral density. These results suggest that therapeutic targeting of the MDL-1 receptor may suppress inflammation and, ultimately, bone resorptive pathways during inflammatory conditions.
In a tissue array gene expression analysis of MDL-1 receptor, we found that human (Fig. 1 A) and mouse (Fig. 1 B) bone marrow cells and joint tissues express the highest levels of Mdl1. Correspondingly, MDL-1 protein is expressed on murine granulocytes (CD11b+ Ly6G+) and monocytes (CD11b+ Ly6G−) from bone marrow and the peripheral blood (Fig. 1 C). We observed that activation with TNF, but not IFN-γ, further enhances Mdl1 mRNA and protein expression in bone marrow–derived macrophage colony-stimulating factor (MCSF)-dependent macrophages (Fig. 1 D). To assess whether triggering the MDL-1 receptor could activate myeloid cells, we generated mAbs that are capable of cross-linking and promoting MDL-1 activation. To test the antibody specificity and function, we performed a bioassay where cellular degranulation can be triggered by MDL-1/DAP12 phosphorylation (see Materials and methods). Treatment of an MDL-1/DAP12-transfected mast cell line with an anti–MDL-1 mAb (clone DX163) induces specific degranulation, demonstrating that clone DX163 is an agonistic mAb that activates the MDL-1–DAP12 signaling pathway (Fig. S1). We next confirmed the activities of the anti–MDL-1 mAb in primary cells. Wild-type, but not Dap12−/−, macrophages produced inflammatory mediators in response to anti–MDL-1 treatment. TNF, G-CSF, IL-1β, and MCP-1 (Fig. 1 E and not depicted) were up-regulated by anti–MDL-1 antibodies, and this was further enhanced in the presence of LPS, a TLR-4 agonist.
The Mdl1 mRNA expression in bone marrow and synovium prompted us to determine which cell types might express this immune regulator in human RA tissue. We found that MDL-1 is highly expressed on myeloid cells in the inflamed pannus. We also observed the same expression pattern in mouse inflamed joint (not depicted). The expression of MDL-1 appears to colocalize with a subset of CD68+ inflammatory macrophages, as indicated by the immunostaining of serial sections from synovial RA samples (Fig. S2). To confirm colocalization of MDL-1 with myeloid cells in inflamed pannus, we performed immunofluorescent staining with anti–MDL-1 (phycoerythrin) and CD11b (FITC). Interestingly, most, but not all, of the CD11b+ cells also coexpress MDL-1 as shown in the merged immunofluorescent images, which appeared yellow (Fig. S2).
Given the expression pattern of MDL-1 in joint tissues, we examined its expression on leukocytes during a collagen antibody-induced arthritis (CAIA) model. This disease is induced by passive transfer of type II collagen-specific antibodies and requires direct myeloid cell activation to promote pathology. We found that CD11b+ Ly6G+ MDL-1+ cells increased from 35 to 50% in the bone marrow 7 d after arthritis induction. Similarly, MDL-1+ cells in peripheral blood increased from 25% in controls to 40% in arthritic mice (Fig. S3). We next determined the function of MDL-1 in CAIA using anti–MDL-1 agonist mAbs that specifically cross-link and activate the MDL-1 receptor pathway. Mice given anti–MDL-1 agonists in conjunction with the arthrogenic antibody cocktail exhibit increased disease incidence and severity (Fig. 2 A). Anti–MDL-1 treatment promoted an increase in the total number of bone marrow CD11b+ Ly6G+ granulocytes and CD11b+ Ly6G− monocytes compared with isotype-treated controls (Fig. 2 B). This increase correlated with higher levels of total MPO activity in the bone marrow (not depicted) and elevated circulating peroxidase-positive (%HPX) neutrophils and monocytes (Fig. 2 C and not depicted), indicating that activation of MDL-1 promoted expansion of “reactive” myeloid cells capable of inducing tissue damage. As early as 1 d after disease onset, anti–MDL-1 agonist-treated mice already showed greater clinical scores compared with the isotype control group. By day 4, histopathology shows a dramatic increase in neutrophil infiltration into the arthritic paws of anti–MDL-1–treated mice (>60% PMNs) compared with isotype-treated controls (20% PMNs), which corresponds with intense cartilage damage, bone erosion, and pannus tissue formation (Fig. 2, D and E). By day 11, the extent of damage in the anti–MDL-1 treatment group is remarkable, with near maximum pathology scores for inflammatory cell infiltrate, articular cartilage destruction, and almost complete cortical bone erosion of the metatarsal-phalange joints. To assess the roles of granulocytes/monocytes in this MDL-1–driven disease, mice were given anti-GR1 mAb, which depletes Ly6G+ granulocytes and a subset of Ly6G+/Ly6C+ monocytes. In vivo depletion was confirmed by flow cytometry shown in Fig. S4. Mice given anti-GR1 treatment 1 d before induction of MDL-1–driven CAIA showed significant disease amelioration, indicating that GR1-positive myeloid cells play an important role in promoting MDL-1–activated joint inflammation (Fig. 2 F).
We also assessed the role of MDL-1 receptor in collagen-induced arthritis (CIA), which is a T, B, and myeloid cell–dependent model of arthritis. Mice were immunized with type II collagen and treated with anti–MDL-1 agonist mAb on the day of clinical disease onset (day 18 after collagen immunization). 2 d after MDL-1 activation, we already noticed enhanced joint swelling response. The disease quickly progressed to a very severe form of arthritis (Fig. S5). These results prompted us to investigate whether specific blockade of MDL-1 could inhibit inflammatory joint disease.
Based on the association of DAP12 and MDL-1 with joint diseases, we determined if blockade of this innate inflammatory pathway could attenuate myeloid cell–mediated joint inflammation and bone erosion. Mice were generated in which all six exons of Mdl1 were deleted via homologous recombination using C57BL/6 embryonic stem cells (Fig. S6). Successful deletion of Mdl1 was confirmed by PCR and flow cytometry. Mdl1−/− mice are viable and born in the expected Mendelian ratios. The number of myeloid and lymphoid cell subsets is similar in Mdl1−/− and wild-type mice (unpublished data). CAIA disease incidence and severity of both Dap12−/− and Mdl1−/− are reduced compared with wild-type mice (Fig. 3 A). In addition, analysis of proinflammatory cytokines and osteoclast markers in arthritic paws show a protective effect of deleting Mdl1 and Dap12 (Fig. 3 B). The absolute values of these inflammatory genes in arthritic and naive control paws are shown in Fig. S7.
Because the endogenous ligand for the MDL-1 receptor has not been identified, we generated a soluble MDL-1 molecule, which would be expected to engage the ligand and inhibit the in vivo activities of MDL-1. This soluble MDL-1 antagonist is composed of a murine FcγRI binding-deficient mutant IgG2a covalently linked to the extracellular portion of MDL-1 (MDL-1–Ig fusion protein). MDL-1–Ig fusion–treated mice were highly resistant to both CIA and CAIA compared with controls (Fig. 3, C and D). In the CIA study, the MDL-1–Ig-fusion treatment was initiated at day 18 when ~40% of the mice (n = 29 from 2 studies) already showed initial clinical signs of disease. Strikingly, only a few days after MDL-1–Ig treatment, the arthritic mice already demonstrated clinical improvement. This contrasts with the rapid disease progression observed in isotype controls and anti–MDL-1 agonist–treated mice (Fig. 3 C). In CAIA studies, MDL-1–Ig treatment also displays similar protection from disease (Fig. 3 D). Histopathological assessment of hind paws showed the isotype control group have mild cellular infiltrate and bone erosion, whereas mice treated with the MDL-1–Ig fusion protein have little or no pathological signs of disease (Fig. S8).
We confirmed the histopathology findings and quantified the magnitude of bone destruction using x-ray microCT analysis. The bone mineral density and the bone structural changes of articular phalangeal joints were assessed at day 11 after CAIA induction. Fig. 4 A shows high resolution three dimensional rendering of microCT scans of hind paws. Anti–MDL-1 agonist treatment induces considerable cortical bone destruction, whereas MDL-1–Ig fusion protein—which functions as an effective antagonist—dramatically blocks bone erosion. Although histopathology findings show intense cortical bone erosion at the joint space of anti–MDL-1–treated mice, the microCT three dimensional image reconstruction produced images suggestive of metaphyseal damage. This may be because if the rendering of a three dimensional dataset into a two dimensional picture and is consistent with previously published MicroCT results in mouse arthritis models (Barck et al., 2004). To quantify the extent of the bone destruction, we performed histomorphometric analysis of cortical bones and determined that MDL-1 agonist mAb-treated mice show substantial loss of bone volume, bone density, and cortical thickness compared with the moderate changes in the Ig control groups (Fig. 4 B). In contrast, MDL-1–Ig fusion–treated mice have bone integrity, density, volume, and bone mass values that are nearly comparable to healthy naive mice, confirming that blocking MDL-1 receptor activation maintains joint integrity. It has been shown that circulating levels of TRAP 5b are proportional to the number of osteoclasts (Scarnecchia et al., 1991; Henriksen et al., 2007). By testing serum samples during the course of disease, we found that the osteoclast-specific TRAP 5b levels were significantly increased after MDL-1 receptor activation (Fig. 4 C). The elevated TRAP 5b levels correlate with the enhanced bone erosion in the anti–MDL-1–treated mice. RANKL levels are also increased in anti–MDL-1 agonist–treated mice, whereas MDL-1-Ig fusion–treated mice have levels comparable to naive animals.
To investigate the immune responses regulated by MDL-1 activation, we assessed the expression of proinflammatory cytokines, osteoclast markers, and myeloid cell markers in arthritic paws. On day 4 after induction of CAIA, which is just before the peak of paw swelling response in the control groups, proinflammatory genes including IL-1β, IL-6, and IL-17 are suppressed in MDL-1–Ig fusion protein–treated mice, whereas the anti–MDL-1–treated group show enhanced cytokine gene expression (Fig. 5 A). Importantly, genes associated with bone destruction such as RANKL, MMP9, ATPV0D2, and TRAP are down-regulated in paws after MDL-1–Ig fusion treatment and up-regulated in anti–MDL-1 agonist treatment. Also, myeloid cell–specific genes including CD11b, RANK, and DAP12 are reduced in the MDL-1–Ig fusion group and elevated in anti–MDL-1 agonist group. In addition, CXCL1, which promotes neutrophil recruitment, is also up-regulated by the MDL-1 agonist. We also determined the gene expression of arthritic paws at day 11 and found similar patterns (unpublished data). Interestingly, even through MDL-1 activation enhanced TNF, IL-6, RANK, and TRAP expression, both type I and II IFNs were undetectable in the inflamed paws (the Q-PCR cycle threshold is ~40), consistent with the concept that MDL-1 is linked with the TNF–RANKL pathway rather than the IFN–STAT1 pathway that inhibits bone resorption mechanisms.
The apparent regulation of the TRAP, RANKL, ATPV0D2, and MMP9 expression after anti–MDL-1 treatment suggests MDL-1 receptor activation may promote osteoclast development and function. To test this, we treated wild-type bone marrow cells with an anti–MDL-1 agonist in the presence of RANKL (10 ng/ml). MDL-1 activation increases the kinetics of cell fusion, resulting in greater size and frequency of mature osteoclasts (Fig. 5 B). These results suggest MDL-1 activation promotes in vitro osteoclastogenesis and cell fusion. TRAP and cathepsin K are osteoclast-specific genes regulated by the NFATc1 transcription factor (Matsumoto et al., 2004; Takayanagi, 2005a). To determine whether MDL-1 directly regulates NFATc1, anti–MDL-1–activated bone marrow cells were prepared for NFATc1 nuclear lysate ELISA. MDL-1 + RANKL induced a significant increase of phospho-NFATc1 nuclear localization over RANKL alone, indicating that MDL-1-DAP12–mediated signaling promotes amplification of this transcription regulator required for osteoclast differentiation (Fig. 5 C). These in vitro osteoclast functional assays, together with our in vivo observations that blockade of MDL-1 function reduces autoimmune joint inflammation and bone erosion, suggest that MDL-1 plays a critical role in joint diseases.
In this study, we have identified MDL-1 receptor as a key mediator of autoimmune joint inflammation. It appears that MDL-1 activation contributes to two distinct cellular mechanisms of tissue destruction. Not only does MDL-1 activation recruit substantial numbers of bone marrow–derived inflammatory macrophages and neutrophils, it also promotes osteoclast activation. Depletion of circulating granulocytes and/or monocytes significantly reduces MDL-1–dependent joint inflammation during CAIA, suggesting that inflammatory macrophages and neutrophils play a key role in MDL-1–mediated pathology. Direct Blockade of MDL-1 function also down-regulates paw swelling responses and inhibits pannus tissue formation while preserving bone volume and mineral density. We also demonstrate that MDL-1 activation increases the expression of NFATc1 and ATPV0D2, which control cell fusion (Lee et al., 2006), as well as regulating bone resorption via TRAP and cathepsin K in osteoclasts (Takayanagi, 2005a). These results suggest that targeting the MDL-1 pathway may modulate several important biological processes that control bone metabolism and inflammatory bone disease.
Previous studies have shown that the pairing partner of MDL-1 receptor—DAP12 has important roles in bone metabolism. Patients with loss of function mutations in DAP12 present with polycystic lipomembranous osteodysplasia and sclerosing leukoencephalopathy, also known as Nasu-Hakola disease. In a linkage disequilibrium analysis, Paloneva et al. (2000) mapped this disease to a 1.8-Mb region of chromosome 19Q13.1. Sequencing the candidate genes in this region revealed Dap12 to carry several disease-associated variants, including a homozygous deletion encompassing exons 1–4. Nasu-Hakola disease is characterized by lipid-filled bone cysts found in articular joints of young adult patients, which leads to bone pain and fractures (Mii et al., 1991). These patients also show signs of presenile dementia associated with loss of myelin in the frontal lobe in addition to the osteoporotic features. However, peripheral blood mononuclear cells from the Dap12-deficient patients exhibit a delayed differentiation of osteoclasts with reduced bone resorption capability (Paloneva et al., 2003). The reduced in vitro osteoclast activity does not match the decreased trabecular bone density in Dap12-deficient patients (Paloneva et al., 2001). In preliminary trabecular bone measurement studies, we found differences between Dap12−/− and Mdl1−/− mice. Consistent with previous studies (Humphrey et al., 2004, 2006), Dap12−/− mice show mild osteopetrosis. Unexpectedly, Mdl1−/− mice show a dysregulated bone phenotype with irregular trabecular bone connectivity (unpublished data). Future studies are needed to address the relative contribution of MDL-1 and DAP12 in bone homeostasis.
Although the endogenous ligands for the MDL-1 receptor have not been identified, a recent study has demonstrated that the dengue virus capsid protein activates the MDL-1–DAP12–ITAM pathways leading to intense immune pathologies during the viral infection (Chen et al., 2008). The hallmarks of dengue “break-bone” fever are cytokine storm, vascular leakage, and severe joint pain (Mathew and Rothman, 2008). Intriguingly, in a mouse model of dengue hemorrhagic disease, specific blockade of MDL-1 receptor inhibited the cytokine storm and vascular leakage. This tissue damage is associated with excessive IL-6, TNF, and MIP-1a production without affecting IFN-α production (Chen et al., 2008). This is consistent with our observation that MDL-1 activation induced TNF, IL-1β, IL-6, (which is linked with NF-κB, TRAF6, and STAT3 activation) but not IFN-α and IFN-γ (STAT1 activation). Resent studies have shown that both type I and II IFNs have profound STAT1-dependent inhibitory effects on immune-mediated arthritis and osteoclast formation (Takayanagi et al., 2005b). This is consistent with our observation that MDL-1 expression on myeloid cells is enhanced by TNF but not IFN-γ (Fig. 1).
A recent study has uncovered the molecular basis for TNF-dependent bone resorption versus tissue inflammation (Ochi et al., 2007). TNF was shown to promote bone loss by inducing osteoclast expression of paired Ig-like receptor A (PIR-A), which partners and signals via ITAM-containing Fc receptor γ (FcRγ). This induced accelerated osteoclastogenesis, which correlated with enhanced bone destruction and osteoporosis. Interestingly, when the PIR-A–FcRγ pathway was inhibited, TNF still promoted soft tissue inflammation, but not bone resorption. In this study, we show that blocking MDL-1–DAP12 predominantly reduced tissue inflammation by reducing TNF, IL-1β, and IL-6 secretion and neutrophil/macrophage infiltration. Further studies are required to confirm the MDL-1–intrinsic role of osteoclast development and bone resorptive function.
It is increasingly evident that merely targeting inflammation alone may not be an adequate treatment for many types of joint disorders because bone resorption is an integral part of these diseases. Therefore, new therapeutic strategies need to incorporate both antiinflammatory and antiresorptive activities. The possibility that MDL-1 may regulate both inflammatory and bone resorptive mechanisms makes this a promising target for treatment of inflammatory arthritis. We have bridged the findings in our mouse studies to human diseases by demonstrating human MDL-1 expression in synovial tissues from RA patients. Further clinical studies are needed to confirm a pathogenic role for MDL-1 in human skeletal disorders and to determine whether this DAP12-paring receptor is a therapeutic target for treatment of inflammatory and/or degenerative bone disorders.
MDL-1 (GenBank/EMBL/DDBJ accession no. BC112099). Anti–mMDL-1 agonist (clone: DX163) was generated from rats using immunogenic fusion proteins consisting of the extracellular domain of the mouse MDL-1 gene, including the amino acid positions 26–166 (GenBank/EMBL/DDBJ accession no. AF139769). Both anti–MDL-1 mAbs are IgG1 isotype. Mouse MDL-1 fusion protein was generated as follows: extracellular (163 amino acids) portion of mouse MDL-1 (GenBank/EMBL/DDBJ accession no. AA186015) was ligated into a pCMV1 expression plasmid containing the Fc portion of mIgG2a that has been mutated (L to E) for low FcγRI binding properties. Protein was expressed in 293 freestyle cells.
Human synovial samples were obtained under informed consent from RA patients under a protocol approved by the Stanford University IRB and performed at the Stanford University Hospital. For the human anatomy panel, depending on the collection protocols established at each site, tissues were acquired either under IRB-approved waiver of consent (NDRI and CHTN) or by informed consent (PAH, Zoion, Ardais, and AGF). All samples have been rendered anonymous, so investigators have no ability to identify the patients. Normal human tissues were obtained from patients undergoing routine surgery (multiple tissue, NDRI; stomach, Ardais Corporation; and colon, Cooperative Human Tissue Network), from short hour autopsy (≤ 5 h, multiple tissues; Zoion Diagnostics), and from transplant donors (lung, Anatomical Gift Foundation, Hanover, MD). All surgical samples were frozen as quickly as possible, typically within an hour of excision. The majority of samples were accompanied by demographic information and pathology reports.
All human tissue experiments were performed in accordance with animal care and use committee–approved protocols. Immunohistochemistry was performed on frozen OCT embedded RA and OA synovia. 8-µm sections were fixed in acetone-methanol-hydrogen peroxide, and blocked with FCS-BSA-rat serum. Tissues were further blocked with avidin (Vector Laboratories) for 15 min and biotin (Vector Laboratories) for another 15 min. Sections were stained with anti–hMDL-1 mAb (clone DX245), anti-hCD68, or isotype control rat antibodies for 3 h and fixed with 1% paraformaldehyde. Tissues were washed and incubated with biotinylated rabbit anti–rat antibodies for 1 h, and Vectastain ABC elite horseradish peroxidase (HRP) complex for 40 min. Cell surface markers (MDL-1 and CD68) were visualized with Nova Red (Vector Laboratories) substrate and counterstained with methyl green.
All animal experiments were performed in accordance with institutional animal care and use committe–approved protocols. Arthritis was induced in 8–16-wk-old (age-matched for a given study) male B10.RIII (Jackson ImmunoResearch Laboratories) with an arthritogenic anti-type II collagen mAb cocktail purchased from Chemicon International or Chondrex. B10RIII mice received 1–1.5 mg of anti-CII mAb cocktail i.v. on day 0. Mice were then treated s.c. with 0.5–1 mg of anti–MDL-1 or IgG1 isotype control. Alternatively, mice were treated s.c. with 0.5 mg of MDL-1 Ig-fusion protein or Ig-fusion control protein at day 0, 2, and 4. C57BL/6 mice received 5 mg arthrogen on day 0 and 10–50 µg of E. coli–derived LPS on day 2. Mice were monitored daily for foot pad swelling through day 11 or up to day 21.
12-16-wk-old B10RIII mice were immunized with 1 mg of bovine type-II collagen in a complete Freund’s adjuvant (Difco) emulsion containing 2 mg/ml H37RA (Chondrex). Initial incidence of disease occurred at day 18 in 33–50% of all mice. On day 18, mice were given a single dose of 0.5 mg of anti–MDL-1 agonist or IgG1 isotype control. MDL-1 Ig-fusion protein (antagonist) or its corresponding mutant mouse Ig-fusion protein control were dosed every other day (starting on day 18) for a total of 6 doses. Mice were monitored for paw swelling through day 35. Paw swelling was measured daily after induction of arthritis. The severity of the disease was graded on a 0–3 scale per paw as follows: 0, normal; 1, swelling of one digit; 2, swelling of two or more digits; 3, swelling of the entire paw. The maximal clinical score per mouse was 12.
12-wk-old B10.RIII mice were dosed s.c. with 0.5 mg of anti-GR1 antibody (clone RB6-8C5) or IgG2b isotype control on day −1 before arthritis induction. Mice were given two subsequent s.c. doses of anti-GR1 or isotype on day 2 and 5 after disease induction.
The paws were removed, fixed, decalcified in Cal-EX II (Thermo Fisher Scientific) for 7 d, and embedded in paraffin. Subsequently, the paw sections were stained with hematoxylin and eosin and examined by light microscopy. A histological analysis of synovial, bone, and cartilage tissues was performed as a blind test. Leukocyte infiltration and percentage of PMNs infiltration were determined in the synovium and joint space. Pannus tissue formation, cartilage destruction, and cortical bone erosions were assessed. The severity was graded on a scale of 0–4. Comparisons between groups were assessed with the two-tailed unpaired Student’s t test with a P value of <0.05 considered as statistically significant. Calculations were performed with the statistical package, GraphPad Prism 4 (GraphPad Software, Inc.).
Histopathology scoring criteria is as follows. Inflammation in synovium and/or joint space: 0 = no inflammation, +1 = minimal, +2 = mild, +3 = moderate, +4 = severe; fibrosis (periarticular or pannus formation): +1 = minimal, +2 = mild, +3 = moderate, +4 = severe; percent PMNs: 1 = <20%, 2 = 20–40%, 3 = 40–60%, 4 = >60%; articular cartilage damage (destruction/pitting): +1 = minimal, +2 = mild, +3 = moderate, +4 = severe; cortical bone erosions/periosteal bone or cartilage proliferation: 0 = normal bone, +1 = minimal erosions, +2 = mild erosions, +3 = moderate, +4 = severe.
Macrophage cultures were generated from C57BL/6 or B10.RIII mice. Bone marrow was extracted from the femurs and tibias of 8–12-wk-old week animals. Cells were cultured for 1–5 d in basal macrophage growth medium, which is comprised of α-Mem media (Invitrogen), supplemented with 10% heat-inactivated fetal bovine serum, 100 IU/ml penicillin, 100 µg/ml streptomycin, 1 mM sodium pyruvate, 2 mM glutamine, and 50 ng/ml of recombinant MCSF (R&D Systems). Bone marrow–derived cells were cultured in various conditions and stained with biotinylated anti–MDL-1 (clone DX192). Samples were analyzed by FACSCalibur and FlowJo software (BD).
Osteoclasts were differentiated from bone marrow cells after 3 d culture in basal macrophage medium. Adherent cells were plated at 1– 5 × 105 per ml in 6-well tissue culture plates and were treated with murine RANKL (10–50 ng/ml) and anti–MDL-1 or isotype control mAb at (10 µg/ml). Anti–MDL-1 activated cells were evaluated for osteoclast formation, gene expression, and TRAP staining (Acid phosphatase staining kit: Sigma) after 6–8 d in culture.
NFATc1 is dephosphorylated upon activation by calcineurin in the cell cytoplasm and then translocated to the nucleus. To determine the ability agonist MDL-1 mAb to activate nuclear migration, 2 × 107 murine bone marrow cells were cultured in 10-mm dishes with 50 ng/ml of MCSF, 50 ng/ml of MCSF plus 30 ng/ml RANKL, and either 10 µg/ml of IgG1 isotype or anti–MDL-1 agonist antibody. Nuclear lysates were prepared from cells harvested at day 6 as described in Active Motif’s nuclear extract kit. Nuclear samples were quantified by Bradford protein determination using lysis buffer as the diluent. 1-µg protein samples were run in duplicate on the NFATc1 assay. Plates were coated with an immobilized NFAT oligonucleotide consensus sequence (5′-AGGAAA-3′). The primary antibody specifically binds the accessible epitope on the NFATc1 protein. Secondary HRP-conjugated antibody allows colorimetric readout. Samples were visualized using SpectraMax (Molecular Devices) plate reader at 450 nm with a reference wavelength of 655. Samples were analyzed using SoftMax pro software (Molecular Devices), and nuclear activation was assessed as compared with a titration PHA-activated Jurkat nuclear extract control.
Blood samples were collected by cardiac puncture from euthanized mice. Serum was separated using serum separation tubes (Sarstedt) centrifuged at 6,000 g. Supernatants were collected from cell cultures and all samples were frozen at −80°C and thawed to room temperature before analysis. Protein and cytokine levels were analyzed by Luminex multiplex assays (LINCO Research). Murine serum TRAP 5b levels were ascertained by enzyme activity assay. (IDS, Inc.). Serum RANKL levels were determined by ELISA (R&D System).
For gene expression analysis, total RNA was isolated using RNA STAT-60 (Tel-Test). Total RNA (5 µg) was subjected to treatment with DNase (Roche). DNase-treated total RNA was reverse-transcribed using Superscript II (Invitrogen). Primers were designed using Primer Express (PE Biosystems) or obtained commercially from Applied Biosystems. Real-time quantitative PCR on 10 ng of cDNA from each sample was performed using either of two methods. In the first method, two gene-specific unlabeled primers were used at 400 nM in a Perkin Elmer SYBR green real-time quantitative PCR assay using an ABI 5700 instrument. In the second method, two unlabeled primers at 900 nM each were used with 250 nM of FAM-labeled probe (Applied Biosystems) in a TAQMAN real-time quantitative PCR reaction on an ABI 7700 sequence detection system. The absence of genomic DNA contamination was confirmed using primers that recognize genomic regions of the CD4 promoter; samples with detectable DNA contamination by real-time PCR were excluded from the study. Ubiquitin levels were measured in a separate reaction and used to normalize the data by the Δ − Δ Ct method, using the mean cycle threshold (Ct) value for ubiquitin and the genes of interest for each sample; the equation 1.8 e (Ct ubiquitin − Ct gene of interest) × 104 was used to obtain the normalized values.
Mice were prepared for microCT analysis 14 d after CAIA disease induction. Hind paws were removed and fixed in 10% neutral buffered formalin. Before CT scanning, paws were washed with running water for 15 min. The imaging of three-dimensional microcomputed tomography was performed with GE eXplore Lotus micro-CT scanner (GE Healthcare). Data were acquired at 27 µm isotropic voxel size with 720 projections by 360-degree scan, integration time of 2,000 ms with three frames, photon energy of 80 KeV, and current of 450 uA. The duration of imaging time was ~100 min per scan and followed by 1 h of projection correction and volume reconstruction of three-dimensional representation. Three-dimensional render images of hind paws were generated through original volumetric reconstructed images by MicroView software (GE Healthcare).
The whole hind paw was scanned to quantify the histomorphometric measurements of the tarsal bones and of the metatarsal phalangeal joint. A three-dimensional region of interest (ROI) 3.2 × 2.0 × 1.8 mm3 volume area was drawn to contain the second, third, and fourth metatarsal phalangeal joints. The profile of voxel densities changed dramatically in the mouse CAIA arthritic joint as inflammation-driven bone resorption gave rise to replacement of dense bone with less dense pannus tissue. The most high-density bone was lost in the metatarsal phalangeal joints of severely inflamed mouse CAIA paws. The greater proportion of “lower density bone” from 800–2,000 HU is caused by demineralization of a percentage of high-density bone within a voxel that gives rise to a lower density voxel after chronic inflammation. Four parameters were assessed to quantify the magnitude of bone loss: the total volume of bone (bone volume; BV), the total bone mineral content, represented by bone mass (bone mineral content; BM), and then the mean density of the bone (bone mineral density; BMD). BMD is the mass (BM) divided by the volume (BV). Total BV measurements in the metatarsal phalangeal joints encompass regions of trabecular and cortical bone. Mean cortical thickness analyses were performed using MicroView 2.2 software package to measure metatarsal phalangeal joint.
Murine blood was harvested by cardiac puncture and collected in EDTA tubes (Terumo Medical Corp.) Blood samples were processed with Advia 120 Automated Hematology Analyzer. Percentage of monocytes, neutrophils, and high peroxidize positive (percentage of HPX) cells were compared with naive control mice.
Fig. S1 demonstrates a mast cell degranulation assay detecting the specific agonist activity of MDL-1. Fig. S2 shows micrographs of human RA synovial tissue stained for myeloid cell markers and MDL-1. Fig. S3 shows murine bone marrow and peripheral blood have increased numbers of MDL-1 positive cells after CAIA induction. Fig. S4 confirms depletion of a CD11b+ subset from blood after treatment with anti-GR1 antibody in CAIA. Fig. S5 shows collagen induced arthritis is exacerbated by agonist MDL-1 antibody treatment. Fig. S6 depicts the Mdl1 −/− mouse gene targeting strategy. Fig. S7 shows the normalized gene expression values for WT, Mdl1 −/−, and Dap12 −/− mice in CAIA model. Fig. S8 shows H&E staining from hind paws of mice in CAIA model where mice were treated with MDL-1 agonist and antagonist reagents. Online supplemental material is available at http://www.jem.org/cgi/content/full/jem.20090516/DC1.
We thank Dr. Craig A. Murphy for sharing his expertise in animal arthritis models. We thank Dr. Stuart Goodman for providing the RA synovial tissues. We also thank Drs. Mandy McGeachy and Cristina Tato for helpful discussion.
This study was funded by Schering-Plough Corporation.
The authors have no conflicting financial interests.