
2023 Impact Factor
Department of Biomedical Laboratory Science, Namseoul University, Cheonan 330-707, Republic of Korea
We tested the hypothesis that micro-computed tomography (micro-CT) analysis provides a better quantitative readout of the therapeutic potential of methotrexate (MTX) for treating collagen-induced arthritis (CIA) in rats and compared to conventional histopathological examination. Rats were divided into three groups: Group 1 (G1) was treated with 0.9% saline, whereas groups 2 (G2) and 3 (G3) were boosted with type II collagen at days 0 and 7. Following the first collagen immunization, rats in G1 and G2 were treated with 0.9% saline and those in G3 were treated with 1.5 mg/kg MTX from day 14 to 28. All rats were sacrificed on day 28, at which point and all hind knee joints were analyzed by micro-CT and histopathological examination. Micro-CT analyses showed that bone volume and trabecular number were significantly decreased in G2 and G3 compared to G1 (
Rheumatoid arthritis (RA) is a chronic inflammatory disease caused by immune reactivity that results in joint destruction and chronic pain (Scott
Autoimmune arthritis is induced by immunization with an emulsion of complete Freund’s adjuvant and type II collagen (Brand
Oral administration of methotrexate (MTX) is widely used method of treating arthritis (Weinblatt
To assess arthritis in joint lesions, the combination of advanced imaging with three-dimensional systems and intravital animal models may provide more informative and disease-relevant platforms (Conway
We tested the hypothesis that micro-CT analysis provided a better quantitative readout of the therapeutic potential of MTX in a rat CIA model and compared to conventional histopathological examination.
Twenty-four female Wistar rats (8 weeks old) were obtained from Orient Bio (Kapyung, Korea) and acclimated for 7 days prior to the study. Rats were maintained in a temperature-controlled environment (22 ± 3°C), 55 ± 5% relative humidity under a 12-h light/dark cycle. Rats were fed a rodent diet and filtered water
Rats were randomly divided into three groups. Rats in group 1 (G1) were treated with 0.9% saline and those in groups 2 (G2) and 3 (G3) were boosted with type II collagen at days 0 and 7 to induce arthritis. Briefly, bovine type II collagen (Chondrex, Redmond, WA, USA) was dissolved in 0.01 M acetic acid overnight at 4°C. Then the mixture was emulsified in an equal volume of incomplete Freund’s adjuvant (Chondrex). Rats in G2 and G3 were immunized intradermally at the tail base with 0.1 mL of emulsion containing 100 μg type II collagen. From day 14 to 28, rats in G1 and G2 were treated orally with 0.9% saline, and those in G3 were treated orally with 1.5 mg/kg MTX. All rats were sacrificed on day 28 after the first collagen immunization, and all hind knee joints were fixed in 10% neutral phosphate-buffered formalin. Then, micro-CT and histopathological analyses were performed. This study was approved by the animal experiment committee of Namseoul University based on the Animal Protection Act.
Quantitative analysis of hind knee joints was performed using a micro-CT system (Skyscan 1172, Bruker, Kontich, Belgium). Specimens were scanned using micro-CT with an X-ray source of 40 kV/250 μV, pixel size 23 μm, and a 0.5 mm aluminum filter. After scanning, cross-sectional slices were reconstructed and each scan result was reconstructed using the 0–0.14 threshold values to distinguish bone from air.
Three-dimensional analysis was performed using CTAn software (Bruker). The fraction of bone volume, percent bone volume, trabecular number, trabecular thickness, bone surface/bone volume and trabecular separation were performed using the built-in software. In addition, osteophytes within each contiguous coronal image section were manually outlined and their volumes were calculated using CTvol software (Bruker).
Hind knee joints were fixed in 10% phosphate-buffered formalin for 24 h and decalcified in 14% EDTA-glycerol for 14 days at room temperature. Samples were routinely processed and embedded in paraffin, and 4 μm sections were stained with hematoxylin and eosin (H&E) for histopathological examination. For cartilage staining, safranin O-fast green was used on hind knee joints. Histopathological analysis of joints was performed to examine infiltration of inflammatory cells, cartilage degradation, bone destruction and synovial proliferation.
The avidin-biotin complex method was used to stain matrix metalloproteinase (MMP) in 4-μm joint sections. Sections were dewaxed with xylene and hydrated through a graded ethanol series, and incubated in hyaluronase (H3506, Sigma Chemical Co., St Louis, MO, USA) for 30 min. Then the sections were sequentially treated with 0.3% hydrogen peroxide, blocking serum, and anti-MMP-13 antibody (ab39012; 1:100; Abcam, Cambridge, MA, USA). Then they were washed with Tris-buffered saline containing Tween 20® (TBS-T) and subjected to ABC-peroxidase procedures (ABC Kit; Santa Cruz Biotechnology, Santa Cruz, CA, USA). Blocking serum, instead of primary antibody, was used as a negative control.
Immune complexes were visualized using 3,3′-diaminobenzidine tetrahydrochloride (DAB; D5637; Sigma-Aldrich, St. Louis, MO, USA) as the chromogen. Sections were counter-stained with Mayer’s hematoxylin to facilitate their examination under a light microscope.
Statistical analysis was performed using GraphPad Prism 6 (GraphPad Software, La Jolla, CA, USA). All data were analyzed using Dunnett’s multiple comparison test following one-way analysis of variance (ANOVA) and Student’s
X-ray, coronal and sagittal micro-CT images showed a normal joint appearance was shown in G1 rats and severe joint destruction was observed in G2 animals. Moreover, this joint destruction was also observed in G3 rats, although no difference in arthritic lesions was obvious in G3 compared to G2 (Fig. 1).
Micro-CT analysis revealed several altered bone parameters (Fig. 2). Bone volume (
No inflammation or tissue destruction was observed in G1. However, in G2 rats, knee joints showed severe joint destruction with inflammatory cell infiltration, and bone and enlarged cavities filled with synovial fibroblasts and inflammatory cells and these changes were also present in G3 animals. However, cartilage destruction was decreased in G3 rats compared to G2 (Fig. 3).
According to safranin O-fast green staining, normal cartilage structures of the joints were noted as red color in G1 animals. However, cartilage staining was remarkable reduced in G2. Although cartilage destruction was present in the joint surface, in G3 animals, safranin O-fast green staining was present around chondrocytes (Fig. 4).
With respect to MMP-13, there was no immunostaining in the joints of G1 animals. In G2 rats, MMP-13 was remarkably increased in the joint surface. However, MMP-13 in joint surface was decreased in G3 rats compared to G2 (Fig. 5).
Micro-CT analysis provided several quantitative parameters for evaluating MTX treatment of RA. It showed that bone volume, percent bone volume, and trabecular number were significantly decreased, and bone surface/bone volume was increased in CIA lesions compared to the control. These results suggest that bony parameters are altered following collagen treatment. However, MTX treatment did not result in therapeutic advantages at these bony parameters. The main therapeutic action of methotrexate was related to the inhibitory effects on the cascade of events initiated by inflammatory cytokines and subsequent joint-destructive enzymes. It was reported that trabecular thickness values was significantly increased in the MTX-treated groups compared to that of the
To evaluate disease-specific regional variables of interest, such as bone volume fraction and joint space, a consistent and reliable spatial sampling method was developed. In general, micro-CT has an advantage for bone detection over other methods. To quantify arthritis progression, micro-CT was utilized in this study. Micro-CT can measure joint space narrowing and reveal trabecular bone structure and osteophyte formation (Koba
Because micro-CT analysis somewhat limited for cartilage detection, H&E and safranin O-fast green staining were utilized. Normal cartilage structures were present in joints in control rats. However, cartilage staining was remarkably reduced in joints from rats treated with collagen. In G3 rats, H&E and safranin O-fast green staining showed that MTX treatment caused a slight reduction in cartilage destruction.
Histopathological examination also showed that knee joints of CIA rats exhibited severe joint destruction with inflammatory cell infiltration. As histopathologic examination provides qualitative or semi-quantitative information, there are some limitations for the quantification of lesions. In this study, MTX treatment did reduce cartilage destruction compared to CIA, although it did not result in therapeutic advantages in bone parameters
Because MMP, collagenases, and gelatinases are involved in joint destruction in arthritis (Ishikawa
While histopathological examination is a valuable method used to evaluate therapeutics (Gerwin
Overall, our results show that MTX treatment caused a reduction in cartilage destruction in rats with CIA, and micro-CT analysis made it possible to quantify bony lesions of arthritis. New technologies associated with histopathological examination should be applied to evaluate cartilage involved in arthritis lesions.
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