Purpose: Facet joint osteoarthritis may be a cause of low back pain in degenerative spine diseases such as lumbar spinal stenosis. While increased bone remodeling is a clinical hallmark of osteoarthritis, the trabecular bone structural parameters of osteoarthritic lumbar facet joints have not been characterized thus far. Interestingly, an age- and gender-specific decrease of trabecular number, thickness and volume fraction has been previously described for lumbar 4/5 facet joints of healthy individuals. Here, we sought to characterize trabecular bone structural parameters and subchondral bone-resident mesenchymal stromal cells (MSC) of osteoarthritic facet joints and compare these with regard to age, gender and healthy controls. Methods: Twenty-one patients scheduled for decompression and stabilization surgery for degenerative spinal stenosis were recruited for this study. Facet joint specimens were harvested during surgery and either fixed in formalin for microcomputed tomography (n = 15) or isolation of MSC by collagenase digestion (n = 6). MicroCT was performed spatial resolution of 20.5 μm. Bone volume fraction (BV/TV), trabecular thickness (Tb.Th), trabecular separation (Tb.Sp) and trabecular number (Tb.N) were evaluated using CT Analyser. Trabecular bone structural parameters of healthy subjects were taken from Wilke and co-workers (J. Anat. 2012). Statistical analysis of differences between gender and age groups (40–60 and 60–80 years) were performed using two-way analysis of variance (ANOVA). Early passage MSC were subjected to adipogenic and osteogenic differentiation for three weeks and evaluated using alkaline phosphatase assay, Alizarin red and Oil red O staining and RT-PCR. Results: Trabecular BV/TV was 0.36 ± 0.14 and 0.35 ± 0.17 for osteoarthritic lumbar facet joints of male and female individuals, respectively. Contrastingly, mean BV/TV in age-matched healthy controls was 0.32 (male) and 0.25 (female). Tb.Th was in the same range for both genders and age-groups (overall mean 0.20 ± 0.07 mm) and did not differ from healthy controls. The overall Tb.Sp averaged 0.52 ± 0.16 mm, which was lower than averages observed for age-matched healthy females (0.60) and males (0.71). Accordingly, Tb.N in osteoarthritic facet joints of male (1.9 ± 1.3/mm) and female (1.7 ± 0.8/mm) patients with lumbar spinal stenosis was higher than reported for healthy controls (1.5–1.0/mm). Statistical analysis did not reveal any age- or gender-specific differences in trabecular bone structural parameters of osteoarthritic lumbar facet joints. Facet joint MSC showed a strongly upregulated alkaline phosphatase activity upon adipogenic (8.1-fold) and osteogenic (4.6-fold) differentiation. Only a low number of lipid vacuoles were detected after adipogenesis. Alizarin red staining revealed varying degrees of in vitro matrix mineralization in MSC, which ranged from blunted to strong mineralization. Conclusions: Subchondral trabecular bone remodeling in lumbar facet joint osteoarthritis is characterized by an increase in bone volume fraction due to a higher trabecular number, but not an increase of trabecular thickness. MSC from osteoarthritic facet joints display impaired adipogenesis and abnormal mineralization during osteogenesis. These data provide a strong rationale for targeting increased bone remodeling in lumbar facet joint osteoarthritis.
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