- Research article
- Open Access
Expression of adiponectin in the subchondral bone of lumbar facet joints with different degrees of degeneration
BMC Musculoskeletal Disorders volume 18, Article number: 427 (2017)
Osteoarthritis research has been most commonly performed in the setting of the articular cartilage of the knee. To the best of our knowledge, no studies have evaluated the role of adiponectin in osteoarthritis of the lumbar facet joint (FJOA). Therefore, in this study, we explored whether adiponectin was expressed in the lumbar facet joints and evaluated the role of adiponectin in FJOA.
We enrolled patients who underwent lumbar computed tomography (CT) and magnetic resonance imaging (MRI) at the Orthopedic Department of the First Affiliated Hospital of Nanchang from May 2015 to June 2016. Lumbar facet joints were obtained from 135 patients at the time of lumbar fusion surgery and divided into three groups according to the Weishaupt grade. Cytokine levels in the subchondral bones were evaluated by enzyme-linked immunosorbent assays (ELISAs), and adiponectin levels were determined by immunohistochemistry, western blotting, and quantitative polymerase chain reaction (qPCR).
By ELISA, adiponectin levels were examined in the subchondral bone for lumbar facet joint, and adiponectin was found to be negatively correlated with BMI in 52 patients (p < 0.001, r = −0.861). By immunohistochemistry analysis, adiponectin was found to be expressed in the subchondral bone of the lumbar facet, whereas the cartilage area was negative for adiponectin expression. Immunostaining intensity and area was related to the degeneration of the lumbar facet joint, and, in our research, considerably decreased staining intensity and area were observed in more severely degenerated lumbar facet joints. Furthermore, the expression of adiponectin was also reduced in degenerated lumbar facet joints, and the level of decline corresponded to degeneration detected by western blotting and qPCR analysis (n = 27, p < 0.0001).
Adiponectin expression was observed in the subchondral bone of the lumbar facet joint and decreased as the degree of degeneration increased. Thus, the results of this study provide new insights into the relationship between adiponectin and osteoarthritis.
Lumbar facet joint osteoarthritis (FJOA) is present in approximately 40% of patients with low back pain [1,2,3]. Therefore, in addition to studies on disc degeneration, studies of FJOA are essential for the prevention of low back pain. The lumbar facet joint is a synovial joint composed of cartilage, synovium, and an articular capsule, and its characteristics are similar to those of other synovial joints, such as the knee [4,5,6]. However, most studies of osteoarthritis (OA) have focused on the knee joint [7,8,9,10]. Some studies have shown that knee OA may be a disease of the entire joint, including articular cartilage, subchondral bone, meniscus, ligament, and neuromuscular groups [11, 12]. Moreover, the subchondral bone plays a major role in knee joint degeneration. However, few studies have evaluated lumbar facet OA or the subchondral bone by basic research, with scholars instead focusing more on clinical research areas [13, 14].
In 2015, we reported a predictive experiment involving cytokine screening in five cases of lumbar facet joint specimens by RayBio® Human Inflammation Antibody Array G3. The screening results showed that interleukin (IL)-1β, TNF α and β, leptin, adiponectin, Chemokine (CCL)-11, CCL-24, colony stimulating factor (CSF)-2, CSF-3, intercellular adhesion molecule (ICAM-1), interferon (IFNg), IL-1–16, monocyte chemotactic protein (MCP), macrophage inflammatory protein (MIP), and others were detected in five cases of lumbar facet joint specimens. The authors discovered that adiponectin showed a strong positive reaction and high expression. Adiponectin is a cytokine secreted by adipose tissue [15, 16] and is abundantly expressed in the circulation in three different molecular forms: trimer, hexamer, and high-molecular-weight (HMW) species . Early studies have suggested that adiponectin plays a key role in the control of energy homeostasis because its plasma levels are inversely correlated with body mass index (BMI), intra-abdominal fat, and indices of insulin resistance [18, 19]. Therefore, adiponectin may be inversely correlated with OA because BMI is a risk factor of OA. In addition, Berner et al.  discovered that adiponectin and its receptors are expressed in bone-forming cells in mice and that adiponectin may affect bone metabolism. Moreover, Berner et al.  suggest that fatty acids have a regulatory effect on adiponectin mRNA expression, and fatty acids provide increased energy supply to cells and enhance adiponectin expression in osteoblasts. Coincidentally, Francin and Presle et al.  reported that the elevated level of adiponectin found in chondrocytes from patients with knee OA might contribute to matrix remodelling during OA; notably, the regulation of bone metabolism by adipokines is largely unknown, and the observed expression and secretion of adiponectin by bone-forming cells serves to add more complexity, as well as redundancy, to this intriguing issue. Therefore, the specific role of adiponectin in FJOA is still unclear and controversial.
Accordingly, in this study, we aimed to evaluate whether adiponectin was expressed in the subchondral bone of lumbar facet joints and to explore the role of adiponectin in FJOA.
Clinical samples and data
Subchondral bone was obtained from the lumbar facet joints of 135 patients (median age: 51.38 years; range: 16–77 years) at the time of lumbar fusion surgery. Additionally, BMI data of 60 of the patients (BMI: 19.4–33.8 kg/m2; mean 23.85 kg/m2),which were part of the 135 patients, were collected to examine the release of adiponectin from the subchondral bone of the lumbar facet joint in relation to BMI. Thirty-two normal facet joint specimens were obtained from L3-L5 vertebral fracture decompression or fusion surgeries, and 103 degenerative samples were obtained from L3-S1 single segment lumbar disc herniation fusion surgeries (60 for ELISAs, 48 for immunohistochemical analysis, and 27 for qPCR and western blotting). Samples were stored at −80 °C after surgery until use. All samples were obtained from the Orthopedic Department of the First Affiliated Hospital of Nanchang University from May 2015 to June 2016. All lumbar facet joints were grouped according to the Weishaupt  grade, as determined by computed tomography (CT) and magnetic resonance imaging (MRI), as follows: 0, normal; 1, slight degeneration; 2, moderate degeneration; 3, severe degeneration (Fig 1). Lumbar facet joints were divided into three groups (normal group [NG]: grade 0; degeneration group [DG]: grades 1 or 2; severe degeneration group [SDG]: grade 3) according to computed tomography (CT) and magnetic resonance imaging (MRI) results based on Weishaupt grading because of subjective interference in grades 1 and 2 .
Inclusion criteria were as follows: L3-L5 vertebral burst fracture or L3-S1 lumbar disc and facet joint degeneration; no history of spinal surgery; underwent lumbar CT and MRI examination. The exclusion criteria were as follows: lumbar spondylolisthesis, scoliosis, lumbar spine infection, spinal tumors and other spine-related diseases; diabetes, hypertension, and other relevant medical history; history of smoking or alcoholism; psychological disorders, mental disorders, or drug use and other history. The study protocol was approved by the Institutional Review Board of the First Affiliated Hospital of Nanchang University, and written informed consent was obtained from all study participants.
Screening of chemical factors by ELISA
Lumbar facet joint samples were obtained from 60 patients (NG, n = 11; DG, n = 34; SDG, n = 15; BMI: 19.4–33.8 kg/m2; mean 23.85 kg/m2). After washing the lumbar facet joint in sterile phosphate buffered saline (PBS), full-depth standardized subchondral bones (120 mg for each specimen) were collected using a scalpel. The subchondral bone (30 mg) was ground with liquid nitrogen into a powder, which was mixed with 1000 μL tissue lysis solution. Then, tissue debris was removed by centrifugation at 12,000×g at 4 °C for 15 min. In addition, 800 μL supernatant samples were obtained. ELISA kits (RayBiotech, Inc.) were used to quantify IL-1β, TNF-α, leptin, and adiponectin in supernatants after centrifugation. Briefly, eight steps were performed according to the instructions of ELISA kits. Finally, the absorbance of the sample was measured at 450 nm. The mean absorbance for each set of duplicate standards, controls, and samples was calculated, and the average zero standard optical density was subtracted. The standard curve was plotted on log-log graph paper, with the standard concentration on the x-axis and the absorbance on the y-axis.
Assessment of adiponectin expression by immunohistochemistry
The lumbar facet joint samples were obtained from 48 patients (NG, n = 12, median age: 45.56 years; DG, n = 12, median age: 47.33 years; SDG, n = 24, median age: 58.75 years) were fixed in 4% buffered paraformaldehyde for 48 h and decalcified with buffered ethylenediaminetetraacetic acid (EDTA, 20%; pH 7.4); the buffer was replaced every 3 days until the pin could be easily pierced. After dehydration and embedding in paraffin, sections were cut to a thickness of 4 μm. Samples were heated for 90 min, deparaffinized with dimethylbenzene, and dehydrated in a graded ethanol series (85%, 90%, and 100%). The sections were then subjected to antigen retrieval using microwave heating in citrate buffer (pH 6.0) for 12 min, and endogenous peroxidases were blocked with 3% H2O2 for 8 min. Serial sections from each case were stained with hematoxylin, hydrochloric acid alcohol, and carbonic acid aluminium and then washed three times with PBS. The sections were incubated with anti-adiponectin antibodies (1:400) or PBS alone as a control at 4 °C for 12 h, followed by washing and incubation with biotinylated secondary antibodies at 37 °C for 30 min. The immunoreaction was finally visualized with diaminobenzidine (DAB) and counterstained with hematoxylin. Human adipocyte tissue was used as a positive control. Specimens were evaluated under a light microscope by an expert pathologist and scored based on a semiquantitative approach of the percentage of positive subchondral bone (0–100%) and the staining intensity (0, negative; 1, weak; 2, moderate; 3, strong) in each subchondral bone sample.
Assessment of adiponectin expression by western blotting
Lumbar facet joint samples were collected from 27 patients (NG, n = 9, median age: 44.44 years; DG, n = 9, median age: 45.33 years; severe SDG, n = 9, median age: 57.22 years). Protease inhibitor (10 μL) and 990 μL RIPA buffer were added to the 50 mg samples, and the samples were then ground on ice and mixed on a rotator for 30 min at 4 °C. Tissue debris was removed by centrifugation at 12,000×g at 4 °C for 15 min, and protein concentrations were measured using a Bio-Rad Protein Assay kit (Bio-Rad, Hercules, CA, USA). Protein samples (20 μg) were subjected to sodium dodecyl sulfate polyacrylamide gel electrophoresis and electrophoretically transferred to polyvinylidene difluoride membranes. The membranes were sequentially blotted with the primary antibody (anti-adiponectin 19F1; ab22554; Abcam, Cambridge, UK) and secondary antibody and developed using enhanced chemiluminescence.
Assessment of adiponectin expression by qPCR
Subchondral bone (50 mg) was ground with liquid nitrogen into a powder, and total RNA was extracted using TRIzol reagent (Transgen Biotechnology Co., Beijing, China), per the manufacturer’s instructions. Total RNA (1 μg) was employed to prepare cDNA via reverse transcription using a PrimeScript RT Reagent kit with gDNA Eraser (Perfect Real Time; DRR047A; TakaRa, Shiga, Japan). cDNA samples (2.8 μL per 20 μL reaction) were analysed for genes of interest and reference genes (h-actin and adiponectin). qPCR was performed using SYBR Premix Ex TaqTM II (Tli RNaseH Plus; DRR820A; TakaRa) with an ABI StepOnePlus system (Applied Biosystems, Inc., Foster City, CA, USA). The cycling profile was as follows: denaturation at 94 °C for 30 s; 40 cycles of annealing at 60 °C for 15 s, primer extension at 72 °C for 60 s, and denaturation at 95 °C for 30 s; and a final extension for 2 min. The comparative RQ value method was used to determine fold changes in expression using β-actin as a control. The following primers were used: H-actin-285, F5′-AGCGAGCATCCCCCAAAGTT-3′ and R5′-GGGCACGAAGGCTCATCATT-3′; ADIPOQ (214 bp), F5′-CATGCCCATTCGCTTTACCA-3′ and R5′-GGAGGCCTGGTCCACATTAT-3′. The primer sequence was selected for high match similarity to Homo sapiens adiponectin gene through NCBI primer blast.
Statistical analysis was conducted with GraphPad Prism 5.0 software (San Diego, California, USA). To study the release of adiponectin from the subchondral bone of the lumbar facet joint in relation to the BMI, Pearson correlation analysis was performed on adiponectin content data determined by ELISA and the BMI measurements of patients. Additionally, data analysis of the immunohistochemistry, western blotting, and qPCR experiments was performed using one-way ANOVA with post hoc examination of significant main effects using the Dunnett method. Data are presented as the mean ± SD, unless stated otherwise. A p value less than 0.05 was considered significant for differences and correlations.
Expression of IL-1β, TNF-α, leptin, and adiponectin in lumbar facet joints
First, we evaluated the expression of several cytokines in lumbar facet joint specimens using ELISA. Since IL-1β, TNF-α, and leptin were detected in only a few specimens, they were not included in the statistical analysis. For the adiponectin content data, extreme values (8 case of specimens) were removed and were analysed via descriptive statistics. The result showed that adiponectin was detected in all facet joint specimens, and adiponectin content was different in the different degeneration groups (Fig. 2a). In addition, adiponectin was negatively correlated with BMI in 52 patients (correlation coefficient: p < 0.001, r = −0.861; Fig. 2b).
Qualitative analysis of adiponectin by immunohistochemistry
Next, we examined whether adiponectin was expressed in the subchondral bone of the lumbar facet joint by immunohistochemistry. We evaluated adiponectin expression in 48 specimens (NG, 12; DG, 12; SDG, 24) by immunohistochemical staining. The results showed that adiponectin was expressed in the subchondral bone but not in the cartilage (Fig 3). Compared to the percentage of immunohistochemical staining in the normal group, significant differences (p < 0.0001) were identified in the severe degeneration group by one-way ANOVA (Fig. 4c). Compared to the percentage of immunohistochemical staining in the normal group, a statistically significant difference (p < 0.05) was observed in the degeneration group by one-way ANOVA (Fig. 4c). In addition, compared to the percentage of immunohistochemical staining in the degeneration group, a significant difference (p < 0.05) was also found in the severe degeneration group by one-way ANOVA (Fig. 4c).
Quantitative analysis of adiponectin expression by western blotting and qPCR in the subchondral bone of the lumbar facet joint
Finally, in order to test our hypothesis that adiponectin plays an important role in FJOA, we further evaluated adiponectin expression by western blotting and qPCR. Western blot analysis demonstrated that adiponectin expression was significantly higher in the normal group than in the degenerative and severe degeneration groups by one-way ANOVA (p < 0.0001; Fig. 4a and b). In addition, adiponectin mRNA levels were significantly lower in the degenerative and severe degeneration groups as compared with those in the normal group when normalized to the expression of β-actin by one-way ANOVA (p < 0.0001; Fig. 4d).
As a part of the three-column structure of vertebrae, facet joints play a key role in maintaining the stability of spinal motion, particularly in the lumbar area . Therefore, most doctors are concerned with the biomechanical and mechanical factors affecting lumbar facet joints. However, the pathogenesis of FJOA has not been fully elucidated. Accordingly, in this study, we evaluated the expression of adiponectin in lumbar facet joints. Our results showed that adiponectin expression was significantly downregulated with increasing degeneration of the lumbar facet joint.
Adiponectin is an adipocyte factor specifically secreted from fat cells. Adiponectin is composed of 244 amino acids; the N-terminus contains one secretory signal sequence, and the C-terminus contains a spherical egg white function threshold. Previous studies have shown that adiponectin is involved in glucose homeostasis, insulin sensitivity, and vascular inflammatory diseases [25, 26]. Adiponectin in human peripheral blood circulation has three different types of polymer, including low- molecular-weight trimers (LMW), a middle-molecular-weight hexamers (MMW), and high numbers of monomers that compose high-molecular-weight multimers (HMW). Yamauchi et al.  reported that the affinity of adiponectin varies between different subtypes and receptors and that the adiponectin monomer, AdipoR1, and AdipoR2 have higher affinity, while MMW and HMW are mainly associated with T-cadherin. Therefore, the biological effects of the different types of adiponectin polymers may vary considerably. In research on metabolic and cardiovascular disease, HMW adiponectin was found to induce proinflammatory cytokine production , whereas LMW adiponectin was shown to inhibit the release of inflammatory factors . Additionally, in studies focusing on arthritis, the adiponectin monomer and OA were negatively correlated, and HMW adiponectin was not associated with the degree of OA . Furthermore, Kang et al.  showed that adiponectin is a potential catabolic mediator of OA in vitro. Therefore, the relationship between adiponectin and OA is of considerable interest.
In this study, the results showed that adiponectin expression was significantly higher than IL-1β, TNF-α, and leptin expression in the lumbar facet joints by ELISA and that adiponectin was negatively correlated with BMI. These findings support a model in which adiponectin is negatively correlated with FJOA. Furthermore, western blotting and qPCR confirmed the down regulation of adiponectin in degenerative joints compared with that in normal joints. Therefore, our findings suggest that degeneration of the lumbar facet joint may be significantly associated with adiponectin expression. However, the specific mechanism is not clear. Berner et al.  found that adiponectin and its receptors are expressed in bone-forming cells of the juvenile mouse mandible and that adiponectin promotes the metabolism of osteoblasts in bone. Chen et al.  provided evidence for the protective role of adiponectin in knee OA. The study found that adiponectin can activate p38 mitogen-activated protein kinase (p38MAPK) pathway, involved in the pathogenesis of OA [33, 34]. However, few studies have evaluated the subchondral bone, which can play an important role in FJOA. The subchondral bone of the lumbar facet is composed of the cortical plate, trabecular bone, bone trabecula, and vascular lacuna. Small veins, small arteries, and sinusoidal ducts enter the subchondral bone area and then into the cartilage and cartilage radiation layer through the cortical plate, providing nutrients to the deeper cartilage [35, 36]. Orth and Cucchiarini  demonstrated that the subchondral bone functions to provide nutrients to articular cartilage, promote the synthesis of protein polysaccharides and collagen fibres, increase the contact surface area, and maintain cartilage. Taken together with the findings of this study, we hypothesize that adiponectin promotes the growth of osteoblasts via the p38 mitogen-activated protein kinase pathway in the subchondral bone of the facet joint that leads to bone remodelling, which results in delayed facet joint degeneration.
There are some limitations in this basic experimental study. In this study, we speculated that adiponectin promotes the growth of osteoblasts via the p38 mitogen-activated protein kinase pathway in the subchondral bone of the facet joint and that this leads to bone remodelling, thereby resulting in delayed facet joint degeneration. However, we have only explored preliminary phenomenon thus far and the specific mechanism involved has not yet been fully determined. Therefore, we will further study the specific mechanism of lumbar facet OA.
Based on our findings in this study, we hold that adiponectin was expressed in the subchondral bone of the lumbar facet joint and that adiponectin may be inversely correlated with the degree of degeneration of the lumbar facet joint. Therefore, we hypothesize that adiponectin may play a role in protection of the lumbar facet joint degeneration via the modulation of osteoblasts and osteoclasts. Studies are currently underway in our laboratory to further investigate this hypothesis.
Body mass index
Enzyme-linked immunosorbent assay
Osteoarthritis of the lumbar facet joint
Magnetic resonance imaging
- p38 MAPK:
p38 mitogen-activated protein kinase
Serious degeneration group
Tumour necrosis factor
Goode AP, Carey TS, Jordan JM. Low back pain and lumbar spine osteoarthritis: how are they related? Curr Rheumatol Rep. 2013;15:305–17.
Schwarzer AC, Aprill C, Derby R, et al. Clinical features of patients with pain stemming from the lumbar zygapophyseal joints. Is the lumbar facet syndrome a clinical entity? Spine. 1994;10:1132–7.
Manchkanti L, Pampati V, Fellows B, et al. Prevalence of facet joint pain in chronic low back pain. Pain Physician. 1999;2:59–64.
Engel R, Bogduk N. The menisci of the lumbar zygapophysial joints. J Anat. 1982;135:795–809.
Glover JR. Arthrography of the joints of the lumbar vertebral arches. Orthop I Clin North Am. 1977;8:37–42.
Giles LGF, Taylor JR. Intra-articular synovial protrusions in the lower lumbar apophyseal joints. Bull Hosp Jt Dis Orthop Inst. 1982;42:248–55.
Hunter DJ, Schofield D, Callander E. The individual and socioeconomic impact of osteoarthritis. Nat Rev Rheumatol. 2014;10:437–41.
Cheng C, Gao S, Lei G. Association of osteopontin with osteoarthritis. Rheumatol Int. 2014;34:1627–31.
Gao SG, Li KH, Zeng KB, et al. Elevated osteopontin level of synovial fluid and articular cartilage is associated with disease severity in knee osteoarthritis patients. Osteoarthr Cartil. 2010;18:82–7.
Gao SG, Zeng C, Li LJ, et al. Correlation between senescence-associated beta-galactosidase expression in articular cartilage and disease severity of patients with knee osteoarthritis. Int J Rheum Dis. 2016;19:226–32.
Lories RJ, Luyten FP. The bone-cartilage unit in osteoarthritis. Nat Rev Rheumatol. 2011;7:43–9.
Brandt KD, Radin EL, Dieppe PA, et al. Yet more evidence that osteoarthritis is not a cartilage disease. Ann Rheumat Dis. 2006;65:1261–4.
Netzer C, Urech K, Hugle T, Benz RM, Geurts J, Schren S. Characterization of subchondral bone histopathology of facet joint osteoarthritis in lumbar spinal stenosis. J Orthop Res. 2016;34(8):1475–80.
Murray KJ, Le Grande MR, Ortega de Mues A, Azari MF. Characterisation of the correlation between standing lordosis and degenerative joint disease in the lower lumbar spine in women and men: a radiographic study. BMC Musculoskelet Disord. 2017;18(1):330.
Maeda K, Okubo K, Shimomura I, et al. cDNA cloning and expression of a novel adipose specific collagen-like factor, apM1 (adipose most abundant gene transcript 1). Biochem Biophys Res Commun. 1996;221:286–9.
Scherer PE, Williams S, Fogliano M, et al. A novel serum protein similar to C1q, produced exclusively in adipocytes. J Biol Chem. 1995;270:26746–9.
Pajvani UB, Du X, Combs TP, et al. Structure–function studies of the adiponectin-secreted hormone Acrp30/adiponectin: implication for metabolic regulation and bioactivity. J Biol Chem. 2003;278:9073–85.
Arita Y, Kihara S, Ouchi N, et al. Paradoxical decrease of an adipose-specific protein, adiponectin, in obesity. Biochem Biophys Res Commun. 1999;257:79–3.
Cnop M, Havel PJ, Utzschneider KM, et al. Relationship of adiponectin to body fat distribution, insulin sensitivity and plasma lipoproteins: evidence for independent roles of age and sex. Diabetologia. 2003;46:459–69.
Berner HS, Lyngstadaas SP, Spahr A, et al. Adiponectin and its receptors and expressed in bone-forming cells. Bone. 2004;35:842–9.
Francin PJ, Abot A, Guillaume C, Presle N. Association between adiponectin and cartilage degradation in human osteoarthritis. Osteoarthr Cartil. 2014;22:519–26.
Weishaupt D, Zanetti M, Boos N, et al. MR imaging and CT in osteoarthritis of the lumbar facet joints. Skelet Radiol. 1999;28:215–9.
Zhou X, Liu Y, Zhou S, et al. The correlation between radiographic and pathologic grading of lumbar facet joint degeneration. BMC Med Imaging. 2016;6:27.
Gellhorn AC, Katz JN, Suri P. Osteoarthritis of the spine: the facet joints. Nat Rev Rheumatol. 2013;9:216–24.
Worf G. Adiponectin: a regulator of energy homeostasis. Nutr Rev. 2003;61:290–2.
Ouchi N, Kihara S, Funahashi T, et al. Obesity, adiponectin and vascular inflammatory disease. Curr Opin Lipidol. 2003;14:561–6.
Yamauchi T, Kamon J, Ito Y, Tsuchida A, Yokomizo T, Kita S, et al. Cloning of adiponectin receptors that mediate antidiabeticmetabolic effects. Nature. 2003;423:762–9.
Hangen F, Drevon CA. Activation of nuclear factor-kappaB by high molecular weight and globular adiponectin. Endocrinology. 2007;148(11):5478–86.
Neumeier M, Weigert J, Schfiffier A, et al. Different effects of adiponectin isoforms in human monocytic cells. J Leukoc Bio. 2006;79(4):803–8.
Klein-Wieringa IR, Andersen SN, Herb-van Toorn L, et al. Are baseline high molecular weight adiponectin levels associated with radiographic progression in the rheumatoid arthritis and osteoarthritis? J Rheumatol. 2014;41(5):853–8.
Kang EH, Lee YJ, Kim TK, et al. Adiponectin is a potential catabolic mediator in osteoarthritis cartilage. Arthritis Res Ther. 2010;12:R231.
Chen TH, Chen L, Hsieh MS, et al. Evidence for a protective role for adiponectin in osteoarthritis. Biochim Biophys Acta. 2006;1762:711–8.
Koskinen A, Juslin S, Nieminen R, et al. Adiponectin associates with markers of cartilage degradation in osteoarthritis and induces production of proinflammatory and catabolic factors through mitogen-activated protein kinase pathways. Arthritis Res Ther. 2011;13(6):184.
Tong KM, Chen CP, Huang KC, et al. Adiponectin increases MMP-3 expression in human chondrocytes through adiporl signaling pathway. J Cell Biochem. 2011;112:143l–40.
Pallante-Kichura AL, Cory E, Bugbee WD, et al. Bone cysts after osteochondral allograft repair of cartilage defects in goats suggest abnormal interaction between subchondral bone and overlying synovial joint tissues. Bone. 2013;57:259–68.
Yu DG, Ding HF, Mao YQ, et al. Strontium ranelate reduces cartilage degeneration and subchondral bone remodeling in rat osteoarthritis model. Acta Pharmacol Sin. 2013;34:393–402.
Orth P, Cucchiarini M, Zurakowski D, et al. Parathyroid hormone [1-34] improves articular cartilage surface architecture and integration and subchondral bone reconstitution in osteochondral defects in vivo. Osteoarthr Cartil. 2013;21:614–24.
We greatly appreciate the assistance of the company Editage in Shanghai, which provided English language editing.
All research costs were supplied by the following three project grants: Gan-Po Talents Project 555 of Jiangxi Province, Jiangxi Provincial Department of Science and Technology (20171BAB205059) and Jiangxi Province Postgraduate Innovation Special Funds(YC2016-S107).
Availability of data and materials
Ethics approval and consent to participate
The study protocol was approved by the Institutional Review Board of the First Affiliated Hospital of Nanchang University, and written informed consent was obtained from all study participants.
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Lai, Q., Liu, Y., Huang, L. et al. Expression of adiponectin in the subchondral bone of lumbar facet joints with different degrees of degeneration. BMC Musculoskelet Disord 18, 427 (2017). https://doi.org/10.1186/s12891-017-1786-8
- Facet joint
- Subchondral bone
- Bone degeneration