Overexpression of MIG-6 in the cartilage induces an osteoarthritis-like phenotype in mice
Arthritis Research & Therapy volume 22, Article number: 119 (2020)
Osteoarthritis (OA) is the most common form of arthritis and characterized by degeneration of the articular cartilage. Mitogen-inducible gene 6 (Mig-6) has been identified as a negative regulator of the epidermal growth factor receptor (EGFR). Cartilage-specific Mig-6 knockout (KO) mice display increased EGFR signaling, an anabolic buildup of the articular cartilage, and formation of chondro-osseous nodules. Since our understanding of the EGFR/Mig-6 network in the cartilage remains incomplete, we characterized mice with cartilage-specific overexpression of Mig-6 in this study.
Utilizing knee joints from cartilage-specific Mig-6-overexpressing (Mig-6over/over) mice (at multiple time points), we evaluated the articular cartilage using histology, immunohistochemical staining, and semi-quantitative histopathological scoring (OARSI) at multiple ages. MicroCT analysis was employed to examine skeletal morphometry, body composition, and bone mineral density.
Our data show that cartilage-specific Mig-6 overexpression did not cause any major developmental abnormalities in the articular cartilage, although Mig-6over/over mice have slightly shorter long bones compared to the control group. Moreover, there was no significant difference in bone mineral density and body composition in any of the groups. However, our results indicate that Mig-6over/over male mice show accelerated cartilage degeneration at 12 and 18 months of age. Immunohistochemistry for SOX9 demonstrated that the number of positively stained cells in Mig-6over/over mice was decreased relative to controls. Immunostaining for MMP13 appeared increased in areas of cartilage degeneration in Mig-6over/over mice. Moreover, staining for phospho-EGFR (Tyr-1173) and lubricin (PRG4) was decreased in the articular cartilage of Mig-6over/over mice.
Overexpression of Mig-6 in the articular cartilage causes no major developmental phenotype; however, these mice develop earlier OA during aging. These data demonstrate that Mig-6/EGFR pathways are critical for joint homeostasis and might present a promising therapeutic target for OA.
Osteoarthritis (OA), a chronic degenerative joint disease, is the most common form of arthritis. OA affects 242 million individuals worldwide, but that number will grow due to increasing life expectancies . This statistic is alarming, considering the disability, the loss of quality of life, and the costs to the health system generated by OA. Currently, there are pharmacological treatments available to manage OA symptoms such as pain [2,3,4] as well as surgical joint replacement at the end stage of disease [5, 6]. Unfortunately, however, there is no cure for OA. Progressive understanding of the pathophysiology of OA suggests that the disease is a heterogeneous condition, so further research is needed to direct the clinical approaches to disease management .
Recent studies have shown that OA is a multifactorial disease of the whole joint; however, its pathogenesis remains still poorly understood . Genetic, environmental, and biomechanical factors can accelerate the onset of OA . The articular cartilage is a highly specialized tissue that forms the smooth gliding surface of synovial joints, with chondrocytes as the only cellular component of the cartilage . The homeostasis of the cartilage extracellular matrix (ECM) involves a dynamic equilibrium between anabolic and catabolic pathways controlled by chondrocytes . The progression of OA is associated with dramatic alteration in the integrity of the cartilage ECM network formed by a large number of proteoglycans (mostly aggrecan), collagen II, and other non-collagenous matrix proteins . In addition, ECM synthesis is regulated by a number of transcriptional regulators involved in chondrogenesis, specifically sex-determining- region-Y box 9 (SOX9), L-SOX 5, and SOX6 that regulate type II collagen (Col2a1) and aggrecan (Acan) gene expression . On the other hand, catabolic events are dominant in OA, and cells are exposed to degenerative enzymes such as aggrecanases (e.g., ADAMTS-4, ADAMTS-5) [12, 14], collagenases (e.g., MMP-1, MMP-3, MMP-8, MMP-13) , and gelatinases (e.g.,MMP-2 and MMP-9), all of which have implications in articular cartilage degeneration . A number of growth factors  play a role in OA pathology, such as transforming growth factor-β , BMP-2 , insulin growth factor 1 (IGF-1) , and fibroblast growth factor (FGF), but the exact regulation of chondrocyte physiology is still not completely understood.
Recent studies in our laboratory [21, 22] have identified the epidermal growth factor receptor (EGFR) and its ligand transforming growth factor alpha (TGFα) as possible mediators of cartilage degeneration [23,24,25]. The human TGFA gene locus was also strongly linked to hip OA and cartilage thickness in genome-wide association studies [26, 27]. TGFα stimulates EGFR signaling and activates various cell-signaling pathways in chondrocytes, including extracellular signal-regulated kinase 1 and 2 (ERK1/2) and phosphoinositide 3-kinase (P13K) . EGFR signaling plays important roles in endochondral ossification [29, 30], growth plate development , and cartilage maintenance and homeostasis [31,32,33], but many aspects of its action in the cartilage are still not well understood. However, both protective and catabolic effects of EGFR signaling in OA have been reported, suggesting context-specific roles of this pathway .
Mitogen-inducible gene 6 (Mig-6) is also known as Gene 33, ErbB receptor feedback inhibitor 1 (ERRFI1), or RALT and is found in the cytosol . Mig-6 protein binds to and inhibits EGFR signaling through a two-tiered mechanism: suppression of EGFR catalytic activity and receptor downregulation . Interestingly, various studies have reported that loss of Mig-6 induces the onset of OA-like symptoms in mice [35, 37,38,39]. Cartilage-specific (Col2-Cre) knockout of Mig-6 mice results in the formation of chondro-osseous nodules in the knee, but also increased thickness of the articular cartilage in the knee, ankle, and elbow . Prx1-Cre-mediated knockout of Mig-6 in the limb mesenchyme results in a similar phenotype as that observed in cartilage-specific knockout mice . These phenotypes appeared to be caused by an increase in chondrocyte proliferation in articular cartilage, supported by the increased expression of Sox9 and EGFR activation in the cartilage . Since our studies suggest dosage- and/or context-specific roles of EGFR signaling in the process of cartilage degeneration in OA, in this study, we used a cartilage-specific (Col2-Cre) to examine effects of Mig-6 overexpression specifically in articular cartilage. We hypothesized that overexpression of Mig-6/EGFR accelerates cartilage degeneration during aging.
Materials and methods
Generation of Mig-6 overexpression mice
Mig-6 overexpression animals on a mixed C57Bl/6 and agouti mouse background, with the overexpression cassette in the Rosa26 locus , and bred for 10 generations into a C57Bl/6 background were used. Transcription of Mig-6 is under the control of a ubiquitously expressed chicken beta actin-cytomegalovirus hybrid (CAGGS) promoter but blocked by a “Stop Cassette” flanked by LoxP sites (LSL) . Mig-6 overexpression mice were bred to mice carrying the Cre recombinase gene under the control of the Collagen 2 promoter , to induce recombination and removal of the Stop Cassette specifically in the cartilage. Throughout the manuscript, animals for homozygote overexpression of Mig-6 from both alleles are termed Mig-6over/over (Mig-6over/overCol2a1-Cre+/−), while control mice are identical but without the Cre gene (noted as “control” in this manuscript for simplicity). Mice were group-housed (at least one pair of littermate-matched control and overexpression animals), on a standard 12-h light/dark cycle, without access to running wheels and with free access to mouse chow and water. Animals were weighed prior to euthanasia by asphyxiation with CO2. All animal experiments were done in accordance with the Animal Use Subcommittee at the University of Western Ontario and conducted in accordance with the guidelines from the Canadian Council on Animal Care.
Genotype was determined by polymerase chain reaction (PCR) analysis using DNA processed from biopsy samples of ear tissue from mice surviving to at least 21 days of age. PCR strategy: primer set P1 and P2 can amplify a 300-bp fragment from the wild-type allele, whereas P1 and P3 can amplify a 450-bp fragment from the targeted ROSA26 locus allele  (Supplementary Figure/Table 1).
RNA isolation and quantitative real-time PCR
Total RNA was isolated from postnatal day 0 (P0) mouse cartilage of Mig-6over/over and control littermates using TRIzol® (Invitrogen) as per the manufacturer’s instructions and as previously described . Complementary DNA (cDNA) was synthesized using the iScript cDNA Synthesis kit (Bio-Rad) with 1 μg of RNA (Bio-Rad Laboratories) and combined with 300 nM of forward and reverse primers (for primer sequences, please see Supplementary Figure 1E) as well as iQ™ SYBR® Green Supermix (Bio-Rad Laboratories) for PCR on a Bio-Rad CFX384 RT-PCR system. Relative gene expression was normalized to the internal control glyceraldehyde 3-phosphate dehydrogenase (Gapdh), calculated using the ΔΔCT method.
Histopathology of the knee
The limbs from Mig-6over/over and control mice were harvested and fixed in 4% paraformaldehyde (Sigma) for 24 h and decalcified in ethylenediaminetetraacetic acid (5% EDTA in phosphate-buffered saline (PBS), pH 7.0. The joints were processed and embedded in paraffin in sagittal or frontal orientation, with the serial sections taken at a thickness of 5 μm. Sections were stained with toluidine blue (0.04% toluidine blue in 0.2 M acetate buffer, pH 4.0, for 10 min) for glycosaminoglycan content and general evaluation of the articular cartilage. All images were taken with a Leica DFC295 digital camera and a Leica DM1000 microscope.
Thickness of proximal tibia growth plate
For early developmental time points such as newborn (P0), the sagittal knee sections stained with toluidine blue were used to measure the width of the zones of the epiphyseal growth plate in the proximal tibia. The average thickness of the resting and proliferative zones combined was evaluated by taking three separate measurements at approximately equal intervals across the width of the growth plate. The average hypertrophic zone thickness was also measured using 3 different measurements across the width of the growth plate, starting each measurement at the border of the proliferative and hypertrophic zones and ending at the subchondral bone interface. The third average measurement was then taken for the thickness of the entire growth plate. The ImageJ software (v.1.51)  was used for all measures, with the observer blinded to the genotype.
Articular cartilage evaluation
Articular cartilage thickness was measured from toluidine blue-stained frontal sections by a blinded observer. Articular cartilage thickness was measured separately for the non-calcified articular cartilage (measured from the superficial tangential zone to the tidemark), and the calcified articular cartilage (measured from the subchondral bone to the tidemark) across three evenly spaced points from all four quadrants of the joint (medial/lateral tibia and femur) in 4 sections spanning at least 500 μm. The ImageJ software (v.1.51)  was used to measure the thickness of the articular cartilage.
Micro-computerized tomography (μCT)
Whole-body scans were collected in 6-week-, 11-week-, 12-month-, and 18-month-old control and Mig-6over/over male and female mice. Mice were euthanized and imaged using the General Electric (GE) SpeCZT microCT machine  at a resolution of 50 μm/voxel or 100 μm/voxel. GE Healthcare MicroView software (v2.2) was used to generate 2D maximum intensity projection and 3D isosurface images to evaluate skeletal morphology. MicroView was used to create a line measurement tool in order to calculate the bone lengths; femur lengths were calculated from the proximal point of the greater trochanter to the base of the lateral femoral condyle. Tibia lengths were measured from the midpoint medial plateau to the medial malleolus. Humerus lengths were measured from the midpoint of the greater tubercle to the center of the olecranon fossa.
Body composition analysis
MicroView software (GE Healthcare Biosciences) was used to analyze the microCT scans at the resolution of 100um/voxel. Briefly, the region of interest (ROI) was used to calculate the mean of air, water, and an epoxy-based, cortical bone-mimicking calibrator (SB3; Gammex, Middleton, WI, USA) (1100 mg/cm3) . A different set of global thresholds was applied to measure adipose, lean, and skeletal mass (− 275, − 40, and 280 Hounsfield units (HU), respectively). Moreover, bone mineral density (BMD) was acquired as the ratio of the average HU (from the value of the skeletal region of interest) in order to calculate the HU value of the SB3 calibrator, multiplied by the known density of the SB3 as described .
OARSI histopathology scoring
Serial sections through the entire knee joint were scored according to the OARSI histopathology scoring system  by two blinded observers on the four quadrants of the knee: lateral femoral condyle (LFC), lateral tibial plateau (LTP), medial femoral condyle (MFC), and medial tibial plateau (MTP). Histologic scoring from 0 to 6 represent the OA severity, from 0 (healthy cartilage) to 6 (erosion of more than 75% of the articular cartilage). Individual scores are averaged first for each observer, then across observers, and OA severity is shown as described for each graph. Scores were compared between male and female Mig-6over/over and control mice at both 12 and 18 months of age. All images were taken with a Leica DFC295 digital camera and a Leica DM1000 microscope.
Frontal paraffin sections of knees were used for immunohistochemical analysis, with slides with “no primary antibody” as a control. All sections were deparaffinized and rehydrated as previously described [40, 48]. Subsequently, the sections were incubated in 3% H2O2 in methanol for 15 min to inhibit endogenous peroxidase activity. After rinsing with water, 5% goat or donkey serum in PBS was applied to reduce non-specific background staining. The sections were incubated overnight at 4 °C with primary antibodies against SOX9 (R&D Systems, AF3075), MMP13 (Protein Tech, Chicago, IL, USA, 18165-1-AP), lubricin (Abcam, ab28484) (primary concentration antibody for all three 1:100), and phospho-EGFR (phosphoTyr-1173; Cell Signaling Technology) (primary concentration antibody 1:50). After washing, the sections were incubated with horseradish peroxidase (HRP)-conjugated donkey anti-goat or goat anti-rabbit secondary antibody (R&D System and Santa Cruz, secondary concentration antibody 1:200), before incubation with diaminobenzidine substrate as a chromogen (Dako, Canada). Finally, the sections were counterstained with 0.5% methyl green (Sigma) and mounted. Cell density of articular cartilage chondrocytes from 6- and 11-week-old male mice was determined by counting all lacunae with evidence of nuclear staining in the lateral and medial femur/tibia using a centered region of interest measuring 200 μm wide and 70 μm deep from the articular surface by a blinded observer. For newborn (P0) animals, the region of interest was measured 200 μm wide and 100 μm deep from the proliferative zone.
All statistical analyses were performed using GraphPad Prism (v6.0). Differences between the two groups were evaluated using Student’s t test, and two-way ANOVA was used to compare the 4 groups followed by a Bonferroni multiple comparisons test. All n values represent the number of cartilage-specific Mig-6-overexpressing mice and control littermates used in each group.
Increased MIG-6 mRNA from overexpression of Mig-6 mice and decreased EGFR staining
We bred mice for conditional overexpression of Mig-6  to mice expressing Cre recombinase under the control of the collagen II promoter. Homozygote mice overexpressed Mig-6 in all collagen II-producing cells (and their progeny) from both Rosa26 alleles and are referred to as Mig-6over/over from here on. Control mice do not express Cre. Genomic DNA was extracted from ear notches to identify homozygous mice Mig-6over/overusing standard PCR analysis. Overexpressing mice were obtained at the expected Mendelian ratios (data not shown). Real-time RT-PCR revealed increased levels of Mig-6 expression in the cartilage of Mig-6over/over mice from postnatal day 0 (PO) (Fig. 1a). Since Mig-6 negatively regulates EGFR signaling [31, 32, 40], immunohistochemistry was performed for phospho-EGFR (Tyr-1173) (pEGFR), with no primary antibody controls. Frontal knee sections from 11-week-old male Mig-6over/over mice showed decreased pEGFR staining in the medial compartment in the knee joint (Fig. 1b–e), as expected upon Mig-6 overexpression.
Overexpression of Mig-6 has minor effects on skeletal phenotypes during development
Male mutant gained weight at the same rate as controls over the examined 10-week period, while female Mig-6over/over mice were slightly lighter than controls starting at 8 weeks of age (Suppl. Fig. 2A-B). These differences persisted at 12 months of age for female mice, while at 18 months, both male and female mutant mice were lighter than their controls (Suppl. Fig. 2C-D). Growth plates of postnatal day 0 (P0) Mig-6over/over and control mice were analyzed by histology. No major differences in the tibia growth plate architecture were seen between genotypes (Suppl. Fig. 3A). While the length of the total growth plate was slightly reduced in Mig-6over/over mice, differences in lengths of either the combined resting/proliferative or hypertrophic zones were not statistically significant (Suppl. Fig. 3B-D).
Mice overexpressing Mig-6 have shorter long bones than control mice
Skeletal morphology and bone length were examined by microCT mice at the ages of 6 weeks and 12 and 18 months. Scans of Mig-6over/over male and female mice and their controls were used to generate 3D isosurface reconstructions of 100 μm/voxel μCT scans, in order to measure long bone lengths (femurs, humeri, and tibiae) in GE MicroView v2.2 software. Mutant bones were slightly shorter throughout life, with the exception of the male humeri at 12 months that did not show any statistically significant difference (Fig. 2a–d). In contrast, male mice did not show any differences in bone mineral density at 11 weeks, 12 months, or 18 months, compared to controls (Suppl. Fig. 4A-C). In addition, no differences in body mass composition were seen in male mutant and control mice at 11 weeks, 12 months, and 18 months of age (Suppl. Fig. 5A1-C2).
Mig-6-overexpressing mice have healthy articular cartilage during skeletal maturity
We next examined articular cartilage morphology in 11-week-old mutant and control mice using toluidine blue-stained paraffin frontal knee sections (Fig. 3a, b). The average thickness of the calcified articular cartilage and non-calcified articular cartilage in the lateral femoral condyle (LFC), lateral tibial plateau (LTP), medial femoral condyle (MFC), and medial tibial plateau (MTP) from control and Mig-6over/over male (Fig. 3c, d) and female (Suppl. Fig. 6A-D) mice did not show statistically significant differences. Histological analyses of the knee sections from male and female mice did not show any loss of proteoglycan, fibrillation, or erosion in the articular cartilage of mutant mice.
Overexpression of Mig-6 in the cartilage induces an osteoarthritis-like phenotype in mice during aging
Since aging is a primary risk factor in OA , we next examined the knee joints in 12- and 18-month-old control and Mig-6over/over mice. Toluidine blue-stained sections were evaluated by two blinded observers, using OARSI recommendations . At 12 months of age, male control mice showed minor signs of cartilage damage, such as loss of proteoglycan staining, but no significant structural degeneration (Fig. 4a). However, seven of nine Mig-6over/over male mice showed more extensive cartilage damage in their medial side (erosion to the calcified layer lesion for 25 to 50% of the medial quadrant) (Fig. 4b). OARSI scoring confirmed increased OA-like damage in mutant mice (Fig. 4c). Similarly, at 18 months of age, the male control group showed minimal cartilage degeneration in 3 of 6 mice (Suppl. Fig. 7A-B). Mig-6over/over male mice showed more severe cartilage erosion in the medial tibial plateau in 3/6 animals. This result was again supported by significantly increased OARSI cartilage damage scores (Suppl. Fig. 7C). Moreover, for the female group at 12 months, control mice did not show cartilage damage. However, Mig-6over/over female mice showed signs of OA-like cartilage damage in 3/8 animals (Suppl. Fig. 8A-C). In addition, at 18 months of age, female control mice showed healthy cartilage, and 3/8 Mig-6over/over female mice showed some proteoglycan loss and cartilage degeneration on the medial side (Suppl. Fig. 9A-C).
Overexpression of Mig-6 decreases Sox9 expression
During chondrogenesis, the transcription factor SOX9 is required for cartilage formation and normal expression of collagen and aggrecan . The sagittal and frontal sections of paraffin-embedded knees from postnatal day 0 (P0), 6-week-old, 11-week-old, 12-month, and 18-month-old male mice were used for SOX9 immunostaining. At P0, nuclear SOX9 expression was observed in the resting and proliferative zone of the growth plate in both genotypes (Fig. 5a, b). Cell density was not different between genotypes (Fig. 5c). In control mice, 78% of chondrocytes were positive for SOX 9 immunostaining, while the proportion of positive cells was only 53% in Mig-6over/over mice (Fig. 5d). At 6 weeks old, the total cell number in control male and Mig-6over/over mice is similar (Fig. 5g), but the percentage of SOX9-positive cells was decreased in mutant mice (Fig. 5h). A similar phenotype was present at 11 weeks (Suppl. Fig. 10A-B). At 12 months of age, SOX9 is present more in the lateral side (LTP and LFC) than the medial side (MTP and MFC) in both strains, with a few positive cells present in the medial side of the control strain. On the other hand, Mig-6over/over mice showed fewer SOX9-positive cells on the medial side due to the articular cartilage damage (Suppl. Fig. 11A-B). Similar results were found at 18 months of age in Mig-6over/over, with decreased SOX9 immunostaining in their medial side compared to the control (data not shown). For all ages, negative controls did not show staining in chondrocytes.
Overexpression of Mig-6 decreases expression of lubricin
Lubricin (aka PRG4/superficial zone protein) is a proteoglycan that plays an important role as a lubricant in the joint . EGFR signaling is crucial for the cartilage lubrication function and regulates the induction of Prg4 expression which is necessary for smooth movement [31, 32]. Immunohistochemistry for lubricin in 11-week-old (Fig. 6a–d) and at 12-month-old animals demonstrated less staining in the superficial zone of the medial side of Mig-6over/over mice than in the control group (Suppl. Fig. 12A-B).
MMP13 immunostaining in Mig-6-overexpressing and control mice
Matrix metalloproteinase (MMP13) is highly expressed in OA [52, 53]. The frontal sections of the knees from 12- and 18-month-old control and Mig-6over/over male mice were used for MMP13 immunohistochemistry. At 12 months, pericellular staining was observed in the lateral articular cartilage of male mice from both genotypes, along with the expected subchondral bone staining (Suppl. Fig. 13A-B). Less staining was observed on the medial side of control mice while advanced cartilage degeneration in mutant mice precluded staining. Negative controls did not show staining in the cartilage or subchondral bone. The articular cartilage from 18-month-old mice showed similar staining patterns and intensity of MMP13 immunostaining in the lateral side of both genotypes; however, in the medial side of Mig-6over/over mice, MMP13 staining is seen on the cartilage surface (lesion sites) and also observed in the subchondral bone (data not shown).
The maintenance of articular cartilage homeostasis relies on a dynamic equilibrium involving growth factors , genetics , mechanical forces , obesity, and injury that all play a role in the onset of osteoarthritis . A better understanding of the underlying molecular mechanism is required to design therapies for preventing the progression of OA. Recent studies from our laboratory and others have identified the epidermal growth factor receptor (EGFR) and Mig-6 as possible mediators of articular cartilage homeostasis [31, 33, 34, 40]. Mig-6 is a cytosolic protein and negative feedback regulator of EGFR signaling ; thus, Mig-6 can be a potential tumor suppressor [41, 59,60,61,62]. In addition, whole-body knockout of the Mig-6 gene in mice results in degenerative joint disease . We also have shown previously that constitutive cartilage-specific deletion of Mig-6 (Mig-6 KO) results in increased articular cartilage thickness and cell density in the joints of 12-week-old mice . Cartilage-specific Mig-6 KO mice show the same anabolic effect in the joint cartilage at 21 months of age (unpublished).
Previous research demonstrates that Mig-6 overexpression acts as a negative feedback regulator of EGFR-ERK signaling ; however, these studies did not yet analyze joint tissues. Since our studies suggest dosage- and/or context-specific roles of EGFR signaling in joint homeostasis and OA , we now examined whether overexpression of Mig-6 alters these processes. Here, we report that cartilage-specific constitutive overexpression of Mig-6 did not cause cartilage degeneration in young mice, but early-onset OA in middle-aged mice. While we observed some effects of Mig-6 overexpression on bone length and weight, these effects were subtle and not accompanied by major morphological or histological changes in the growth plate cartilage, overall skeletal morphology, or body composition. A previous study showed that the deletion of EGFR in bone tissue (Col1-Cre EgfrWa5/f) resulted in shorter femurs compared to wild-type mice , consistent with our findings. The EGFR network is essential during long bone development, since previous studies have shown that EGFR- or TGFα-deficient mice exhibit a widened zone of hypertrophic chondrocytes [23, 64]. Moreover, Qin and colleagues have shown that the administration of the EGFR inhibitor, gefitinib, into 1-month-old rats results in an enlarged hypertrophic zone due downregulation of MMP-9, MMP-13, and MMP-14 . Together, these data suggest a critical role of EGFR during endochondral ossification and elucidate the downstream mechanism of EGFR . Further research is required to provide more evidence of EGFR/Mig-6over/over signaling during bone formation, but many of these effects are relatively subtle and transient, and likely unrelated to the much more severe phenotypes observed later. Histologically, our findings showed that mice with cartilage-specific Mig-6 overexpression showed healthy articular cartilage with no significant difference in articular cartilage thickness from the control group at the ages of 6 weeks and 11 weeks. However, Mig-6over/over mice developed severe degeneration of the articular cartilage with aging. More prevalent, the knee joints of Mig-6over/over male mice showed significantly advanced cartilage degeneration. The same pattern, but with more severe damage, was seen in 18-month-old mice. As previously described, sex hormones play a role in OA disease where male mice develop more severe OA . SOX9 is crucial in chondrogenesis during endochondral bone formation, articular cartilage development, and cartilage homeostasis . Previous in vivo models using cartilage (Col2)-Cre- or limb mesenchyme (Prx1)-Cre-specific ablation of Mig-6 showed increased expression of SOX9 in the articular cartilage. Consistent with these data, we show that the percentage of SOX9-positive chondrocytes was decreased in the knee joints of 6- and 11-week-old male Mig-6over/over mice compared to controls, despite the absence of histological defects in articular cartilage. The percentage of SOX9-expressing cells was also reduced in Mig-6over/over mice at later ages. However, our previous in vitro studies suggested that TGFα suppresses the expression of anabolic genes such as Sox9, type II collagen, and aggrecan in primary chondrocytes . A potential explanation for these conflicting results is the context-specific role of EGFR signaling in the cartilage, as discussed previously ; this pathway can both promote cartilage degeneration and confer protection of the cartilage, depending on the context. Another potential explanation is the difference between in vivo and in vitro experiments. Our data from the current study suggest that reduction in Sox9 expression precedes the degeneration of articular chondrocytes in our mutant mice. In addition, we observed decreased expression of lubricin/PRG4 in these joints, which might also contribute to the observed joint pathologies. PRG4 has been shown to be regulated by EGFR signaling before [31, 32], in support of our findings. While the EGFR is the best characterized substrate of Mig-6, other substrates have been described. Mig-6 binds to different proteins such as the cell division control protein 42 homolog (Cdc42) , proto-oncoprotein (c-Abl) , and the hepatocyte growth factor receptor (c-Met) . While we cannot exclude that deregulation of these other substrates contributes to the observed phenotypes, the similarities of defects in our mice with those seen upon cartilage-specific deletion of EGFR suggest that decreased EGFR signaling is the main cause for the advanced OA observed in our mutant mice. Nevertheless, it will be important to determine whether signaling through cMet and other pathways is altered as well.
Future studies will include an examination of Mig-6-overexpressing mice in other models of OA, such as the post-traumatic model of DMM (destabilization of the medial meniscus) surgery. As discussed above, the role of the EGFR/Mig-6 pathway in OA is context-specific. Thus, we cannot extrapolate from our aging model to all forms of OA. In addition, the role of Mig-6 in human OA will require further studies. While there is plenty of evidence for crucial roles of the EGFR pathway in human OA, and Mig-6 is a crucial regulator of this pathway, more direct analyses of this role in human cartilage are required [21, 70, 71].
Mig-6 expression is heavily regulated. While its expression in human OA has not been studied thoroughly, one can easily imagine upregulation by a number of biochemical (such as EGFR and other growth factors, as in other tissues) or biomechanical factors. Mig-6 overexpression has been demonstrated in OA cartilage in dogs , suggesting that the same could occur in human OA. More generally, the EGFR pathway, through which Mig-6 primarily acts, has been shown to be deregulated in human OA in several studies [21, 34, 71]. Thus, the current study is highly relevant to the pathogenesis of human OA.
In conclusion, we show for the first time that cartilage-specific Mig-6 overexpression in mice results in reduced EGFR activity in chondrocytes, reduced SOX9 and PRG4 expression, and accelerated development of OA. These data highlight the important and context-specific role of the EGFR-Mig-6 signaling pathway in joint homeostasis and point towards potential targeting of this pathway for OA therapy.
Availability of data and materials
The dataset of the current manuscript is available upon request from the corresponding author.
- Acan :
Bone mineral density
- c-Abl :
Non-receptor tyrosine kinase proto-oncoprotein
Chicken beta actin-cytomegalovirus hybrid
Cell division control protein 42
Hepatocyte growth factor receptor
- Col2a1 :
Type II collagen gene
Epidermal growth factor receptor
Extracellular signal-regulated kinase 1 and 2
ErbB receptor feedback inhibitor 1
- Gadph :
Glyceraldehyde 3-phosphate dehydrogenase gene
Insulin growth factor 1
Lateral femoral condyle
“Stop Cassette” flanked by LoxP (LoxP-Stop Cassette-LoxP)
Lateral tibial plateau
PRG4/superficial zone protein
Medial femoral condyle
- Mig-6 :
Mitogen-inducible gene 6; RALT; Gene 33
Matrix metalloproteinase 13
Osteoarthritis Research Society International
Newborn mouse (postnatal day 0)
Phosphorylated epidermal growth factor receptor
Region of interest
Cortical bone-mimicking calibrator
Sex-determining-region-Y box 9
Transforming growth factor alpha
Woolf AD, Pfleger B. Burden of major musculoskeletal conditions. Bull World Health Organ. 2003;81:646–56.
Kramer WC, Hendricks KJ, Wang J. Pathogenetic mechanisms of posttraumatic osteoarthritis: opportunities for early intervention. Int J Clin Exp Med. 2011;4:285–98.
Ruan MZ, et al. Treatment of osteoarthritis using a helper-dependent adenoviral vector retargeted to chondrocytes. Mol Ther—Methods Clin Dev. 2016;3:16008.
Sokolove J, Lepus CM. Role of inflammation in the pathogenesis of osteoarthritis: latest findings and interpretations. Ther Adv Musculoskel Dis. 2013;5:77–94.
Mcalindon TE, et al. OARSI guidelines for the non-surgical management of knee osteoarthritis. Osteoarthr Cartil. 2014;22:363–88.
Hunter DJ, et al. Best Pract Res Clin Rheumatol. 2011;25:801–14.
Driban JB, Sitler MR, Barbe MF, Balasubramanian E. Is osteoarthritis a heterogeneous disease that can be stratified into subsets? Clin Rheumatol. 2010;29:123–31.
Man GS, Mologhianu G. Osteoarthritis pathogenesis - a complex process that involves the entire joint. J Med Life. 2014;7:37–41.
Felson DT. Osteoarthritis as a disease of mechanics. Osteoarthr Cartil. 2013;21:10–5.
Fox AJS, et al. The basic science of articular cartilage: structure, composition, and function. Sports Health. 2009;1:461–8.
Saha AK, Kohles SS. A cell-matrix model of anabolic and catabolic dynamics during cartilage biomolecule regulation. Int J Comput Healthc. 2012;1:214–28.
Goldring MB, et al. Cartilage homeostasis in health and rheumatic diseases. Arthritis Res. Ther. 2009;11:224.
Tsang KY, Tsang SW, Chan D, Cheah KSE. The chondrocytic journey in endochondral bone growth and skeletal dysplasia. Birth Defects Res Part C Embryo Today Rev. 2014;102:52–73.
Gilbert AM, Bikker JA, O’Neil SV. Advances in the development of novel aggrecanase inhibitors. Expert Opin Ther Pat. 2011;21:1–12.
Parks WC, Wilson CL, López-Boado YS. Matrix metalloproteinases as modulators of inflammation and innate immunity. Nat Rev Immunol. 2004;4:617–29.
Yoon YM, et al. Epidermal growth factor negatively regulates chondrogenesis of mesenchymal cells by modulating the protein kinase C-alpha, Erk-1, and p38 MAPK signaling pathways. J Biol Chem. 2000;275:12353–9.
Fortier LA, Barker JU, Strauss EJ, McCarrel TM, Cole BJ. The role of growth factors in cartilage repair. Clin Orthop Relat Res. 2011;469:2706–15.
van der Kraan PM. Differential role of transforming growth factor-beta in an osteoarthritic or a healthy joint. J Bone Metab. 2018;25:65.
Gamer LW, et al. The role of Bmp2 in the maturation and maintenance of the murine knee joint. J Bone Miner Res. 2018;33:1708–17.
Wei F-Y, Lee JK, Wei L, Qu F, Zhang J-Z. Correlation of insulin-like growth factor 1 and osteoarthritic cartilage degradation: a spontaneous osteoarthritis in guinea-pig. Eur Rev Med Pharmacol Sci. 2017;21:4493–500.
Appleton CTG, Usmani SE, Bernier SM, Aigner T, Beier F. Transforming growth factor α suppression of articular chondrocyte phenotype andSox9 expression in a rat model of osteoarthritis. Arthritis Rheum. 2007;56:3693–705.
Appleton CTG, et al. Global analyses of gene expression in early experimental osteoarthritis. Arthritis Rheum. 2007;56:3693–705.
Usmani SE, et al. Transforming growth factor alpha controls the transition from hypertrophic cartilage to bone during endochondral bone growth. Bone. 2012;51:131–41.
Appleton CTG, et al. Reduction in disease progression by inhibition of transforming growth factor α-CCL2 signaling in experimental posttraumatic osteoarthritis. Arthritis Rheumatol. 2015;67:2691–701.
Usmani SE, et al. Context-specific protection of TGFα null mice from osteoarthritis. Sci Rep. 2016;6:30434.
Cui G, et al. Association of common variants in TGFA with increased risk of knee osteoarthritis susceptibility. Genet Test Mol Biomarkers. 2017;21:586–91.
Zengini E, et al. Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis. Nat Genet. 2018;2018(1). https://doi.org/10.1038/s41588-018-0079-y.
Appleton CTG, Usmani SE, Mort JS, Beier F. Rho/ROCK and MEK/ERK activation by transforming growth factor-α induces articular cartilage degradation. Lab Investig. 2010;90:20–30.
Wang K, Yamamoto H, Chin JR, Werb Z, Vu TH. Epidermal growth factor receptor-deficient mice have delayed primary endochondral ossification because of defective osteoclast recruitment. J Biol Chem. 2004;279:53848–56.
Zhang X, et al. The critical role of the epidermal growth factor receptor in endochondral ossification. J Bone Miner Res. 2011;26:2622–33.
Jia H, et al. EGFR signaling is critical for maintaining the superficial layer of articular cartilage and preventing osteoarthritis initiation. Proc Natl Acad Sci U S A. 2016;113:14360–5.
Shepard JB, Jeong J-W, Maihle NJ, O’Brien S, Dealy CN. Transient anabolic effects accompany epidermal growth factor receptor signal activation in articular cartilage in vivo. Arthritis Res. Ther. 2013;15:R60.
Zhang X, et al. Reduced EGFR signaling enhances cartilage destruction in a mouse osteoarthritis model. Bone Res. 2014;2:14015.
Qin L, Beier F. EGFR signaling: friend or foe for cartilage? JBMR Plus. 2019;3:e10177.
Jin N, Gilbert JL, Broaddus RR, Demayo FJ, Jeong J-W. Generation of a Mig-6 conditional null allele. Genesis. 2007;45:716–21.
Frosi Y, et al. A two-tiered mechanism of EGFR inhibition by RALT/MIG6 via kinase suppression and receptor degradation. J Cell Biol. 2010;189:557–71.
Zhang Y-W, et al. Targeted disruption of Mig-6 in the mouse genome leads to early onset degenerative joint disease. Proc Natl Acad Sci U S A. 2005;102:11740–5.
Mateescu RG, Todhunter RJ, Lust G, Burton-Wurster N. Increased MIG-6 mRNA transcripts in osteoarthritic cartilage. Biochem Biophys Res Commun. 2005;332:482–6.
Joiner DM, et al. Accelerated and increased joint damage in young mice with global inactivation of mitogen-inducible gene 6 after ligament and meniscus injury. Arthritis Res Ther. 2014;16:R81.
Pest MA, Russell BA, Zhang Y-W, Jeong J-W, Beier F. Disturbed cartilage and joint homeostasis resulting from a loss of mitogen-inducible gene 6 in a mouse model of joint dysfunction. Arthritis Rheumatol. 2014;66:2816–27.
Kim TH, et al. Mig-6 suppresses endometrial cancer associated with pten deficiency and ERK activation. Cancer Res. 2014;74:7371–82.
Terpstra L, et al. Reduced chondrocyte proliferation and chondrodysplasia in mice lacking the integrin-linked kinase in chondrocytes. J Cell Biol. 2003;162(1):139–48.
Ratneswaran A, et al. Nuclear receptors regulate lipid metabolism and oxidative stress markers in chondrocytes. J Mol Med (Berl). 2017;95:431–44.
Schneider CA, Rasband WS, Eliceiri KW. NIH Image to ImageJ: 25 years of image analysis. Nat Methods. 2012;9:671–5.
Beaucage KL, Pollmann SI, Sims SM, Dixon SJ, Holdsworth DW. Quantitative in vivo micro-computed tomography for assessment of age-dependent changes in murine whole-body composition. Bone Rep. 2016;5:70–80.
White DR. Tissue substitutes in experimental radiation physics. Med Phys. 1978;5:467–79.
Glasson SS, Chambers MG, Van Den Berg WB, Little CB. The OARSI histopathology initiative – recommendations for histological assessments of osteoarthritis in the mouse. Osteoarthr Cartil. 2010;18:S17–23.
Ratneswaran A, et al. Peroxisome proliferator-activated receptor δ promotes the progression of posttraumatic osteoarthritis in a mouse model. Arthritis Rheumatol. 2015;67:454–64.
Zhang M, Egan B, Wang J. Epigenetic mechanisms underlying the aberrant catabolic and anabolic activities of osteoarthritic chondrocytes. Int J Biochem Cell Biol. 2015;67:101–9.
Lefebvre V, Dvir-Ginzberg M. SOX9 and the many facets of its regulation in the chondrocyte lineage HHS Public Access. Connect Tissue Res. 2017;58:2–14.
Waller KA, et al. Role of lubricin and boundary lubrication in the prevention of chondrocyte apoptosis. Proc Natl Acad Sci U S A. 2013;110:5852–7.
Wang M, et al. MMP13 is a critical target gene during the progression of osteoarthritis. Arthritis Res Ther. 2013;15:R5.
Blaney Davidson EN, et al. Correction: increase in ALK1/ALK5 ratio as a cause for elevated MMP-13 expression in osteoarthritis in humans and mice. J Immunol. 2010;185:–2629.
Mariani E, Pulsatelli L, Facchini A. Signaling pathways in cartilage repair. Int J Mol Sci. 2014;15:8667–98.
Lee A, et al. A current review of molecular mechanisms regarding osteoarthritis and pain. Gene. 2013;527:440–7.
Bader DL, Salter DM, Chowdhury TT. Biomechanical influence of cartilage homeostasis in health and disease. Arthritis. 2011;2011:979032.
Richmond SA, et al. Are joint injury, sport activity, physical activity, obesity, or occupational activities predictors for osteoarthritis? A Systematic Review. J Orthop Sport Phys Ther. 2013;43:515–B19.
Hackel PO, Gishizky M, Ullrich A. Mig-6 is a negative regulator of the epidermal growth factor receptor signal. Biol Chem. 2001;382:1649–62.
Maity TK, et al. Loss of MIG6 accelerates initiation and progression of mutant epidermal growth factor receptor-driven lung adenocarcinoma. Cancer Discov. 2015;5:534–49.
Li Z, et al. Downregulation of Mig-6 in nonsmall-cell lung cancer is associated with EGFR signaling. Mol Carcinog. 2012;51:522–34.
Zhang Y-W, et al. Evidence that MIG-6 is a tumor-suppressor gene. Oncogene. 2007;26:269–76.
Sasaki M, Terabayashi T, Weiss SM, Ferby I. The tumor suppressor MIG6 controls mitotic progression and the G2/M DNA damage checkpoint by stabilizing the WEE1 kinase. Cell Rep. 2018;24:1278–89.
Zhang X, et al. Epidermal growth factor receptor plays an anabolic role in bone metabolism in vivo. J Bone Miner Res. 2011;26:1022–34.
Sibilia M, et al. Correction: mice humanised for the EGF receptor display hypomorphic phenotypes in skin, bone and heart. Development. 2017;143:–4755.
Zhang X, et al. Epidermal growth factor receptor (EGFR) signaling regulates epiphyseal cartilage development through β-catenin-dependent and -independent pathways. J Biol Chem. 2013;288:32229–40.
Ma H-L, et al. Osteoarthritis severity is sex dependent in a surgical mouse model. Osteoarthr Cartil. 2007;15:695–700.
Jiang X, et al. Inhibition of Cdc42 is essential for Mig-6 suppression of cell migration induced by EGF. Oncotarget. 2016. https://doi.org/10.18632/oncotarget.10205.
Hopkins S, et al. Mig6 is a sensor of EGF receptor inactivation that directly activates c-Abl to induce apoptosis during epithelial homeostasis. Dev Cell. 2012;23:547–59.
Pante G, et al. Mitogen-inducible gene 6 is an endogenous inhibitor of HGF/Met-induced cell migration and neurite growth. J Cell Biol. 2005;171:337–48.
Castaño-Betancourt MC, et al. Novel genetic variants for cartilage thickness and hip osteoarthritis. PLoS Genet. 2016;12:e1006260.
Sun H, et al. Gefitinib for epidermal growth factor receptor activated osteoarthritis subpopulation treatment. EBioMedicine. 2018;32:223–33.
We would like to thank Julia Bowering for kindly performing the articular cartilage sectioning.
This study was funded by a fellowship from Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)/Brazil (201342/2014-6) to MB. Also, FB is supported by a grant from the Canadian Institutes of Health Research (Grant #332438). FB holds the Canada Research Chair in Musculoskeletal Research.
Ethics approval and consent to participate
All experiments were conducted under the supervision of the Animal Care Committee (ACC) at the University of Western Ontario under the Animal Use Protocol (AUP) 2019-035:1: titled “The Regulation of Endochondral Bone Growth by Hormones.”
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The authors declare that they have no competing interests.
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Bellini, M., Pest, M.A., Miranda-Rodrigues, M. et al. Overexpression of MIG-6 in the cartilage induces an osteoarthritis-like phenotype in mice. Arthritis Res Ther 22, 119 (2020). https://doi.org/10.1186/s13075-020-02213-z
- Mitogen inducible gene-6
- Epidermal growth factor receptor
- Articular cartilage