Patellar tendinopathy (PT), is an exercise-associated injury that results in significant disability and can compromise the career of an athlete (Peers and Lysens, 2005). The prevalence of PT is high in sports, such as volleyball (44.6% ± 6.6%) and basketball (31.9% ± 6.8%) (Lian et al., 2005) and it accounts for up to 15% of the soft tissue injuries reported in military cohorts (Rutland et al., 2010). Recently, a study by Bode et al. (2017) found prevalence rates as high as 13.4% in young elite level soccer players (Bode et al., 2017). Furthermore, in addition to the type of sports participation, the duration of training, female gender and hamstring flexibility have all been shown to affect the risk of PT (Morton et al., 2017). There is also some evidence to suggest that both back pain and a family history of tendon problems might be related to the risk of PT (Morton et al., 2017).

From a histological perspective, the development of PT is associated with neovascularisation, an increase in collagen type III fibers and an accumulation of glycosaminoglycans (Rosso et al., 2015). Such changes may, in part, be due to the altered expression of matrix metalloproteinase (MMP) enzymes that have been shown to have an important role in regulating tendon extracellular matrix (ECM) homeostasis (Del Buono et al., 2013). Interestingly, genetic variation within genes (like the MMPs), that code for enzymes that regulate ECM homeostasis, are known to impact on Achilles tendinopathy risk (Raleigh and Collins, 2012; Collins and Raleigh, 2009). However, genetic association studies conducted to identify risk variants have sometimes yielded conflicting data. For example, Raleigh et al. (2009) demonstrated that the G allele of the rs679620 variant within the MMP3 gene increased the risk of Achilles tendinopathy in a South African study, whereas the same variant in a British cohort did not increase risk (El Khoury et al., 2016). Likewise, the COL5A1 rs12722 T variant has been shown to increase risk of Achilles tendinopathy in both South African and Australian cohorts (September et al., 2009) but in British Caucasians this variant does not modify risk (Brown et al., 2017).

We recently suggested that epigenetic modifications, such as DNA methylation, might explain discrepant association signals sometimes obtained in studies on human patellar tendinopathy (El Khoury et al., 2018). Indeed, we demonstrated that methylation changes to a CpG site upstream of the ADAMTS4 promoter were associated with patellar tendinopathy (El Khoury et al., 2018). However, to date, and as far as we are aware, no other research has been published to address the impact of DNA methylation on the risk of human tendinopathy.

The MMP11 enzyme catalytically degrades several components of the extracellular matrix (ECM) including aggrecan, fibronectin and laminin (Araki and Mimura, 2017). Although the detailed role that MMP11 plays in ECM homeostasis is poorly understood, the expression of MMP11 in Achilles tendinopathy is substantially affected. For example, it has been shown that MMP11 RNA levels are both five and six-fold higher in painful and ruptured Achilles tendon respectively, compared to control tissue (Jones et al., 2006). Furthermore, MMP11 expression decreases nearly twofold in human Achilles tenocytes that have been subjected to mechanical strain (Jones et al., 2013). Although these observations may infer a role for MMP11 in tendinopathy, the mechanisms underlying the observations are unknown.

The MMP11 gene was originally mapped to chromosome 22 (Anglard et al., 1995). Multiple transcripts are encoded within the region 24,110,413-24,126,503 (GRch37-hp19 at: https://grch37.ensembl.org/index.html) and expression is known to be altered by DNA methylation (Navarro et al., 2012). Specifically, hypomethylation is associated with transcriptional upregulation of MMP11 (Navarro et al., 2012). With this in mind, we hypothesized that the methylation status of the MMP11 promoter might differ in DNA isolated from patellar tendinopathy compared to normal tendon. If this were the case, such differences in methylation might explain why MMP11 expression is substantially altered in tendinopathy and lead the way to novel strategies that could reduce the incidence of these injuries.

Patellar tendon tissue was obtained from 10 males with healthy patellar tendons (CON) and 10 males with patellar tendinopathy (PT). The CON samples were from patients undergoing ACL reconstruction surgeries using a patellar tendon graft and had no history of tendinopathy. Controls also had magnetic resonance imaging (MRI) to confirm their injury. The PT samples were from patients undergoing surgical debridement for recalcitrant overuse patellar tendinopathy (Parkinson et al., 2010). The PT specimens all had ultrasound scans (US) or MRI confirmation of the diagnosis by a medical doctor. PT samples were taken from the proximal tendon. Normal (CON) tendons were also taken from the proximal end, at the margins of the graft. Participants were Caucasian, aged from 19 to 41 years and they were all otherwise healthy. All participants provided written informed consent and approval for this study was obtained from the University of Northampton’s School of Health Research Ethics Committee.

We originally extracted, and bisulfite treated, the DNA from these samples as described in our previous study (El Khoury et al., 2018). Hence for this study we re-interrogated the same DNA samples using a pyrosequencing assay specific for the MMP11 gene (Hs_CHCHD10_01_PM) promoter that was selected from the Pre-Designed PyroMark^® CpG Assays (Qiagen, Hilden, Germany). Using this assay, we measured the methylation statuses of 4 separate CpG sites that were -38 (CpG 1), -55 (CpG 2), -58 (CpG 3) and -65 (CpG 4) bp respectively from the first exon of the MMP11 gene (transcript 003, GRch37, hg19).

The bisulfite treated DNA samples were amplified on a Techne TC-512 thermocycler (Bibby Scientific Ltd, Staffordshire, UK), using the PCR primer sets of the PyroMark^® CpG Assay. This amplified the specific region of interest (141 bp amplicon product) within the MMP11 gene promoter at 31 bp from the first exon. PCR amplification was confirmed by running the products on a 1x agarose gel alongside a GeneRuler™ 100 bp ladder (MBI Fermentas, UK).

Following gel electrophoresis, the biotinylated PCR products were immobilized to Streptavidin-coated Sepharose high-performance beads (GE Healthcare, Buckinghamshire, UK). The PyroMark^® Q24 vacuum (Qiagen, Hilden, Germany) was used to capture the immobilized PCR products, before releasing them into a 24 well PyroMark^® Q24 plate containing 1x sequencing primer diluted in 25 μl PyroMark^® Annealing Buffer. In order for the sequencing primer to anneal to samples, the PyroMark^® Q24 plate was placed on a hot-plate at 80 °C for 2 min, followed by 10 min incubation at room temperature. The samples were then loaded into the PyroMark^® Q24 for pyrosequencing. Each run included hypo and hyper methylated DNA control samples.

We used PyroMark^® Q24 (Version 2.0.6) software to analyse the percent methylation of each CpG site in both PT and CON groups. An independent samples t-test was used to establish whether significant differences (p<0.05) existed between each CpG site in PT and CON groups, based on a normal distribution of our data. We also determined the effect of age on methylation status by conducting a Pearson’s correlation analysis for each CpG site in the PT, CON and combined groups. All data analyses were performed using SPSS Version 20 (IBM Corp. Armonk, NY).

The recruited CON and PT groups were similarly matched for age (p = 0.449). Typical pyrograms showing the percentage DNA methylation at the 4 CpG cites within the MMP11 gene promoter (panels A and B) are shown in Figure 1. We found a significant difference (p = 0.045) in DNA methylation between the CON and PT group at the CpG 4 site that sits 65 bp upstream of the MMP11 first exon (Figure 2). At this CpG site, the mean percentage methylation in the PT samples was 4.8 ± 0.4 (95% CI 3.98 to 5.66) compared to the CON value of 3.6 ± 0.4, (95% CI 2.88 to 4.33). The affect size (Cohens d) for this difference was 0.966. We were unable to quantify the methylation status at CpG site 3 in both the CON and PT groups as the data did not meet an acceptable quality control standard. The reason for this, at present, is unknown. Finally, we found no additional differences in methylation status, for each CpG site measured, between the CON and PT groups.

In addition, for the CON group, we found a tentative correlation (r = 0.77; p = 0.009) between participant age and degree of methylation at the CpG 2 site (Figure 3A). However, the correlation failed to reach significance (p > 0.05) when a potential outlier was removed. By comparison there was no correlation (r = 0.11; p = 0.764) between participant age and degree of methylation at the CpG 2 site in the PT group (Figure 3B). Furthermore, there were no other correlations between age and degree of methylation at any of the other CpG sites measured in both the CON and PT groups. Indeed, when the analyses were pooled to contain both groups, there were no additional correlations. The mean age of the CON and PT groups was 25.1 ± 6.4 and 23.2 ± 4.4 years respectively.

We have shown a statistically significant difference (p = 0.045) in DNA methylation at a CpG site (CpG 4) in the MMP11 gene promoter in patellar tendinopathy, compared to controls. This CpG site lies 65 bp upstream of the MMP11 gene and showed higher methylation in the PT group. At present we do not know why this change takes place but methylation changes to the MMP11 gene are known to alter MMP11 RNA expression levels (Navarro et al., 2012). For example, hypomethylation causes an increase in MMP11 (Navarro et al., 2012). Indeed, it is possible that hypomethylation of the MMP11 gene promoter may, in part, explain the elevated levels of MMP11 mRNA expression previously observed in both ruptured and painful Achilles tendon (Jones et al., 2006) compared to normal tendon.

Interestingly, we found a hypermethylation (not hypomethylation) event within the MMP11 promoter in PT samples compared to controls. Hypermethylation is typically associated with reduced gene expression (Roach et al., 2005). Therefore it might be expected that MMP11 substrates accumulate within PT, as the amount of MMP11 enzyme available for catalysis would become limited. Indeed, proteoglycan accumulation has been observed in PT. Specifically, Parkinson and colleagues found increased levels of proteoglycans such as aggrecan in the tendon samples from patients that were used in this study (Parkinson et al., 2011). Normally aggrecan can protect tendon from damage as it binds to water molecules, aiding hydration and reducing the effect of over compression (Riley, 2004; Cook and Purdam, 2012). However over-hydration can lead to swelling in tendinopathy (Parkinson et al., 2011) and it is possible that hypermethylation of the MMP11 promoter might exacerbate this process.

It is interesting that we found a tentative correlation between age and degree of methylation at CpG site 2 that sits 55 bp upstream of the MMP11 first exon. This correlation was apparent in the CON group but not in DNA from those with PT. However, this result must be considered preliminary as when we removed a potential outlier from the data set the correlation disappeared. Although we cannot yet comment on the significance of this finding, it is possible that an increase in methylation in the promoter of the MMP11 gene might be necessary to allow for ECM adaptions as a person ages. Therefore, the lack of correlation between age and CpG methylation observed by us in the PT group may indicate an abnormal promoter methylation pattern that precedes tendinopathy. However, this will need to be verified by additional research.

In this study, we looked at the methylation statuses of several CpG sites upstream of the MMP11 gene in DNA from males with PT and compared them to controls. We found a significant difference (hypermethylation) in the methylation profile between these two groups for the CpG site 4 that is -65 bp away from the start of the gene. Although most studies relating to DNA methylation in musculoskeletal disorders report more extensive methylation changes over numerous CpG rich regions (Reynard, 2017), there is compelling evidence that methylation changes at single CpG sites can also have profound effects. For example, we have previously shown that methylation change at a single CpG site within the ADAMTS4 gene promoter also associates with PT (El Khoury et al., 2018). Furthermore, Nile and colleagues (2008) have shown that single CpG site methylation changes alter interleukin-6 expression, which impacts on the pathogenesis of rheumatoid arthritis (Nile et al., 2008). Methylation of single CpG sites upstream of the SLC23A and NCOR2 genes are also known to influence the severity of spinal muscular atrophy (Zheleznyakova et al., 2015).

Although we have shown that the degree of methylation, at a single CpG site -65 bp away from the start of the MMP11 gene differs in patellar tendinopathy compared to healthy tendons our study does have limitations. Firstly, as we only had access to a limited amount of sample for each patient we were unable to measure the mRNA expression levels of MMP11. However, previous studies have shown that MMP11 promoter methylation does influence its expression (Navarro et al., 2012; Veerla et al., 2008). Secondly, we only investigated a small section of the promoter for MMP11 transcript 003 and additional work should focus on other regions. Thirdly, the clinical samples available for this study were from a small group of male Caucasians and the same results might not be obtained in female or non-Caucasian groups. Indeed, we would recommend repeating this study in different population cohorts to establish whether similar DNA methylation events are observed across populations. Finally, although there were no differences between age in our PT and control groups, we were unable to control for both weight and height as these data were not available to us at the time of sampling.

We provide the first preliminary data that suggests DNA methylation of a member of the MMP family of genes differs in patellar tendinopathy compared to healthy tendon. Our data add to our earlier work on the epigenetics of human tendinopathy and suggest that risk assessment, on the basis of genetics alone, is incomplete without a knowledge of epigenetic factors.