Enpp1 inhibits ectopic joint calcification and maintains articular chondrocytes by repressing hedgehog signaling

ABSTRACT

The differentiated phenotype of articular chondrocytes of synovial joints needs to be maintained throughout life. Disruption of the articular cartilage, frequently associated with chondrocyte hypertrophy and calcification, is a central feature in osteoarthritis (OA). However, the molecular mechanisms whereby phenotypes of articular chondrocytes are maintained and pathological calcification is inhibited remain poorly understood. Recently, the ecto-enzyme Enpp1, a suppressor of pathological calcification, was reported to be decreased in joint cartilage with OA in both human and mouse, and Enpp1 deficiency causes joint calcification. Here, we found that hedgehog (Hh) signaling activation contributes to ectopic joint calcification in the Enpp1^−/− mice. In the Enpp1^−/− joints, Hh signaling was upregulated. Further activation of Hh signaling by removing the patched 1 gene in the Enpp1^−/− mice enhanced ectopic joint calcification, whereas removing Gli2 partially rescued the ectopic calcification phenotype. In addition, reduction of Gα_s in the Enpp1^−/− mice enhanced joint calcification, suggesting that Enpp1 inhibits Hh signaling and chondrocyte hypertrophy by activating Gα_s-PKA signaling. Our findings provide new insights into the mechanisms underlying Enpp1 regulation of joint integrity.

Summary: Activation of hedgehog signaling contributes to the joint calcification that is induced by loss of Enpp1 function, offering a new therapeutic target for osteoarthritis.

INTRODUCTION

The joint connects neighboring skeletal elements together as a functional unit. The joint cartilage protects the underlying bone from excessive mechanical load, which is distributed across the entire joint surface. The healthy synovial joint is composed of articular cartilage and other joint tissues such as synovial membrane and joint ligaments (Lories and Luyten, 2011). In the healthy joint, the matrix of articular cartilage maintains a relatively low turnover rate and chondrocytes exhibit low proliferation rates, without hypertrophy or terminal differentiation (Dreier, 2010).

The integrity of the complex joint structures has to be maintained throughout life; its disruption causes arthritis, a joint disease that affects >50% of people over the age of 65 and is among the leading causes of disability throughout the world (Guilak, 2011). Osteoarthritis (OA) is the most common type of arthritis (Arai et al., 2004). It is primarily characterized by cartilage breakdown, which is associated with new bone formation at the joint margins (osteophytosis), subchondral bone sclerosis, variable degrees of mild synovitis and thickening of the joint capsule (Sellam and Berenbaum, 2010). Articular cartilage loss is the first sign of OA; the breakdown of cartilage extracellular matrix leads to an early and high incidence of OA (Heinegård and Saxne, 2011). In the osteoarthritic joint, there is ectopic chondrocyte hypertrophy evidenced by the expression of collagen 10a1 (Col10, also known as Col10a1) and matrix metalloproteinase 13 (Mmp13) (Kamekura et al., 2006; Neuhold et al., 2001) in articular cartilage, and these ectopic hypertrophic chondrocytes form calcified cartilage zones (Tchetina, 2011). However, despite detailed histological characterization of OA, the underlying molecular mechanisms whereby articular cartilage degeneration is initiated and advanced, leading to OA, remain poorly understood. This has severely hampered development of pharmacological agents that can prevent or reduce the articular cartilage degeneration and ectopic calcification associated with OA. Multiple risk factors such as hormones, age and levels of calcium (Ca²⁺), phosphate (P_i) and pyrophosphate (PP_i) in the blood have been found to contribute to the onset and progression of OA. As OA heritability has been suggested to be 50% or more, genetic susceptibility contributes significantly (Spector and MacGregor, 2004; Valdes et al., 2008).

Ectonucleotide pyrophosphatase/phosphodiesterase 1 (Enpp1) is an ecto-enzyme that converts ATP to AMP and PP_i outside of cells. Enpp1 plays an essential role in phosphate homeostasis (Goding et al., 2003). Enpp1 has been found to be expressed in various cells, including chondrocytes and osteoblasts (Goding et al., 1998), and Enpp1 protein has been detected in articular cartilage in both human and mouse joints (Bertrand et al., 2012). Enpp1 inhibits hydroxyapatite formation by generating PP_i, and thereby inhibits soft tissue calcification (Stefan et al., 2005). In humans, loss-of-function ENPP1 mutations cause generalized arterial calcification of infancy (GACI) (Ruf et al., 2005; Rutsch et al., 2003) or pseudoxanthoma elasticum (Nitschke and Rutsch, 2012). Enpp1 also represents an important genetic susceptibility factor in OA of the hand, which is the third most common OA, after knee OA and hip OA. A family-based association study showed that genetic variation at the ENPP1 locus is involved in the etiology of hand OA (Gabay and Gabay, 2013). In mice, loss of function of Enpp1 results in ectopic calcification of articular cartilage, the joint capsule and certain tendons (Babij et al., 2009; Harmey et al., 2004; Zhang et al., 2016). Enpp1^−/− mice also exhibit OA-like changes (Bertrand et al., 2012).

Hedgehog (Hh) signaling plays an essential and pivotal role in the regulation of chondrocyte proliferation and hypertrophy during endochondral bone development, in which Indian hedgehog is expressed in prehypertrophic and early hypertrophic chondrocytes (Long et al., 2001; Mak et al., 2008b; St-Jacques et al., 1999; Vortkamp et al., 1996). We have shown previously that Hh signaling activation promotes chondrocyte hypertrophy in articular cartilage, and has also been found in human OA (Lin et al., 2009; Mak et al., 2008b). Blockade of Hh signaling can reduce the severity of OA in mice (Lin et al., 2009). We have also found that Gα_s inhibits Hh signaling (Regard et al., 2013). In addition, loss of Gnas, which encodes Gα_s, leads to premature chondrocyte hypertrophy (Bastepe et al., 2004). As ATP and its derived products, such as adenosine, which are generated by Enpp1, can signal through G-protein-coupled receptors (GPCR) that can be coupled to Gα_i or Gα_s, Enpp1 may inhibit joint calcification by inhibiting Hh signaling through reducing Gα_i signaling and/or upregulating Gα_s signaling. To test this hypothesis, we have determined whether Hh signaling is altered in the Enpp1^−/− joint. We found ectopic upregulation of Hh signaling activity in the articular cartilage of the Enpp1^−/− mice. Activation of Hh signaling by removing one copy of patched 1 (Ptch1), or reduction of Hh signaling by removing one copy of Gli2, led to enhanced or reduced ectopic joint calcification in the Enpp1^−/− mice, respectively. In addition, heterozygous loss of Gnas function also enhanced the joint calcification phenotypes of the Enpp1^−/− mice. Our work suggests that, apart from regulating ATP, PP_i and P_i homeostasis, Enpp1 deficiency may also cause OA by promoting calcification via activation of the Hh signaling pathway.

RESULTS

Loss of Enpp1 alters cell differentiation in joints

The Enpp1^−/− mice developed stiffened joints at ∼4 weeks of age on a standard rodent diet, with progressively mineralized articular cartilage detected from 9 weeks of age (Bertrand et al., 2012; Li et al., 2013; Zhang et al., 2016). To test whether mineralization of the articular cartilage is caused simply by deposition of hydroxyapatite on the articular surfaces, or whether there is loss of articular chondrocyte differentiation and ectopic chondrocyte hypertrophy associated with OA in the joints of the Enpp1^−/− mice, we first examined gene expression by quantitative real time PCR (qRT-PCR) in the metacarpophalangeal joints of the Enpp1^−/− and wild-type (WT) control mice at 1 month of age, when there is no joint mineralization (Zhang et al., 2016) (Fig. 1A). In this study, the phalangeal joints between the metacarpal bone and the proximal phalanx of digit three were used for analysis, unless otherwise indicated in the text. The joint tissue was a mixture of cartilage, tendon and synovium. Normal articular chondrocytes strongly express Col2 (also known as Col2a1), aggrecan (Acan) and Sox9, but not Col10, a marker for hypertrophic chondrocytes. In the joints of the Enpp1^−/− mice, we found that, whereas Col2, Acan and Sox9 expression was reduced, Col10 expression was significantly upregulated. To further examine whether there was hypertrophic chondrocyte differentiation in the articular cartilage of the Enpp1^−/− mice, we examined the presence of hypertrophic chondrocyte cells using the osterix (Osx, also known as Sp7) promoter-driven GFP-fused cre recombinase (OsxGFPcre) mouse line (Rodda and McMahon, 2006). Osx is expressed in hypertropic chondrocytes and is an early marker of committed osteoblast cells (Nakashima et al., 2002). To detect whether Osx was ectopically expressed in the phalangeal joint, we generated OsxGFPcre; Enpp1^−/− mice. The GFP⁺ cells should be either hypertrophic chondrocytes or osteoblasts, which express Osx. Whereas the control WT OsxGFPcre mice had almost no GFP⁺ cells in the joint, the number of GFP⁺ cells increased ∼20-fold in the articular cartilage and in the joint capsule of the metacarpophalangeal joint of the 4-month-old Enpp1^−/− mice (Fig. S1A-1A″), in which joint mineralization started at ∼8-9 weeks of age (Hajjawi et al., 2014; Zhang et al., 2016). In addition, we performed immunofluorescent staining of Osx and Sox9 in sections of the 1-month-old WT and Enpp1^−/− metacarpophalangeal joints. Osx expression was detected in the articular cartilage of the metacarpophalangeal joints of the Enpp1^−/− mice, but not in that of the WT mice (Fig. 1B-C′). Conversely, Sox9 expression was reduced the Enpp1^−/− mice compared with the WT control (Fig. 1D-E′). These results indicate that in addition to deposition of hydroxyapatite crystals, the Enpp1^−/− mice formed ectopic hypertrophic chondrocytes and/or osteoblasts in the articular cartilage and joint capsule.

Fig. 1.

Ectopic expression of hypertrophic chondrocyte and osteoblast markers in the Enpp1^−/− metacarpophalangeal joint. (A) qRT-PCR analysis of cartilage-specific markers and hypertrophic markers expressed in the metacarpophalangeal joints of Enpp1^−/− and WT control mice (Enpp1^+/−) at 1 month of age (n=3). (B-E′) Phalangeal joint sections from 1-month-old WT and Enpp1^−/− mice were stained with antibodies against Osx (B-C′) and Sox9 (D-E′). Nuclei are stained with DAPI. (F-F″) Col1a1 mRNA expression detected by ISH with RNAscope technology in the metacarpophalangeal joint surface of newborn pups (P2). Arrows indicate ectopic expression of Col1a1 in the Enpp1^−/− joint cartilage and capsule. Col1a1-expressing cells in the articular cartilage of the metacarpophalangeal joints were quantified as the number of Col1a1⁺/field of view under 40× objective magnification (n=4). (G-G″) Mmp13 expression in the joints of P2 WT and Enpp1^−/− mice. Arrows indicate ectopic expression of Mmp13. Mmp13⁺ cells were quantified as the number of Mmp13⁺ cells/field of view (G″). (H-I″) Opn expression in the joints of 1 month old WT and Enpp1^−/− mice. Opn⁺ cells were quantified as the number of Opn⁺ cells/field of view (500×400 µm) (H‴). *P<0.05, **P<0.01 (Student's t-test). Dashed lines indicate the surface of articular cartilage.

To further confirm that there was ectopic chondrocyte and/or osteoblast differentiation in the joints of the Enpp1^−/− mice, we examined expression of other hypertrophic and osteoblast cell markers. We performed in situ hybridization (ISH) using postnatal day (P) 2 Enpp1^−/− forelimb joints and found ectopic expression of collagen1a1 (Col1a1) in the articular cartilage of the Enpp1^−/− mice and increased Col1a1 expression in the joint capsule (Fig. 1F,F′). Furthermore, using immunofluorescent staining, we found that expression of Mmp13 and osteopontin (Opn, also known as Spp1) were both upregulated in the articular cartilage in the metacarpophalangeal joints of the P2 and 1-month-old Enpp1^−/− mice, respectively (Fig. 1G,G″ and H-I″). Taken together, these results indicate that in the phalangeal joints of the Enpp1^−/− mice, there is ectopic chondrocyte hypertrophy and osteoblastic differentiation before ectopic mineralization could be detected.

Loss of Enpp1 leads to upregulation of Hh signaling in development

Previous studies have demonstrated that Hh signaling promotes chondrocyte hypertrophy and osteoblast differentiation (Lin et al., 2009; Mak et al., 2006; Regard et al., 2013). We hypothesized that Enpp1 may inhibit chondrocyte hypertrophy and/or osteoblast differentiation in the joint by inhibiting Hh signaling. Loss of Enpp1 may have resulted in activated Hh signaling, causing ectopic calcification. To test this hypothesis, we first examined the expression of the Hh target genes Gli1 (Bai et al., 2002), Hhip (Chuang and McMahon, 1999) and Ptch1 (Goodrich et al., 1996) in embryonic day (E) 15.5 forelimbs by whole-mount in situ hybridization (WISH). Gli1, Hhip and Ptch1 expression were all upregulated in the forelimbs of the E15.5 Enpp1^−/− embryos compared with the WT controls (Fig. 2A-D, Fig. S1B,B′). However, we did not detect obvious ectopic expression of Hh target genes outside their normal expression domains in the Enpp1^−/− embryos. Upregulation of Hh target gene expression in the forelimbs was further confirmed by qRT-PCR analysis of the E15.5 Enpp1^−/− and WT embryos (Fig. 2E). In addition, chondrocyte hypertrophy and/or osteogenic differentiation in the forelimbs was increased as shown by qRT-PCR analysis of the E15.5 Enpp1^−/− and WT embryos (Fig. 2F). These results show that, early in skeletal formation during embryonic development, Hh signaling is already upregulated in the Enpp1^−/− limbs.

Fig. 2.

Increased Hh signaling activity in the Enpp1^−/− embryo. (A-D) Expression of Hh signaling targets Gli1 (A,B) and Hhip (C,D) in E15.5 WT and Enpp1^−/− forelimbs shown, by WISH. Gli1 and Hhip mRNA levels were upregulated in the limbs of the Enpp1^−/− embryos. (E-F) qRT-PCR analysis of Hh target gene expression in the forelimbs of E15.5 embryos (n=3). *P<0.05, **P<0.01 (Student's t-test).

As ectopic mineralization in the Enpp1^−/− mice occurs 9 weeks after birth (Zhang et al., 2016), we asked whether ectopic Hh signaling activation in the joint of the Enpp1^−/− mutants could be detected before ectopic mineralization. We dissected the limbs from the P2 Enpp1^−/− and WT mice, and gene expression was examined by qRT-PCR. Hh target gene (Gli1, Hhip and Ptch1) expression was increased in the Enpp1^−/− mutant (Fig. 3A). Chondrocyte hypertrophy and/or osteogenic differentiation was also increased in the Enpp1^−/− mutant, as shown by increased expression of osteoblast differentiation markers such as Osx, Col1a1 and osteocalcin (Oc, also known as Bglap) (Fig. 3A). We then further examined Hh signaling activity in situ in the joint. A lacZ ‘knock-in’ null allele of Ptch1 (Mak et al., 2008b) was used to examine Ptch1 expression. X-gal staining of the Ptch1^+/− metacarpophalangeal joints at P2 showed Ptch1-lacZ expression in the growth plate and perichondrium region as expected (Fig. 3B,C, Fig. S2E). Ptch1-lacZ expression in the articular cartilage was much weaker. Interestingly, clustered strong ectopic Ptch1-lacZ expression was detected in the articular cartilage and perichondrum (Fig. 3B′-C″, Fig. S2F-F′) in the P2 Ptch1^+/−; Enpp1^−/− mouse pups. These results indicate that Hh signaling is indeed ectopically activated early after birth in the joint cartilage of the Enpp1^−/− mice.

Fig. 3.

Increased Hh signaling activity in postnatal Enpp1^−/− mutant mice. (A) qRT-PCR analysis of gene expression of Hh targets and osteoblast markers in the front paws of P2 mice (n=3). (B-C″) β-galactosidase staining (blue) of the metacarpophalangeal (B,B′) and carpo-metacarpal joints (C,C′) of P2 Enpp1^−/− and Enpp1^−/−; Ptch1^+/− mice. Ectopic Ptch1-lacZ expression is indicated by red arrows (articular cartilage) and black arrows (perichondrium). The number of lacZ⁺ cells in the articular cartilage of the metacarpophalangeal joints was quantified as the number of lacZ⁺cells/field of view under 40× objective magnification (n=3) (C″). (D) qRT-PCR analysis of Hh target and osteogenic genes expressed in the front paws of 1-month-old Enpp1^−/− mice (n=3). (E-F′) Hh signaling activity was detected by lacZ expression (β-galactosidase staining, blue) in the metacarpophalangeal joints from 3-week-old Ptch1^+/− and Ptch1^+/−; Enpp1^−/− mice. Black arrows indicate Hh activity in the perichondrium of metacarpal bone. The articular cartilage is shown in higher magnification in E′ and F′. Red arrows indicate the lacZ⁺ chondrocytes. (G-H‴) Phalangeal joint sections from 2-month-old WT (G-G″) and Enpp1^−/− (H-H″) mice were stained with antibodies against Gli1. Nuclei are stained with DAPI. Gli1 expression was detected in the articular chondrocyte of Enpp1^−/− (yellow arrows), but not in WT mice. The number of Gli1⁺ cells in the articular cartilage was quantified as the number of Gli1⁺ cells/field of view under 40× objective magnification (n=3) (H‴). *P<0.05, **P<0.01 (Student's t-test). Dashed lines indicate the surface of articular cartilage.

As joint mineralization was observed later than Hh signaling upregulation in the Enpp1^−/− mice, we hypothesized that upregulation of Hh signaling activity may be progressively more severe, which eventually leads to ectopic joint mineralization. To test this, we performed qRT-PCR analysis with forelimb tissues from 1-month-old WT, Enpp1^+/− and Enpp1^−/− mice (Fig. 3D). A more pronounced increase in the expression of Hh signaling target genes and osteoblast markers was observed in the limbs of Enpp1^−/− mice compared with that seen in the limbs of the WT control. The WT control and Enpp1^+/− mice, which never developed a stiff joint phenotype, had similar expression levels of the Hh target genes. To examine ectopic activation of Hh signaling in situ in older mice, we examined Ptch1-lacZ expression again in the metacarpophalangeal joint of 3-week-old mice, before the detection of ectopic mineralization. We found that Ptch1-lacZ expression was increased in the perichondrium and periosteum of the Enpp1^−/− mutant digit close to the growth plate (compare Fig. 3F with E). In the articular cartilage, more cells, particularly those lining the joint surface, showed stronger lacZ expression (β-galactosidase staining) in the Enpp1^−/−; Ptch1^+/− mice (Fig. 3F′) compared with the Ptch1^+/− control (Fig. 3E′). It has been reported that the articular cartilage and tendon of the joints were mineralized in the Enpp1^−/− mutants mice at 3 months of age (Hajjawi et al., 2014; Harmey et al., 2004; Okawa et al., 1998; Zhang et al., 2016). To examine Hh signaling activities at this stage, qRT-PCR analysis was performed using the Enpp1^−/− forelimb tissue. The results confirmed our finding that Hh target genes were highly expressed in the Enpp1^−/− joints compared with the controls (Fig. S1C). Our results indicate that, in the Enpp1^−/− joints, Hh activity is increased and detected ectopically before ectopic mineralization occurs in the postnatal phalangeal joint.

As ectopic calcification and Ptch1-lacZ expression were found in the digit joint of the Enpp1^−/− mice, we further examined Gli1 protein expression in the Enpp1^−/− and WT joint at 2 months and 4 months using immunofluorescent staining. Gli1 expression is also a readout of Hh signaling activity (Ingham and McMahon, 2001) and we found it was indeed ectopically detected in the nucleus of chondrocytes in the articular cartilage of digit joints of both 2-month-old (Fig. 3G-H‴) and 4-month-old (Fig. S2A-D″) Enpp1^−/− mice. Taken together, these results suggest that, in the phalangeal joints of the Enpp1^−/− mice, Hh signaling was upregulated, and that this change was associated with ectopic osteoblast differentiation in the phalangeal joints.

Activation of Hh signaling enhances joint calcification in the Enpp1^−/− mice

Our observation that the loss of Enpp1 leads to Hh signaling activation in the phalangeal joint suggests that Hh signaling may be a functional target of Enpp1 in regulating joint integrity. To test this hypothesis genetically, we first set out to determine whether there were genetic interactions between Ptch1 and Enpp1 that cause OA. As Ptch1 encodes an inhibitory receptor of the Hh signaling pathway (Stone et al., 1996), removing one allele of Ptch1 provides a sensitized genetic background to better reveal the effects of Hh signaling activation. We reasoned that the digit joint calcification phenotype of the Enpp1^−/− mice should be enhanced by the loss of one copy of Ptch1, if activation of Hh signaling is causative for this phenotype. Therefore, the Ptch1^+/−; Enpp1^−/− mice were generated and Col1a1 expression was examined by ISH (Fig. 4A-C′, Fig. S3A-C). Col1a1 expression was further increased in the articular cartilage on both sides of the metacarpophalangeal joint of the P2 Ptch1^+/−; Enpp1^−/− mice compared with the Enpp1^−/− mice. Ectopic expression of Osx, Opn and Oc was determined by immunohistochemistry and found to be further increased in the Ptch1^+/−; Enpp1^−/− joints compared with the Enpp1^−/− joints (Fig. 4D-F‴, Fig. S3D-D‴). These results indicate that phenotypes of ectopic chondrocyte hypertrophy and/or osteoblast differentiation in the Enpp1^−/− mutant joint were further enhanced by genetic enhancement of Hh signaling.

Fig. 4.

Enhanced joint calcification by increasing Hh signaling in the Enpp1^−/− mice. (A-C) Col1a1 expression was detected using ISH of the phalangeal joint sections from P2 mice. (C′) The number of Col1a1⁺ cells in the articular cartilage of the metacarpophalangeal joints was quantified as the number of Col1a1⁺ cells/field of view under 40× objective magnification (n=3). (D-F‴) Fluorescent immunostaining of Osx and Opn in the phalangeal joint sections of WT, Enpp1^−/− and Enpp1^−/−; Ptch1^+/− mice, which were P2 littermates. Osx⁺ and Opn⁺ cells were quantified as the number of Osx⁺ cells/field of view (500×300 µm) (D″″) and Opn⁺ cells/field of view (500×300 µm) (E″″). (G-I′) Representative images of Alcian Blue- and Alizarin Red-stained forelimbs from 3-month-old Enpp1^+/− (G), Enpp1^−/− (H), and Enpp1^−/−; Ptch1^+/− (I) mice. Phalangeal joints are shown at higher magnification (G′,H′,I′). Arrows indicate the enlarged metacarpophalangeal joints. (J) Quantification of the size of metacarpophalangeal joints in WT, Enpp1^+/−, Enpp1^−/−; Ptch1^+/− and Enpp1^−/− mice. Littermates of Enpp1^−/−; Ptch1^+/− and Enpp1^−/− were used in this experiment (n=3). (K-N) Representative X-ray images of the hindlimbs of 4-month-old mice. Arrow indicates enhanced calcification in the phalangeal joint of Enpp1^−/−; Ptch1^+/− mice. (O-Q′) Safranin-O staining of sections of the metacarpophalangeal joints from forelimbs of 3-month-old Enpp1^+/− (O,O′), Enpp1^−/− (P,P′), Enpp1^−/−; Ptch1^+/− (Q,Q′) mice. Arrows indicate reduced Safranin-O staining. O′,P′,Q′ are enlargements of the boxed areas in O,P,Q, respectively. NS, not significant, *P<0.05, **P<0.01 (Student's t-test). Dashed lines indicate the surface of articular cartilage.

Consistent with increased expression of osteoblast markers in the metacarpophalangeal joint of the Ptch1^+/−; Enpp1^−/− neonatal mice, in the 3-month-old Ptch1^+/−; Enpp1^−/− mice, joint calcification indicated by Alizarin Red staining was enhanced compared with the Enpp1^−/− mice (Fig. 4G-J). The joint size was quantified by measuring the relative size of the metacarpophalangeal joints using ImageJ (imagej.nih.gov/ij/) (Fig. S3E). The relative sizes of the metacarpophalangeal joints of digits two and four were further increased in the Ptch1^+/−; Enpp1^−/− mice compared with those in the Enpp1^−/− mice (Fig. 4G-J, n=4). There was no significant difference in the relative size of WT and Enpp1^+/− joints, and both were smaller than the Enpp1^−/− and Ptch1^+/−; Enpp1^−/− joints. In addition, we compared mineralization levels of the hindlimbs from 4-month-old mice by X-ray imaging, which also showed that the loss of one copy of Ptch1 enhanced calcification in the joint area of the Enpp1^−/− mice (compare Fig. 4N with L). These results indicate that activation of Hh signaling in the Enpp1^−/− mice further promoted osteoblast differentiation in the joint. We then examined cartilage matrix integrity by Safranin-O staining of the articular cartilage sections (Kim et al., 2014) (Fig. 4O-Q′). More-severe loss of Safranin-O staining was observed in the metacarpophalangeal joint sections from the Ptch1^+/−; Enpp1^−/− mice than from the Enpp1^−/− mice at 3 months (Fig. 4P-Q′). These results indicate that increased Hh signaling further enhanced the articular cartilage damage and joint calcification that is caused by Enpp1 loss.

Reduced Hh signaling activity partially rescues joint calcification in the Enpp1^−/− mice

As Hh signaling promotes chondrocyte hypertrophy as well as osteoblast differentiation (Lin et al., 2009; Mak et al., 2008b; Regard et al., 2013), we next asked whether joint calcification in the Enpp1^−/− mice can be reduced by inhibiting Hh signaling activity. Gli2 is mainly responsible for the activated form of the Gli transcription factors that activate Hh signaling target gene expression (Ahn and Joyner, 2004; Bai et al., 2002, 2004; Corrales et al., 2004; Joeng and Long, 2009). To reduce Hh activity in the Enpp1^−/− mice, we removed one copy of Gli2 (Fig. 5D,D′,H), and found that this led to a decrease in joint sizes compared with those in the Enpp1^−/− mice (n=4 in each group) (Fig. 5A-D′,I, Fig. S4A-C). Enpp1^+/−; Gli2^+/− mice or Enpp1^+/− mice did not show joint calcification and they were considered control groups (Fig. 5A-B′). As Hh signaling promotes osteoblast differentiation from mesenchymal progenitor cells, we next tested whether Enpp1 inhibits osteoblast differentiation from mesenchymal progenitor cells by inhibiting Hh signaling. Subcutaneous mesenchymal progenitors (SMPs) were isolated from the Enpp1^−/−; Gli2^+/−, Enpp1^−/−, Enpp1^+/−; Gli2^+/− and Enpp1^+/− mice, and cultured under osteogenic conditions. Osteoblast differentiation was determined by alkaline phosphatase (ALP) staining and qRT-PCR assays. ALP activity was similar in the control Enpp1^+/−; Gli2^+/− and in the Enpp1^+/− SMPs, but increased in the Enpp1^−/− SMPs. This increase was ameliorated in the Enpp1^−/−; Gli2^+/− cells (Fig. 5E-H). Consistently, expression of Hh target genes and osteogenic markers were all decreased in the Enpp1^−/−; Gli2^+/− SMPs compared with the Enpp1^−/− SMPs (Fig. 5J). Therefore, reduction of Hh signaling indeed led to a reduction in osteoblast differentiation from mesenchymal progenitor cells promoted by loss of Enpp1.

Fig. 5.

Reduced Hh signaling activity partially rescued joint calcification of Enpp1^−/− mice. (A-D) Representative images of Alcian Blue and Alizarin Red stained forelimbs from 3-month-old Enpp1^−/− (A), Enpp1^+/−; Gli2^+/− (B), Enpp1^−/− (C) and Enpp1^−/−; Gli2^+/− (D) mice. (A′,B′,C′,D′) Phalangeal joints shown at higher magnification. (E-G) Representative ALP staining of SMPs from WT (E), Enpp1^+/−; Gli2^+/− (F), Enpp1^−/− (G) and Enpp1^−/−; Gli2^+/− mice (H) cultured in osteogenic medium for 7 days. (I) Quantification of the relative metacarpophalangeal joint sizes. Littermates were used in this experiment, n=4. (J) qRT-PCR analysis of Hh target and osteoblast genes expressed in SMPs of indicated genotypes. SMPs were cultured in osteogenic medium for 7 days (n=3). NS, not significant, *P<0.05, **P<0.01, ***P<0.001 (Student's t-test).

Loss of Gnas-enhances joint calcification in the Enpp1^−/− mice

As Hh signaling activation due to Enpp1 loss contributed to joint calcification in the Enpp1^−/− mice, we next asked how Enpp1 inhibits Hh signaling. The Hh signaling pathway can be inhibited by Gα_s signaling (He et al., 2014; Regard et al., 2013) and ATP can signal through Gα_i- or Gα_s-coupled receptors (Burnstock, 2007; Di Virgilio, 2012). We therefore tested whether ectopic joint calcification in the Enpp1^−/− mice can be enhanced by loss of Gnas function. The Enpp1^−/−; Gnas^+/− mice were generated, and ectopic calcification of the metacarpal bones and interphalangeal joints were examined at 2 months of age (Fig. 6A-D) (n=3 in each group). Ectopic calcification was not detected in the Gnas^+/− mice (Fig. 6C), but the loss of one copy of Gnas enhanced joint calcification of the Enpp1^−/− mice (compare Fig. 6D with B). This was also confirmed by Alizarin Red and Alcian Blue staining of the skeleton of 2.5-month-old mice (Fig. 6E,F). The Enpp1^−/−; Gnas^+/− mice showed the most-severe calcification and enlargement of the interphalangeal joints, with reduced space in the phalangeal joint cavity.

Fig. 6.

Ectopic joint calcification in Enpp1^−/− mutants was enhanced by reduced Gnas. (A-D) Representative X-ray images of the forelimbs of 2-month-old WT, Enpp1^−/−, Gnas^+/− and Enpp1^−/−; Gnas^+/− mice. Gnas^+/− enhanced the joint calcification of the Enpp1^−/− mice. These data indicated that Enpp1 may signal through Gα_s in regulating cartilage calcification. Arrows indicate calcified joints. (E-F) Representative Alizarin Red and Alcian Blue staining of forelimbs from the Enpp1^−/− and the Enpp1^−/−; Gnas^+/− mice at 2.5 months of age. More ectopic mineralization can be found around the joints of the Enpp1^−/−; Gnas^+/− mice compared with the Enpp1^−/− mice. (G-I) Representative Safranin-O staining of phalangeal joint sections from forelimbs of 1-month-old mice. Arrows indicate reduced Safranin-O staining and reduced cartilage thickness. (J-R″) Sections of phalangeal joints from 1-month-old WT, Enpp1^−/− and Enpp1^−/−; Gnas^+/− mice were stained with antibodies against Gli1 (J-L′), Osx (M-O′) and Sox9 (P-R′). Gli1, Osx and Sox9 positive cells were counted and quantified as the number of Gli1⁺/field of view, Osx⁺/field of view and Sox9⁺/field of view (500×400 µm) (R′′). Nuclei are stained with DAPI. (S) Western blot PKA activity measured using p-Creb levels in MEF cells from WT mice. Cells were treated for 5 min with ATP of indicated concentration. (T) Chondrocytes isolated from P0 WT and Enpp1^−/− mice were treated with 1 mM ATP for 5 min. P-Creb and total Creb protein levels were detected using western blotting. (U) WT MEF cells were treated with 100 nM SAG, 0.1 mM ATP or 0.1 mM NHATP for 10 min. p-Creb, total Creb and tubulin protein levels were detected using western blotting. Protein bands in the blot were quantified by densitometry and analyzed using ImageJ. The numbers indicate relative grayscale values of P-Creb and Creb in each lane, and P-Creb/Creb ratio was calculated. **P<0.01 (Student's t-test). Dashed lines indicate the surface of articular cartilage.

We then performed Safranin-O staining of the phalangeal joint sections to detect the cartilage matrix integrity. Articular cartilage was thinner at 1 month in the Enpp1^−/−; Gnas^+/− joints compared with the joint from the Enpp1^−/− mice (Fig. 6G-I). A thinner articular cartilage layer in the joint was also found in the Ptch1^c/c; Col2a1-CreER mice (Mak et al., 2008b), consistent with the notion that upregulated Hh signaling contributes to the joint phenotypes. To test whether a reduction of Gnas is associated with Hh signaling upregulation, we examined expression of Gli1, Osx and Sox9 by immunohistochemistry. We found that, whereas Gli1 and Osx were expressed at higher levels in the articular cartilage of the Enpp1^−/−; Gnas^+/− mice than in the Enpp1^−/− mice, Sox9 expression was reduced (Fig. 6J-R″). These results indicate that Gnas genetically interacts with Enpp1 to inhibit joint calcification, and support the suggestion that Enpp1 may act through Gα_i to inhibit Hh signaling in the joint cartilage.

The P2 purinergic receptors (i.e. P2X and P2Y receptors) mediate ATP signaling (Erb et al., 2006; Khakh and North, 2006). Eight P2Y family members are GPCRs (P2Y1, P2Y2, P2Y4, P2Y6, P2Y11, P2Y12, P2Y13 and P2Y14) and they respond to the extracellular ATP and ADP (North, 2002). In addition, adenosine receptors, which are also GPCRs, respond to adenosine derived from ATP and ADP after hydrolysis. To test whether ectopic calcification in the Enpp1^−/− mice may be caused by increased extracellular ATP, which can act through Gα_i-coupled P2 purinergic receptors to inhibit cAMP production and protein kinase A (PKA) activity, we treated mouse embryonic fibroblast (MEF) cells with ATP and measured p-Creb levels as an indication of PKA activities, which are positively or negatively regulated by Gα_s or Gα_i through cAMP, respectively. MEF cells were treated with 1 mM or 1 µM of ATP for 5 min. The p-Creb levels were significantly decreased by both ATP treatments, especially after the 1 mM ATP treatment (Fig. 6S). To test whether joint cells were similarly regulated, ATP treatment of primary synovial cells was performed, which also resulted in reduction of Creb phosphorylation (Fig. S4D). These results suggest that increased extracellular ATP can decrease cAMP and PKA levels, leading to a reduction of p-Creb levels. To further test whether chondrocytes were regulated by Enpp1 through ATP, primary chondrocytes were isolated from the WT or Enpp1^−/− mice and treated with vehicle (doubly distilled H₂O) or 1 mM ATP for 5 min. ATP treatment of WT chondrocytes also reduced Creb phosphorylation, and Enpp1^−/− chondrocytes with vehicle treatment showed a much lower p-Creb/total Creb ratio compared with those from the WT chondrocytes (Fig. 6T), indicating that the loss of Enpp1 in chondrocytes leads to a reduction of PKA activity due to increased extracellular ATP levels. Furthermore, Enpp1^−/− chondrocytes did not respond to ATP treatment (Fig. 6T), possibly because of saturated ATP levels. These results suggest that, in chondrocytes and possibly other synovial tissues, Enpp1 regulates PKA activity, which in turn regulates Hh signaling, as has been previously reported in other contexts (He et al., 2014; Regard et al., 2011, 2013).

ATP can be hydrolyzed by Enpp1 to form PP_i and AMP, which can be further hydrolyzed to form adenosine and P_i. To further test whether loss of Enpp1 leads to increased ATP signaling through Gα_i to decrease p-Creb, we treated MEF cells with ATP and a non-hydrolyzeable ATP (NHATP; β, γ-CH₂-ATP), which functions as a selective inhibitor of human ENPP1 (Lecka et al., 2013). In the MEF cells, we found that both ATP and NHATP can efficiently reduce the phosphorylation of Creb at the concentration of 0.1 mM for 10 min (Fig. 6U). NHATP appears to have a slightly stronger action than ATP, possibly due to its resistance to hydrolysis. Interestingly, treatment with SAG, an agonist of Hh receptor smoothened (a seven transmembrane protein), also reduced Creb phosphorylation. These results suggest that Enpp1 in the extracellular space may promote Gα_s signaling activity by reducing ATP-induced Gα_i signaling, thereby inhibiting joint calcification.

DISCUSSION

Here, we show that upregulated Hh signaling activity contributes to the joint calcification phenotypes of Enpp1^−/− mice. Increased Hh signaling activity was observed early in development of the Enpp1^−/− embryos. Ectopic expression of Hh target genes, together with upregulation of chondrocyte hypertrophy and/or osteogenic markers, preceded calcification in the joint of the postnatal Enpp1^−/− mice. Genetic enhancement or reduction of Hh signaling enhanced or reduced the joint calcification phenotypes in the Enpp1^−/− mice, respectively. Our work suggests that inhibition of Hh signaling may lead to a therapeutic strategy to reduce ectopic calcification caused by loss or reduced ENPP1 functions in humans.

Extracellular PP_i is a crucial factor that inhibits calcification. Enpp1 deficiency directly leads to reduced PP_i levels, causing the deposition of hydroxyapatite (Murshed et al., 2005; Harmey et al., 2004). In this current study, we observed activation of Hh signaling and expression of chondrocyte hypertrophy and/or osteoblast markers in the Enpp1^−/− joint, indicating that calcification caused by Enpp1 deficiency is not only a process of passive deposition of hydroxyapatite on the joint surface, but is also driven by an active process due to ectopic chondrocyte hypertrophy and/or osteoblast differentiation driven by activated Hh signaling. As recent studies show that chondrocytes can transdifferentiate into osteoblasts (Dy et al., 2012; Park et al., 2015; Yang et al., 2014a,b; Zhou et al., 2014), it will be interesting to further determine whether osteoblast transdifferentiation indeed occurs in the articular cartilage of Enpp1^−/− mice. Our evidence suggests that Hh signaling upregulation is a primary outcome of Enpp1 deficiency, not a secondary effect of decreased PP_i, as both ATP and NHATP inhibited PKA activity, shown by reduced Creb phosphorylation (Fig. 6U). It is likely that decreased PPi levels and Hh signaling activation are two parallel processes that induced calcification. This is further supported by partial rescue of ectopic calcification in the Enpp1^−/− mice by removing one copy of Gli2. There are several possibilities for why Gli2^+/− only partially rescued the Enpp1^−/− stiff joint phenotype. First, whole-body PP_i levels were decreased in the Enpp1-deficient mice (Johnson et al., 2003). Removal of Gli2 cannot change the circulating P_i/PP_i ratio in the Enpp1^−/−; Gli2^+/− mice, as Hh signaling and PP_i act in parallel downstream of Enpp1. Second, although we removed Gli2, Gli1 and Gli3 are still there to transduce Hh signaling. Lastly, Enpp1 may regulate other signaling pathways to inhibit osteoblast differentiation.

Hh signaling plays crucial roles in regulating chondrocyte proliferation and hypertrophy during embryonic development and after birth. Ectopic activation of Hh signaling causes OA in long bone synovial joints (Lin et al., 2009; Mak et al., 2008a). Our findings extend these previous studies by showing that Enpp1 is an important regulator of Hh signaling. Joint calcification was detected in the phalangeal joint cartilage and the soft tissue, such as the joint capsule in the Enpp1^−/− mice. Similar observations have been made in a recent study showing that Enpp1 loss of function leads to ectopic mineralization in cartilage and soft tissues, such as tendons and ligaments (Hajjawi et al., 2014; Harmey et al., 2004; Zhang et al., 2016). Our results suggest that upregulated Hh signaling activity in the absence of Enpp1 may be a common mechanism underlying ectopic calcification that is found in distinct tissues. In addition to joint calcification, the loss of Enpp1 function also results in vascular calcification (Lorenz-Depiereux et al., 2010; Rutsch et al., 2003), a degenerative process that is associated with an increased risk of cardiovascular problems. Humans who carry the ENPP1 loss of function mutations develop the vascular calcification GACI (Nitschke et al., 2012), which is a rare autosomal-recessive disorder with calcification of the internal elastic lamina and fibrotic myointimal proliferation of muscular arteries (Rutsch et al., 2001). It would be interesting to determine whether arterial calcification and joint calcification share similar mechanisms involving the activation of Hh signaling, and whether inhibition of Hh signaling could reduce vascular calcification.

MATERIALS AND METHODS

Animals and diet

The mouse lines have been described previously: Enpp1^−/− mice (C57BL/6-Enpp1tm1) (Serrano et al., 2014); Gnas ^f/f (Chen et al., 2005), Ptch1^+/− (Mak et al., 2008a), Gli2^+/− (Bai and Joyner, 2001) and Osx-GFP::Cre mice (Rodda and McMahon, 2006). Genotyping was carried out using tail genomic DNA by standard PCR-based procedures. Mice were maintained on normal laboratory diet. Mice of the same genetic background were generated and raised under identical conditions. Female and male mice exhibited similar phenotypes. As the genetic experiments require a large number of females to breed the appropriate number of mice with desired genotypes, we only used males for experiments. Sex-matched littermate mice were compared. All mouse experiments were approved by the Institutional Animal Care and Use Committee of the National Institutes of Health and Harvard Medical School.

Histological analysis of the interphalangeal joints

Histological analysis was performed on the paraffin sections of the metacarpophalangeal joints of the forelimbs. Skeletal tissues were fixed in 4% paraformaldehyde (PFA) (wt/vol) overnight at 4°C, decalcified for 1 week in 0.5 M EDTA (pH 8.0) and dehydrated. Paraffin-embedded tissue was sectioned at 7 µm and stained with Safranin-O and Hematoxylin & Eosin according to standard procedures. Whole-mount X-gal staining was performed as has been previously described (Topol et al., 2003).

Radiography of skeleton

X-ray images of the fixed forelimbs were taken using the Bruker MS FX PRO Imager.

Immunostaining

Forelimbs were collected and immediately fixed in 4% PFA (wt/vol) overnight at 4°C. Then limbs were decalcified in 0.5 M EDTA (pH 7.4) for 2 weeks at 4°C, changing EDTA every 3-4 days. The limbs were placed in 30% (wt/vol) sucrose at 4°C overnight, embedded in optimal cutting temperature compound and sectioned at 16 µm. The slides were blocked in 5% bovine serum albumin (BSA) (wt/vol) in PBST (PBS with 0.02% Tween-20) at room temperature for 1 h, then incubated with primary antibodies diluted in blocking buffer overnight at 4°C. The slides were washed in PBST for 3×10 min, incubated in secondary antibodies for 1 h at room temperature and washed in PBST for 3×10 min before imaging. Primary antibodies that were used in immunostaining include: anti-Gli1 (Santa Cruz Biotechnology, sc-6152) at 1:50, anti-Col1a1 (Santa Cruz Biotechnology, sc-59772) at 1:500, anti-Osx (Abcam, 22552) at 1:400, anti-Opn (R&D Systems, AF808) at 1:500, anti-Oc (LifeSpan BioSciences, LS-C42094) at 1:100 and anti-Sox9 (Abcam, 185966) at 1:400. To quantify immunostaining, the immunopositive cells in a field of view that had a greater intensity than the background were counted using Photoshop CS6. The total area of each field of view was calculated using ImageJ, and at least three fields of view were counted for each immunostaining.

Isolation, culturing and analyses of SMP, MEF, chondrocytes and synoviocytes

Subcutaneous skin tissue containing adipose deposits were dissected from 6-week-old mice. The subcutaneous tissue was prepared under sterile conditions and washed in PBS supplemented with 100 U/ml penicillin and 100 µg/ml streptomycin on ice. Tissue was minced and digested with 1 mg/ml collagenase type 1 and 0.5% trypsin in 0.1% BSA at 37°C for 2 h, then centrifuged at 650 g for 10 min. The floating fat depots were removed, and the cell pellets were collected, dissociated and centrifuged a second time at 650 g for 10 min. The SMP cell pellet was dissociated and filtered through a 100 µm mesh filter. SMP cells were cultured in Alpha-MEM with 20% fetal bovine serum, 100 U/ml penicillin, 100µg/ml streptomycin and 2 mM glutamine. Cells were seeded at a density of 2.5×10⁵ per well in 12-well plates and switched into osteogenic medium with ascorbic acid and glycerophosphate after reaching super confluence. MEF cells were isolated from E12.5-13.5 mouse embryos. The internal organs of the embryos were removed from the abdominal cavity. Embryos were rinsed in 10-20 ml Dulbecco's phosphate-buffered saline and transferred to a 15 ml tube containing 3-5 ml trypsin/EDTA solution and incubated for 20 min at 37°C. The digested cells were collected and large tissue pieces were avoided. The suspended cells were then centrifuged for 5 min at 1000 g at room temperature. The cells in the pellets were dissociated in 10-50 ml fresh MEF medium with penicillin/streptomycin and plated in 100 mm tissue culture plates or 75 cm² flasks. Primary chondrocytes were isolated from P0 mice. The rib cages were incubated with pronase for 30 min at 37°C, followed by 3 mg/ml collagenase in Dulbecco's modified eagle medium (DMEM) at 37°C for 1 h 30 min until all soft tissues could be detached from the cartilage by a small amount of pipetting. The cartilage was digested with collagenase for 4-5 h and chondrocytes were harvested by centrifugation. Synovial cells were isolated from synovial membranes of the knee joints of 10-week-old mice after digestion with 0.2% collagenase in DMEM at 37°C for 1 h. The treatment was carried out using ATP (Sigma FLAAS-1VL), NHATP (Sigma-Aldrich, A2647) and SAG (MedChem Express, HY-12848). Western blotting analysis was performed according to standard protocols (Jin et al., 2012). Antibodies used were: rabbit anti-p-Creb (1:2000; Millipore, 06-519), rabbit anti-Creb (1:2000; Santa Cruz Biotechnology, sc-25785), mouse anti-GAPDH (1:5000; Sigma-Aldrich, G8795) and mouse anti-tubulin (1:5000; Sigma-Aldrich, T5168).

Quantitative RT-PCR

Quantitative RT-PCR was performed to measure the relative mRNA levels. RNA samples were prepared from the forelimbs without skin using Trizol (Invitrogen) with the RNeasy kit (Qiagen). The phalangeal joints between the metacarpal bone and the proximal phalanx of digit three were used for analysis, unless otherwise indicated in the text. cDNA was generated by the SuperScript2 reverse transcriptase kit (Invitrogen) and digested with DNase1 (Invitrogen). Primers used for amplification have been described previously (Regard et al., 2013). Samples were normalized with GAPDH expression.

Whole-mount skeletal preparation and joint size measurements

Mice were skinned and placed in 100% ethanol overnight, then in 100% acetone for 1 day. Whole-mount skeletal preparations were performed as described (McLeod, 1980). Mice were then stained with Alcian Blue and Alizarin Red solution (50 ml staining solution=2.5 ml 0.3% Alcian Blue, 2.5 ml 0.1% Alizarin Red, 2.5 ml 100% glacial acetic acid and 42.5 ml 70% ethanol) for 2 days at 37°C. The mice were then cleared in 1% KOH for 2 days and transferred to 20% glycerol with 1% KOH until soft tissue was transparent. The cleared mice were stored in 80% glycerol. Four mice of each genotype were used for quantification of the forelimb metacarpophalangeal joints size. Statistics shown in text are mean±s.d. The joint sizes were measured using ImageJ as follows: the length of a straight line indicates the diameter of metacarpophalangeal joint size (D1) on the frontal view of the forelimb and is measured as pixels. The midpoint of the proximal phalange was visually determined and the diameter of the proximal phalanges (D2) was similarly measured. Then the ratio of D1/D2 of each digit was calculated as the relative joint size and used in the statistical analysis.

In situ hybridization

Forelimbs for ISH were fixed in 10% (vol/vol) formalin at room temperature for 24-36 h. Paraffin sections at 8 µm were used to perform RNA ISH using an RNAscope (ACDBio) (Wang et al., 2012) 2.0HD Detection Kit according to the manufacturer's instructions. The probe used in the study is mCol1α1 (Ref: 319371, Lot:15258A, ACDBio). The intensity of ISH signal across the various anatomical locations was compared. WISH was performed according to an established protocol (Andre et al., 2015).

Statistical analysis

Quantification was performed from at least three independent experimental groups and presented as mean±s.d. Statistical analysis between groups was performed by two-tailed Student's t-test to determine significance when only two groups were compared. P<0.05 was considered statistically significant (*P<0.05, **P<0.01, ***P<0.001). The signal of immunohistochemistry was calculated as the number of positive cells/field of view.