Diseases of ectopic calcification of the vascular wall range from lethal orphan diseases such as generalized arterial calcification of infancy (GACI), to common diseases such as hardening of the arteries associated with aging and calciphylaxis of chronic kidney disease (CKD). GACI is a lethal orphan disease in which infants calcify the internal elastic lamina of their medium and large arteries and expire of cardiac failure as neonates, while calciphylaxis of CKD is a ubiquitous vascular calcification in patients with renal failure. Both disorders are characterized by vascular Mönckeburg’s sclerosis accompanied by decreased concentrations of plasma inorganic pyrophosphate (PPi). Here we demonstrate that subcutaneous administration of an ENPP1-Fc fusion protein prevents the mortality, vascular calcifications and sequela of disease in animal models of GACI, and is accompanied by a complete clinical and biomarker response. Our findings have implications for the treatment of rare and common diseases of ectopic vascular calcification.
Generalized arterial calcification of infancy (GACI) is an ultra-rare neonatal disease characterized by infantile onset of widespread arterial calcifications in large and medium-sized vessels resulting in cardiovascular collapse and death in the neonatal period. The disease presents clinically with heart failure, respiratory distress, hypertension, cyanosis and cardiomegaly. The prognosis is grave, with older reports of an 85% mortality rate at 6 months1, while recently intensive treatment with bisphosphonates has lowered mortality to 55% at 6 months2. Tempering this apparent progress is the severe skeletal toxicity associated with prolonged use of etridonate in patients with GACI (ref. 3), the observation that the limited available data makes it difficult to determine if bisphosphonate treatment is truly protective or reflects the natural history of the disease in less effected patients, and the ineffectiveness of bisphosphonates to prevent mortality in some patients even when instituted early4,5,6,7.
The overall incidence of GACI is rare, with 200 reported cases in the medical literature8 and a disease frequency of one in 391,000 (ref. 9). Although the disease was first described by Bryant and White in 1901 (ref. 10), it was not until 2000 that Rutsch et al.11 noted that serum plasma inorganic pyrophosphate (PPi) levels and ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) enzymatic activity were significantly impaired in GACI patients. ENPP1 (also known as PC-1) is the founding member of the ENPP or NPP family of enzymes, which are characterized by phosphodiesterase activity12, and is a type II extracellular membrane bound glycoprotein located on the mineral-depositing matrix vesicles of osteoblasts and chondrocytes, as well as the vascular surface of cerebral capillaries13. ENPP1 is the primary source of extracellular PPi in the body, and hydrolyzes extracellular ATP into AMP and PPi (refs 12, 14). PPi acts as a potent inhibitor of mineralization, presumably by occupying some of the Pi sites on the surface of nascent or growing hydroxyapatite crystals, thereby creating irregularities that slow or terminate crystal growth14,15. Rutsch et al. discovered that inactivating mutations in ENPP1 account for 75% of GACI patients2,11,16 and have contributed to recent observations that a sizable fraction of the remaining patients result from inactivating mutations in the ATP dependent membrane transporter ABCC6 (refs 17, 18, 19, 20, 21, 22). ABCC6 mutations result in decreased extracellular concentrations of nucleoside triphosphates through an unknown mechanism23, thereby limiting ENPP1’s metabolism of ATP into extracellular PPi. The identification of both ENPP1 and ABCC6 inactivating mutations as genetic etiologies for GACI therefore links the same biochemical pathway to unregulated tissue mineralization in both genetic variants of GACI.
Despite the multiple genetic etiologies and multifactorial nature of the expression, progression, and severity of medial wall vascular calcification, we hypothesized that disruption of ENPP1’s extracellular purinergic metabolism accounts for the pathologic sequela and mortality associated with GACI and that enzyme replacement therapy with ENPP1 is a tractable therapeutic approach. To test this hypothesis, we employed ENPP1-asj mice (Jackson Laboratory), which carry an inactivating mutation in enpp1 such that homozygotes (enpp1asj/asj) have markedly reduced ENPP1 function. To enhance the disease phenotype, the mice were maintained on the an ‘acceleration diet’ in utero24,25. Here we demonstrate that daily subcutaneous doses of a biologic agent comprising the extracellular domain of ENPP1 fused to the Fc region of human IgG1 eliminates the vascular calcifications, mortality, myocardial infarctions, and sequela of GACI in enpp1asj/asj mice, and that this clinical response is accompanied by normalization of serum and tissue PPi concentrations.
Natural history study of GACI in enpp1asj/asj mice
When fed an acceleration diet, the daily weights of enpp1asj/asj mice diverged from wild-type (WT) siblings pairs at day 26, when the ENPP1-asj/asj mice experienced a ‘failure to thrive’ event and began to lose weight (Fig. 1a). After day 26 the enpp1asj/asj animals displayed progressive stiffness and reductions in physical activity. All of the enpp1asj/asj animals died between days 35–71, with a median lifespan of 58 days (Fig. 1b). The presence of calcifications in enpp1asj/asj and enpp1wtj mice was evaluated via post-mortem by micro-computed tomography (CT) scans (Fig. 1c) and histologic sections taken from the heart, aorta and kidneys (Fig. 1d–g). Approximately one-third of the enpp1asj/asj mice had visible calcifications in their hearts, and two-thirds had calcifications in their aortas visible by micro-CT imaging (Table 1). These percentages increased to 100% on histologic examination, which also showed that many of the animals had dramatic nearly circumferential calcifications in their aortic walls (Fig. 1d,e). Histologic examination also revealed that 100% of the coronary arteries possessed arterial wall calcifications and that 70% of the animals had focal or confluent areas of myocardial necrosis consistent with myocardial infarction (Fig. 1f,g). Conversely, the enpp1wt mice displayed none of these abnormalities. These findings demonstrate that the animal model recapitulates GACI in humans, which is characterized by prominent calcifications of the large and medium sized arteries and a cardiac demise.
Design and characterization of therapeutic
To produce soluble, recombinant ENPP1 for in vivo use, we modified our previous expression construct26 by fusing ENPP1 to the Fc domain of IgG1 (hereafter referred to as hENPP1-Fc and mENPP1-Fc for the human and mouse protein isoforms, respectively, Fig. 2b) and expressed the fusion protein in stable mammalian (HEK293) cell lines (Supplementary Note 1). The effect of expressing the hENPP1-Fc in mammalian, as compared to our previous studies in insect cells26, altered the Michaelis–Menton kinetics by reducing (tightening) the Michaelis constant KM for ATP substrate by over two orders of magnitude, while also reducing (slowing down) the kcat by a factor of 2–3 (Fig. 3a–c). The altered Michaelis–Menton constants could reflect either the change in expression system from baculovirus-infected insect cells to mammalian cells or the addition of the Fc tag. To differentiate between these two possibilities, we expressed hENPP1 without an Fc tag in mammalian (HEK293) cell lines to directly compare the kinetics of ENPP1 with and without an Fc tag. We found that the kinetic constants of the hNPP1-Fc and hNPP1 enzymes expressed in mammalian cells were essentially identical (Fig. 3d), suggesting that the alteration in kinetic constants was due to the change in expression systems.
To understand the pharmacokinetics of ENPP1-Fc we determined plasma concentrations of drug following a single subcutaneous injection over time. Fifteen mice were administered a single subcutaneous dose of 10 mg kg−1 and blood was collected from tail veins to quantitate ENPP1-Fc in the plasma. The concentration ENPP1-Fc reaches a maximal plasma concentration of ∼300 nM (Cmax) within 8 h (tmax) and remains elevated at 100 nM for 72 h after dosing (Fig. 4a). The integral of the plotted concentration–time curve, or area under the curve, is 9 μM h−1. Plotting the data as fraction of drug absorbed over time allows for the determination of the elimination (ke) and absorption (ka) constants by fitting the data to the equation for the total systemic absorption of a drug administered at a subcutaneous depot at time zero,
This analysis yield a ke=0.107±0.016 h−1 and a ka=0.048±0.008 h−1, which yields an elimination half life (t1/2)=6.5 h (Fig. 4b).
The activity of ENPP1-Fc was noted to diminish over a 30 day period when stored at 4 °C, but the enzyme could be frozen at −80 °C and retain nearly complete activity on thawing (Fig. 4c). The enzyme was therefore stored as a frozen stock solution after purification until needed. The oligomerization state of ENPP1-Fc at 1 μM and 100 nM was determined by size exclusion chromatography coupled with light scattering, refractive index, and absorbance (ultraviolet) detection (SEC-MALLS/RI/UV)27, which allows for a determination of the molecular weight (MW) of glycosylated proteins from the relationship of molecular weight and the ratio of laser light scattering, ultraviolet and refractive index (RI) signals in the absence of knowledge of the extend of glycosylation28. The results of the SEC-MALLS analysis revealed that the MW of the ENPP1-Fc protein represents a dimer over the concentration range of 100 nM–1 μM, with an experimentally determined MW of 274±38 KDa (Fig. 4d). This agrees well with the calculated MW of 252 KDa for an ENPP1-Fc dimer. The experimental approach also allows for an independent estimation of the glycosylation level of the fusion protein, which was determined to be ∼5% according to the method of Hayashi et al.29
Following purification, ENPP1-Fc was dialysed into PBS supplemented with Zn and Ca2+ (PBSplus) concentrated to between 5 and 7 mg ml−1 and frozen at −80 °C in aliquots of 200–500 μl. Aliquots were thawed immediately before use, and the specific activity of the solution was adjusted to 31.25 a.u. ml−1 (or ≈0.7 mg ml−1 depending on the preparation) by dilution in PBSplus.
Therapeutic proof of concept in enpp1asj/asj mice
Dosing was performed according to activity units (a.u.) per kg animal weight to account for variations in specific activity in different protein preparations. The specific activity of the enzyme varied with each protein preparation, and because the clinical response was noted to be highly dependent on enzyme specific activity, we rejected protein preparations with specific activities of <40 a.u. mg−1. To establish initial dosing levels for the proof of concept study we performed dose escalation trials in limited numbers of animals (1–2 per dose level). While both the human and mouse version ENPP1 were used in the dose escalation trials, the proof of concept study was performed with the mouse isoform of ENPP1-Fc (mENPP1-Fc). enpp1asj/asj mice were dosed daily on the fourteenth day of life with subcutaneous injections of mENPP1-Fc and weekly with intra-peritoneal injections of GK 1.5, the latter added to minimize immune rejection of recombinant protein30. Subcutaneous doses of mEnpp1-Fc at 500 a.u. kg−1 qD demonstrated a strong early response in weight with an absence of the observed ‘failure to thrive’ crisis observed in undosed enpp1asj/asj animals (Supplementary Fig. 1). This dose corresponded to between 6–10 mg kg−1 of ENPP1-Fc, depending on the specific activity of the protein preparation.
On the basis of the results of the dose escalation trials we chose to enrol a cohort of 8 enpp1asj/asj animals dosed with mENPP1-Fc at 500 a.u. kg qD and weekly intra-peritoneal injections with GK 1.5 (Fig. 5). We included a control groups (enpp1wt and enpp1asj/asj) dosed daily with vehicle and weekly with GK 1.5 in an identical manner as the dosed cohort, and the study duration was shortened to 55 days. All 8 treated enpp1asj/asj animals survived the full 55 days of the trial, with a dramatic clinical response observed in treated animals (Supplementary Movie 1), while the median lifespan of the untreated enpp1asj/asj animals decreased from 58 to 35 days in the therapeutic trial, perhaps resulting from the weekly intra-peritoneal injections of the GK 1.5 immunosuppressant. The untreated enpp1asj/asj animals also all experienced a failure to thrive crisis at day 26, followed by weight loss and mobility restriction progressing variably to paralysis and death over the next 30 days. All but one untreated enpp1asj/asj animal expired over the 55 day trial, while in contrast all treated enpp1asj/asj mice gained weight comparable to the enpp1wt mice and displayed no signs of reduced mobility or stiffness (Supplementary Movie 1).
At the conclusion of the study, 100% of the enpp1asj/asj mice treated with vehicle displayed calcifications in their hearts, aortas and coronary arteries, and 77% of the animals displayed histologic evidence of myocardial infarction (Table 2). In most cases this took the form of small areas of myocardial cell necrosis and single cell drop out in the vicinity of the cardiac calcifications (Figs 5d and 6f–h), but in two animals (22%) there were large, full thickness myocardial infarctions in the free wall of the right ventricle (Fig. 6c–e). Myocardial fibrosis in the myocardial tissue adjacent to regions of coronary artery calcification was a common finding (Fig. 6g,h), illustrating that ischaemia from coronary artery calcification likely accounts for a substantial burden of the myocardial disease. Some untreated enpp1asj/asj animals displayed dramatic calcifications of coronary arteries, heart, ascending and descending aorta (Supplementary Movie 2). In contrast, none of the enpp1asj/asj animals treated with ENPP1-Fc displayed cardiac, arterial, or aortic calcification on histology or post-mortem micro-CT (Table 2 and Figs 5e, 6b and 7a). Although renal calcifications are not a feature of human GACI, the enpp1asj/asj mouse model is noted to have calcifications in the kidneys. Similar to previous findings, we noted light calcifications in the kidneys of ≈60% of the WT animals and 100% of the dosed enpp1asj/asj mice. The calcifications in these animals were centred in the renal medulla. 100% of the undosed enpp1asj/asj animals had heavy, extensive calcifications, centred in the outer medulla, with extension into the renal cortex. In comparison to previous reports, the renal calcifications in the dosed animals seem to approximate renal calcifications seen in the heterozygous enppWT/asj animals.
In addition to survival, daily animal weights, and terminal histology, treatment response was also assessed via post-mortem high-resolution micro-CT scans to image vascular calcifications, plasma PPi concentrations, and 99mTc PPi (99mPYP) uptake (Fig. 7a–f and Table 2). The biochemical and physiologic response was complete as measured by all of these parameters. None of the WT or treated enpp1asj/asj animals were noted to possess any vascular calcifications via micro-CT, in contrast to the dramatic calcifications noted in the aortas, coronary arteries, and hearts of the untreated enpp1asj/asj cohort (Fig. 7a). In addition, serum PPi concentrations of treated enpp1asj/asj animals (≈5.2 μM) were elevated to WT levels (4.4 μM) and significantly above untreated enpp1asj/asj levels (<0.5 μM) (Fig. 7b).
99mPYP, an imaging agent typically employed in cardiac imaging and bone remodelling, was used as a marker for treatment response. It is sensitive to areas of unusually high-bone rebuilding activity since it localizes to the surface of hydroxyapatite and then may be taken up by osteoclasts. One would expect increased 99mPYP uptake in animals lacking functional ENPP1 since they have reduced plasma [PPi] and correspondingly elevated rates of mineralization. To test this hypothesis, we performed weekly in vivo99mPYP imaging in enpp1wt and undosed enpp1asj/asj animals to detect differences in 99mPYP uptake between the sibling pairs (Fig. 7c,d). We limited analysis of 99mPYP uptake to the head, which is comprised of both enchondral bone (skull) and soft tissue (vibrissae), which are known sites of ectopic calcification in enpp1asj/asj mice. This also simplified data analysis as the head does not overlap with internal organs showing transient 99mPYP uptake (such as the bladder, heart and diaphragm) during the 180° camera rotation that occurs during data collection.
Weekly serial imaging of enpp1wt and untreated enpp1asj/asj animals demonstrated that, as expected, uptake of 99mPYP in the heads as per cent injected dose was greater in enpp1asj/asj animals than in enpp1wt animals, and that changes in 99mPYP uptake within experimental groups did not vary significantly over the course of the study (Fig. 7c,d). We therefore chose to measure 99mPYP uptake in treated and untreated enpp1asj/asj animals at two time points—days 30–35 and at the completion of the study (days 50–65). Comparison of these experimental groups demonstrates that ENPP1-Fc treatment returned 99mPYP uptake in GACI mice to WT levels (Fig. 7e,f), suggesting that ENPP1-Fc treatment is able to abrogate unregulated tissue, vibrissae and skull mineralization in enpp1asj/asj mice by raising the extracellular PPi concentrations.
Reappearance of calcifications following cessation of dosing
To address questions regarding the reappearance of calcifications following the cessation of dosing, we enrolled two animals in a limited dosing trial in which enpp1asj/asj animals were dosed with hENPP1-Fc starting on day 14 and ending on day 27. On day 28 and thereafter the animals were dosed with PBSplus and the appearance of vascular calcifications were followed with weekly in vivo CT scans (Fig. 8a). Both animals were free of calcifications until day 64, when one animal developed calcifications in the heart, which were noted on day 79 to progress to the aorta, spleen, kidney, and liver. The second animal developed renal calcifications on day 79. Surprisingly both animals remained alive past day 84. The limited dosing study demonstrates that calcifications reappear following the cessation of dosing and that treatment in the 14–27 day window significantly extends survival in enpp1asj/asj animals maintained on the acceleration diet in utero.
Diseases of ectopic tissue calcification range from ultra-rare diseases such as GACI to nearly ubiquitous maladies in the aging population such as hardening of the arteries. The genetic aetiology of human GACI suggests that the lethal arterial calcifications result from impairment of extracellular purinergic metabolism, either through loss of function mutations in ENPP1 or upstream reductions in nucleotide triphosphates metabolized by ENPP1 into extracellular PPi. Here we demonstrate that daily subcutaneous injections of ENPP1-Fc fusion protein eliminate the mortality, cardiac and arterial calcifications, and other sequela of disease in rodent models of GACI. ENPP1 is the enzyme responsible for the generation of extracellular PPi, and we demonstrate that ENPP1-Fc raises plasma pyrophosphate levels from the nearly undetectable levels present in enpp1asj/asj mice to concentrations comparable to those seen in WT sibling pairs. Our findings suggest that ENPP1-Fc may be effective in other diseases of ectopic calcification in which plasma PPi concentrations are decreased.
Extracellular PPi is a potent inhibitor of mineralization. ENPP1 is the major producer, and tissue-nonspecific alkaline phosphatase (TNAP) is the primary degrader, of extracellular PPi (Fig. 2a). In blood, [PPi] is ∼320 times lower than [Pi], therefore small changes in [PPi] have large effects in the [Pi]/[PPi] ratio, whereas similar magnitude changes in [Pi] would not. If the [Pi]/[PPi] ratio is the mechanism governing hydroxyapatite mineralization, as has been proposed, attention should be given to plasma [PPi] in patients suffering from disorders in ectopic mineralization.
The contribution of AMP generation and purinergic signalling to the suppression of vascular calcification is incompletely understood but has been addressed previous studies of enpp1asj/asj mice using aortic allografts of WT into enpp1asj/asj mice and vice versa31. These studies demonstrated that normal levels of extracellular pyrophosphate were sufficient to prevent vascular calcification over the entire surface of a transplanted enpp1asj/asj aortic allograft. The suppression of calcification in aortic allografts was throughout the entire length of the allograft with no gradient of suppression of calcification observed. Because purinergic signalling is believed to be autocrine or paracrine in nature (and not systemic), the authors concluded that purinergic signalling was either not important for vascular calcification suppression or was not substantially altered by ENPP1 deficiency. Our observations that enpp1asj/asj mice dosed with ENPP1-Fc are free of vascular calcifications and have normal plasma PPi concentrations supports the notion that plasma PPi levels may be primarily responsible for suppression of vascular calcification in ENPP1 deficiency.
Reduced plasma PPi levels are also present in vascular calcification associated with end stage renal disease (ESRD)31,32. One in ten adults suffer from chronic kidney disease (CKD), and it is estimated that 80% of patients with CKD on dialysis and 47–83% of patients with CKD not on dialysis possess vascular calcifications compromising their quality of life and endangering their health. Vascular calcifications associated with ESRD contributes to poor outcomes by increasing pulse pressure, causing or exacerbating hypertension, and inducing or intensifying myocardial infarctions and strokes. Most patients with ESRD do not die of renal failure, but from the cardiovascular complications of ESRD, and it is important to note that many very young patients with ESRD on dialysis possess coronary artery calcifications. The histologic subtype of vascular calcification associated with CKD is known as Mönckeburg’s sclerosis, which is a form of vessel hardening in which calcium deposits are found in the muscular layers of the medial vascular wall. This form of calcification is histologically distinct from intimal or neo-intimal vascular wall calcification commonly observed in atherosclerosis but identical to the vascular calcifications observed in human GACI patients, and in the rodent models of the disease described herein. The similar pathophysiology of vascular calcification present in GACI and CKD suggests that these disorders may be treated by a common therapeutic.
To this point, the current medical strategies treating ectopic vascular calcification of CKD are typically ineffective and are directed at reducing hyperphosphatemia and minimizing serum calcium concentrations. Continuous intra-peritoneal infusions of exogenous PPi substantially inhibits vascular calcifications in rodent models of ESRD, but the rapid hydrolysis of PPi in vivo prevents translation of this therapy to the clinic33. Attempts treating vascular calcifications in rodent models of ESRD with non-hydrolyzable PPi analogues (bisphosphonates) required doses above those known to inhibit bone formation, and the anticipated bone toxicity coupled with a renal mechanism of clearance discourages the use of bisphosphonates as therapeutic agents in CKD34. It appears that we are able to circumvent both the poor pharmacokinetics of PPi and the bone toxicity of bisphosphonates by fusing the PPi generating enzyme ENPP1 to the Fc domain of IgG1, and demonstrated that the biologic is effective in GACI. We suspect that it may also be effective in vascular calcification associated with CKD.
ENPP1-asj GACI mouse model
Animal care and maintenance were provided through Yale University Animal Resource Center at Yale University (New Haven). All procedures were approved by the Animal Care and Use Committee of Yale University and complied with the US National Institutes of Health guide for the care and use of laboratory animals. Heterozygous enpp1asj/+ (genotype C57BL/6J-Enpp1asj/GrsrJ, Jackson Laboratory stock number 012810) breeding pairs were maintained on the ‘acceleration diet’ (TD.00442, Harlan Laboratories, Madison WI) throughout the entire experiment and food and water were delivered ad libitum. The animal colony was housed in pathogen free conditions. All experimental animals were maintained on the acceleration diet in utero through completion of the study. Litters were genotyped on day 8 and weaned at day 21. Following weaning, sibling pairs were sequentially divided into cohorts as described below and enrolled in experimental trials. Animals were consecutively enrolled in experimental trials without regard to gender, and the gender of the experimental animals was not recorded. On the basis of the trial dosing we estimated that statistically significant survival differences could be determined between dosed and undosed animals using a sample size of eight animals in each experimental group. We used identical breeding pairs throughout the study, and all experimental groups were enrolled sequentially beginning with the enpp1wt and undosed enpp1asj/asj cohorts and ending with the dosed enpp1asj/asj cohort. Enrolment of the dosed and undosed enpp1asj/asj cohorts spanned 4 months. Once the enrolment of an experimental group began both sexes of the appropriate genotype were consecutively enrolled in an experimental cohort with the exclusion of severely runted animals weighing <5.5 g at 14 days of life. Following weaning, all experimental animals were housed with littermates to allow for cooperative grooming and nesting. Experimentalists were not blinded during the study.
Human and mouse NPP1 (Human: NCBI accession NP_006199; Mouse: NCBI accession NP_03839) modified to express soluble, recombinant protein as described previously26 were fused to IgG1 by subcloning into pFUSE-h IgG1-Fc1 or pFUSE-m IgG1-Fc1 plasmids (InvivoGen, San Diego, CA), respectively. The final human protein sequence is listed in Supplementary Fig. 1.
Protein production with shaking flasks
Stable transfections of the ENPP1-Fc were established in HEK293 cells under zeocin selection. Briefly, adherent HEK293 cells were adapted for suspension growth by progressive dilution of fetal bovine serum from 10 to 1% over 5–6 passages35. Zeocin selection (450 μg ml−1) was maintained throughout the adaptation process, and cultures were supplemented with 1% insulin-transferrin-selenium (Mediatech 25–800-CR), and cells were passaged when they reached confluence in 175 cm2 tissue culture flasks. Adapted cells were used to seed liquid culture growths in FreeStyle medium (Gibco, Waltham MA) in shaker flasks at 37°F and 5% CO2, agitated at 120 r.p.m. with high humidity. Cell density in liquid culure was maintained between 0.5 and 2.5 × 106 cells per ml and zeocin selection was maintained in liquid culture at 450 μg ml−1 until the cells reached a volume of 4 l in liquid culture, and then reduced to 225 μg ml−1 thereafter. The culture was gradually expanded to 8 l and then maintained for another 12 days to accumulate extracellular protein. During the maintenance phase, cultures were supplemented with CD EfficientFeed C AGT (Gibco #A13275-05) to enhance protein production.
Protein production with bioreactor
Cells were propagated in a 10 l bioreactor equipped with dissolved oxygen and pH control. Dissolved oxygen was kept at 40% air saturation by supplying the culture with mixture of air and oxygen not exceeding 3 l minute at an agitation rate of 80 RPM. pH was controlled at 7.4 by sparging CO2 when the pH was higher than 7.4. Culture growth was followed by measuring cell number, cell viability, glucose and lactate concentrations. Final yields for both methods of production were ∼5 mg of purified ENPP1-Fc per liter of culture.
The liquid cultures were centrifuged at 4,300g for 15 min and the supernatants were filtered through a 0.2 μm membrane and concentrated via tangential low using a Pellicon3 0.11 m2 Ultracell 30 kD cassette (Millipore, Billerica MA). The concentrated supernatant was loaded onto a protein-A column, then washed using 50 mM Tris pH8, 150 mM NaCl2, 1 mM ZnCl2 and 1 mM CaCl2. The recombinant protein was eluted using Elution Buffer (150 mM Sodium Citrate; pH=4.3, 150 mM NaCl2, 1 mM ZnCl2 and 1 mM CaCl2), then immediately neutralized using a 1/10th volume of 1 M Tris pH 9.2, 150 mM NaCl2, 3 mM ZnCl2 and 3 mM CaCl2. Fractions containing enzymatic activity were pooled and dialysed against PBSplus buffer (1 × PBS buffer pH 7.4, 11 uM ZnCl2, 20 uM CaCl2), then concentrated to ∼6 mg ml−1, distributed into small aliquots and stored at −80 °C. Resulting protein samples were then tested with Pierce LAL Chromogenic Endotoxin Quantitation Kit (cat. 88282) to verify that all were free of endotoxin.
The steady state hydrolysis of ATP by human NPP1 was determined by high performance liquid chromatography (HPLC; refs 26, 36). Briefly, enzyme reactions were started by addition of 10 or 50 nM NPP1 to varying concentrations of ATP in the reaction buffer containing 20 mM Tris, pH 7.4, 150 mM NaCl, 4.5 KCl, 14 uM ZnCl2, 1 mM MgCl2 and 1 mM CaCl2. At various time points, 50 μl reaction solution was removed and quenched with an equal volume of 3 M formic acid. The quenched reaction solution was loaded on a C-18 (5 μm 250 × 4.6 mm) column (Higgins Analytical) equilibrated in 15 mM ammonium acetate (pH 6.0) solution and eluted with a 0–20% methanol gradient. Substrate and products were monitored by ultraviolet absorbance at 259 nm and quantified according to the integration of their correspondent peaks and standard curves.
Size exclusion chromatography coupled with static laser light scattering
The light scattering data were collected using a Superose 6, 10/30, HR Size Exclusion Chromatography (SEC) column (GE Healthcare, Piscataway, NJ), connected to high performance liquid chromatography system (HPLC), Agilent 1200, (Agilent Technologies, Wilmington, DE) equipped with an autosampler. The elution from SEC was monitored by a photodiode array (PDA) UV/VIS detector, UV, (Agilent Technologies, Wilmington, DE), differential refractometer, RI, (OPTI-Lab rEx Wyatt Technology, Santa Barbara, CA), static and dynamic, multiangle laser light scattering (LS) detector (HELEOS II with QELS capability, Wyatt Technology, Santa Barbara, CA). The SEC-MALLS/UV/RI system was equilibrated in PBSplus buffer at the flow rate of 0.3 ml/min. Two software packages were used for data collection and analysis: the Chemstation software (Agilent Technologies, Wilmington, DE) controlled the HPLC operation and data collection from the multi-wavelength ultraviolet /VIS detector, while the ASTRA software (Wyatt Corp., Santa Barbara, CA) collected data from the refractive index detector, the light scattering detectors, and recorded the ultraviolet trace from the PDA detector. The weight average molecular weights, Mw, were determined across the entire elution profile in the intervals of 1 s from static light scattering (LS) measurement using ‘three detector approach’27,28,29.
Mouse ENPP1-Fc (mENPP1-Fc) was formulated in vehicle such that the volume of vehicle delivered was 16 μl vehicle per gram of body weight. Vehicle consisted of americanBio 10X PBS (Stock# AB11072) diluted to 1 × with endotoxin free water and supplemented with 14 μM CaCl2 and 14 μM ZnCl2.
Animals in the proof of concept study (Figs 5, 6, 7) were dosed either with vehicle or with mouse ENPP1-Fc (mENPP1-Fc) formulated in vehicle. Mice were dosed with daily subcutaneous injections starting on day 14 at dose levels of 500 a.u. kg−1 mENPP1-Fc. Animals in the limited dosing study (Fig. 8a) were dosed with human ENPP1-Fc (hENPP1-Fc) formulated in vehicle beginning on the fourteenth day of life and ending on the twenty-seventh day of life. To tolerize the mice to human protein, the mice were dosed intraperitoneally with 75 μg of GK 1.5 (eBioscience, San Diego, CA) on the thirteenth day of life, and 50 μg of GK 1.5 on the twentieth day of life. Between days 28 and 83 the mice received vehicle. Inactive hENPP1-Fc protein (Fig. 8b) was generated by exposure to EDTA. The specific activity hENPP1-Fc following EDTA exposure was < 20 a.u. mg−1, or <50% of the activity of native protein.
Clearance rate of ENPP1-Fc
Briefly, 15 male C57BI/6J mice aged 8 weeks or older were administered a single subcutaneous dose of 10 mg kg−1 of mENPP1-Fc. Blood was collected from tail veins into heparin-containing tubes before the injection and at different time points post injection. Mice were divided into three groups for blood collection: (1) 1 h, 8 h, 48 h, 96 h. (2). 3 h, 24 h, 45 h and 72 h. (3). 6 h and 32 h. Enpp1 activity in plasma were measured with pNP-TMP assay in the following buffer: 100 mM Tris·HCl (pH 9.0), 500 mM NaCl, 5 mM MgCl2, 0.05% (vol/vol) Triton X-100 and 4 mM pNp-TMP. Plasma activity units were converted into protein mass using an empirically determined conversion factor of 0.332 units per μg protein. To derive plasma concentrations and fraction of subcutaneous drug absorbed into plasma, the total blood volume of each mouse was estimated at 1.5 ml. Clearance rate constants were derived as detailed in the text.
Definition of activity unit
Animals were dosed according to total activity of enzyme delivered rather than concentration of enzyme to account for varying activity among batches of enzyme used. One activity unit (1 a.u.) is defined as pM of pNP-TMP substrate hydrolyzed min−1 mg−1 enzyme. The activity assay was performed in a buffer consisting of 50 mM Tris pH9, 150 mM NaCl, 0.1 mM ZnCl2, 0.1 mM CaCl2, 0.1 mM MgCl2. The activity of acceptable protein preparations varied between 40 and 43 a.u. mg−1, and preparations with <40 a.u. mg−1 were discarded. A dose of 500 a.u. kg−1 corresponds to between 6 and 10 mg kg−1, depending on the specific activity of the protein preparation.
Quantification of plasma PPi
Animals were terminally bled retro-orbitally using heparinized, micropipets, and the blood was immediately dispensed into heparin-treated eppendorf tubes and placed on wet ice. The samples were spun in a 4 °C pre-cooled microcentrifuge at 4,000 r.p.m. for 5 min, and plasma was collected and diluted in one volume of 50 mM Tris-Acetate pH=8.0. Plasma was then filtered through a 300 KDa membrane via ultracentrifugation (NanoSep 300 K, Pall Corp., Ann Arbour, MI) and frozen at −80 °C. Pyrophosphate was quantitated using standard three-step enzymatic assays using uridine 5’ diphospho[14C]glucose to record the reaction product, uridine 5’ diphospho[14C]gluconic acid37. Briefly, a reaction mixture (100 μl) containing 5 mM MgCl2, 90 mM KCL, 63 mM Tris-HCL (pH 7.6), 1 nmol NADP+, 2 nmol glucose 1,6-diphosphate, 400 pmol uridine 5’-diphosphoglucose, 0.02 μCi uridine 5’ diphospho[14C]glucose, 0.25 units of uridine 5’-diphosphoglucose pyrophosphorylase, 0.25 units of phosphoglucose mutase, 0.5 units of glucose 6-phosphate dehydrogenase, and inorganic pyrophosphate (50–200 pmol) is incubated for 30 min at 37 °C. The reaction is terminated by the addition of 200 μl of 2% charcoal well suspended in water. The mixture is kept on ice, vortexed three times over 15 min and clarified by centrifugation for 5 min. An aliquote of 200 μl of supernatant is then counted in scintillation solution.
In vivo99mPYP imaging
The bone imaging agent 99mTc-pyrophosphate (Pharmalucence, Inc) was evaluated in cohorts of animals using a preclinical microSPECT/CT hybrid imaging system with dual 1 mm pinhole collimators (X-SPECT, Gamma Medica-Ideas)38. Each animal was injected intraperitoneally with 2–5 mCi of the radiolabelled tracer and imaged 1–1.5 h after injection. A CT scan (512 projections at 50 kVp, 800 uA and a magnification factor of 1.25) was acquired for anatomical co-localization with the SPECT image. The SPECT imaging was acquired with 180° per collimator head in a counter-clockwise rotation, 32 projections, 60 s per projection with an ROR of 7.0 cm, FOV of 8.95 cm and an energy window of 140 keV±20. CT images were reconstructed with the FLEX X-O CT software (Gamma Medica-Ideas) using a filtered back-projection algorithm. SPECT images were reconstructed using the FLEX SPECT software (5 iterations, 4 subsets) and subsequently fused with the CT images and analysed using the AMIRA software and offline in-house script. Data were corrected for decay and injected dose to achieve % injected dose.
Quantification of 99mPYP uptake
For the 99mPYP murine scans, the animals were imaged two hours postinjection. The resulting SPECT scans were imported into NIH’s ImageJ image processing software and regions of interest were drawn around each animal’s head (target organ) and whole body. Per cent injected activity (PIA), often referred to as ‘per cent injected dose’ was calculated by comparing the ratio of counts in the head to the counts in the whole body, and expressed as per cent injected dose to give a measure as of the affinity with which the radiotracer is taken up by the region of interest (head). The total counts in each scan were taken as the whole body measure of injected dose.
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These studies were financially supported by research grants from Alexion Pharmaceuticals Inc., The Connecticut Bioscience Innovation Fund, and Yale University Department of Pathology. DTB acknowledges helpful conversations with Michael Hodsdon (Eli Lily), Elias Lolis (Yale), and John Louis (NIH/NIDDK/Laboratory of Chemical Physics), and Dr Jon Morrow (Yale) for his enthusiastic support and encouragement throughout the course of this study. This material is based on work supported in part by the State of Connecticut under the Connecticut Bioscience Innovations Fund. Its contents are solely the responsibility of the authors and do not necessarily represent the official views of the State of Connecticut or Connecticut Innovations, Incorporated.
R.A.A. and D.T.B. are co-inventors of a pending patent application owned by Yale University related to these studies. Z.C., K.B. and Z.-X.Y. are employees of Alexion Pharmaceuticals, Inc. The remaining authors declare no competing financial interest.
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Albright, R., Stabach, P., Cao, W. et al. ENPP1-Fc prevents mortality and vascular calcifications in rodent model of generalized arterial calcification of infancy. Nat Commun 6, 10006 (2015). https://doi.org/10.1038/ncomms10006
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