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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptHHS Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
 
Nat Med. Author manuscript; available in PMC 2010 March 29.
Published in final edited form as:
Published online 2008 November 30. doi:  10.1038/nm.1888
PMCID: PMC2846458
NIHMSID: NIHMS187710

BMP type I receptor inhibition reduces heterotopic ossification

Abstract

Fibrodysplasia ossificans progressiva (FOP) is a congenital disorder of progressive and widespread postnatal ossification of soft tissues14 and is without known effective treatments. Affected individuals harbor conserved mutations in the ACVR1 gene that are thought to cause constitutive activation of the bone morphogenetic protein (BMP) type I receptor, activin receptor-like kinase-2 (ALK2)5. Here we show that intramuscular expression in the mouse of an inducible transgene encoding constitutively active ALK2 (caALK2), resulting from a glutamine to aspartic acid change at amino acid position 207, leads to ectopic endochondral bone formation, joint fusion and functional impairment, thus phenocopying key aspects of human FOP. A selective inhibitor of BMP type I receptor kinases, LDN-193189 (ref. 6), inhibits activation of the BMP signaling effectors SMAD1, SMAD5 and SMAD8 in tissues expressing caALK2 induced by adenovirus specifying Cre (Ad.Cre). This treatment resulted in a reduction in ectopic ossification and functional impairment. In contrast to localized induction of caALK2 by Ad.Cre (which entails inflammation), global postnatal expression of caALK2 (induced without the use of Ad.Cre and thus without inflammation) does not lead to ectopic ossification. However, if in this context an inflammatory stimulus was provided with a control adenovirus, ectopic bone formation was induced. Like LDN-193189, corticosteroid treatment inhibits ossification in Ad.Cre-injected mutant mice, suggesting caALK2 expression and an inflammatory milieu are both required for the development of ectopic ossification in this model. These results support the role of dysregulated ALK2 kinase activity in the pathogenesis of FOP and suggest that small molecule inhibition of BMP type I receptor activity may be useful in treating FOP and heterotopic ossification syndromes associated with excessive BMP signaling.

Individuals with FOP typically present within the first decade of life with progressive ectopic calcification of muscles and connective tissues after physical trauma, surgery, viral illness or myositis14. FOP results in severe debilitation and reduced life expectancy due to joint fusion and restrictive lung disease with thoracic involvement. A recent linkage and sequencing analysis identified heterozygous mutations in ACVR1, the gene encoding the BMP type I receptor ALK2, in all affected members from seven families5,7. BMP ligands facilitate the phosphorylation and activation of BMP type I receptors (ALK2, ALK3 and ALK6) by BMP type II receptors (BMPRII, ActRIIA and ActRIIB). Activated BMP type I receptors phosphorylate BMP-responsive SMAD1, SMAD5 and SMAD8, which translocate to the nucleus to regulate the transcription of genes, including the Inhibitor of DNA binding (ID) gene family, with broad effects on growth and differentiation8. The classic FOP-associated ALK2 mutation, R206H, is predicted to disrupt an α-helix in the glycine-serine regulatory domain and alter local electrostatic potential to perturb intra- or intermolecular interactions required for kinase regulation5,9, rendering ALK2 constitutively active. Heterozygous mutations affecting the adjacent residue, Q207E, have been identified in phenotypic variant FOP10. The Q207E mutation and a well described man-made ALK2 mutation affecting the same residue, Q207D11, may exert similarly disruptive effects on the glycine-serine domain structure and to cause constitutive activation of ALK2. In vivo, transfer of the gene encoding ALK2Q207D but not wild-type ALK2 induces chondrogenic differentiation in chick embryos and promotes endochondral bone growth in cortical allografts12,13, consistent with potent osteogenic effects of constitutively activating ALK2 mutations.

To further explore the ability of constitutively active ALK2 to induce ectopic calcification, we took advantage of the availability of transgenic mice expressing an inducible ALK2Q207D (CAG-Z-EGFP-caALK2, or conditional caALK2). When the transgene is globally expressed during embryogenesis, mice are arrested at mid-gestation14, in contrast to individuals with FOP, who appear essentially normal at birth except for shortened great toes2. To circumvent the embryonic lethality of this transgene, we induced postnatal over-expression of ALK2Q207D in the left hindlimbs of mice with retro-popliteal injection of Ad.Cre (1 × 108 plaque-forming units (PFU)) on postnatal day 7 (P7). High-frequency, Cre-mediated recombination was evident by P11, with loss of nuclear β-galactosidase staining and gain of cytoplasmic GFP expression in myocytes, ligaments and vasculature only in the injected area (Fig. 1a). Mononuclear infiltrates and myofiber edema were apparent in the left gastrocnemius, soleus and hamstring muscles, consistent with myositis induced by intramuscular adenovirus injection15, whereas muscles of uninjected limbs appeared normal (Fig. 1a).

Figure 1
Mouse model of FOP. (a) Staining of muscle sections from Ad.Cre-injected conditional caALK2–expressing (ALKQ207D) mice. The injection done at P7 induced recombination in myocytes of the left (L) gastrocnemius and soleus muscles at P11, as evidenced ...

Conditional caALK2–expressing mice injected with Ad.Cre in the left hindlimb developed severely decreased mobility in the injected limb by P30, with loss of passive flexion in hip, knee and ankle joints when examined under anesthesia, whereas wild-type mice injected with Ad.Cre retained normal posture and range of motion (Fig. 1b). By radiography and micro-computed tomography (μCT), bony calluses were evident in injected hindlimbs of conditional caALK2–expressing mice, circumferentially encasing the tibia and fibula (Fig. 1b,c). These calluses frequently fused with the pelvis and femur, rendering hip, knee and ankle joints immobile and extended and preventing the use of those limbs during locomotion (Supplementary Videos 1 and 2 online). At P30, the penetrance of heterotopic ossification and immobility associated with local induction of caALK2 by this technique was 100% (data not shown).

We recently identified a small-molecule inhibitor of BMP type I receptors, dorsomorphin (Fig. 2a), which selectively blocks ALK2, ALK3 and ALK6 activity16. We subsequently described the synthesis of potent and specific derivatives of dorsomorphin6. By reiteratively testing modifications of the parent molecule, we found that replacement of the pendent pyridine ring with a 4-quinolinyl group could improve potency that replacement of the 2-(1-piperidinyl)ethoxy group with piperazine improved metabolic stability and that, in general, modifications of the pyrazolo[1,5-a]pyrimidine core were not tolerated6. An optimized molecule, LDN-193189 (Fig. 2a), inhibited BMP4-mediated Smad1, Smad5 and Smad8 activation with greater potency than did dorsomorphin (half-maximal inhibitory concentration (IC50) = 5 nM versus 470 nM) while retaining 200-fold selectivity for BMP signaling versus transforming growth factor-β (TGF-β) signaling (IC50 for TGF-β ≥ 1,000 nM; Fig. 2a–c). LDN-193189 efficiently inhibited transcriptional activity of the BMP type I receptors ALK2 and ALK3 (IC50 = 5 nM and 30 nM, respectively), with substantially weaker effects on activin and the TGF-β type I receptors ALK4, ALK5 and ALK7 (IC50 ≥ 500 nM, Supplementary Fig. 1 online) and increased selectivity for BMP signaling versus AMP-activated protein kinase, platelet-derived growth factor receptor and mitogen–activated protein kinase signaling pathways as compared to the parent compound16 (Supplementary Fig. 2 online). LDN-193189 blocked the transcriptional activity induced by either constitutively active ALK2R206H or ALK2Q207D mutant proteins (Fig. 2d,e). These findings suggest that LDN-193189 might affect BMP-induced osteoblast differentiation. In fact, LDN-193189 inhibited the induction of alkaline phosphatase activity in C2C12 cells by BMP4 even when administered 12 h after BMP stimulation (Fig. 2f), indicating sustained BMP signaling activity is needed for osteogenic differentiation, as we have previously observed in vascular smooth muscle cells17.

Figure 2
Effect of LDN-193189 on BMP signaling and function. (a) Structures of dorsomorphin and LDN-193189. (b) Quantitative immunoblotting of PASMCs showing differential effects of dorsomorphin or LDN-193189 on BMP4–induced (10 ng ml−1) phosphorylation ...

To assess the impact of ALK2Q207D on BMP signaling, we isolated and cultured pulmonary artery smooth muscle cells (PASMCs) from conditional caALK2–expressing mice. Baseline phosphorylation of Smad1, Smad5 and Smad8 was increased in cells infected with Ad.Cre compared to those infected with Ad.GFP (Fig. 2g), consistent with increased basal BMP signaling after Cre-mediated induction of ALK2Q207D. PASMCs expressing ALK2Q207D also showed hyperresponsiveness to BMP ligands, consistent with observations in cells that express the mutant ALK2R206H protein18,19. Enhanced Smad1, Smad5 and Smad8 activation in cells expressing ALK2Q207D was effectively inhibited by treatment with LDN-193189 (Fig. 2g).

To determine the pharmacokinetics of LDN-193189, we measured its plasma concentration after administration of a single dose (3 mg kg−1 intraperitoneally (i.p.)) in C57BL/6 mice. LDN-193189 remained at levels several fold higher than its in vitro IC50 for >8 h (Supplementary Fig. 3 online), suggesting sustained inhibition of BMP signaling might be obtained by bolus dosing. To assess the effect of ALK2 kinase inhibition on ectopic calcification in vivo, we injected conditional caALK2–transgenic and wild-type mice with Ad.Cre on P7 and then treated them with LDN-193189 (3 mg kg−1 i.p. every 12 h) or with vehicle. Ad.Cre injection of conditional caALK2–transgenic mice led to mild calcifications surrounding the left tibia and fibula first visible at P13 on X-ray (Fig. 3a). By P15, these lesions were more prominent and extended to involve the distal femur (Fig. 3a). Lesions that effectively joined the hip, femur and tibia-fibula were present in all vehicle-treated, Ad.Cre-injected mice by P30, progressing to fusion of the left hip, knee and ankle joints by P60 (Fig. 3a and Supplementary Fig. 4 online). Treatment of Ad.Cre-injected, caALK2-expressing mice with LDN-193189 prevented radiographic lesions at P15 in all mice examined (Fig. 3a). At P30, LDN-193189 prevented ectopic bone in approximately two-thirds of mice and attenuated lesions in the remainder, whereas at P60 LDN-193189 prevented ectopic bone in one-third of mice and attenuated lesions in the remainder (Supplementary Fig. 4). In contrast to vehicle-treated mice, LDN-193189–treated mice appeared to preserve knee and ankle joints at P30 and P60. Alizarin red and Alcian blue staining of vehicle-treated caALK2-expressing mice at P15 revealed ectopic bone encasing the tibia and fibula and increased cartilage formation in surrounding tissues (Fig. 3b,c). LDN-193189-treated mice showed no ectopic bone at P15 but did show enhanced cartilage formation in surrounding soft tissues compared to wild-type mice. Vehicle-treated, caALK2-expressing mice developed extensive ossification and fusion by P30 on μCT, whereas LDN-193189-treated, caALK2-expressing mice had small ectopic ossifications without joint fusion (Fig. 3d). Radiographic lesions in vehicle-treated mice correlated with abnormal hindlimb posture and decreased passive range of motion of hip, knee and ankle joints when the mice were examined under anesthesia, all of which were attenuated in LDN-193189-treated mice (Fig. 3e). A quantitative measure of passive range of motion in the ankle joint (Fig. 3f) appeared to be a sensitive marker of functional impairment (Fig. 3g), correlating with severe lesions found in vehicle-treated mutant mice while demonstrating significant rescue of function in LDN-193189–treated mice. In fact, LDN-193189–treated mice showed at least mildly impaired range of motion even in the absence of radiographically visible disease at P30, perhaps reflecting enhanced cartilage formation or early calcification (Fig. 3a–c,g). Consistent with this functional end point, vehicle-treated mice progressively lost use of the left hindlimb owing to joint fusion, whereas LDN-193189–treated mice retained use of the left hindlimb during ambulation at P15 and P30 (Supplementary Videos 3–6 online). Treatment of wild-type or mutant mice with LDN-193189 under this regimen did not cause weight loss or growth retardation (Supplementary Fig. 5 online), spontaneous fractures, decreased bone density (Fig. 3a) or lead to other skeletal, morphologic, hematological or behavioral abnormalities (data not shown).

Figure 3
Impact of LDN-193189 on ectopic ossification in vivo. (a) Conditional caALK2–expressing mice receiving vehicle after Ad.Cre injection on P7 developed radiographic disease at P13, progressing to fusion of left hindlimb joints by P30–P60, ...

Vehicle-treated, Ad.Cre-injected, caALK2-expressing mice showed increased amounts and nuclear accumulation of phosphorylated Smad1, Smad5 and Smad8 in the left gastrocnemius, soleus and hamstring muscles (Fig. 4a), whereas the uninjected right gastrocnemius had little detectable phosphorylated Smad1, Smad5 and Smad8. Consistent with enhanced Smad1, Smad5 and Smad8 signaling, Id1 expression was more than threefold greater in the hindlimb muscles of Ad.Cre-injected, caALK2-expressing mice than in wild-type or uninjected mutant controls (Supplementary Fig. 6 online). Within Ad.Cre-injected muscle tissues, but not controls, a subset of myocyte-like cells was observed to express the osteogenic runt-related transcription factor-2 (Runx2; Fig. 4a). Treatment of conditional caALK2–transgenic mice with LDN-193189 did not have an impact on recombination efficiency, myocyte edema or inflammation, but did result in diminished phosphorylated Smad1, Smad5 and Smad8 and Runx2 staining in the left gastrocnemius (Fig. 4a). By P15, maturing endochondral bone, marked by alkaline phosphatase–positive osteoblasts, chondrocyte-like cells and marrow cells were evident in Ad.Cre-injected muscles of conditional caALK2–expressing mice (Fig. 4b). The hindlimbs of Ad.Cre-injected, conditional caALK2–expressing mice treated with LDN-193189 developed substantially less endochondral bone but retained evidence of inflammation and myocyte injury (Fig. 4b). Histological evolution of lesions in affected mice thus paralleled that of human intramuscular FOP lesions, showing myocyte injury and inflammatory infiltrate followed by elaboration of a chondrogenic matrix, osteoblast-mediated mineralization and maturation into endochondral bone20. This process of ectopic ossification, beginning with activation of Smad1, Smad5 and Smad8, was markedly attenuated by LDN-193189 treatment.

Figure 4
Impact of pharmacologic inhibition of BMP signaling and inflammation in the mouse FOP model. (a) Immunofluorescence showing enhanced nuclear p-Smad1/5/8 and expression of Runx2 in a number of recombined (β-gal–negative) myocytes from left ...

To test the sufficiency of transgenic expression of caALK2 for the development of ectopic bone, we used an alternate recombination strategy. We achieved global postnatal expression of ALK2Q207D by mating conditional caALK2–transgenic mice with CAGGS-CreER mice, which express a tamoxifen-inducible Cre recombinase ubiquitously21. Double-transgenic mice were injected with tamoxifen (0.5 mg i.p.) on P7, inducing high-frequency recombination of the gene segment encoding CAG-Z-EGFP-caALK2 throughout hindlimb muscle and vascular and connective tissues, as indicated by the loss of nuclear β-galactosidase staining (Fig. 4c). Muscle tissues undergoing recombination by this technique did not show edema or mononuclear cell infiltrates. In contrast to Ad.Cre-induced recombination, global postnatal overexpression of ALK2Q207D did not lead to detectable radiological ossification by P60 (Fig. 4d). When double-transgenic mice were injected with tamoxifen on P7 and injected with a control adenovirus (Ad.GFP, 1 × 108 PFU, left popliteal fossa) on P8, mildly decreased left hindlimb range of motion and small ectopic calcifications appeared by P14 (Fig. 4e). These data suggest that expression of caALK2 is by itself insufficient to produce ectopic bone, and that inflammation or tissue injury from viral immunogenicity or cytotoxicity might be required for bone formation. To test this hypothesis, we treated conditional caALK2–expressing mice with dexamethasone (10 mg kg−1 d−1 i.p.) starting 1 d after Ad.Cre injection at P7 and assessed them for ectopic calcification. By P30, ectopic calcifications and immobility were markedly reduced in corticosteroid-treated mice compared with vehicle-treated mice (Fig. 4f,g). The impact of corticosteroid treatment suggests that inflammation and caALK2 expression are both required to form ectopic bone. Unlike LDN-193189 administration, dexamethasone administration was accompanied by toxicity, reflected by severely impaired weight gain during drug administration (Supplementary Figs. 5 and 7 online).

These studies provide a model of heterotropic ossification that recapitulates key features of human FOP, including the evolution of intramuscular endochondral bone and radiological and functional outcomes. Episodes of ectopic ossification in afflicted humans are frequently precipitated by viral prodromes and accompanying viral myositis22. Formation of ectopic bone in conditional caALK2–transgenic mice in conjunction with local adenovirus infection and the response to corticosteroid treatment support a similar relationship between ossification and inflammation in the mouse model as suggested in previous reports23,24. These studies confirm the role of dysregulated ALK2 kinase activity in the molecular pathogenesis of FOP19 while demonstrating the potential of rational therapy mediated through inhibition of ALK2. Despite this promising result, it is worthwhile to note that before any human therapy can be considered using this approach, comprehensive and long-term toxicity studies in multiple species and further drug refinement and optimization will be necessary to ensure adequate safety of both the compound and chronic or intermittent inhibition of BMP signaling in vivo. Moreover, the ability of LDN-193189 to prevent ectopic ossification in conditional caALK2–transgenic mice was incomplete. It is possible that LDN-193189, in the manner it was administered, was insufficient to completely suppress activation of SMAD signaling. It is also conceivable that activation of SMAD-independent pathways, which were not blocked by dorsomorphin (ref. 16) and may not be inhibited by LDN-193189, can contribute to the ectopic ossification associated with caALK2 expression.

BMP signals have pivotal roles in vertebrate development, regulating gastrulation, patterning and organogenesis by specifying the fate of multipotent cells25. In contrast, the postnatal roles of BMP signals are most essential in the contexts of injury repair, inflammation or remodeling, in the skeleton as well as in connective and vascular tissues26,27. Given the apparent requirement for injury and enhanced BMP signaling for FOP lesions in humans and mice, it is possible that abnormal ossification results from diversion of an injury repair program toward bone formation, perhaps deviating the normal adaptive response of cells with regenerative potential. Understanding the cellular basis of endochondral bone formation in FOP could yield insights into the mechanism of heterotopic ossification of auto-immune, post-traumatic or postsurgical etiologies and reveal how BMPs specify plasticity of mesenchyme-derived tissues in physiology and in disease.

METHODS

Chemical, protein and viral agents

We purchased dorsomorphin (Compound C, 6-[4-(2-piperidin-1-yl-ethoxy)phenyl]-3-pyridin-4-yl-pyrazolo[1,5-a]pyrimidine) from EMD Biosciences. We synthesized LDN-193189 (4-[6-(4-piperazin-1-ylphenyl)pyrazolo[1,5-a]pyrimidin-3-yl]quinoline) as previously described6, determined its purity (99.8%) by HPLC and confirmed its structure by 1H-NMR and high-resolution mass spectrometry. The vehicle was 2% (wt/vol) (2-hydroxypropyl)-β-cyclodextrin in PBS, pH 7.4. We purchased dexamethasone from Sigma. Recombinant human BMP4, platelet-derived growth factor-BB and TGF-β were obtained from R&D Systems. We produced adenoviruses expressing GFP and Cre and quantified them by the plaque-titer method.

Conditionally-expressed, constitutively-active ALK2–transgenic mice

The construction of mice expressing a single conditionally expressed allele of the gene encoding constitutively-active ALK2Q207D (CAG-Z-EGFP-caALK2) on a C57BL/6 background was previously described14. We obtained CAGGS-CreER mice, which express a tamoxifen-inducible Cre recombinase ubiquitously under the control of the cytomegalovirus immediate-early enhancer and the chicken β-actin promoter/enhancer20, from the Jackson Laboratory. All mouse experiments were approved by the Massachusetts General Hospital Subcommittee on Research Animal Care.

Cell culture

We isolated PASMCs from wild-type and CAG-Z-EGFP-caALK2–transgenic mice as previously described28 and cultured them in RPMI medium (Invitrogen) supplemented with 10% FBS. We induced recombination of PASMCs expressing conditional caALK2 in vitro by infecting with Ad.Cre (multiplicity of infection of 50) or Ad.GFP as a control and then culturing for 3 d and passaging. We cultured C2C12 myofibroblast cells (American Type Culture Collection) in DMEM (Invitrogen) supplemented with glutamine and 10% FBS. We preincubated cells with pharmacological inhibitors for 10 min and then exposed them to BMP4, TGF-β or platelet-derived growth factor-BB ligands for 30 minutes at 37 °C.

Immunoblot analysis of Smad1, Smad5 and Smad8 phosphorylation

We mechanically homogenized cell extracts in SDS-lysis buffer (62.5 mM Tris-HCl (pH 6.8), 2% SDS, 10% glycerol, 50 mM dithiothreitol and 0.01% bromophenol blue), separated the proteins by SDS-PAGE, immunoblotted with polyclonal antibodies specific for phosphorylated Smad1, Smad5 and Smad8, phosphorylated Smad2 (Cell Signaling Technology) or rabbit monoclonal antibodies specific for Smad1 (Epitomics) or Smad2 (Cell Signaling), and visualized the immunoreactive proteins with ECL Plus (GE Healthcare).

Alkaline phosphatase activity

We seeded C2C12 cells into 96-well plates at 2,000 cells per well in DMEM supplemented with 2% FBS. We treated the wells in quadruplicate with BMP ligands and LDN-193189 or vehicle. We collected the cells after 6 d in culture in 50 μl Tris-buffered saline and 1% Triton X-100. We added the lysates to p-nitro-phenylphosphate reagent in 96-well plates (Sigma) for 1 h and then evaluated alkaline phosphatase activity (absorbance at 405 nm). We measured cell viability and quantity by Cell Titer Aqueous One (absorbance at 490 nm, Promega), using replicate wells treated identically to those used for alkaline phosphatase measurements.

Visualization of skeletal mineralization

We fixed soft tissues and bone and stained them with Alizarin red and Alcian blue as previously described29.

Radiography

For plain film radiography, we anesthetized the mice with ketamine and xylazine and then immobilized them and X-rayed them. For three-dimensional images, we killed the mice and analyzed them with a desktop microtomographic imaging system (μCT40, Scanco Medical AG) equipped with a 10-mm focal spot microfocus X-ray tube. We acquired transverse CT slices of the lower pelvis and hindlimbs with a 12-μm isotropic voxel size. We reconstructed, filtered and thresholded the images with a specimen-specific threshold.

Histology

We killed mice and fixed their limbs in 0.5% paraformaldehyde in PBS overnight and then decalcified them in 14% EDTA disodium salt solution with daily changes for 3 d. We incubated the limbs overnight in 30% sucrose with PBS, embedded them in optimal cutting-temperature medium and prepared 12-μm sections with the Cryo-Jane system (Instrumedics). We stained sections for β-galactosidase or alkaline phosphatase activity (X-Gal and BM purple stains, respectively, Roche), and/or with hematoxylin or eosin counter-stains. For immunofluorescence, we post-fixed sections in cold methanol to disrupt GFP fluorescence and incubated them with polyclonal antibodies specific for phosphorylated Smad1, Smad5 and Smad8 (1:100, Cell Signaling) or Runx2 (M-70, 1:200, Santa Cruz Biotechnology), followed by Alexa Fluor 488–labeled goat Fab specific for rabbit IgG (Invitrogen).

Id1 and plasminogen activator inhibitor-1 promoter luciferase reporter assays

We transiently transfected mouse PASMCs grown to 50% confluence in six-well plates with 0.3 μg Id1 promoter luciferase reporter construct (BRE-Luc30, kindly provided by P. ten Dijke) in combination with 0.6 μg of plasmid expressing constitutively active forms of BMP type I receptors (caALK2, caALK3 or caALK631, kindly provided by K. Miyazono), using Fugene6 (Roche). To assess activin and TGF-β type I receptor function, we transiently transfected PASMCs with 0.3 μg PAI1 (plasminogen activator inhibitor-1) promoter luciferase reporter construct (CAGA-Luc32, provided by P. ten Dijke) in combination with 0.6 μg of plasmid expressing constitutively active forms of type I receptors (caALK4, caALK5 and caALK733, provided by K. Miyazono). For both reporter plasmids, we used 0.2 μg of pRL-TK Renilla luciferase (Promega) to control for transfection efficiency. We incubated PASMCs with LDN-193189 (2 nM–32 μM) or vehicle starting 1 h after transfection. We harvested cell extracts and quantified relative promoter activity by the ratio of firefly to Renilla luciferase activity with the dual luciferase assay kit (Promega).

Range of motion analyses

To quantify impaired mobility via passive range of motion, we anesthetized transgenic and control mice and assessed them for the ability to passively dorsiflex the left ankle joint. Scores were assessed by two independent observers blinded to genotype and treatment. The observers scored the minimum angle formed by the ankle and the tibia with passive dorsiflexion under light manual pressure as follows: 0, normal flexion with a minimal angle of < 20°; 1, mildly impaired flexion with a minimal angle of ≥ 20° but < 90°; 2, moderately impaired flexion with a minimal angle of ≥ 90° but < 135°; and 3, severely impaired flexion with a minimal angle of ≥ 135° (depicted in Fig. 3f).

Statistical analyses

We measured the statistical significance of compared measurements with the Student’s two-tailed t-test.

Supplementary Material

Supplemental Figures

Acknowledgments

We thank P. ten Dijke (Leiden University Medical Center) for providing BRE-Luc and CAGA-Luc and K. Miyazono (University of Tokyo) for providing caALK2, caALK3, caALK4, caALK5, caALK6 and caALK7. We are grateful to H. Beppu, E. Schipani, H. Kronenberg, A. Wagers, J. Groppe, W. Zapol and F. Kaplan for insightful discussions and technical expertise, A. Graveline and D. Panus for technical assistance and E. Buys for technical expertise. This work was supported by US National Institutes of Health grants HL079943 (P.B.Y.) and HL074352 (K.D.B.), the US National Institute of Environmental Health Sciences Intramural Research Program grant ES071003-10 (Y.M.) and Partners Healthcare. This work was also supported by a Howard Hughes Medical Institute Early Career Award (P.B.Y.), a Pulmonary Hypertension Association Mentored Clinical Scientist Award (P.B.Y.), a grant from the GlaxoSmithKline Research & Education Foundation for Cardiovascular Disease (P.B.Y.) and a Developmental Grant from the Center for Research in Fibrodysplasia Ossificans Progressiva and Related Disorders at the University of Pennsylvania (C.C.H.).

Footnotes

Note: Supplementary information is available on the Nature Medicine website.

AUTHOR CONTRIBUTIONS

P.B.Y. wrote the manuscript. P.B.Y., D.Y.D. and C.S.L. designed and performed experiments and analyzed data. G.D.C., P.B.Y., K.D.B. and R.T.P. helped to design, synthesize and evaluate dorsomorphin derivatives, and G.D.C. provided pharmacokinetic data. M.L.B. provided technical expertise and μCT tomography data. D.W.H. and P.M.M. performed experiments. C.S. tested the efficacy of the dorsomorphin derivative with additional assays. N.K. performed control experiments. Y.M. and T.F. provided key experimental reagents. T.K. provided reagents and experimental advice. C.C.H., Y.M. and K.D.B. provided feedback and experimental advice, and P.B.Y. and K.D.B. edited the manuscript.

Reprints and permissions information is available online at http://npg.nature.com/reprintsandpermissions/

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