Mutations in SFRP4 cause Pyle’s bone disease with wide metaphyses and increased skeletal fragility. The WNT signaling pathway plays important roles in determining skeletal architecture and SFRP4 is a secreted Frizzled decoy receptor that inhibits WNT signaling. Seven cohorts of male and female Sfrp4 gene knockout mice, examined through 2 years of age, had a normal lifespan but showed cortical and trabecular bone phenotypes. Mimicking human Erlenmeyer flask deformities, bone cross-sectional areas were elevated 2-fold in the distal femur and proximal tibia but only 30% in femur and tibia shafts. Reduced cortical bone thickness was observed in the vertebral body, midshaft femur and distal tibia. Elevated trabecular bone mass and numbers were observed in the vertebral body, distal femur metaphysis and proximal tibia metaphysis. Midshaft femurs retained extensive trabecular bone through 2 years of age. Vertebral bodies had increased compressive strength, but femur shafts had reduced bending strength. Trabecular, but not cortical, bone parameters in heterozygous Sfrp4 mice were modestly affected. Ovariectomy resulted in similar declines in both cortical and trabecular bone mass in wild-type and Sfrp4 KO mice. SFRP4 is critical for metaphyseal bone modeling involved in determining bone width. Sfrp4 KO mice show similar skeletal architecture and bone fragility deficits observed in patients with Pyle’s disease with SFRP4 mutations.
Pyle’s disease, OMIM #265900, is an autosomal recessive familial metaphyseal dysplasia first identified in 19311,2,3,4,5 with 51 subsequent reports describing 87 subjects from 21 countries. Radiographic abnormalities universally include Erlenmeyer flask deformities6,7,8 at the distal femur and humerus. Genu valgum of varying severity is present and the tibia has an S-shaped deformity at the midshaft. Cortical bone in limbs, clavicles, ribs and digits is exceptionally thin. Bone fractures, spine platyspondyly, and sclerosis of the skull base are often observed. A key observation is that height is normal, indicating there are no disturbances in longitudinal bone growth.
Mutations in the Secreted Frizzled-Related 4 gene (SFRP4) were shown to be responsible for Pyle’s disease in 20169 and three independent confirmations have subsequently been reported.10,11,12 SFRP4 is a secreted WNT decoy receptor, structurally related to WNT Frizzled receptors, that binds WNTs to inhibit both canonical and non-canonical WNT signaling.13,14,15,16
Global Sfrp4 gene disruption in Lexicon Pharmaceutical´s Genome 5000™ high-throughput phenotypic screen of 3 762 viable gene knockout (KO) mouse lines resulted in high trabecular bone mass but low cortical bone thickness.17 Additional Sfrp4 KO mice were examined in a Sfrp4/Wnt16 double KO study and the elevated trabecular bone mass with Sfrp4 KO was not influenced by simultaneous Wnt16 deletion. Midshaft femurs from these DKO mice had intermediate femur cortical cross-sectional area between elevated Sfrp4 KO and reduced Wnt16 KO values, indicating these two genes have independent actions on bone width. Bones from DKO mice had lower cortical thickness than the already reduced values in both single KOs but spontaneous fractures were not observed.
The first publication linking Pyle’s disease to human SFRP4 mutations9 included Lexicon data showing Sfrp4 KO mice have reduced midshaft femur cortical thickness from 4 weeks through 68 weeks of age and reduced femur shaft breaking strength at 24 weeks of age. We subsequently showed that Sfrp4 KO mice have dramatically increased bone trabecularization in the femoral neck18 and mice with simultaneous KO of both Sfrp4 and Notum have reduced cortical bone thickness, like values in Sfrp4 KO mice rather than elevated values observed in Notum KO mice.19
Two independent laboratories also examined Sfrp4 KO mice9,20,21 with agreement concerning greatly elevated trabecular bone mass, increased cortical bone width, and reduced cortical bone thickness. Here, we confirm and extend these observations to multiple ages and skeletal sites. Sfrp4 KO mice have increased spine compressive breaking strength and normal ovariectomy-induced bone loss. Treating young adult Sfrp4 KO mice with zoledronic acid, an inhibitor of osteoclastic bone resorption, does not influence normal gains in trabecular bone mass.
Lexicon’s high-throughput bone phenotyping campaign examining 3 762 viable gene KO mouse lines9 identified several skeletal abnormalities in Sfrp4 KO mice. Body vBMD (Z score = minus 1.6) was reduced but spine LV5 trabecular bone volume (Z score = plus 2.6) and midshaft femur total area (Z score = plus 2.1) were elevated. Midshaft femur cortical thickness had the lowest value of all 3 343 genes examined. Figure S1 shows histograms with these data.
Further studies examined 7 cohorts of Sfrp4 KO mice to determine the effects of age, sex, heterozygosity, ovariectomy, zoledronic acid treatment, and simultaneous KOs of Wnt16 and Notum (Table S1). The numbers of Sfrp4 mutant mice reaching weaning followed expected Mendelian inheritance ratios with 1 101 weanlings divided among 290 wildtype, 560 heterozygous and 251 homozygous mice (P = 0.21 by Chi-squared analysis). Sfrp4 KO mice remained generally healthy with normal viability through 2 years of age (Fig. S2), but 6 of 14 KO mice (7 males and 7 females) displayed a hunchback with stiff thoracic spine when examined visually at 77 weeks of age. Sfrp4 KO mice had normal body weight, fat content and lean body mass (Table S2). Apart from elevated platelet levels in female mice, clinical chemistry and blood cell count values were normal in Sfrp4 KO mice at 2 years of age (Tables S3, S4).
The following phenotypes were consistently observed in multiple cohorts: (1) elevated trabecular bone mass (BV/TV) in LV5 and distal femoral metaphysis (Fig. 1), (2) elevated LV5 trabecular number (Fig. S3), (3) elevated midshaft femur cross-sectional area (Fig. 1), (4) reduced midshaft femur cortical thickness (Fig. 1), and (5) reduced midshaft femur mBMD and vBMD measured by microCT (Fig. S4). LV5 trabecular thickness was normal (data not shown). Femur lengths, measured at 17, 24, and 60 weeks of age were within 2% of control values (Table S5), indicating these skeletal phenotypes did not result from alternations in longitudinal bone growth. Although DXA body BMD values were minimally reduced with Sfrp4 KO, spine BMD was generally elevated and femur BMD was generally reduced (Table S6).
Male Sfrp4 heterozygous and KO mice were examined at 60 weeks of age (Table S7). In addition to the parameters described above, KO mice had increased metaphyseal trabecular numbers in the distal femur and proximal tibia. Metaphyseal trabecular thickness was reduced at both skeletal sites. Consistent with phenotypes observed in the midshaft femur, tibial cortical bone (at the tibia-fibula junction) had elevated total area (mineralized bone plus marrow) and reduced cortical thickness. Metaphyseal cross-sectional areas were elevated 2-fold in both distal femur and proximal tibia. Sfrp4 heterozygous mice had elevated LV5 trabecular BV/TV, elevated metaphyseal trabecular numbers in both distal femur and proximal tibia and reduced trabecular thickness in the proximal tibia metaphysis. All other bone parameters were normal in Sfrp4 heterozygous mice.
A longitudinal microCT slice image of a representative male Sfrp4 KO femur at 2 years of age shows extensive marrow cavity trabecularization (Fig. 2). Representative midshaft femur cross-section images are also shown in Fig. 2, with multiple trabeculae present in bones from all 5 Sfrp4 KO mice but few or no marrow cavity trabeculae for the 8 wild-type (WT) mice. Histological observations (data not shown) from plastic-embedded sections of midshaft femurs of these mice showed no fluorochrome labels, indicating the absence of ongoing periosteal bone formation in wild-type (WT) or KO mice. Endocortical surfaces of bones from WT mice were undergoing minimal focal remodeling.
In an 8-week ovariectomy study (Fig. 3) KO of Sfrp4 in sham-OVX mice led to increased trabecular bone volume in the LV5 vertebral body (74%), distal femur metaphysis (3.5-fold) and proximal tibia metaphysis (3.1-fold). In WT mice, ovariectomy resulted in loss of trabecular bone in the LV5 vertebral body (48%), distal femur metaphysis (66%) and proximal tibia metaphysis (44%). In Sfrp4 KO mice, ovariectomy led to similar fractions of trabecular bone loss, being 65% in the LV5 vertebral body, 44% in the distal femur metaphysis and 44% in the proximal tibia metaphysis. Compression strength testing of the LV5 vertebral body demonstrated the expected effects of ovariectomy and Sfrp4 KO. Maximum load of the vertebral body was increased by 43% in Sfrp4 KO mice and decreased by 34% and 27% following ovariectomy in WT and Sfrp4 KO mice, respectively. Compared to WT control values, trabecular bone following OVX in Sfrp4 KO mice was similar in the proximal tibia, 13% higher in LV5 and 2-fold higher in the distal femur. Compression strength of LV5 vertebral body (including contributions from the cortical shell) was similar in sham-WT and OVX-Sfrp4 KO mice.
OVX-induced loss of cortical bone occurred in the midshaft femur, midshaft tibia and LV5 vertebral body for both control and Sfrp4 KO mice (Fig. 4). Femoral cortical thickness losses were 8% (21 µm) in WT and 19% (36 µm) in Sfrp4 KO mice. Similarly, tibial cortical thickness losses were 4% (10 µm) in WT and 14% (24 µm) in Sfrp4 KO mice. For all four groups, midshaft femur and tibia cortical thickness values were highly correlated (Fig. S5). LV5 cortical BV/TV losses were 15% in WT and 21% in Sfrp4 KO mice. OVX-induced reductions in midshaft femur breaking strength were 11% (3.9 N) in WT and 31% (8.6 N) in KO mice. Compared to WT control values, the combination of OVX and Sfrp4 KO reduced LV5 cortical BV/TV by 36%, femoral cortical thickness by 43%, tibial cortical thickness by 40% and femoral strength by 46%. Femoral 4-point bending strength across all bones (Fig. S6) was correlated to cortical thickness (R2 = 0.70) but neither total area (R2 = 0.27), nor polar moment of inertia (R2 = 0.08).
Male and female WT and Sfrp4 KO mice were treated with the bisphosphonate zoledronic acid at 8 weeks of age. At this age Sfrp4 KO mice have reduced cortical bone thickness, but normal trabecular bone mass (Fig. 1). Male and female mice were treated for 60 and 16 weeks, respectively. For male mice, analyses of serum levels of PINP and CTX at 50 weeks of age to assess bone turnover (remodeling) showed no effect of Sfrp4 KO but 40% reductions with zoledronic aid treatment (Table S8).
Both male and female Sfrp4 KO mice had elevated trabecular bone mass in both LV5 vertebral body and the distal femur metaphysis, with zoledronic acid treatment resulting in further additive increases in trabecular bone mass (Fig. 5). These findings demonstrate that zoledronic acid treatment does not interfere with the development of elevated trabecular bone mass with Sfrp4 disruption. Zoledronic acid treatment did not differentially affect midshaft femur cortical bone width or thickness, nor LV5 cortical bone mass, in WT or KO mice (Fig. S7). These findings suggest simultaneous treatment with a SFRP4 neutralizing antibody and a bisphosphonate in adult osteoporosis patients might promote trabecular bone gain while inhibiting further cortical bone loss.
Analysis of published gene expression databases showed that Sfrp4 expression was stimulated 7-fold during BMP2-induced differentiation of murine C2C12 myoblasts into osteoblasts (Fig. S8).
Pyle’s disease is a developmental familial skeletal dysplasia resulting from disturbances in metaphyseal bone modeling (Fig. 6), a complex process involving periosteal bone resorption, endocortical bone formation and coalescence of calcified cartilage trabeculae into cortical bone.22,23,24,25,26 Serial wrist radiographs obtained during healthy adolescence showed distal radius rates of periosteal resorption and endocortical apposition averaged 8 μm·d−1 and 10 μm·d−1, respectively.27 Although human short stature can result from disruptions in at least 60 genes influencing longitudinal bone growth,28 bone lengths are unaffected in Pyle´s disease subjects and Sfrp4 KO mice. Therefore, SFRP4 does not appear to influence formation and maintenance of articular cartilage and epiphyseal bone, nor growth plate dynamics.
Failure of normal metaphyseal bone modeling results in radiographic Erlenmeyer flask deformities,6 also known as metaphyseal widening, clubbing, flaring and undermodeling. Besides Pyle’s disease, human skeletal dysplasias with normal bone lengths and Erlenmeyer flask deformities occur with mutations in ANKH (craniometaphyseal dysplasia,29 COL10A1 (Schmid metaphyseal dysplasia,30,31 FLNA (frontometaphyseal dysplasia,32 GBA (Gaucher’s disease,33 LRRK1 (osteosclerotic metaphyseal dysplasia,34 PTH1R (Jansen’s metaphyseal chondrodysplasia,35 and CLCN7,36,37 PLEKHM1,38 and SNX1039 each resulting in osteopetrosis. COL10A1 is a cartilage structural component; PTH1R and SFRP4 are involved in cell signaling pathways; with ANKH, CLCN7, FLNA, GBA, LRRK1, PLEKHM1 and SNX10 all having roles in bone resorbing osteoclasts. Osteoclast dysfunction contributes to failure of metaphyseal periosteal bone resorption leading to the Erlenmeyer flask deformity.
There are no apparent bone architecture differences between male and female Pyle’s disease subjects nor Sfrp4 KO mice. Bone dysplasias in Pyle’s disease subjects and Sfrp4 KO mice appear during growth and are not progressive in adults. SFRP4 is unlikely to be involved in postmenopausal osteoporosis as cortical and trabecular bone losses following ovariectomy in adult mice was unaffected by Sfrp4 KO. These observations suggest that inhibition of SFRP4, for example with a therapeutic neutralizing antibody, would not be a viable therapy for postmenopausal osteoporosis.
Standard clinical radiographs obtained in living Pyle’s disease subjects cannot show trabecular bone abnormalities occurring within bones. Iliac crest biopsies and 3-dimensional bone CT scans have not been performed to provide insights into trabecular bone architecture. Fortunately, Ingalls obtained a femur and tibia from a cadaver, first described in 1910,40 having classic Erlenmeyer flask deformities. He sectioned these bones longitudinally and published his descriptions in 1933 with a photograph of the sectioned bones.41 Extensive trabecular bone was observed within the distal three-fifths of this femur and proximal three-fifths of this tibia. Femoral Erlenmeyer flask enlargement was greater in the coronal than the sagittal plane.42 Similar observations were subsequently made on a human femur and tibia recovered from an archeological site in Peru.43 These bone phenotypes are consistent with SFRP4 mutations but other genetic metaphyseal dysplasias are possible.
Sfrp4 KO mouse limbs exhibit Erlenmeyer flask deformities observed in Pyle’s disease subjects. Metaphyseal cross-sectional areas are elevated 2-fold in the mouse distal femur and proximal tibia (Table S7) but by only 30% in the midshaft femur (Fig. 1) and tibia shaft at the fibula junction (Table S7). These observations are consistent with the excessively wide proximal tibiae and distal femurs previously observed in Sfrp4 KO mice.9,20
Mouse clavicles, ribs, digits, and the cranial base, sites with radiographic abnormalities in Pyle’s subjects, have not been examined as all mouse studies were performed prior to the 2016 identification of SFRP4 mutations being responsible for Pyle’s disease.9 During development growth plates (synchondroses) separate the sphenoid, ethmoidal and basioccipital bones at the base of the skull.44 Presumably, disturbances in metaphyseal bone modeling similar to those observed in limbs is responsible for cranial base sclerosis observed in Pyle’s disease subjects. Skull shape appears normal as SFRP4 does not affect longitudinal growth. The femoral neck growth plate is located just below the femoral head and femoral necks in WT mice consist of predominately cortical bone but are extensively trabecularized in Sfrp4 KO mice.18
Consistent with the autosomal recessive inheritance of Pyle’s disease, except for modestly elevated trabecular bone mass in spine, femur, and tibia, we did not observe skeletal phenotypes in heterozygous Sfrp4 mice. Studies employing pQCT would presumably show excess trabecular bone within limbs of both subjects and possibly their heterozygous relatives.
The lifelong persistence of extensive trabecular bone networks within limb diaphyses from two human adult cadavers presumed to have Pyle’s disease40,42 and aged Sfrp4 KO mice is unusual. We suggest that the normal resorption of entire trabeculae at the metaphyseal-diaphyseal junction does not occur in the absence of SFRP4, resulting in marrow cavity trabecularization within the diaphysis. Extensive trabecularization of the diaphyseal marrow cavity also occurs in adult mice with genetic disruptions of Kindlin3,45 Lrrk146, Schnurri3,47 Sgpl1,17,48 Slc37a249, and Vhl.50 Consistent with our suggestion, diaphyseal trabeculae in adult Lrrk1 and Vhl KO mice contain remnants of calcified cartilage, presumably originating from the metaphyseal growth plate region. The extent of trabecular bone remodeling in adults is unclear. Levels of serum bone turnover markers PINP and CTX are normal in Sfrp4 KO mice at 50 weeks of age, adult Vhl KO mice50 and in the few adult Pyle’s disease subjects examined.9
Normal gains in trabecular bone mass in both the distal femur metaphysis and LV5 vertebral body after 8 weeks of age in Sfrp4 KO mice following treatment with zoledronic acid, an osteoclast inhibitor, are consistent with elevated trabecular bone formation in Sfrp4 KO mice observed by others.9 Endocortical and trabecular bone loss in femurs, tibias and vertebral bodies following ovariectomy were unaffected by Sfrp4 gene disruption. These results suggest SFRP4 specifically inhibits metaphyseal endocortical bone resorption during longitudinal growth.
Metaphyseal bone dysmorphology observed with SFRP4 disruption is consistent with the expression patterns of Sfrp4 in mouse bone. Robust Sfrp4 expression in embryonic51 and neonatal52 mouse femoral metaphysis is observed by in situ mRNA hybridization. Similarly, robust skeletal Sfrp4 expression, viewed in whole-mount mouse bones after LacZ-driven X-Gal staining, occurs in embryonic mouse midshaft femur and the femur metaphysis at 3 weeks20 and 12 weeks of age.53 Sfrp4 expression in adult mouse bone lining cells was identified by RT-PCR after FACS isolation.54 SFRP4 is highly expressed in primary cultures of human osteoblasts.55 Sfrp4 expression is stimulated 5-fold following PTH treatment of osteocyte Ocy454 cells56 and, as described above, 7-fold during BMP2-induced differentiation of murine C2C12 myoblasts into osteoblasts.57 These studies all suggest Sfrp4 is expressed by bone cells. Overexpression of Sfrp4 in mice reduces trabecular bone mass.52,58
Results from the present study, our previously published data,17,18,19 and findings by two independent laboratories9,20,21 all support Sfrp4 KO mice are a good model for human Pyle’s disease resulting from human SFRP4 mutations. Bone dysplasias, including Erlenmeyer flask deformities, occur during growth and persist in adults. Human height and mouse bone length are normal. Partially penetrant hunchback posture occurs in adult mice and platyspondyly has been reported in humans.8 There are extensive trabecular bone networks within adult diaphyseal marrow cavities and cortical bone thickness is reduced. Mouse longevity and serum chemistry values are both unaffected. Human fragility fractures are common and we previously reported17 that mouse femur shafts have reduced 4-point bending strength.
Knockout mice were generated by homologous recombination techniques with disruption of the first exon of the Sfrp4 gene (Fig. S9). All studies examined F2 hybrid littermate/cagemate mice derived from C57BL/6 J and 129SvEv parental strains generated and studied within the Lexicon vivarium.19 Mice were group-housed in micro-isolator cages within a barrier facility at 24 °C on a fixed 12-h light and 12-h dark cycle and fed Purina rodent chow No. 5001 (Purina, St. Louis, MO). The high-fat diet (45 kcal percent fat) employed in the primary screen was D12451i from Research Diets (New Brunswick, NJ USA). Diets and acidified water were provided ad libitum. All procedures involving use of live mice were conducted in conformance with Lexicon’s Institutional Animal Care and Use Committee guidelines that were in compliance with the state and federal laws and the standards outlined in the Guide for the Care and Use of Laboratory Animals (National Research Council, 1996). Quarterly sentinel surveillance showed no evidence of pathogenic rodent viruses, Mycoplasma, or Helicobacter species in the source colonies. All mice and samples were analyzed after investigator blinding to genotypes and experimental treatments.
Spine BMD and body composition were measured under isoflurane anesthesia using a PIXImus DXA (InsideOutside Sales, Fitchburg, WI) by standard techniques. Bone architecture was determined by microCT using a µCT40 (Scanco Medical, Brüttisellen, Switzerland) scanner employing a threshold of 240, an X-ray tube voltage of 55 keV, a current of 145 microamperes and an integration time of 200 microseconds. For cortical bone analyses in the femur (midshaft) and tibia (tibia-fibula junction), twenty slices were analyzed and total area of mineralized bone plus marrow was determined as an estimate of bone cross-sectional area. For LV5, the vertebral body was analyzed for trabecular bone and, in four cohorts, also for cortical bone. Trabecular bone analyses included the region inside the cortical shell. When cortical analyses were performed, the scans were first analyzed for trabecular bone and then a second contour was traced to include the cortical region of the (Fig. S10).
Bilateral ovariectomy or sham surgery was performed at 16 weeks of age, with bones examined 8 weeks later. Mice were administered 20 µg·kg−1 single doses of zoledronic acid intraperitoneally at 8 weeks of age, with bones examined at 24 weeks for females and 68 weeks for males. Zoledronic acid (Zometa, Novartis, Basel, Switzerland) was purchased from a pharmacy and diluted with sterile saline before use.
For male mice examined at 105 weeks of age, subcutaneous injections of sterile solutions of calcein (10 mg·kg−1) and demeclocycline (30 mg·kg−1) were given 26 and 5 days, respectively, prior to necropsy to label bone forming surfaces. Both calcein and demeclocycline were purchased from SigmaAldrich (St. Louis, MO USA). Femur shafts were embedded in methacrylate, sectioned at ~80 µm with a SP1600 Saw Microtome (Leica Biosystems, Buffalo Grove, IL USA) and visually examined by fluorescent microscopy.
For the ovariectomy study, LV5 vertebral body ultimate compression strength and femur shaft 4-point ultimate breaking strength were measured using an Instron 5500 Testing Unit at Numira Biosciences (Salt Lake City, UT USA). LV5 vertebral bodies were compressed at a rate of 0.6 mm·min−1. Femurs were mounted with a 2.5 mm inner support and a 7.0 mm outer support and 4-point loading was applied at a displacement rate of 3 mm·min−1.
The EMBL-EBI Expression Atlas59 was employed to search for relevant published mouse Sfrp4 gene expression data. This search identified a dataset providing expression data (GeneChip™ Mouse Genome 430 2.0 Array for 45 000 probes) during BMP2-induced differentiation of murine C2C12 myoblasts into osteoblasts.57
Statistical evaluations were by Student’s t-test, one-factor ANOVA (with Dunnett’s test for multiple comparisons) or two-factor ANOVA, as appropriate. Sample numbers were determined from power calculations using values from Lexicon’s extensive database of skeletal phenotypes in KO mice.17
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Pyle, E. A case of unusual bone development. J. Bone Jt. Surg. Am. 13, 874–876 (1931).
Jackson, W. P., Albright, F., Drewry, Hanelin, J. & Rubin, M. I. Metaphyseal dysplasia, epiphyseal dysplasia, diaphyseal dysplasia, and related conditions. I. Familial metaphyseal dysplasia and craniometaphyseal dysplasia; their relation to leontiasis ossea and osteopetrosis; disorders of bone remodeling. AMA Arch. Intern. Med. 94, 871–885 (1954).
Gorlin, R. J. & Koszalka, M. F. Pyle’s disease (familial metaphyseal dysplasia). J. Bone Jt. Surg. (Am.) 52, 347–353 (1970).
Beighton, P. Pyle disease (metaphyseal dysplasia). J. Med. Genet. 24, 321–324 (1987).
Turra, S., Gigante, C., Pavanini, G. & Bardi, C. Spinal involvement in Pyle’s disease. Pediatr. Radio. 30, 25–27 (2000).
Faden, M. A., Krakow, D., Ezgu, F., Rimoin, D. L. & Lachman, R. S. The Erlenmeyer flask bone deformity in the skeletal dysplasias. Am. J. Med. Genet. A 149A, 1334–1345 (2009).
Rubin, P. & Squire, L. Clinical concepts in bone modeling. Am. J. Roentgenol. Radium Ther. Nucl. Med. 82, 217–228 (1959).
Stark, Z. & Savarirayan, R. Osteopetrosis. Orphanet J. Rare Dis. 4, 5 (2009).
Simsek Kiper, P. O. et al. Cortical-bone fragility - Insights from sFRP4 deficiency in Pyle’s disease. N. Engl. J. Med. 374, 2553–2562 (2016).
Chatron, N. et al. A novel homozygous truncating mutation of the SFRP4 gene in Pyle’s disease. Clin. Genet. 92, 112–114 (2017).
Galada, C., Shah, H., Shukla, A. & Girisha, K. M. A novel sequence variant in SFRP4 causing Pyle disease. J. Hum. Genet. 62, 575–576 (2017).
Sowińska-Seidler, A. et al. The first report of biallelic missense mutations in the SFRP4 gene causing Pyle disease in two siblings. Front. Genet. 11, 593407 (2020).
Wawrzak, D. et al. Wnt3a binds to several sFRPs in the nanomolar range. Biochem. Biophys. Res. Commun. 357, 1119–1123 (2007).
Carmon, K. S. & Loose, D. S. Development of a bioassay for detection of Wnt-binding affinities for individual frizzled receptors. Anal. Biochem. 401, 288–294 (2010).
Pawar, N. M. & Rao, P. Secreted frizzled related protein 4 (sFRP4) update: A brief review. Cell Signal 45, 63–70 (2018).
Guan, H. et al. Secreted frizzled related proteins in cardiovascular and metabolic diseases. Front. Endocrinol. (Lausanne) 12, 712217 (2021).
Brommage, R. et al. High-throughput screening of mouse gene knockouts identifies established and novel skeletal phenotypes. Bone Res. 2, 14034 (2014).
Brommage, R., Jeter-Jones, S., Xiong, W. & Liu, J. MicroCT analyses of mouse femoral neck architecture. Bone 145, 115040 (2021).
Brommage, R. et al. NOTUM inhibition increases endocortical bone formation and bone strength. Bone Res. 7, 2 (2019).
Haraguchi, R. et al. sFRP4-dependent Wnt signal modulation is critical for bone remodeling during postnatal development and age-related bone loss. Sci. Rep. 6, 25198 (2016).
Chen, K. et al. Sfrp4 repression of the Ror2/Jnk cascade in osteoclasts protects cortical bone from excessive endosteal resorption. Proc. Natl. Acad. Sci. USA 116, 14138–14143 (2019).
Enlow, D. H. A study of the post-natal growth and remodeling of bone. Am. J. Anat. 110, 79–101 (1962).
Cadet, E. R. et al. Mechanisms responsible for longitudinal growth of the cortex: coalescence of trabecular bone into cortical bone. J. Bone Jt. Surg. Am. 85A, 1739–1748 (2003).
Rauch, F., Neu, C., Manz, F. & Schoenau, E. The development of metaphyseal cortex-implications for distal radius fractures during growth. J. Bone Min. Res. 16, 1547–1555 (2001).
Wang, Q., Ghasem-Zadeh, A., Wang, X. F., Iuliano-Burns, S. & Seeman, E. Trabecular bone of growth plate origin influences both trabecular and cortical morphology in adulthood. J. Bone Min. Res. 26, 1577–1583 (2011).
Ip, V., Toth, Z., Chibnall, J. & McBride-Gagyi, S. Remnant woven bone and calcified cartilage in mouse bone: differences between ages/sex and effects on bone strength. PLoS One 11, e0166476 (2016).
Rauch, F., Neu, C., Manz, F. & Schoenau, E. The development of metaphyseal cortex - Implications for distal radius fractures during growth. J. Bone Min. Res. 16, 1547–1555 (2001).
Costantini, A., Muurinen, M. H. & Mäkitie, O. New gene discoveries in skeletal diseases with short stature. Endocr. Connect. 10, R160–R174 (2021).
Nürnberg, P. et al. Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia. Nat. Genet. 28, 37–41 (2001).
Wallis, G. A. et al. Amino acid substitutions of conserved residues in the carboxyl-terminal domain of the alpha 1(X) chain of type X collagen occur in two unrelated families with metaphyseal chondrodysplasia type Schmid. Am. J. Hum. Genet. 54, 169–178 (1994).
McIntosh, I., Abbott, M. H., Warman, M. L., Olsen, B. R. & Francomano, C. A. Additional mutations of type X collagen confirm COL10A1 as the Schmid metaphyseal chondrodysplasia locus. Hum. Mol. Genet. 3, 303–307 (1994).
Clark, A. R., Sawyer, G. M., Robertson, S. P. & Sutherland-Smith, A. J. Skeletal dysplasias due to filamin A mutations result from a gain-of-function mechanism distinct from allelic neurological disorders. Hum. Mol. Genet. 18, 4791–4800 (2009).
Tsuji, S. et al. A mutation in the human glucocerebrosidase gene in neuronopathic Gaucher’s disease. N. Engl. J. Med. 316, 570–575 (1987).
Iida, A. et al. Identification of biallelic LRRK1 mutations in osteosclerotic metaphyseal dysplasia and evidence for locus heterogeneity. J. Med. Genet. 53, 568–574 (2016).
Schipani, E., Kruse, K. & Jüppner, H. A constitutively active mutant PTH-PTHrP receptor in Jansen-type metaphyseal chondrodysplasia. Science 268, 98–100 (1995).
Cleiren, E. et al. Albers-Schönberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel gene. Hum. Mol. Genet. 10, 2861–2867 (2001).
Kornak, U. et al. Loss of the ClC-7 chloride channel leads to osteopetrosis in mice and man. Cell 104, 205–215 (2001).
Van Wesenbeeck, L. et al. Involvement of PLEKHM1 in osteoclastic vesicular transport and osteopetrosis in incisors absent rats and humans. J. Clin. Invest. 117, 919–930 (2007).
Aker, M. et al. An SNX10 mutation causes malignant osteopetrosis of infancy. J. Med. Genet. 49, 221–226 (2012).
Hamann, C. A. An abnormality in the form of the femur. Clevel. Med. J. 9, 710–712 (1910).
Ingalls, N. W. Bone growth and pathology as seen in the femur (and tibia). VIII. Studies on the femur. Arch. Surg. 26, 787–795 (1933).
Ingalls, N. W. & Grossberg, M. H. Studies on the femur. VI. The distal part of the diaphysis. Am. J. Phys. Anthropol. 26, 475–495 (1932).
Urteaga, O. & Moseley, J. E. Craniometaphyseal dysplasia (Pyle’s disease) in an ancient skeleton from the Mochica culture of Peru. Am. J. Roentgenol. Radium Ther. Nucl. Med. 99, 712–716 (1967).
Hallett, S. A., Ono, W., Franceschi, R. T. & Ono, N. Cranial base synchondrosis: Chondrocytes at the hub. Int. J. Mol. Sci. 23, 7817 (2022).
Dudiki, T. et al. Progressive skeletal defects caused by Kindlin3 deficiency, a model of autosomal recessive osteopetrosis in humans. Bone 160, 116397 (2022).
Xing, W. et al. Targeted disruption of leucine-rich repeat kinase 1 but not leucine-rich repeat kinase 2 in mice causes severe osteopetrosis. J. Bone Min. Res. 28, 1962–1974 (2013).
Hofstaetter, J. G. et al. Biomechanical and bone material properties of Schnurri-3 null mice. JBMR 3, e10226 (2019).
Vogel, P. et al. Incomplete inhibition of sphingosine 1-phosphate lyase modulates immune system function yet prevents early lethality and non-lymphoid lesions. PLoS One 4, e4112 (2009).
Ng, P. Y. et al. Sugar transporter Slc37a2 regulates bone metabolism via a dynamic tubular lysosomal network in osteoclasts https://www.biorxiv.org/content/10.1101/2022.04.28.489831v1
Dirckx, N. et al. Vhl deletion in osteoblasts boosts cellular glycolysis and improves global glucose metabolism. J. Clin. Invest. 128, 1087–1105 (2018).
Witte, F., Dokas, J., Neuendorf, F., Mundlos, S. & Stricker, S. Comprehensive expression analysis of all Wnt genes and their major secreted antagonists during mouse limb development and cartilage differentiation. Gene Expr. Patterns 9, 215–223 (2009).
Nakanishi, R. et al. Osteoblast-targeted expression of Sfrp4 in mice results in low bone mass. J. Bone Min. Res. 23, 271–277 (2008).
Mastaitis, J. et al. Loss of SFRP4 alters body size, food intake, and energy expenditure in diet-induced obese male mice. Endocrinology 156, 4502–4510 (2015).
Matic, I. et al. Quiescent bone lining cells are a major source of osteoblasts during adulthood. Stem Cells 34, 2930–2942 (2016).
Spencer, G. J., Utting, J. C., Etheridge, S. L., Arnett, T. R. & Genever, P. G. Wnt signalling in osteoblasts regulates expression of the receptor activator of NFkappaB ligand and inhibits osteoclastogenesis in vitro. J. Cell Sci. 119, 1283–1296 (2006).
Wein, M. N. et al. SIKs control osteocytes response to parathyroid hormone. Nat. Commun. 7, 13176 (2016).
Hupkes, M., Sotoca, A. M., Hendriks, J. M., van Zoelen, E. J. & Dechering, K. J. MicroRNA miR-378 promotes BMP2-induced osteogenic differentiation of mesenchymal progenitor cells. BMC Mol. Biol. 15, 1 (2014).
Cho, H. Y. et al. Transgenic mice overexpressing secreted frizzled-related proteins (sFRP)4 under the control of serum amyloid P promoter exhibit low bone mass but did not result in disturbed phosphate homeostasis. Bone 47, 263–271 (2010).
Petryszak, R. et al. Expression Atlas update - an integrated database of gene and protein expression in humans, animals and plants. Nucleic Acids Res. 44, D746–D752 (2016).
All studies were supported by Lexicon Pharmaceuticals. Wendy Xiong sectioned plastic-embedded femurs and Andrea Y. Thompson examined the cortical bone sections by fluorescent microscopy. Victor Shen and Vonn Wright of Numira Biosciences performed the bone strength measurements. Hiroaki Saito, Francesca Gori, Eric Hesse and Roland Baron provided insights from their Sfrp4 KO mouse studies.
The authors declare no competing interests.
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Brommage, R., Liu, J. & Powell, D.R. Skeletal phenotypes in secreted frizzled-related protein 4 gene knockout mice mimic skeletal architectural abnormalities in subjects with Pyle’s disease from SFRP4 mutations. Bone Res 11, 9 (2023). https://doi.org/10.1038/s41413-022-00242-9