The Rb and Pten tumor suppressor genes are important regulators of bone development and both are frequently mutated in the bone cancer osteosarcoma (OS). To determine if Rb1 and Pten synergize as tumor suppressor genes for osteosarcoma, we co-deleted them in osteoprogenitor cells. Surprisingly, we observed rapid development of adipogenic but not osteosarcoma tumors in the ΔRb1/Pten mice. ΔPten solo deleted mice also developed lipoma tumors but at a much reduced frequency and later onset than those co-deleted for Rb1. Pten deletion also led to a marked increase in adipocytes in the bone marrow. To better understand the function of Pten in bone development in vivo, we conditionally deleted Pten in OSX+ osteoprogenitor cells using OSX-Cre mice. μCT analysis revealed a significant thickening of the calvaria and an increase in trabeculae volume and number in the femur, consistent with increased bone formation in these mice. To determine if Pten and Rb1 deletion actively promotes adipogenic differentiation, we isolated calvarial cells from Ptenfl/fl and Ptenfl/fl; Rb1fl/fl mice, infected them with CRE or GFP expressing adenovirus, treated with differentiation media. We observed slightly increased adipogenic, and osteogenic differentiation in the ΔPten cells. Both phenotypes were greatly increased upon Rb1/Pten co-deletion. This was accompanied by an increase in expression of genes required for adipogenesis. These data indicate that Pten deletion in osteoblast precursors is sufficient to promote frequent adipogenic, but only rare osteogenic tumors. Rb1 hetero- or homo-zygous co-deletion greatly increases the incidence and the rapidity of onset of adipogenic tumors, again, with only rare osteosarcoma tumors.
Citation: Filtz EA, Emery A, Lu H, Forster CL, Karasch C, Hallstrom TC (2015) Rb1 and Pten Co-Deletion in Osteoblast Precursor Cells Causes Rapid Lipoma Formation in Mice. PLoS ONE 10(8): e0136729. https://doi.org/10.1371/journal.pone.0136729
Editor: Xing-Ming Shi, Georgia Regents University, UNITED STATES
Received: January 16, 2015; Accepted: August 8, 2015; Published: August 28, 2015
Copyright: © 2015 Filtz et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: This work was funded by grants to T.H. from National Institutes of Health (R01CA168622) and the Children’s Cancer Research Fund, Minneapolis, MN. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Mammalian bone formation occurs in a coordinated, sequential process that is characterized by the commitment of osteoprogenitor cells into pre- and mature osteoblasts whose function is to synthesize the bone matrix that later becomes mineralized. Osteoblasts originate from pluripotent mesenchymal stem cells that can also differentiate into other mesenchymal cell lineages such as adipocytes, chondrocytes, myoblasts, and fibroblasts depending on the nature of the activated transcriptional differentiation program, and if triggered prior to their commitment to the osteoblastic lineage. For example, MyoD transcription factors are critical for the maturation of muscle cell lineages , whereas the peroxisome proliferator-activated receptor γ (PPARγ) is necessary for the differentiation of adipocyte lineage cells . Several transcription factors are critical for the commitment of mesenchymal stem cells into the osteoblast cell lineage, such as the runt-related genes Cbfa1 and Runx2 [3–5]. SP7, also known as Osterix and OSX, is a bone-specific transcription factor that regulates osteoblast development and is expressed in precursors at an early stage in the osteoblast lineage . Understanding the regulation of mesenchymal stem cells into distinct lineages is critical because dysregulation or reactivation of these pathways have an important role in the pathogenesis of human disorders such as osteoporosis and osteosarcoma bone tumors.
Osteosarcoma (OS) is the most common primary bone cancer and is associated with excess osteoblastic proliferation. Mutations in several common human cancer genes such as TP53, RB1, CDKN2A, MYC, and PTEN drive OS development [7, 8]. OS incidence is increased several hundred-fold in patients with RB1 germline mutations and patients with hereditary retinoblastoma through loss of the Rb tumor suppressor protein, a key regulator of E2F transcription factors and cell cycle progression, and thus its deletion is often accompanied by defects in cell cycle exit and can result in an undifferentiated cellular phenotype [9–11]. In addition, pRB controls mesenchymal cell differentiation through interactions with RUNX2 to promote osteogenic differentiation , or through blocking PPAR-γ expression to suppress adipogenesis .
PTEN (phosphatase and tensin homolog) is a tumor suppressor gene that is mutated at high frequency in a wide variety of human cancers, such as glioblastoma, prostate, breast, osteosarcoma and was recently identified as a key driver of osteosarcoma in a murine forward genetic screen [8, 14, 15]. PTEN encodes a lipid phosphatase that dephosphorylates phosphatidylinositol (3,4,5)- triphosphate (PIP3) to oppose the activity of phosphatidylinositol 3-kinase (PI3K), which functions as a PIP3 kinase that is constitutively activated and functions as an oncogene in many cancer types . Loss of PTEN causes persistent activation of the Akt serine-threonine kinase which promotes cell growth and proliferation, disables apoptosis, and controls metabolism by directly phosphorylating numerous downstream targets such as BAD, FOXO transcription factors, CASP9, MTOR, MDM2, and others .
We recently identified a functional connection between Rb1 and Pten in murine retinal progenitor cells, where Rb1 deletion deregulates E2F dependent cell cycle entry and cell death, and co-deleting Pten inactivates an E2F/FOXO transcriptional complex in vivo to prevent apoptosis and promote rapid retinal tumorigenesis in retinal progenitor cells . We tested if co-deleting Rb1 and Pten in mouse osteo-progenitors resulted in osteosarcoma development. We surprisingly observed rapid lipoma formation and increased marrow adipocyte size and numbers in mice with Rb1 and Pten co-deleted in osteoprogenitor cells. Consistent with these observations, deleting Pten or co-deleting Rb1 and Pten in calvarial osteoblast cells significantly promoted adipocyte differentiation and adipogenic differentiation gene expression. These data indicate that Pten deletion in osteoblast precursors is sufficient to promote frequent adipogenic, but only rare osteogenic tumors. Rb1 hetero- or homo-zygous co-deletion greatly increases the incidence and the rapidity of onset of adipogenic tumors, again, with only rare osteosarcoma tumors.
Materials and Methods
Experimental Animals & Ethics Statement
Osx1-GFP::Cre mice , Rb1lox/lox mice , p107-/- mice , and Ptenlox/lox mice  and associated PCR genotyping protocols have been described. Animals were housed in the University of Minnesota animal facility. All mouse experiments were performed in accordance with University of Minnesota Institutional Animal Care and Use Committee procedures and guidelines under IACUC protocols #1309-30948A (2013-present), and previously #0711A20882 (2010–2013). No analgesic or anesthetics were used. Mice were monitored at least three times weekly during the survival study for evidence of surface irritation, infection, inability to obtain feed or water, accompanying weight loss, but these symptoms were not observed. Mice were humanely euthanized with CO2 when tumors reached a size of 1cm3, or immediately if tumors began to ulcerate the skin, or if a general moribund status evidenced by a reluctance to stand or move around the cage was observed. The University of Minnesota Comparative Pathology Shared Resource assisted with H&E staining, Ki-67 & TUNEL immunohistochemistry (IHC) staining. Kaplan-Meier curves were calculated using GraphPad Prism software, and p-values were determined by Student’s t-test. Marrow fat percentage, adipocyte density and size were determined by histomorphometry of mouse tibial sections as described [22, 23].
Microcomputed tomography (μCT) analysis
Mouse femurs and calvaria were subjected to micro-CT scanning (model XT H 225, Nikon Metrology, Inc.) using the conditions of 90 kV, 90 μA, 0.5° steps with a pixel size at 12 μm and exposure time of 708 ms as described . CT Pro 3D (Nikon metrology) software was used to reconstruct original three-dimensional images. VG Studio Max 2.1 (Volume Graphics GmbH) was used for visualization and three-dimensional rendering and creation of bmp files. Finally, histomorphometry analyses were performed using SkyScan CT-Analyzer Version 1.12 (Bruker micro-CT).
Calvarial osteoblast isolation, adenovirus infection and cell differentiation
Calvarial osteoblasts were harvested as described . Briefly, calvaria were removed from newborn pups and rinsed in warmed MEM to remove excess tissue. Calvaria were shaken for 20 minutes at 37°C in collagenase digestion mixture and the first fraction was discarded. Calvaria were shaken with another 10 ml aliquot of digestion mix for 40 minutes, and a third aliquot for 90 minutes. Trypsin was quenched with 10% FBS after each digestion, and cells from fractions 2 and 3 were resuspended in 10% FBS MEM and plated on 60mm plates at an approximate density of 1 calvaria/1.5 plates. Adenovirus infections were performed as described . Cells were infected 24 hours after isolation (60–80% confluence) with control, or CRE expressing adenovirus at a multiplicity of infection (MOI) of 100. Adipogenic Media (α-MEM containing 10% FBS, 1% anti-microbial, 0.5 mM 3-isobutyl-1-methylxanthine (IBMX), 5 ug/ml h-insulin, and 0.1 μM dexamethasone) or osteogenic media (α-MEM containing 10% FBS, 1% anti-microbial, 100 mM L-ascorbic acid, 0.01M sodium phosphate) differentiation media was added five days after adenovirus infections. Cells were grown in differentiation media for 25 days, and media was changed every three days.
Oil Red O (ORO) and Alizarin Red staining of differentiated calvarial cells
ORO stock solution (3mg/mL in isopropanol) was prepared fresh each experiment and mixed at a 3/2 ratio to make the working solution, which was filtered and used within 2 hours. Cells were rinsed with PBS, fixed in 10% formalin for 30 minutes at room temperature, rinsed with water and treated with 60% isopropanol for 5 minutes. ORO working solution was added to cells for 5 minutes and then rinsed with water. Cells that had been treated with osteogenic differentiation media were fixed (10% formalin for 30 minutes). After rinsing fixed cells, alizarin red solution (2% Alizarin Red S in distilled water, pH adjusted to 4.2 with ammonium hydroxide) was added to cells for 15 seconds and then rinsed with water before imaging.
Quantitative real-time PCR
RNA was prepared from cells for quantitative real-time PCR using RNeasy, QIAshredder, and QuantiTect SYBR Green RT-PCR kits from QIAGEN. Each RT-PCR experiment was performed in triplicate and normalized against expression of GAPDH expression levels and fold changes were calculated using ΔΔCT method . p-values were determined by Student’s t–test. p < 0.05 were considered significant. Primers are listed in S1 Table.
Combined deletion of Pten and Rb1 in osteoblast precursor cells accelerates adipogenic tumor formation
Because the Rb1 and Pten tumor suppressor genes are frequently mutated in bone cancer, we predicted that their combined deletion might provoke a stronger tumor phenotype than individual deletion of either gene. The Osx-Cre transgenic mouse was chosen to conditionally delete Rb1 and Pten in these studies because Osterix is expressed in committed osteoprogenitor cells and because Osx-Cre has successfully been utilized to generate osteosarcoma mouse models that co-deleted Rb1 and the p53 tumor suppressor genes [6, 27, 28]. We generated Osx-Cre; Rb1fl/fl; Ptenfl/fl mice and aged them to determine if they develop OS.
We unexpectedly observed rapid development of large, bilateral adipogenic tumors in 100% (37/37) of the Osx-Cre; Rb1fl/fl; Ptenfl/fl mice within the subcutaneous space of the axillae and interscapular/dorsal thoracic region. These unencapsulated, non-invasive masses were detectable before one month of age, and grew rapidly until the tumor burden required mice to be euthanized. Tumors were composed of a multilobulated mass of well-differentiated white and brown fat that was interspersed and supported by multifocal to coalescing thin bands of fibrous connective tissue, stroma, and rare macrophages (Fig 1A). The mass was composed mainly of white fat (large vacuoles with eccentric nuclei) and rare, interspersed brown fat (small multi-vacuolated cells). The surrounding tissues were largely skeletal muscle and brown fat. These animals displayed little subcutaneous, retroperitoneal, or mesenteric fat stores, besides the large tumors. Detailed radiographic and histologic examination of the bones (skull, mandible, thoracic vertebrae and femur) from control and Osx-Cre; Rb1fl/fl; Ptenfl/fl mice revealed no bone lesions in any of these animals (data not shown).
(A) H&E staining of sections from lipoma tumors derived from Osx-Cre; Rb1fl/fl; Ptenfl/fl mice. Scale bars, 200 μM (Left), 50 μM (Right). (B) Kaplan-Meier survival curve analysis for the indicated genotypes: Osx-Cre (n = 21), Osx-Cre; Rb1fl/fl; p107-/- (n = 37), Osx-Cre; Ptenfl/fl (n = 17), Osx-Cre; Rb1fl/+; Ptenfl/fl (n = 43), and Osx-Cre; Rb1fl/fl; Ptenfl/fl (n = 37). p-values were determined by log rank test comparing a genotype with that of the control mice. *, p < 0.05; **, p < 0.01; ***, p < 0.005; N.S., not significant.
Because the RB protein is a reported positive regulator of osteogenic differentiation, we predicted that retaining one copy of the Rb1 gene in the Osx-Cre Rb1fl/+; Ptenfl/fl mice might shift the tumor formation away from adipogenic and towards osteogenic tumors. Cohorts of control, Osx-Cre; Ptenfl/fl, and Osx-Cre; Rb1fl/+; Ptenfl/fl mice were generated and aged to around 18 months to assess tumor incidence. We also generated Osx-Cre; Rb1fl/fl; p107-/- mice to test the effect of co-deleting the Rbl1 (p107) gene, a pRB pocket protein family member, because its deletion augments other Rb driven tumors like retinoblastoma in mice . However, we found that the Osx-Cre Rb1fl/+; Ptenfl/fl mice still developed adipogenic tumors, albeit at a lower incidence and reduced rapidity compared to those arising in the Osx-Cre; Rb1fl/fl; Ptenfl/fl mice (Fig 1B). Retention of both copies of Rb1 (Osx-Cre; Ptenfl/fl) reduced the formation and delayed onset of lipoma formation even further, and only 4 of 17 mice developed them at around 9–12 months old. We detected a single sternal OS on the Osx-Cre; Ptenfl/fl (1/7 mice analyzed) and a single OS, also sternal, on one of the Osx-Cre Rb1fl/+; Ptenfl/fl mice (S1 Fig). No detectable OS or adipogenic tumors or other abnormal phenotype were detected on the control or Osx-Cre; Rb1fl/fl; p107-/- mice. These data indicate that Pten deletion in osteoblast precursors strongly promotes lipoma tumor formation, that Rb1 hetero- or homo-zygous co-deletion greatly increases the incidence and the rapidity of onset of adipogenic tumors, with only a modest increase in detectable osteosarcoma tumors compared to control mice.
Pten loss in osteoprogenitor cells leads to accumulation of bone marrow adipocytes
Osx-Cre expresses Cre in several mesenchymal cell types in the bone marrow of post-natal mice, including osteoblasts, osteocytes, chondrocytes, adipocytes, and stromal cell . Thus, it is not entirely clear if Osx-Cre targets a common MSC progenitor of these cell types or if it targets discrete progenitor cell types. We analyzed sections of tibias from 12 month-old control, Osx-Cre; Ptenfl/fl and Osx-Cre; Rb1fl/+; Ptenfl/fl mice by hematoxylin and eosin (H&E) staining to determine the consequences of homozygous deletion of Pten with, or without, heterozygous deletion of Rb1. We observed a striking increase in the number of adipocytes in the proximal tibial sections of Osx-Cre; Ptenfl/fl and Osx-Cre; Rb1fl/+; Ptenfl/fl compared with control mice (Fig 2A). We used histomorphometry to quantify the differences in marrow adipocytes between the three strains. Total marrow fat increased from 3% in control mice to over 50% in Osx-Cre; Ptenfl/fl and Osx-Cre; Rb1fl/+; Ptenfl/fl mice (Fig 2B). This difference was due to significant increases in adipocyte density (Fig 2C) and average adipocyte size (Fig 2D). These differences were due to Pten deletion because additional heterozygous loss of Rb1 did not augment the phenotype.
(A) Tibias from 12-month old Osx-Cre (control), Osx-Cre; Ptenfl/fl, and Osx-Cre; Rb1fl/+; Ptenfl/fl, were cut for H&E staining and proximal end displayed. Scale bars, 500 μM. Tibial marrow contents from 12-month old mice were compared using NIH ImageJ. (B) Percentage of marrow fat; (C) adipocyte number (#/mm2); (D) adipocyte size (μm2) were measured using histomorphometry. Data are the mean ± SD from six mice. *, p < 0.05; **, p < 0.01; ***, p < 0.005.
Pten deletion in mouse osteoblast precursors results in increased calvaria thickness and bone volume
We evaluated the effects of Pten deletion on skeletal anatomy using three-dimensional micro-computed tomography (μCT) analysis and histology. μCT analysis revealed a significant thickening of the calvaria of 12-month-old Osx-Cre; Ptenfl/fl mice compared to those from control mice (Fig 3A). We also analyzed calvaria by histology from control, Osx-Cre; Ptenfl/fl and Osx-Cre; Rb1fl/+; Ptenfl/fl mice (Fig 3B). Calvaria were on average 3-times thicker in both the Osx-Cre; Ptenfl/fl and Osx-Cre; Rb1fl/+; Ptenfl/fl compared to control mice (Fig 3C).
(A) μCT analysis was performed on 12-month-old Osx-Cre (control) and Osx-Cre; Ptenfl/fl calvaria. (B) Representative coronal calvarial sections from 12-month old mice. Scale bar, 500 μM. (C) Bar graphs showing the calvarial thickness (mean ± SD; n = 6). ***, p < 0.005.
We next analyzed femurs by μCT from control, Osx-Cre; Ptenfl/fl and Osx-Cre; Rb1fl/+; Ptenfl/fl mice. Whereas the cortical thickness of the Osx-Cre; Ptenfl/fl and Osx-Cre; Rb1fl/+; Ptenfl/fl femurs was unchanged compared to control (Fig 4a), both the trabecular volume density and trabecular number were significantly increased in Osx-Cre; Ptenfl/fl and Osx-Cre; Rb1fl/+; Ptenfl/fl mice compared to control animals (Fig 4a and 4b). Bone volume over total volume (BV/TV %) significantly increased from 5% in control mice to 10% in Osx-Cre; Ptenfl/fl and Osx-Cre; Rb1fl/+; Ptenfl/fl 12-month-old mice. Likewise, trabecular number increased from 0.7 (1/mm) to 1.5 (1/mm) at one year in the Pten-deleted and Osx-Cre; Rb1fl/+; Ptenfl/fl mice (Fig 4b). Neither trabecular thickness nor trabecular separation showed any significant differences between control and experimental animals. These results indicate that Pten deletion in OSX+ osteoprogenitor cells results in increased bone mass in vivo. Additional heterozygous loss of the Rb1 tumor suppressor gene (Osx-Cre; Rb1fl/+; Ptenfl/fl) did not increase any of these parameters compared to Pten deletion alone.
(A) μCT analysis was performed on the distal femur of control, Osx-Cre; Ptenfl/fl and Osx-Cre; Rb1fl/+; Ptenfl/fl mice. (B) Bar graphs showing the trabecular volume (BV/TV%), trabecular number (1/mm), trabecular thickness (mm), trabecular separation (mm) (mean ± SD; n = 6). *, p < 0.05; **, p < 0.01; ***, p < 0.005; N.S., not significant.
Rb1 and Pten control adipocyte and osteoblast differentiation
Since Pten deletion in osteoprogenitor cells caused an increase in adipocytes in vivo, it is possible that it directly regulates adipocytic differentiation. We tested this using an established in vitro osteoblast differentiation assay. Primary cells were isolated from the calvaria of newborn mice carrying conditional Ptenfl/fl or Rbfl/fl/Ptenfl/fl and grown to confluence. Cells were then infected with control or Cre-recombinase expressing adenovirus, and gene deletion was confirmed by PCR (data not shown). Primary plated cells were treated with standard adipogenic or osteogenic differentiation media for 25 days. Using this approach, cells that differentiate into adipocytes contain lipid droplets that can be detected by staining with Oil red O. Likewise, differentiated osteoblasts secrete calcium deposits which can be detected by staining with alizarin red. Oil red O staining on calvarial cells lacking Pten showed increased adipocyte differentiation compared with control cells (Fig 5a). Adipocyte differentiation was more pronounced by co-deleting Rb1 and Pten. Deletion of Pten also increased osteoblast differentiation as detected by alizarin red staining (Fig 5b). The Rbfl/fl/Ptenfl/fl cells differentiated to a greater extent than Ptenfl/fl cells by alizarin red staining. These data show that loss of Pten acts in an intrinsic manner to increase calvarial cell differentiation into adipocytes and osteoblasts, and that co-deleting Rb1 with Pten augments differentiation into both cell types.
(A) Primary calvarial osteoblasts were grown to confluence, infected with control or Adeno-Cre, and grown for 25 days with adipogenic differentiation media and measured for adipocyte differentiation by Oil red O staining. Scale bar: 50 μM. (B) Cells were cultured as in (A) but were treated with osteoblastic differentiation media. Terminal osteoblastic differentiation was measured by alizarin red staining. Results are representative of 6 experiments.
We then measured changes in expression of several adipogenic and osteogenic genes by qPCR to further examine the differentiation characteristics of these cells. Gene expression was assessed 48 hours after adding adipogenic or osteogenic media to detect early effects on differentiation. Deletion of Pten had no effect on any of the pro-adipogenic Cebpa, Ppargc1a, Pparg, or Fabp4 genes tested at this time point (Fig 6a). Co-deleting Rb1 with Pten, however, significantly induced expression of Cebpa, Pparg, and Fabp4, but not Ppargc1a, at this timepoint. Pten deletion caused slight, but non-significant decreased expression of the Bglap, Runx2 and Col1a1 but significantly decreased Alp pro-osteoblastic gene expression. Rb1 and Pten co-deletion, however, significantly reduced expression of each gene. These findings suggest that Pten deletion had only modest effects on adipogenic and osteogenic gene expression at early timepoints but was capable of promoting both adipogenic and osteogenic differentiation in longer assays. Second, co-deleting both Rb1 and Pten significantly increased adipogenic gene expression, concomitant with increased adipogenesis. It is unclear why Rb1 and Pten co-deletion reduced osteogenic gene expression at early time points but robustly induced osteogenesis in this in vitro model.
Calvarial osteoblasts were isolated, cultured, and infected with control or Adeno-Cre and differentiated with adipogenic (A) or osteogenic (B) differentiation media for 48 hours. Quantitative PCR was performed on isolated RNA and displayed as fold-change in relative expression. Data are the mean ± SD from three independent experiments. *, p < 0.05.
In this study we deleted Rb1 and Pten from osteoprogenitor cells to determine the consequences for bone development and tumor formation. We show that Pten loss significantly increased bone accumulation over time, but also caused a greatly increased adipocyte population and size in the bone marrow. Pten deletion also caused lipoma formation outside the marrow, which was robustly accelerated by co-deleting Rb1. A variety of other cre-deleter mouse strains have also been used to demonstrate that Pten is an important contributor to normal skeletal growth. Pten deletion in mature osteoblasts using an Osteocalcin-cre driver increased bone cell proliferation and skeletal mass over the lifespan of the animal . Several groups conditionally deleted Pten in osteochondroprogenitor cells using Col2a1-cre transgenic mice, leading to Pten deletion in cartilage and perichondrium. These mice too exhibited skeletal overgrowth, and also chondrocyte dysplasia, and one displayed increased lipoma formation [32–34]. Deletion of Pten in mesenchymal cells using Dermo-cre caused early lethality in the majority of mutant mice, but surviving mice exhibited increased osteoblast differentiation and bone mass [35, 36]. Thus, Pten deletion across all stages of osteoblast formation, from early mesenchyme, partially differentiated progenitors, and mature osteoblasts, consistently increases bone growth in vivo. Mechanistically, Pten loss may promote bone growth by inactivating the FOXO transcription factors. FOXOs are phosphorylated and inactivated by the AKT serine/threonine kinase, which is constitutively activated following Pten loss. Foxo1, -3, and -4 co-deletion using Osx1-Cre leads to increased osteoblast numbers and high bone mass by increasing β–catenin/TCF mediated transcription, indicating a critical role for FOXOs in suppressing bone formation and osteoblast proliferation .
Despite Pten deletion strongly promoting osteoblast proliferation and significantly increasing bone mass, and the genomic region containing the Pten locus being commonly lost in human and canine osteosarcomas [38, 39], Pten deletion in mature osteoblasts or osteoblast precursor cells only rarely leads to osteosarcoma formation. For example, just 2/12 Col2a1-Cre; Ptenfl/fl mice developed OS , and likewise, we observed only one osteosarcoma formation from 17 Osx1-Cre; Ptenfl/fl mice aged to 18 months. Intriguingly, the Pten gene was recovered as one of the key drivers of OS in a murine transposon-based forward genetic screen . Thus, it seems likely that although Pten loss is associated with OS progression in various species, Pten loss is insufficient to initiate OS without other cooperating mutations. Additionally, complete deletion of Pten may favor differentiation towards other lineages, whereas heterozygous deletion of Pten may instead favor OS .
We observed a striking increase in marrow adipogenesis in the Pten deleted mice. Pten deletion in the cartilage and perichondrium mesenchymal lineages of Col2a1-cre transgenic mice also displayed increased marrow adipocytes and lipoma formation . In contrast, Pten deletion in mature osteoblasts using Osteocalcin-cre was not reported to affect adipogenesis . Foxo1, -3, and -4 co-deletion using the Osx1-Cre line leads to decreased marrow adiposity, in contrast with our findings that ΔPten increases marrow adiposity, indicating that Pten deletion regulates adipose levels in the marrow through FOXO independent targets . Pten deletion also promotes adipogenesis in other tissues and cell types. For example, hepatocyte-specific deletion of Pten in mice promotes accumulation of adipocytes . Likewise, Pten deletion in the endometrium by Amhr2-Cre results in accumulation of adipocytes in the myometrium . This pro-adipogenic effect is tissue specific, and is not observed when Pten is deleted from skeletal muscles or cardiomyocytes [42, 43]. Deletion of Pten in adipocytes leads to striking lipoma formation when targeting MYF5 expressing cells, but surprisingly did not affect lipid mass when deleted from mature aP2-cre targeted fat cells [44, 45]. The effects of Pten deletion on adipogenesis and fat production appear to depend on the timing of Pten deletion and potentially also of the capacity of the targeted cells to trans- or de-differentiate into adipocytes.
Although the Rb1 gene is also frequently mutated in human osteosarcoma , previous studies indicated that Rb1 deletion in osteoblast precursors only has modest effects and does not promote OS [27, 28]. In general, Rb1 promotes osteogenesis through interactions with the RUNX2 transcription factor, and inhibits adipogenesis by repression expression of PPARγ[12, 13]. Accordingly, Rb1 deletion in the embryo using Meox1-Cre reduces bone formation and osteogenic gene expression, and simultaneously increases expression of adipogenic markers and adipogenesis . The ability of pRB to suppress adipogenesis has also been observed in the context of mesenchymal p53 deletion. p53 is a major osteosarcoma tumor suppressor, and its homozygous deletion in early mesenchymal precursors (Prx1-cre) or partially differentiated osteoblasts (Osx1-cre) leads to robust osteosarcoma emergence [11, 27, 28]. Consistent with a role for Rb1 in suppressing adipogenesis, homozygous Rb1 co-deletion dramatically shifted the tumor spectrum towards fatty tumors and reduced incidence of OS. Surprisingly, retaining a single copy of Rb1 in p53 deleted cells shifted the tumor spectrum strongly back towards osteosarcomas, consistent with the notion that Rb1 is a positive regulator of osteogenesis.
Because Pten deletion was insufficient to drive robust OS onset, we tested if co-deleting Rb1 and Pten could synergistically promote osteosarcoma formation. Co-deleting Rb1 with Pten greatly accelerated lipoma formation and increased the incidence to 100%, but did not induce osteosarcoma. It is possible that we failed to observe osteosarcoma because the rapid enlargement of lipoma tumors required mice to be euthanized around 3–4 months of age. We also aged Osx1-Cre; Rbfl/+; Ptenfl/fl mice to determine of retaining a single copy of Rb1 promoted osteosarcoma formation. However, these mice only induced osteosarcoma in a single mouse (1/7), and developed lipomas at a rate and size intermediate between Osx1-Cre; Ptenfl/fl and Osx1-Cre Rbfl/fl; Ptenfl/fl mice. These findings suggest that Osx1-Cre expresses cre in certain fat cells, or adipocyte precursors, outside the marrow, and that co-deleting Rb1 and Pten in these cells promotes their sustained proliferation. In contrast, Rb1 heterozygous co-deletion with Pten did not affect marrow adiposity or Pten driven bone outgrowth in the calvaria or femur trabeculation. Thus, mesenchymal cell fate outcomes, in regards to lipoma- vs osteosarcoma-genesis appear to depend heterozygous vs. homozygous gene deletion, the timing of gene loss during mesenchymal cell specification, and the capacity of the target cell to trans- or de-differentiate into other mesenchymal lineages.
S1 Fig. Osteosarcoma presentation and tumor histology.
A. Representative presentation of OS on the sternum of 12 month-old (A) Osx-Cre; Ptenfl/fl and (B) Osx-Cre; Rb1fl/+; Ptenfl/fl mice. C. Tumor histology of OS from Osx-Cre; Ptenfl/fl mouse. Bar = 500 μm. D. Tumor histology of OS from Osx-Cre; Rb1fl/+; Ptenfl/fl mouse. Bar = 500 μm. E & G. Histology of OS from Osx-Cre; Ptenfl/fl mouse. Bar = 50 μm. Arrow notes adipocytes within the OS. F. Histology of OS from Osx-Cre; Rb1fl/+; Ptenfl/fl mouse. Bar = 50 μm. Arrow notes adipocytes within the OS. H. Osteoid-rich section of the tumor. Bar = 50 μm.
Conceived and designed the experiments: AE TCH. Performed the experiments: EAF AE HL CLF CK TCH. Analyzed the data: EAF AE TCH. Contributed reagents/materials/analysis tools: AE HL CK. Wrote the paper: TCH.
- 1. Weintraub H. The MyoD family and myogenesis: redundancy, networks, and thresholds. Cell. 1993;75(7):1241–4. Epub 1993/12/31. 0092-8674(93)90610-3 [pii]. pmid:8269506.
- 2. Tontonoz P, Hu E, Spiegelman BM. Stimulation of adipogenesis in fibroblasts by PPAR gamma 2, a lipid-activated transcription factor. Cell. 1994;79(7):1147–56. Epub 1994/12/30. 0092-8674(94)90006-X [pii]. pmid:8001151.
- 3. Otto F, Thornell AP, Crompton T, Denzel A, Gilmour KC, Rosewell IR, et al. Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development. Cell. 1997;89(5):765–71. Epub 1997/05/30. S0092-8674(00)80259-7 [pii]. pmid:9182764.
- 4. Hoshi K, Komori T, Ozawa H. Morphological characterization of skeletal cells in Cbfa1-deficient mice. Bone. 1999;25(6):639–51. Epub 1999/12/11. S8756-3282(99)00223-9 [pii]. pmid:10593408.
- 5. Lee JS, Thomas DM, Gutierrez G, Carty SA, Yanagawa S, Hinds PW. HES1 cooperates with pRb to activate RUNX2-dependent transcription. J Bone Miner Res. 2006;21(6):921–33. Epub 2006/06/07. pmid:16753023.
- 6. Rodda S, McMahon A. Distinct roles for Hedgehog and canonical Wnt signaling in specification, differentiation and maintenance of osteoblast progenitors. Development. 2006;133:3231–44. pmid:16854976
- 7. Chen X, Bahrami A, Pappo A, Easton J, Dalton J, Hedlund E, et al. Recurrent somatic structural variations contribute to tumorigenesis in pediatric osteosarcoma. Cell Rep. 2014;7(1):104–12. Epub 2014/04/08. S2211-1247(14)00165-X [pii] pmid:24703847.
- 8. Moriarity BS, Otto GM, Rahrmann EP, Rathe SK, Wolf NK, Weg MT, et al. A Sleeping Beauty forward genetic screen identifies new genes and pathways driving osteosarcoma development and metastasis. Nat Genet. 2015;47(6):615–24. Epub 2015/05/12. ng.3293 [pii] pmid:25961939.
- 9. Dyson N. The regulation of E2F by pRB-family proteins. Genes & Dev. 1998;12:2245–62.
- 10. Gutierrez GM, Kong E, Sabbagh Y, Brown NE, Lee JS, Demay MB, et al. Impaired bone development and increased mesenchymal progenitor cells in calvaria of RB1-/- mice. Proc Natl Acad Sci U S A. 2008;105(47):18402–7. Epub 2008/11/21. pmid:19020086.
- 11. Calo E, Quintero-Estades JA, Danielian PS, Nedelcu S, Berman SD, Lees JA. Rb regulates fate choice and lineage commitment in vivo. Nature. 2010;466(7310):1110–4. Epub 2010/08/06. pmid:20686481.
- 12. Thomas DM, Carty SA, Piscopo DM, Lee JS, Wang WF, Forrester WC, et al. The retinoblastoma protein acts as a transcriptional coactivator required for osteogenic differentiation. Mol Cell. 2001;8(2):303–16. Epub 2001/09/08. pmid:11545733.
- 13. Fajas L, Landsberg RL, Huss-Garcia Y, Sardet C, Lees JA, Auwerx J. E2Fs regulate adipocyte differentiation. Dev Cell. 2002;3(1):39–49. pmid:12110166
- 14. Li J, Yen C, Liaw D, Podsypanina K, Bose S, Wang SI, et al. PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer. Science. 1997;275(5308):1943–7. pmid:9072974
- 15. Stambolic V, Suzuki A, de la Pompa JL, Brothers GM, Mirtsos C, Sasaki T, et al. Negative regulation of PKB/Akt-dependent cell survival by the tumor suppressor PTEN. Cell. 1998;95(1):29–39. Epub 1998/10/20. S0092-8674(00)81780-8 [pii]. pmid:9778245.
- 16. Cantley L. The phosphoinositide 3-kinase pathway. Science. 2002;296(5573):1655–7. pmid:12040186
- 17. Manning BD, Cantley LC. AKT/PKB signaling: navigating downstream. Cell. 2007;129(7):1261–74. Epub 2007/07/03. pmid:17604717.
- 18. Xie C, Lu H, Nomura A, Hanse EA, Forster CL, Parker JB, et al. Co-deleting Pten with Rb in retinal progenitor cells in mice results in fully penetrant bilateral retinoblastomas. Mol Cancer. 2015;14(1):93. Epub 2015/04/25. pmid:25907958.
- 19. Sage J, Miller AL, Perez-Mancera PA, Wysocki JM, Jacks T. Acute mutation of retinoblastoma gene function is sufficient for cell cycle re-entry. Nature. 2003;424:223–8. pmid:12853964
- 20. Lee M-H, Williams BO, Mulligan G, Mukai S, Bronson RT, Dyson N, et al. Targeted disruption of p107: functional overlap between p107 and Rb. Genes Dev. 1996;10:1621–32. pmid:8682293
- 21. Trotman L, Niki M, Dotan Z, Koutcher J, Di Cristofano A, Xiao A, et al. Pten dose dictates cancer progression in the prostate. PLoS Biology. 2003;1(3):385–96.
- 22. Egan KP, Brennan TA, Pignolo RJ. Bone histomorphometry using free and commonly available software. Histopathology. 2012;61(6):1168–73. Epub 2012/08/14. pmid:22882309.
- 23. Parlee SD, Lentz SI, Mori H, MacDougald OA. Quantifying size and number of adipocytes in adipose tissue. Methods Enzymol. 2014;537:93–122. Epub 2014/02/01. B978-0-12-411619-1.00006–9 [pii] pmid:24480343.
- 24. Broege A, Pham L, Jensen ED, Emery A, Huang TH, Stemig M, et al. Bone morphogenetic proteins signal via SMAD and mitogen-activated protein (MAP) kinase pathways at distinct times during osteoclastogenesis. J Biol Chem. 2013;288(52):37230–40. Epub 2013/11/16. pmid:24235143.
- 25. Lu H, Hallstrom TC. The nuclear protein UHRF2 is a direct target of the transcription factor E2F1 in the induction of apoptosis. J Biol Chem. 2013;288(33):23833–43. Epub 2013/07/09. pmid:23833190.
- 26. Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods. 2001;25(4):402–8. Epub 2002/02/16. S1046-2023(01)91262-9 [pii]. pmid:11846609.
- 27. Walkley CR, Qudsi R, Sankaran VG, Perry JA, Gostissa M, Roth SI, et al. Conditional mouse osteosarcoma, dependent on p53 loss and potentiated by loss of Rb, mimics the human disease. Genes Dev. 2008;22(12):1662–76. pmid:18559481
- 28. Berman SD, Calo E, Landman AS, Danielian PS, Miller ES, West JC, et al. Metastatic osteosarcoma induced by inactivation of Rb and p53 in the osteoblast lineage. Proc Natl Acad Sci U S A. 2008;105(33):11851–6. Epub 2008/08/14. pmid:18697945.
- 29. Wirt SE, Sage J. p107 in the public eye: an Rb understudy and more. Cell Div. 2010;5:9. Epub 2010/04/03. pmid:20359370.
- 30. Chen J, Shi Y, Regan J, Karuppaiah K, Ornitz DM, Long F. Osx-Cre targets multiple cell types besides osteoblast lineage in postnatal mice. PLoS One. 2014;9(1):e85161. Epub 2014/01/24. pmid:24454809.
- 31. Liu X, Bruxvoort KJ, Zylstra CR, Liu J, Cichowski R, Faugere MC, et al. Lifelong accumulation of bone in mice lacking Pten in osteoblasts. Proc Natl Acad Sci U S A. 2007;104(7):2259–64. pmid:17287359
- 32. Ford-Hutchinson AF, Ali Z, Lines SE, Hallgrimsson B, Boyd SK, Jirik FR. Inactivation of Pten in osteo-chondroprogenitor cells leads to epiphyseal growth plate abnormalities and skeletal overgrowth. J Bone Miner Res. 2007;22(8):1245–59. Epub 2007/04/26. pmid:17456009.
- 33. Hsieh SC, Chen NT, Lo SH. Conditional loss of PTEN leads to skeletal abnormalities and lipoma formation. Mol Carcinog. 2009;48(6):545–52. Epub 2008/11/01. pmid:18973188.
- 34. Yang G, Sun Q, Teng Y, Li F, Weng T, Yang X. PTEN deficiency causes dyschondroplasia in mice by enhanced hypoxia-inducible factor 1alpha signaling and endoplasmic reticulum stress. Development. 2008;135(21):3587–97. Epub 2008/10/04. pmid:18832389.
- 35. Guntur AR, Reinhold MI, Cuellar J Jr, Naski MC. Conditional ablation of Pten in osteoprogenitors stimulates FGF signaling. Development. 2011;138(7):1433–44. Epub 2011/03/10. pmid:21385768.
- 36. Tiozzo C, Carraro G, Al Alam D, Baptista S, Danopoulos S, Li A, et al. Mesodermal Pten inactivation leads to alveolar capillary dysplasia- like phenotype. J Clin Invest. 2012;122(11):3862–72. Epub 2012/10/02. pmid:23023706.
- 37. Iyer S, Ambrogini E, Bartell SM, Han L, Roberson PK, de Cabo R, et al. FOXOs attenuate bone formation by suppressing Wnt signaling. J Clin Invest. 2013;123(8):3409–19. Epub 2013/07/23. pmid:23867625.
- 38. Freeman S, Allen S, Ganti R, Wu J, Ma J, Su X, et al. Copy number gains in EGFR and copy number losses in PTEN are common events in osteosarcoma tumors. Cancer. 2008;113(6):1453–61. pmid:18704985
- 39. Levine R, Forest T, Smith C. Tumor Suppressor PTEN is mutated in canine osteosarcoma cell lines and tumors. Vet Pathol. 2002;39(3):372–8. pmid:12014501
- 40. Horie Y, Suzuki A, Kataoka E, Sasaki T, Hamada K, Sasaki J, et al. Hepatocyte-specific Pten deficiency results in steatohepatitis and hepatocellular carcinomas. J Clin Invest. 2004;113(12):1774–83. Epub 2004/06/17. pmid:15199412.
- 41. Daikoku T, Jackson L, Besnard V, Whitsett J, Ellenson LH, Dey SK. Cell-specific conditional deletion of Pten in the uterus results in differential phenotypes. Gynecol Oncol. 2011;122(2):424–9. Epub 2011/05/17. pmid:21570712.
- 42. Crackower MA, Oudit GY, Kozieradzki I, Sarao R, Sun H, Sasaki T, et al. Regulation of myocardial contractility and cell size by distinct PI3K-PTEN signaling pathways. Cell. 2002;110(6):737–49. Epub 2002/09/26. pmid:12297047.
- 43. Wijesekara N, Konrad D, Eweida M, Jefferies C, Liadis N, Giacca A, et al. Muscle-specific Pten deletion protects against insulin resistance and diabetes. Mol Cell Biol. 2005;25(3):1135–45. Epub 2005/01/20. pmid:15657439.
- 44. Sanchez-Gurmaches J, Hung CM, Sparks CA, Tang Y, Li H, Guertin DA. PTEN loss in the Myf5 lineage redistributes body fat and reveals subsets of white adipocytes that arise from Myf5 precursors. Cell Metab. 2013;16(3):348–62. Epub 2012/09/04. pmid:22940198.
- 45. Kurlawalla-Martinez C, Stiles B, Wang Y, Devaskar SU, Kahn BB, Wu H. Insulin hypersensitivity and resistance to streptozotocin-induced diabetes in mice lacking PTEN in adipose tissue. Mol Cell Biol. 2005;25(6):2498–510. Epub 2005/03/04. pmid:15743841.
- 46. Wadayama B, Toguchida J, Simizu T, Ishizaki K, Sasaki MS, Kotoura Y, et al. Mutation spectrum of the retinoblastoma gene in osteosarcomas. Cancer Res. 1994;54(11):3042–8. pmid:8187094