Physiologic and molecular consequences of endothelial Bmpr2 mutation
© Majka et al; licensee BioMed Central Ltd. 2011
Received: 28 June 2010
Accepted: 22 June 2011
Published: 22 June 2011
Pulmonary arterial hypertension (PAH) is thought to be driven by dysfunction of pulmonary vascular microendothelial cells (PMVEC). Most hereditary PAH is associated with BMPR2 mutations. However, the physiologic and molecular consequences of expression of BMPR2 mutations in PMVEC are unknown.
In vivo experiments were performed on adult mice with conditional endothelial-specific expression of the truncation mutation Bmpr2delx4+, with age-matched transactivator-only mice as controls. Phenotype was assessed by RVSP, counts of muscularized vessels and proliferating cells, and staining for thromboses, inflammatory cells, and apoptotic cells. The effects of BMPR2 knockdown in PMVEC by siRNA on rates of apoptosis were assessed. Affymetrix expression arrays were performed on PMVEC isolated and cultured from triple transgenic mice carrying the immortomouse gene, a transactivator, and either control, Bmpr2delx4+ or Bmpr2R899X mutation.
Transgenic mice showed increased RVSP and corresponding muscularization of small vessels, with histologic alterations including thrombosis, increased inflammatory cells, increased proliferating cells, and a moderate increase in apoptotic cells. Expression arrays showed alterations in specific pathways consistent with the histologic changes. Bmpr2delx4+ and Bmpr2R899X mutations resulted in very similar alterations in proliferation, apoptosis, metabolism, and adhesion; Bmpr2delx4+ cells showed upregulation of platelet adhesion genes and cytokines not seen in Bmpr2R899X PMVEC. Bmpr2 mutation in PMVEC does not cause a loss of differentiation markers as was seen with Bmpr2 mutation in smooth muscle cells.
Bmpr2 mutation in PMVEC in vivo may drive PAH through multiple, potentially independent, downstream mechanisms, including proliferation, apoptosis, inflammation, and thrombosis.
Pulmonary arterial hypertension (PAH) is a lethal disorder characterized by pulmonary vasoconstriction and vascular remodeling, leading to progressively worsening right ventricular strain, and eventual right heart failure. Early molecular and physiologic events in the development of the idiopathic form of PAH (IPAH) are not known. However, in most theories of etiology, the pulmonary microvascular endothelial cell (PMVEC) plays a central role, either because of aberrant signaling to the smooth muscle, excess proliferation which fills in vessels, or excess apoptosis which causes vessels to drop out.
The familial form of PAH is usually caused by mutations in the type 2 receptor for the bone morphogenetic protein signaling pathway, BMPR2[5, 6], and there is substantial evidence that suppression of the BMP pathway is involved in all idiopathic PAH. However, detailed effects of BMPR2 mutation in endothelium, either in vivo or in vitro, are not known.
BMPR2 signals through multiple downstream pathways. In canonical signaling, when a dimer of BMPR2 receptors forms a complex with a dimer of type 1 receptors in the presence of ligand, the type 2 receptors phosphorylate and thus activate the type I receptor, allowing the type 1 receptor to phosphorylate SMAD transcription factors 1, 5, or 8. The SMAD transcription factor complexes with SMAD4, and enters the nucleus to transcribe targets. However, BMPR2 also possesses a long cytoplasmic tail, well conserved by evolution but found in no other TGFb superfamily receptor. This tail domain is not required for SMAD signaling, and signals through other, currently poorly understood, pathways[10, 11]. Mutations in human patients can fall anywhere in the gene. Determining the common molecular consequences of SMAD dependent and cytoplasmic tail dependent signaling is thus important to determining how BMPR2 mutation predisposes to disease.
We have previously reported physiologic and molecular consequences in smooth muscle of inducible transgenic overexpression of Bmpr2 mutants with defects in SMAD-dependent (and cytoplasmic tail-dependent (Bmpr2R899X) signaling[9, 13, 14]. These transgenic mice rely on the fact that the Bmpr2 receptor works as a dimer; thus, overexpression of a mutant protein inhibits expression of the native protein in two ways - by acting as a decoy receptor, and by binding native receptor into a nonfunctional complex.
The goal of this study is to complete a first description of the physiologic and molecular consequences of the different classes of Bmpr2 mutation in endothelium. Yelle et al have already reported physiologic consequences of our Bmpr2R899X mutant under an endothelial promoter. In this report we thus express our doxyycline-inducible Bmpr2delx4+ mutant in adult mice under the control of a previously published Tie2 promoter[16–18] and perform hemodynamic and histologic examination of consequences. To determine molecular consequences, we cultured PMVEC from control, Bmpr2R899X, and Bmpr2delx4 mice, and performed expression analyses using Affymetrix arrays. We found that Tie2-rtTA x TetO7-Bmpr2delx4 mice developed variably elevated RVSP, associated with increased muscularization particularly of small arteries, increased proliferation, infiltration of a variety of inflammatory cell types, increased thrombosis, and increased apoptosis. Expression analysis found that Bmpr2delx4 and Bmpr2R899X mutations caused very similar changes in proliferation, apoptosis, adhesion, and metabolism, but were quite different in their effect on inflammatory and thrombotic genes.
Generation of Tie2-rtTA x TetO7-Bmpr2delx4+ mice
Both transgenes used for this double-transgenic mice have been independently previously published. The Tie2-rtTA mouse was originally generated for study of neovascular retinopathy, and was shown to be endothelial specific in that context[16–18]. The TetO7-Bmpr2delx4+ mice were first described and validated crossed to a smooth muscle-specific SM22-rtTA second transgene. Both mice were on an Fvb/n strain background. Double transgenic mice are doxycycline inducible; they express very little transgene until fed doxycycline, with expression levels in whole lung roughly equivalent to expression in the lungs of our previously published SM22-rtTA x TetO7-Bmpr2delx4+ model.
Mouse Phenotyping Protocol
Mice were given Avertin (500 mg/kg IP) to induce a surgical plane of anesthesia. The animals were then shaved to expose the surgical area. Mice were placed on a heated surgical table (Harvard Apparatus 872/1, 872/H, Holliston, MA) and secured with surgical tape. Systemic blood pressure and pulse was measured via a tail cuff and pulse transducer run through a PowerLab NIBP Controller (ADInstruments, Colorado Springs, CO). The surgical site was viewed using a Zeiss OpMi 1 surgical microscope. An incision of approximately 1 inch in length was made extending from the animal's chin down to the right armpit. The thyroid gland was then blunt dissected upwards to expose the underlying tissue and the right jugular vein. The jugular vein was then separated from surrounding tissue using dissecting forceps until the body of the vessel was completely free from adherent tissues. The cranial end of the jugular was tied off completely and a loose tie was then made at the caudal end of the exposed jugular using 4-0 braided silk suture. 4" Micro-dissecting scissors were then used to make a small incision in the medial aspect of the right jugular vein. A Millar 1.4 French pressure/volume micro-tip catheter transducer (SPR-839, Millar Instruments, Houston, TX) connected to a PowerLab/8S (ADInstruments) was then inserted through the incision and gently threaded down into the right ventricle. Proper placement within the ventricle was determined through observation of the pressure volume loop obtained from the catheter. The loose caudal suture was then tightened to secure the catheter in place. Once the catheter is properly placed, data was collected using Chart 5 for Windows (ADInstruments). Once blood pressure and volume data was collected, the caudal suture was re-loosened and the catheter removed for tissue inflation. 100U of heparin was then injected through the jugular incision to prevent clotting. The suture was then re-tightened to prevent bleeding. The animals were then removed from the surgical table to a dissecting area. All animal procedures were approved by the UCHSC animal care and use committee (IACUC).
Mouse tissue collection and morphometry
After checking for insensitivity to toe-pinch, a paramedian sternotomy was performed, lungs were flushed with saline injected through the RV, the right lung was tied off, and the left lung was inflated using low-melt agarose injected through the trachea. The left lung was removed and fixed in 10% formalin and paraffin embedded. The right lung was flash-frozen in liquid nitrogen. Hearts were collected for weighing to determine right ventricular muscularization. Lung sections were stained for smooth muscle actin (SMA), counterstained with hematoxylin, and imaged using a Zeiss Axioscop 2 microscope. Twelve 20x microscopic fields were collected from each animal from which counts of fully or partially (less than 50%) muscularized vessels and vessel diameter were collected.
Immunoflourescence and Carstair's Stain
Immunofluorescence was done as previously described using the following antibodies and dilutions. Monoclonal anti-alpha smooth muscle actin antibody was purchased from Sigma (St. Louis, MO) and used at a dilution of 1:1000. Rabbit polyclonal anti-smooth muscle actin was purchased from Abcam (Cambridge, MA) and used at a dilution of 1:250. Rabbit polyclonal anti CD45 was purchased from Santa Cruz Biotechnology (Santa Cruz, CA) and used at 1:100. Rabbit polyclonal CD3 epsilon was purchased from Abcam (Cambridge, MA) and used at a dilution of 1;200. Mac-3 antibody was purchased from BD Pharmingen (San Jose, CA) and used at a dilution of 1:200. Tissues processed for immunofluorescence were rinsed and placed in either Alexa Fluor 488 or 594 (Invitrogen, Carlsbad, CA) secondary antibody at a 1:1000 dilution for 1 hour at room temperature in the dark. Slides were then rinsed with PBS and coverslipped with Vectashield with DAPI (Vector Laboratories, Burlingame, CA). All staining was evaluated and digital images acquired using a Zeiss Axioskop 2 equipped with an AxioCam (Carl Zeiss Microscopy, Jena Germany). Carstairs' stain for fibrin and platelets was done by IHC tech (LLC12635 Montview Blvd. Ste. 215 Aurora CO, 80045) Briefly, deparaffinized slides were incubated 5 minutes in ferric aluminum, rinsed, stained with Mayer's hematoxylin 5 minutes, rinsed, stained in picric acid- orange G solution for 30 minutes, rinsed, differentiated with 1% phosphotungstic acid, rinsed and stained with aniline blue solution for 1 hr and rinsed before mounting. This is a modification of picro-Mallory staining, resulting in orange to red fibrin, gray-blue platelets, bright blue collagen, red muscle, and red, green, or yellow red blood cells.
Cell culture and siRNA
Murine pulmonary microvascular endothelial cells (MVECs) were isolated by collagenase digest of whole lung tissue and selected by cytometry using PECAM-1. The isolated cells were grown to ~60% confluency on 10 cm cell culture dishes in Endothelial Growth Media 2 (EGM2) containing 5% serum. Following VE-Cadherin and diLDL staining to confirm EC phenotype, transfections were done at passage 3 using 100 nM scrambled siRNA control (Qiagen, Valencia, CA) or siRNA to BMPR2 (Ambion). Lipofectamine and Plus reagents (Invitrogen, Carlsbad, CA) were mixed with Optimem media (Invitrogen) and siRNA as per manufacturer's instructions. EGM2 media was replaced with Optimem before lipid-RNA complexes were added to the cells and incubated for 2 hours at 37°C. A volume of EGM2 media containing 10% serum equal to that already on the plate was then added to the existing transfection media and the cells were incubated for and additional 24-48 hrs. Cells were subsequently harvested using the PARIS kit from Ambion (Austin, TX). To extract the BMPR2 from the membrane, SDS was added to a final concentration of 6%. Equal amounts of protein determined using BCA protein assay (Pierce, Rockford, IL) was loaded onto a 10% polyacrylamide gel with 10% glycerol and transferred to Hybond-P membrane (Amersham, Piscataway, NJ). BMPR2 is detected with a mouse monoclonal antibody diluted 1:150 (BD Transduction Laboratories, San Jose, CA) and visualized by chemiluminescence (ECL, Amersham, Piscataway, NJ).
Apoptosis - Tissue
The fluorescein FragEL DNA fragmentation detection kit (Calbiochem, San Diego, CA) was used to look at fragmented DNA signifying apoptosis. The manufacturer's protocol was followed. Briefly, paraffin embedded lung tissue from Tie2- BMPR2delx4+ and control mice were cut, put onto slides and deparaffinized as described above. Fragmented DNA was labeled using terminal deoxynucleotidyl transferase which binds to exposed 3'-hydroxyl ends left after fragmentation of DNA in response to apoptotic signals and catalyzes the addition of fluorescein-labeled and unlabeled deoxynucleotides allowing for visualization.
Apoptosis - Cells
Plates (60 mm) were seeded with 3 × 105 mouse pulmonary microvascular endothelial cells in Minimum Essential-alpha (MEM-a) media (Invitrogen, Carlsbad, CA) supplemented with 20% FBS and incubated overnight. BMPR2 siRNA or scrambled siRNA (100 nM, Ambion) was transfected using Lipofectamine and Plus reagent (Invitrogen, Carlsbad, CA), cells were recovered with complete media at 2 h. At 72 h cells were trypsinized, washed with ice-cold PBS and resuspended in 1 ml of PBS. Apoptotic cells were labeled with YO-PRO-1, Vybrant Apoptosis Assay (Invitrogen, Carlsbad, CA) which stains apoptotic cells green fluorescent while necrotic cells stain red fluorescent with propidium iodide separating early apoptosis and necrosis using flow cytometry. To prevent apoptosis through the BMPR2 pathway, cells were seeded as described above. After overnight incubation, cells were washed with PBS and media replaced with MEM-a without FBS. At 24 h, 150 ng/ml BMP-2 (R&D systems, Minneapolis MN) was added and at 72 h cells were trypsinized, washed with ice-cold PBS and resuspended in 1 ml of PBS. Apoptotic cells were labeled with YO-PRO-1 (Vybrant Apoptosis Assay, Molecular Probes) and analyzed by flow cytometry.
Generation of murine PMVEC
Immortomouse X Rosa26-rtTA2 X TetO7-Bmpr2R899X or Immortomouse X Rosa26-rtTA2 X TetO7-Bmpr2delx4+ triple transgenic mice (Immorto-Bmpr2R899X) were bred with transgenes verified by PCR genotyping of tail DNA. The immortomouse contains a transgenic insertion of the SV40 large T antigen, tsA58, under control of an interferon-inducible promoter. When cells are grown at 33°C and interferon is added, the transgene is activated and the cells are immortalized and proliferate freely; at 37°C, this transgene is inert. The immortomouse therefore produces cells which proliferate as though they were immortalized at 33°C, but revert to a more normal phenotype when cultured at 37°C. Immorto-Bmpr2R899X PMVEC were collected from adult mice as previously described, and verified by staining for endothelial markers VWF, PECAM, and VE-Cadherin.
Mouse Gene 1.0 microarrays (Affymetrix, Foster City, CA) were performed on pooled RNA from three plates each. Array results were submitted to the NCBI gene expression and hybridization array data repository (GEO, http://www.ncbi.nlm.nih.gov/geo/), accession number pending. Arrays were analyzed using a combination of Affymetrix Expression Console, comparisons within Microsoft Excel, and Webgestalt for gene ontology groupings.
Statistical analysis was performed with Statview 5.0 (SAS Institute, Cary NC). Specific tests used are listed in figure legends, with p < .05 considered significant.
Tie2-Bmpr2delx4+ mice have increased RVSP, muscularization of vessels, and cellular proliferation
Tissues were collected from additional groups of Tie2-Bmpr2delx4+ with transgene activated 2.5 and 8 weeks to allow more complete analysis of histologic changes. There was an increase in muscularization of very small (<25 mm) vessels by 2.5 weeks, and an increase in both small and mid-sized vessels (25-50 mm) by 8 weeks; larger vessels never had a statistically significant increase in muscularization (Figure 1B-F).
Tie2-Bmpr2delx4+ mice have increased pulmonary inflammatory cells and thromboses
Thrombosis and perivascular inflammation could be found together (Additional File 2, Figure S2B), but this was uncommon.
Loss of endothelial BMP signaling results in apoptosis in vivo and in culture
Molecular consequences of Bmpr2delx4+ and Bmpr2R899X mutations in PMVEC
PMVEC were cultured from double and triple transgenic mice, expressing the Immortomouse transgene, the Rosa26-rtTA2 transgene, and either no additional transgenes (control PMVEC), the TetO7-Bmpr2R899X, or the TetO7-Bmpr2delx4+ transgene. The immortomouse transgene was added because it is otherwise impractical to collect enough PMVEC from mice to perform experiments. Affymetrix Mouse Gene 1.0 microarrays were used to determine molecular consequences of Bmpr2delx4+ and Bmpr2R899X mutations in PMVEC. Two arrays were run for each cell type, with RNA for each array consisting of a pool of three independently grown plates (total of six arrays).
Using a requirement of a minimum of a 1.4x change, a minimum expression intensity of the higher of the pair of at least 128 (arbitrary Affymetrix units), and average expression values separated by more than the sum of their standard deviations (which equates to roughly a p < .05 for difference), we found 840 unique genes with gene ontology information differentially expressed in Bmpr2delx4+ compared to controls (Additional File 3, Table S1), and 1692 differentially expressed in Bmpr2R899X mutants compared to controls (Additional File 4, Table S2).
In contrast, expression of Bmpr2delx4+ and Bmpr2R899X mutations in PMVEC had very different effects on inflammatory and thrombotic genes. Bmpr2delx4+ mutation resulted in induction of multiple cytokines not upregulated in Bmpr2R899X (Figure 7E). There were many of these, but examples upregulated only in Bmpr2delx4+ include the angiogenic chemokine Cxcl12, the interleukin 27 receptor Il27ra, and the inflammatory cell adhesion molecule CD24a. Some inflammatory genes were changed only in Bmpr2R899X, including downregulation of MAP kinase p38δ (Mapk13) and upregulation of the TH1 inducer interleukin 18 (Il18). We also tested expression of interleukin 6, which we had previously found to be regulated by Bmpr2delx4+ mutation in smooth muscle; we found it upregulated in Bmpr2delx4+ mutant PMVEC, but not in Bmpr2R899X (Additional File 5, Figure S3).
Effects of the two mutations were also very different in thrombosis related genes (Figure 7F), with increases in prothrombotic genes in Bmpr2delx4+ but not Bmpr2R899X; examples include 4x increases in platelet/endothelial cell adhesion molecule (PECAM1) and platelet chemokine ligand Ccl5, a 28x increase in platelet adhesion molecule selectin P (Selp), and an 18x increase in Entpd1, a nucleotidase involved in response to thrombosis. In contrast, the anticoagulant thrombomodulin (Thbd) is downregulated, but only in Bmpr2delx4+.
Endothelial markers are not consistently changed by Bmpr2 mutation.
Post Hoc (p < .05)
Delx4 > Control
Delx4 > Control > R899X
Endothelial-Specific Marker 1
Delx4 = R899X > Control
Flk1 (VEGF receptor 2)
Delx4 = Control > R899X
Flt1 (VEGF receptor 1)
Control > R899X > Delx4
Delx4 > Control = R899X
Delx > Control = R899X
Selectin, endothelial cell
Delx4 = Control > R899X
Delx4 > R899X > Control
Delx4 > Control = R899X
R899X > Control = Delx4
Von Willebrand factor
This study analyzed the physiologic and molecular effects of Bmpr2 mutation in endothelium. We found that most Tie2-Bmpr2delx4+ mice developed elevated RVSP, although with large variability in degree. This was associated with increased muscularization of small arteries (Figure 1), an increase in proliferating cells (Figure 2), inflammatory cells(Figure 3), thrombosis (Figure 4), and apoptosis (Figure 5). Molecular changes substantially matched the physiologic changes, with an increase in gene ontology groups related to proliferation (Figure 7B), apoptosis (Figure 7A), and thrombosis (Figure 7F). The increase in inflammatory cells seen is probably related both to the increase in cytokines (Figure 7E, Additional File 5) and the decrease in cell-cell adhesion genes (Figure 7C). BMPR2 has been previously shown to regulate endothelial barrier function in the context of leukocyte transmigration. We also saw large scale alteration in metabolic genes, including response to oxidative stress (Figure 6); this matches our previous findings in smooth muscle and whole animals. Unlike expression of Bmpr2delx4+ mutation in smooth muscle, expression in PMVEC did not cause loss of differentiation markers. Overall, this is the first report of the molecular effects of Bmpr2 mutation in PMVEC, with results consistent with both our current physiology and our previous findings.
Physiologic results from this mouse were similar to results from an endothelial-specific BMPR2 knockout mouse described by Hong et al, despite having very different methods of generation. The only difference was higher penetrance in our model (~80% as opposed to ~30%). Histologic details such as thromboses and perivascular inflammatory cells and levels of increased proliferating cells were all almost identical between the models, which strongly increases confidence that both models accurately represent the consequences of complete suppression of signaling through BMPR2 in the endothelium.
Both of these models are quite different in histologic detail than expression of a different Bmpr2 mutation, Bmpr2R899X, in endothelium. Endothelial expression of Bmpr2R899X, which retains intact Smad signaling, results in vascular pruning and increased RVSP, but without the obvious increase in thromboses. This also matches our molecular data; increases in thrombotic pathways were not seen in PMVEC with Bmpr2R899X mutation (Figure 7F). Our molecular results imply that neither increased thrombosis nor increased inflammation are required for the development of Bmpr2-mediated PAH, although obviously both could exacerbate disease.
Broadly, we believe that the sum of the data to date suggests that the normal role of BMPR2 in the adult pulmonary vasculature is as a master switch mediating injury response. After injury, suppression of BMPR2 signaling through its cytoplasmic tail results in a decrease in cell-cell adhesion to improve migration and leukocyte recruitment, a metabolic shift towards glycolysis to support production of proteins and lipids needed for proliferation, and an increase in propensity for both proliferation and apoptosis to support tissue remodeling and angiogenesis or angeogenic repair. Suppression of BMPR2 signaling through SMAD results in an increase in thrombosis and an increase in expression of cytokines, and in smooth muscle but not endothelium, dedifferentiation. In those with intact BMPR2, this naturally resolves as the injury is repaired. In the case of BMPR2 mutation, these injury responses can never be successfully resolved, leading to a pathologic continuation of the pro-thrombotic and pro-proliferative pathways which would have been adaptive in acute injury.
Decades ago, long before molecular origins of PAH were known, there was controversy over whether the initiating events in the disease involved inflammation, proliferation, thrombosis, or vasoconstriction through defective endothelial-smooth muscle communication. The discovery of BMPR2 as the familial PAH gene had promised a resolution to this controversy. However, the current study, as well as its predecessors in the literature, indicate that all of these are consequences of BMPR2 mutation alone, and our expression arrays suggest that they may all be relatively direct consequences of BMPR2 mutation, not an in vivo cascade. Our study does not address the issue of whether any are dispensable for the development of PAH. However, since each of these individually is capable of driving PAH in animal models, it is possible that inflammation, proliferation, thrombosis, and vasoconstriction in the context of pulmonary vascular injury can not be easily separated; it is not that one is the cause and the other are bystanders, but rather they are inextricably linked.
We present here a relatively comprehensive first look at the physiologic and molecular consequences of Bmpr2 mutation. These data support an important role for Bmpr2 signal in maintaining endothelial homeostasis, and support our broad hypothesis that a normal role for Bmpr2 is in injury response. Future studies will be needed to determine the specific roles of and alterations in pathways identified, including, p53-mediated proliferation, MSX1-mediated apoptosis, a shift to glycolysis, and a loss of cell-cell adhesion.
List of abbreviations
BCL2-associated X protein
BCL2/adenovirus E1B interacting protein 3
cell adhesion molecule 2
chemokine (C-C motif) ligand 5
chemokine (C-X-C motif) ligand 12
Death Associated Protein 1
diacylglycerol kinase a
diacylglycerol kinase h
enolase 2, gamma neuronal
ectonucleoside triphosphate diphosphohydrolase 1
glutamine-fructose-6-phosphate transaminase 2
interleukin 27 receptor, alpha
idiopathic pulmonary arterial hypertension
integrin, alpha 1 [
- Lhx2 - LIM:
homeobox protein 2
mitogen activated protein kinase 13
homeobox, msh-like 1
pulmonary arterial hypertension
proliferating cell nuclear antigen
platelet/endothelial cell adhesion molecule 1
phosphoglycerate kinase 1
pulmonary microvascular endothelial cell
prostaglandin e synthase
protein tyrosine phosphatase, receptor type, V
serpin peptidase inhibitor, clade E, member 1
transforming growth factor, beta 1
vav 3 oncogene
vascular cell adhesion molecule 1
This work was supported by National Institute of Health HL82694, HL071596, HL079315, HL014985, and HL091105.
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