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Loeys-Dietz syndrome (LDS) is a connective tissue disorder that is characterized by a high risk for aneurysm and dissection throughout the arterial tree and phenotypically resembles Marfan syndrome. LDS is caused by heterozygous missense mutations in either TGF-β receptor gene (TGFBR1 or TGFBR2), which are predicted to result in diminished TGF-β signaling; however, aortic surgical samples from patients show evidence of paradoxically increased TGF-β signaling. We generated 2 knockin mouse strains with LDS mutations in either Tgfbr1 or Tgfbr2 and a transgenic mouse overexpressing mutant Tgfbr2. Knockin and transgenic mice, but not haploinsufficient animals, recapitulated the LDS phenotype. While heterozygous mutant cells had diminished signaling in response to exogenous TGF-β in vitro, they maintained normal levels of Smad2 phosphorylation under steady-state culture conditions, suggesting a chronic compensation. Analysis of TGF-β signaling in the aortic wall in vivo revealed progressive upregulation of Smad2 phosphorylation and TGF-β target gene output, which paralleled worsening of aneurysm pathology and coincided with upregulation of TGF-β1 ligand expression. Importantly, suppression of Smad2 phosphorylation and TGF-β1 expression correlated with the therapeutic efficacy of the angiotensin II type 1 receptor antagonist losartan. Together, these data suggest that increased TGF-β signaling contributes to postnatal aneurysm progression in LDS.
Loeys-Dietz syndrome (LDS) is a connective tissue disorder with significant phenotypic overlap with Marfan syndrome (MFS) (1, 2). Patients with MFS and LDS typically share skeletal features, including long fingers, chest wall deformity, scoliosis, and joint laxity. Both syndromes also present with dural ectasia and mitral valve prolapse. While most patients with MFS or LDS typically present with early and progressive aortic root enlargement, patients with LDS uniquely show widespread arterial tortuosity and a high risk for aneurysm and dissection throughout the arterial tree (1, 2). Aortic dissection in LDS often occurs at vascular dimensions below thresholds recommended for surgical intervention in MFS (2). This complex and aggressive vascular pathology makes LDS difficult to manage surgically and highlights the need for the development of medical therapies.
LDS is caused most often by heterozygous mutations in the gene encoding either the TGF-β receptor type I (TGFBR1) or TGF-β receptor type II (TGFBR2) subunit (TβRI and TβRII, respectively) (1–3). Most of these mutations, which substitute conserved amino acids in the serine/threonine kinase domain, are missense (1, 2). Receptors carrying LDS mutations fail to propagate signaling when expressed in cells naive for the corresponding subunit. Cotransfection of equal amounts of wild-type and mutant receptors results in approximately 50% reduction in TGF-β signaling output (3, 4), indicating that the mutant receptors are unable to propagate signal even in the presence of their wild-type counterpart.
Human genetics and animal studies have provided strong evidence for the involvement of the TGF-β pathway in aortic aneurysm. Upon TGF-β ligand binding to TβRII, TβRI (also known as ALK5) is recruited to and phosphorylated by TβRII. This event activates TβRI, which propagates signaling through phosphorylation of the receptor-regulated Smads (R-Smads), Smad2 and Smad3. Upon activation, R-Smads form heteromeric complexes with the Co-Smad, Smad4, and shuttle into the nucleus, in which they regulate expression of target genes (5). Our studies of both MFS mouse models and patients with MFS have shown that fibrillin-1 contributes to regulation of TGF-β signaling and that many manifestations of MFS, including aortic aneurysm (6–8), can be linked to overactivation of the TGF-β signaling pathway. Significantly, aortic root aneurysm in a Marfan mouse model could be attenuated by pharmacological antagonism of the TGF-β signaling pathway (8). A role for TGF-β signaling in aortic aneurysm has also been confirmed by the discovery that heterozygous inactivating mutations in genes encoding both positive (SMAD3 and TGFB2) and negative effectors (SKI) of this pathway cause aneurysmal disorders very similar to LDS (9–11). These findings have caused controversy regarding whether excessive or diminished activation of the TGF-β pathway is the primary driver of aortic root aneurysm (12, 13). In this light, the therapeutic use of agents with known TGF-β–suppressive properties, such as the angiotensin II type 1 receptor blocker (ARB) losartan (14), has remained controversial despite evidence for efficacy in MFS (8). To address these issues, we have developed and characterized mouse models of LDS and tested the therapeutic potential of losartan.
In transfection studies, LDS mutant receptor subunits fail to propagate signaling (3). It is therefore possible that loss of function of one allele of either TGF-β receptor gene might be sufficient to cause LDS. We therefore analyzed 2 mouse lines heterozygous for null alleles for either Tgfbr1 or Tgfbr2 and compared their phenotype to that of mice in which LDS-associated missense mutations were introduced in the endogenous genomic locus (Figure (Figure1A).1A). Both Tgfbr1+/– and Tgfbr2+/– mice showed an approximately 50% reduction in the expression of the corresponding TGF-β receptor transcript in the aortic wall when compared with that of wild-type littermates (Figure (Figure1A).1A). Mouse models that genetically mimic LDS were generated by targeting 2 missense mutations, which cause classic and severe manifestations of LDS in patients (1, 2), to their respective endogenous locus in either the Tgfbr1 (M318R) or Tgfbr2 (G357W) gene. Heterozygous mice resulting from homologous recombination are designated Tgfbr1M318R/+ and Tgfbr2G357W/+, respectively (Figure (Figure1,1, B and C). RT-PCR and restriction digest of the PCR product confirmed approximately equal expression of the mutant and wild-type alleles in the aortic walls of heterozygous animals (Figure (Figure1,1, B and C). Comparison of these 4 mouse strains revealed that mice carrying heterozygous missense LDS mutations, but not mice haploinsufficient for TGF-β receptor alleles, phenotypically recapitulate LDS. Aortic root size and growth in Tgfbr1+/– and Tgfbr2+/– mice was similar to that observed in wild-type mice, while Tgfbr1M318R/+ and Tgfbr2G357W/+ mice showed enlarged aortas and accelerated aortic root growth (Figure (Figure2,2, A and B, and Supplemental Figure 1, A and B; supplemental material available online with this article; doi: 10.1172/JCI69666DS1). Aortic root enlargement in both Tgfbr1M318R/+ and Tgfbr2G357W/+ mice progressively worsened between 4 and 24 weeks of age, with subtle but significant deviation from wild-type mice detectable at 4 weeks but highly reproducible and dramatic deviation at 24 weeks of age (Supplemental Figure 1). At 24 weeks of age, elastic fiber fragmentation was detectable in the aortic roots of LDS knockin mice but not in those of haploinsufficient strains (Figure (Figure2,2, C and D). The aortic wall also showed progressive thickening with excessive collagen deposition in LDS mice (Supplemental Figure 1C). Both Tgfbr1M318R/+ and Tgfbr2G357W/+ mice, but not haploinsufficient animals, showed elongation and tortuosity of the aortic arch and coronary arteries as well as predisposition for aortic dissection and early death (hemothorax or hemopericardium was observable in approximately 60% of deaths) (Figure (Figure2,2, E and F). Knockin mice uniquely showed craniofacial and skeletal manifestations of LDS (Supplemental Figure 2, A and B). These findings indicate that haploinsufficiency for either TGF-β receptor gene is not sufficient to recapitulate LDS, while knockin LDS mouse models manifest many of the phenotypic features observed in patients.
The absence of phenotype in mice haploinsufficient for TGF-β receptor, but recapitulation of pathology in knockin LDS mice, suggests that the presence of mutant TGF-β receptor protein is necessary to cause disease. To test whether expression of a mutant receptor subunit was sufficient to cause LDS, we engineered transgenic mice to ubiquitously overexpress either wild-type or mutant (G357W) TβRII (1x Tg-Tgfbr2 and 1x Tg-Tgfbr2GW mice, respectively) (Figure (Figure3A).3A). Aortic tissue from both 1x Tg-Tgfbr2 and 1x Tg-Tgfbr2GW mice showed similar amounts of endogenous and transgene-derived Tgfbr2 transcript. A higher mutant-to-endogenous transcript ratio was observed when the mutant transgene was bred to homozygosity, generating 2x Tg-Tgfbr2GW mice (Figure (Figure3B).3B). Both hemizygous and homozygous mutant transgenic mice displayed typical LDS vascular pathology, including aortic root dilatation (Figure (Figure3C),3C), elastic fiber fragmentation (Figure (Figure3D),3D), and arterial tortuosity (Figure (Figure3E),3E), although 2x Tg-Tgfbr2GW mice showed a more severe phenotype than 1x Tg-Tgfbr2GW mice. Additionally, 2x Tg-Tgfbr2GW mutant transgenic mice also died prematurely (hemothorax or hemopericardium was observable in approximately 70% of cases) (Figure (Figure3F).3F). Control transgenic mice (1x Tg-Tgfbr2 mice) resembled wild-type littermates and showed no evidence of aortic aneurysm, vascular tortuosity, or premature death (Figure (Figure3,3, C–F).
In order to analyze the signaling alterations caused by LDS mutations, we generated primary aortic VSMCs cultures derived from the roots and proximal ascending aortas of Tgfbr2G357W/+, Tgfbr2+/–, and 2x Tg-Tgfbr2GW mice. RNA analysis of Tgfbr2G357W/+ VSMCs showed levels of Tgfbr2 mRNA comparable to those in wild-type VSMCs (Supplemental Figure 3A). In addition, pyrosequencing analysis showed that about 50% of Tgfbr2 mRNA expressed in Tgfbr2G357W/+ VSMCs carried the G357W mutation (Supplemental Figure 3B). Tgfbr2G357W/+ VSMCs also showed normal surface levels of TβRII (Supplemental Figure 3C). In order to confirm normal expression and trafficking of the mutant receptor to the cell surface, we also assessed TβRII expression in T47D cells (which normally lack expression of TβRII) transfected with constructs expressing wild-type and Tgfbr2G357W mRNA as well as a GFP from an internal ribosomal entry site (IRES) on the same transcript. Expression of TβRII in GFP+ cells transfected with wild-type construct was comparable to that of cells transfected with the mutant construct (Supplemental Figure 3D). Taken together, these data suggest that the G357W mutation does not affect expression or surface presentation of the derived TβRII protein and are consistent with previous reports indicating that most LDS-causing mutations do not affect receptor trafficking or surface expression (4). A similar analysis conducted on Tgfbr2+/– and 2x Tg-Tgfbr2GW VSMCs showed that these cells have decreased and increased expression of Tgfbr2 mRNA, respectively (Supplemental Figure 4A). Approximately 50% of Tgfbr2 mRNA in 2x Tg-Tgfbr2GW VSMCs harbors the G357W mutation (Supplemental Figure 4B). Surface expression of TβRII protein correlated with Tgfbr2 mRNA expression, with Tgfbr2+/– and 2x Tg-Tgfbr2GW VSMCs showing lower and higher levels of TβRII surface expression compared with control VSMCs, respectively (Supplemental Figure 4C).
Tgfbr2G357W/+, Tgfbr2+/–, and 2x Tg-Tgfbr2GW VSMCs were starved and then stimulated with 10 ng/ml or 1 ng/ml TGF-β1 for 1 hour prior to assessment of Smad2 phosphorylation (pSmad2) by Western blot analysis (Figure (Figure4,4, A–C). Both Tgfbr2G357W/+ and 2x Tg-Tgfbr2GW VSMCs showed reduced signaling capacity in the acute response to administered ligand, with a maximal and significant deviation from that of wild-type cells (~50% reduction) at lower concentrations of ligand, while haploinsufficient Tgfbr2+/– VSMCs showed normal signaling. A similar reduction in pSmad2 was observed in human VSMCs derived from patients with LDS at the time of aortic surgery (Supplemental Figure 5A).
We next assessed the levels of pSmad2 in VSMCs grown in 5% serum at steady state. VSMCs derived from Tgfbr2G357W/+ mice and from patients with LDS showed normal levels of pSmad2 when analyzed under these conditions (Figure (Figure4D4D and Supplemental Figure 5B). In order to assess whether mutant VSMCs might compensate for their signaling deficiency by upregulation of TGF-β ligands, we measured their expression by qPCR. VSMCs derived from Tgfbr2G357W/+ mice or patients with LDS showed either a trend toward increased expression of Tgfb1 (P = 0.09) or significant upregulation of Tgfb2 under steady-state conditions when compared with control VSMCs, respectively (Figure (Figure4E4E and Supplemental Figure 5C).
The in vitro signaling experiments seemingly point to decreased TGF-β–dependent signaling, while we and others have observed increased signaling in aortic tissue samples from patients with LDS obtained at autopsy or surgery (1, 2, 9, 15). In this light, we monitored the status of TGF-β signaling in the proximal aortas of LDS mice at early and later stages of aneurysm development. Analysis of TGF-β signaling, as assessed by pSmad2 levels and expression of TGF-β target genes, showed apparently normal activation of this pathway in the aortic roots of LDS mice up to 8 weeks of age (Supplemental Figure 6). By 12 weeks of age, increased pSmad2 was observed in the aortic media of LDS mice when compared with that in wild-type littermates; this was most reliably monitored by in situ methods (such as immunofluorescence), as opposed to averaging techniques (i.e., immunoblot of tissue lysates), due to a variable but often intense proliferation and/or infiltration of cells within the adventitia of mutant mice (Figure (Figure5B5B and Supplemental Figure 7, A and B). The increase in pSmad2 in the aortic media of LDS mice was further accentuated by 24 weeks of age (Figure (Figure5C).5C). Further analysis of the thickened and hyperplastic aortic root adventitia in LDS mice revealed infiltration of CD45+ (bone marrow–derived) cells (Supplemental Figure 7C). Both CD45+ adventitial cells and CD45– medial cells showed enhanced pSmad2 when compared with wild-type littermates (Figure (Figure5D);5D); adventitial cells also showed higher levels of total Smad2 (Supplemental Figure 7C). At this age, we also detected increased ERK phosphorylation (pERK) in the medial layer of the LDS aortic root (Supplemental Figure 8). This signaling profile correlated with increased expression of Tgfb1 and collagen (Figure (Figure6,6, A and B).
Many of the phenotypic features of MFS that overlap with LDS, such as aortic root aneurysm, correlate with dysregulated TGF-β signaling and can be prevented by ARB therapy in mouse models (8, 16). We therefore tested whether the ARB losartan was an effective therapy in LDS mice. Mice were treated with hemodynamically equivalent oral doses (Supplemental Figure 9) of either losartan or the β-adrenergic receptor blocker propranolol from 4 weeks to 24 weeks of age. Losartan normalized aortic root growth and prevented deterioration of aortic wall architecture in LDS mice (Figure (Figure7).7). The therapeutic efficacy of losartan correlated with reduced levels of pSmad2 and pERK in the medial layers of LDS mice (Figure (Figure8A8A and Supplemental Figure 10). Propranolol had no effect on aortic root growth or aortic wall architecture (Figure (Figure7)7) and failed to restore a normal signaling profile (Figure (Figure8A8A and Supplemental Figure 10). In addition to reducing pSmad2, losartan treatment also normalized expression of Tgfb1 and Col1a1 and prevented cellular infiltration into the adventitia (Figure (Figure8).8). In an attempt to directly assess the role of TGF-β in aneurysm progression in LDS mice, we performed a third trial with the pan-specific TGF-β–neutralizing monoclonal antibody (NAb) 1D11. The 1D11 NAb had only a modest effect in attenuating elastic fiber fragmentation in LDS mice and had no effect on aortic root dilatation (Supplemental Figure 11, A–C). Failure of the 1D11 NAb to rescue the aortic phenotype in LDS correlated with its failure to reduce pSmad2 in the aortic root media (Supplemental Figure 10A and Supplemental Figure 11D). Of note, LDS mice treated with the 1D11 NAb were chronically ill and died prematurely with severe cachexia in association with pronounced gastrointestinal inflammation but no aortic dissection.
In this study we show that mouse strains haploinsufficient for either Tgfbr1 or Tgfbr2 do not recapitulate LDS. This is not surprising given that the vast majority of LDS mutations are predicted to give rise to mutant receptor subunits that traffic to the surface and bind ligands but are unable to propagate signal (2). Indeed, heterozygous mutations in TGFBR1 that prevent ligand-binding or induce nonsense-mediated mRNA decay cause autosomal dominant Ferguson-Smith disease, characterized by focal self-healing squamous epitheliomas due to somatic loss of the wild-type allele, but no features of LDS (17). VSMCs derived from haploinsufficient mice also show normal TGF-β signaling potential in culture, despite half the normal levels of receptor at the cell surface, suggesting that this degree of reduced expression is not limiting.
Such findings are apparently at odds with a traditional antimorphic effect in which mutant protein interferes with the function of its wild-type counterpart owing to direct physical association, a plausible scenario given that heterotetrameric TGF-β receptor complexes are composed of 2 TβRI and 2 TβRII subunits (5). In this circumstance, it would be predicted that 3 out of 4 receptor complexes would lack the ability to propagate signal in the heterozygous state. In contrast, if each TβRI/TβRII dimer within the heterotetramer binds ligand and signals independently, as recently proposed (18), then half of the dimers would retain full signaling potential in heterozygous cells. In this scenario, one would predict normal signaling in the presence of high levels of ligand (as seen in haploinsufficient cells), with a maximal signaling reduction of 50% when mutant and wild-type dimers compete for a limiting amount of ligand. This mechanistic hypothesis appears to best match our observations.
Demonstration of a decline in TGF-β signaling potential by LDS VSMCs in vitro, albeit conditional and relative, still offers the null hypothesis that vascular disease in LDS is simply driven by low TGF-β signaling, a view apparently supported by the finding that other LDS-like phenotypes are caused by heterozygous loss-of-function mutations in genes encoding positive effectors of TGF-β signaling, including SMAD3 and TGFB2 (9, 10). However, a number of observations make this position difficult to defend. First, the phenotypic overlap between LDS and MFS, a condition consistently associated with high TGF-β signaling, is undeniable (13). Second, many studies have documented a tissue signature for high TGF-β signaling in the aortic walls of patients with LDS (caused by mutations in TGFBR1, TGFBR2, SMAD3, or TGFB2) during phases of postnatal aneurysm progression, and no study has provided evidence for low TGF-β signaling in LDS in vivo (1, 9, 10, 15). Third, Shprintzen-Goldberg syndrome, a condition that includes virtually every manifestation of LDS, is caused by mutations in or near the Smad binding domain of SKI (a potent inhibitor of TGF-β signaling) — an event predicted and observed to cause high TGF-β signaling (11).
Our analysis of the aortic tissue of LDS mice has failed to detect any evidence of impaired signaling but rather showed increased levels of pSmad2 and TGF-β target gene expression, which are detectable by 12 weeks of age and progressively accentuate with worsening of the disease. Importantly, the striking protection afforded by losartan correlates with reduced pSmad2 and TGF-β ligand expression within both the adventitial and medial compartments. While apparently normal TGF-β signaling was observed at 8 weeks of age despite evolving evidence of aneurysms, young mice remained responsive to losartan; this could reflect either lack of sensitivity of our assays to subtle perturbations in TGF-β signaling or an independent influence of angiotensin II signaling at this age.
It remains possible that some LDS phenotypes might in fact be caused by a simple decrease in TGF-β signaling. In support of this notion, some of the phenotypic manifestations in LDS, such as cleft palate, have been associated with abrogation of TGF-β signaling in mice (19, 20). This would also explain the susceptibility of LDS mice treated with TGF-β–neutralizing antibody to overt gastrointestinal inflammation, a known TGF-β deficiency phenotype in mice (21, 22).
Despite this progress, a number of issues remain. First, what is the mechanism for the paradoxically enhanced signaling, and, second, why did TGF-β–neutralizing antibody fail to afford protection in LDS mice? We observe no in vitro evidence for a cell-autonomous gain of function for mutant TGF-β receptor subunits. Rather, cell culture and in vivo studies suggest that chronic compensatory events may contribute to maintenance or enhancement of TGF-β signaling by LDS cells, respectively. It seems notable that tissue from patients or mice with various etiologies of LDS, including mutations in SMAD3 and TGFB2, shows increased expression of TGF-β1 (9, 10). The high TGF-β1 expression seen in LDS could lead to enhanced TGF-β signaling due to the absolute amount of ligand being expressed and/or the contribution of alternative activators of TGF-β, such as integrins, which contribute to activation of TGF-β1 but not TGF-β2 (23). The specific source of TGF-β1 in LDS has not been fully explored. We previously proposed that specific cell types that are particularly vulnerable to the impaired function imposed by heterozygous LDS mutations might attempt to compensate for this deficiency by secreting excessive amounts of TGF-β ligand into their immediate environment (13). This could lead to paracrine overdrive of TGF-β signaling in neighboring cells, with relatively preserved signaling capacity despite expression of mutant receptors. In the aortic root, the 2 critical cell populations might be second heart field– and neural crest–derived VSMCs (13, 24, 25). Additionally, infiltrating CD45+ cells, whose presence correlates with the severity of the aneurysm pathology, might also contribute to signaling overdrive.
In contrast to MFS, in which TGF-β–neutralizing antibody suppressed TGF-β signaling and afforded relative but significant protection (8, 26), this reagent neither improved nor accentuated aortic pathology and had no effect on TGF-β signaling in LDS mice. While 1D11 is described as a pan-specific TGF-β–neutralizing antibody, it is possible that it has differential effects on the various TGF-β ligands and that the predominant ligand underlying LDS pathology is relatively resistant. In addition, systemically delivered 1D11 might have limited capacity to penetrate the overtly thickened, collagen-rich, and hypercellular LDS vessel wall, as previously proposed for hypertrophic cardiac tissue (27). Alternatively, an excess of pSmad2 may relate to an accentuation of other pathways capable of mediating this event, such as angiotensin II or activin signaling (28, 29); both could remain responsive to losartan.
LDS is associated with aggressive and diffuse vascular disease, with involvement of arterial segments that are difficult to approach surgically. While it is clear that the pathogenesis of LDS is complex and requires additional study and refinement, we provide critical preclinical evidence for the use of ARBs in the treatment of LDS. Hemodynamically equivalent doses of the beta-blocker propranolol, which lowers blood pressure but does not affect Smad2 signaling, failed to preserve aortic wall architecture and had only a modest effect on the rate of aortic root dilation. This suggests that losartan-dependent amelioration of pathologic aortic growth and medial degeneration is not solely dependent on its antihypertensive properties and might in fact depend on its ability to circumvent or suppress whatever mechanism is driving excessive TGF-β signaling in LDS mice. The therapeutic efficacy of losartan in the treatment of aortic disease in LDS mice suggests that therapies developed for MFS may find broader application in additional inherited disorders of vessel wall homeostasis.
Tgfbr1+/– mice were generated by chemical mutagenesis by Ingenium and obtained from The Jackson Laboratory. These mice harbor a nonsense mutation in exon 7 (cytosine to adenine at nucleotide 1134). Tgfbr2+/– mice (30) were provided by Makoto Taketo (Kyoto University, Kyoto, Japan). For the generation of Tgfbr1M318R/+ and Tgfbr2G357W/+ mice, murine genomic fragments of Tgfbr1 (9 kb, exons 5–8) and Tgfbr2 (8.4 kb, exon 4) were obtained by long-range PCR of 129S6/SvEvTac ES cell DNA. Both were separately subcloned into plasmid pSL301 (Life Technologies). Site-directed mutagenesis was performed using the QuikChange Mutagenesis Kit (Stratagene), substituting arginine for methionine at codon 318 of Tgfbr1 and substituting tryptophan for glycine at codon 357 of Tgfbr2. A neomycin resistance cassette (NeoR) was amplified from pEGFP-C1 (Life Technologies) using PCR primers with the loxP sequence flanking either end by AgeI linkers (Tgfbr1) or BamHI linkers (Tgfbr2). Each of the floxed NeoR amplicons were then separately subcloned into pCR2.1-TOPO (Life Technologies). AgeI and BamHI digestion fragments containing the NeoR and flanking loxP sequences were ligated into either a unique Age1 site in Tgfbr1 intron 6–7 or a unique BamHI site in Tgfbr2 intron 3–4. Both vectors were linearized by a unique restriction site (XmaI and AgeI for Tgfbr1 and Tgfbr2, respectively) prior to electroporation into 129S6/SvEvTac ES cells by the Johns Hopkins Transgenic Core Facility. Positive clones were identified by Southern blot analysis. Briefly, Southern probes derived from genomic DNA 5′ and 3′ to the targeting vector were designed to recognize the insertion of a novel NcoI site in the NeoR. Sequencing of 5′ and 3′ long-range PCR products from the NeoR to outside the targeting construct confirmed proper targeting. Positive clones were injected into C57BL6/J blastocysts at E3.5 and transferred into pseudopregnant females by the Johns Hopkins Transgenic Core Facility. Chimeric offspring were mated to C57BL6/J mice, and germline transmission was confirmed by RT-PCR and restriction digest. The loxP-flanked NeoR was removed by mating Tgfbr1M318R/+ and Tgfbr2G357W/+ founder mice with CAG-Cre recombinase transgenic mice (31). Experimental mice were backcrossed onto a 129S6/SvEvTac background at least 5 times. Wild-type littermates were used as controls. For the generation of 1x Tg-Tgfbr2 and 1x Tg-Tgfbr2GW transgenic mice, murine Tgfbr2 cDNA was cloned into pBROAD3 vector (Invivogen). This plasmid enables ubiquitous transgene expression in transgenic mice by virtue of its ROSA26 promoter. For the mutant Tgfbr2 transgenic mouse, site-directed mutagenesis was performed using the QuikChange Mutagenesis Kit (Stratagene), substituting tryptophan for glycine at codon 357 as described above. Both vectors were linearized by PacI digestion prior to pronuclear injection into C57B6/SJL F1 embryos by the Johns Hopkins Transgenic Core Facility. Founder mice were confirmed by Southern blot analysis. Transgenic mice were backcrossed at least 4 times onto a C57B6 background prior to experimentation. Wild-type littermates were used as controls. All constructs were validated by Sanger sequencing. All animal experiments were approved by the Johns Hopkins Animal Care and Use Committee.
For RNA extraction, tissue was processed using the RNeasy Fibrous Tissue Kit (Qiagen) or TRIzol (Life Technologies) plus an automatic bead homogenizer (FastPrep24, MP Biomedicals). In all cases, an on-column DNAse digest was performed using RNeasy mini columns (Qiagen). Protein was extracted using the Total Protein Extraction Kit (Millipore) and a pestle motor (Kimble-Kontes) or using an automatic bead homogenizer in conjunction with reagents from the Protein Extraction Kit (Full Moon Biosystems). All protein lysis buffers contained protease and phosphatase inhibitors (Millipore).
Transcript levels for the gene or transgene of interest were determined by RT-PCR, followed by incubation with a radioactive probe specific for the corresponding cDNA, or by amplification with prevalidated TaqMan probes. For quantification with radioactive probes, cDNA was generated with the SuperScript III First-Strand Synthesis System (Life Technologies) using oligo-dT primers. A PCR of 25 cycles was then performed on the resultant cDNA with primers specific for the cDNA of interest. After electrophoresis, the PCR products were Southern blot transferred to a membrane and subsequently hybridized with a 32P-γ–dATP–labeled oligonucleotide from the original PCR using UltraHyb (Ambion). Relative quantification was determined using a phosphoimager. Differential restriction patterns were exploited to discriminate between mutant and endogenous transcripts. An NciI restriction and an AlwI restriction site are introduced by the M318R mutation and the G357W mutation, respectively, in the corresponding mutant cDNA; a MfeI site is present in the endogenous Tgfbr2 cDNA but not in the transgenically expressed control or mutant cDNA. For cDNA quantification using prevalidated TaqMan probes, cDNA was generated using TaqMan High-Capacity cDNA Reverse Transcription reagents. Quantitative PCR was performed in triplicate with TaqMan Universal PCR Master Mix using an ABI Prism 7900HT QPCR machine (all from Applied Biosystems). The following prevalidated TaqMan probes were used to detect specific transcripts: Mm99999915_g1 (Gapdh), Mm01545399_m1 (Hprt), Mm01178820_m1 (Tgfb1), Mm00436955_m1 (Tgfb2), Mm00436960_m1 (Tgfb3), Mm00801666_g1 (Col1a1), Mm01192932_g1 (Ctgf), and Mm00435860_m1 (Serpine1). For human samples, the following probes were used: Hs00998133_m1 (Tgfb1), Hs00234244_m1 (Tgfb2), Hs01086000_m1 (Tgfb3), and Rn01775763_g1 (Gapdh). Reactions were run in triplicate, and relative quantification for each transcript was obtained by normalizing against housekeeping control transcript.
Following halothane-induced euthanasia, the abdominal and chest walls were dissected away, the left common iliac artery was transected to facilitate drainage, and the left ventricle was then flushed with 5 ml PBS (pH 7.4). Approximately 2 ml yellow latex (Ward’s Natural Science) was injected directly into the apex of the left ventricle. Mice were then kept moist at 4°C for 3 to 4 hours to facilitate setting of the injected latex. Whole mice were subsequently fixed overnight in 10% neutral buffered formalin (Fisher Scientific) and then stored in 70% ethanol prior to performance of dissections. The heart and thoracic aorta were dissected out en bloc. Transverse sections (~3 mm long) of the entire thoracic aorta (root, ascending, transverse, and descending segments) were mounted in 4% agar prior to paraffin embedding. Five-micron sections were stained with Verhoeff–van Gieson (VVG) for elastin and with Movat or Masson trichrome for collagen. Slides were examined using an Eclipse E400 microscope (Nikon Inc.). The number of elastic fiber breaks per high power field was calculated from VVG-stained aortic sections. For each genotype, age, and treatment group, entire aortic rings (with many high-power fields per ring) were analyzed at 4 distinct sites of the aortic root and proximal ascending aorta. Genotype and treatment groups were determined only after this analysis was concluded.
Mice were first euthanized by halothane inhalation then skinned and eviscerated. Carcasses were then sequentially placed in 95% ethanol for 2 days, Alcian blue staining solution (0.015% Alcian Blue 8X [Sigma-Aldrich], 80% ethanol, 20% acetic acid) for 10 days, 95% ethanol for 2 days, 1% potassium hydroxide for 4 days to facilitate tissue clearing, and Alizarin red staining solution (0.001% Alizarin Red [Sigma-Aldrich] in 1% potassium hydroxide) for 3 days. Whole skeleton photography was performed by the Pathology Photography and Computer Graphic Department of Johns Hopkins.
For murine samples, aortic VSMC cultures were established from roots and proximal ascending aortas of 8-week-old mice. Aortas were digested in 300 U/ml collagenase II (Worthington Biochemical Corp.) in HBSS (Life Technologies) for 10 minutes at 37°C to facilitate removal of the endothelium and adventitia. Following an overnight incubation in DMEM (Life Technologies) with 20% FBS, aortas were washed with HBSS and digested with 300 U/ml collagenase II and 3 U/ml elastase for 45 minutes at 37°C. Aortas were triturated with a Pasteur pipette and incubated with DMEM plus 20% FBS. Four days were allowed for the VSMCs to adhere to the plate, after which the media was changed to DMEM plus 10% FBS. Human aortic VSMC cultures were established from aortic root samples obtained at surgery. After removal of the adventitial and intima layer, a “clean” piece of media was minced into small pieces and SmGM-2 media (Lonza, product CC-3182) was added to the dish. Cells growing out of the pieces of tissue were grown to approximately 80% confluence prior to freezing and/or further experiments. Control human ascending aorta VSMCs were obtained from Lonza and PromoCell. For stimulation experiments, murine and human aortic VSMC cultures were grown to approximately 80% confluence in 10% DMEM or SmGM-2 media (Lonza, product CC-3182), respectively. Cultures were then starved in 2% DMEM or SmBm-2 media (Lonza, product CC-3182) for 24 hours before the addition of recombinant human TGF-β1 (R&D Systems, product 240-B-010) or vehicle. For “steady-state” studies, VSMCs were grown in SmGM-2 media (Lonza, product CC-3182) to approximately 80% confluence. Protein lysates were harvested and lysed in M-PER buffer (Pierce) plus protease and phosphatase inhibitors (Millipore).
VSMCs were grown to approximately 70% confluence in DMEM plus 10% FBS. Cultures were then starved in 2% serum for 24 hours before analysis. Cells were lifted from culture plates by adding ice-cold 0.5 mM EDTA for 10 minutes, washed twice with PBS, and then resuspended in PBS containing 0.5% BSA (Flow Cytometry Staining Buffer). Cells were stained with APC-conjugated anti-mouse TβRII antibody (R&D Systems, FAB532A) or APC-conjugated isotype control antibody (R&D Systems, IC108A) by adding 10 μl of antibody to 106 cells in 100 μl. Cells were incubated for 60 minutes on ice in the dark. Unbound antibody was removed by washing the cells in Flow Cytometry Staining Buffer twice. Stained cells were then fixed for 10 minutes at room temperature in 4% PFA in PBS, washed with Flow Cytometry Staining Buffer, and resuspended in 1 ml Flow Cytometry Staining Buffer prior to acquisition. Flow cytometry data were acquired on a BD FACSVerse flow cytometer (BD Biosciences). Results were evaluated, including median fluorescent intensity calculations, using FlowJo software (Tree Star Inc.).
Tgfbr2 cDNA was obtained from Open Biosystems (Thermo Scientific) and cloned into a pIRES2-AcGFP1 vector (Clontec); site-directed mutagenesis (QuikChange II XL Site-Directed Mutagenesis Kit, Stratagene, Agilent Technologies) was used to introduce the G357W mutation in the Tgfbr2WT-IRES-GFP construct and thus generate the Tgfbr2G357W-IRES-GFP construct. T47D cells were obtained from ATCC. Transfection was performed using Lipofectamine 2000 (Invitrogen, Life Technologies) according to the manufacturer’s protocol. Cells were grown to approximately 90% confluence prior to transfection. GFP and TβRII expression was assayed 24 hours after transfection.
Western blotting was performed using LI-COR buffer and species-appropriate secondary antibodies conjugated to IRdye-700 or IRdye-800 (LI-COR Biosciences), according to the manufacturer’s guidelines, and analyzed using LI-COR Odyssey. The following primary antibodies were used: anti-phospho Smad2 (Millipore, clone A5S), anti-GAPDH (Abcam, Ab9483), anti-actin (Sigma-Aldrich, clone AC-74), anti-Smad2 (Cell Signaling Technology, 3103), anti-phospho Erk1/2 (Cell Signaling Technology, 4370), anti-phospho p38 (Cell Signaling Technology, 4511), and anti-phospho JNK (Cell Signaling Technology, 9251).
Mice were euthanized by halothane inhalation. Following sacrifice, the abdominal and chest walls were dissected away and the left common iliac artery was transected to facilitate drainage. The left ventricle was then flushed with 20 ml PBS (pH 7.4) and then approximately 20 ml PBS containing 4% paraformaldehyde. The heart and thoracic aorta were then dissected out en bloc and fixed in fresh 4% paraformaldehyde in PBS at 4°C overnight. The following day, tissue blocks were immersed in antigen retrieval solution (10 mM sodium citrate buffer, pH 6.0) at 4°C overnight and then immersed in boiling antigen retrieval solution for 3 minutes. Tissue was then immediately placed in cold 30% sucrose in PBS and incubated at 4°C overnight, embedded in Tissue-Tek O.C.T. Compound, and frozen using ethanol mixed with dry ice and stored at –80°C. Frozen 10-μm long-axis view (“candy cane”) sections were obtained with a cryostat and mounted on glass slides. Sections were dried for at least 1 day at room temperature prior to staining. Sections were permeabilized in staining buffer (PBS containing 0.1% Triton-X 100) for 15 minutes and then incubated with Fc Receptor Block from Innnovex for 30 minutes at room temperature, washed briefly in staining buffer, and then incubated again in blocking solution (0.1% Triton-X 100, 1:50 goat serum, 0.3 M glycine) for 30 minutes. Primary antibodies were diluted at 1:100 in staining buffer and incubated overnight at 4°C. Three consecutive washes with staining buffer were performed prior to incubation with goat anti-rabbit secondary antibody conjugated to Alexa Fluor 594 (Life Technologies) at 1:200 for 1 hour. If double staining for the CD45 antigen was performed, slides were then incubated with anti-CD45 antibody overnight at 4°C and then again washed 3 times prior to mounting with VECTASHIELD Hard Set Mounting Media with DAPI. Images were acquired on Zeiss AxioExaminer with 710NLO-Meta multiphoton confocal microscope at a ×25 magnification. The following primary antibodies were used: anti-phosho Smad2 (Millipore, clone A5S), anti-phospho ERK1/2 (Cell Signaling Technology, 4370), anti-Smad2 (Abcam, Ab33875), anti–pan-leukocyte marker CD45–Alexa Fluor 488 (Biolegend, 103121), and anti–smooth muscle myosin heavy chain (Abcam, ab53219).
Losartan (100 mg/kg) and propranolol (80 mg/kg) dosing was performed daily by oral gavage or by administration of losartan food diet (Harlan) designed to deliver 3 mg drug per day (8). The mouse monoclonal antibody against TGF-β1, TGF-β2, and TGF-β3 (R&D Systems, clone 1D11) was given 3 times per week by intraperitoneal injection (5 mg/kg). Mice were treated from 4 to 24 weeks of age. Similar numbers of males and females were used in each treatment group.
Blood pressures were measured by tail cuff plethysmography in the week prior to the completion of drug treatment. Mice were habituated to the system for 5 days, and, on the fifth day, 3–5 blood pressures were obtained and averaged. Echocardiograms were undertaken on conscious mice, whose hair had been removed with Nair cream, using Visualsonics Vevo 660 V1.3.6 imaging system (VisualSonics). Echocardiographic recordings were taken using a parasternal long-axis view; 3 independent measurements of the maximal internal dimension at the sinus of Valsalva were made and averaged. All imaging and measurements were performed by a cardiologist who was blinded to genotype and treatment arm.
Data are presented as box-and-whiskers plots. The upper and lower margins of the box define the 75th and 25th percentiles, respectively; the internal line defines the median, and the whiskers define the range. For experiments including multiple comparisons, P values refer to 1-way ANOVA followed by Tukey’s honestly significant difference (HSD) test. For experiments including only one comparison, P values refer to unpaired 2-tailed Student’s t test. Survival curves were compared with log-rank (Mantel-Cox) test. P ≤ 0.05 was considered statistically significant.
Patients were recruited from the Connective Tissue Clinic at Johns Hopkins Hospital. Recovery of aortic tissue samples at surgery for the generation of primary VSCM cultures was performed in compliance with the Johns Hopkins School of Medicine Institutional Review Board and after informed consent.
We thank Makoto Taketo for providing critical reagents. We thank N. Barker from the Pathology Photography and Computer Graphic Department of Johns Hopkins for photography of the mouse skeletons, the Johns Hopkins Transgenic Core Facility for assistance in generation of new mouse strains, and the Johns Hopkins Microscope Facility for assistance in acquisition of immunofluorescence images. This work was supported by NIH grant AR41135-18. H.C. Dietz is also supported by the Howard Hughes Medical Institute. E.M. Gallo was also supported by a Helen Hay Whitney Foundation postdoctoral fellowship.
Conflict of interest: The authors have declared that no conflict of interest exists.
Citation for this article: J Clin Invest. 2014;124(1):448–460. doi:10.1172/JCI69666.
David C. Loch’s present address is: Fisher Adam Kelly, Patent and Trademark Attorneys, Brisbane, Queensland, Australia.
Mark E. Lindsay’s present address is: Massachusetts General Hospital Thoracic Aortic Center, Boston, Massachusetts, USA.
See the related Commentary beginning on page 79.