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Klotho is a potent regulator of 1,25-hydroxyvitamin D3 [1,25(OH)2D3] formation and calcium-phosphate metabolism. Klotho-hypomorphic mice (kl/kl mice) suffer from severe growth deficits, rapid aging, hyperphosphatemia, hyperaldosteronism, and extensive vascular and soft tissue calcification. Sequelae of klotho deficiency are similar to those of end-stage renal disease. We show here that the mineralocorticoid receptor antagonist spironolactone reduced vascular and soft tissue calcification and increased the life span of kl/kl mice, without significant effects on 1,25(OH)2D3, FGF23, calcium, and phosphate plasma concentrations. Spironolactone also reduced the expression of osteoinductive Pit1 and Tnfa mRNA, osteogenic transcription factors, and alkaline phosphatase (Alpl) in calcified tissues of kl/kl mice. In human aortic smooth muscle cells (HAoSMCs), aldosterone dose-dependently increased PIT1 mRNA expression, an effect paralleled by increased expression of osteogenic transcription factors and enhanced ALP activity. The effects of aldosterone were reversed by both spironolactone treatment and PIT1 silencing and were mitigated by FGF23 cotreatment in HAoSMCs. In conclusion, aldosterone contributes to vascular and soft tissue calcification, an effect due, at least in part, to stimulation of spironolactone-sensitive, PIT1-dependent osteoinductive signaling.
Cardiovascular events are the leading cause of death in patients suffering from chronic kidney disease (CKD), and patients with CKD are considered among the highest risk group for cardiovascular events independent of traditional risk factors (1). Vascular calcification contributes substantially to the risk for cardiovascular events, and the extent of vascular calcification is a strong predictor of cardiovascular and all-cause mortality (2, 3). Vascular calcification is part of the mineral bone disorder (MBD) in CKD (4). Vascular calcification in patients with CKD differs from atherosclerotic calcification and affects the elastic lamellae in the artery (5).
The vascular calcification in CKD is similar to that of klotho-hypomorphic mice (kl/kl mice) (6). Klotho participates in the tight regulation of 1,25-hydroxyvitamin D3 [1,25(OH)2D3] formation and renal tubular transport of phosphate and calcium, which in turn determines plasma phosphate and Ca2+ concentration (7). kl/kl mice carry a disruption in the promoter sequence of the Klotho gene, leading to severe klotho depletion with extensive soft tissue calcification and eventual early death (8). The tissue calcification is considered to result from excessive 1,25(OH)2D3 formation and subsequent hypercalcemia and hyperphosphatemia (9). Increased extracellular phosphate concentration induces vascular calcification (10), and elevated plasma phosphate concentration is recognized as a powerful predictor of mortality (11). In patients with CKD, a strong reduction of klotho expression is paralleled by elevated plasma phosphate levels, and klotho is considered a biomarker for kidney function in renal disease (6).
Vascular calcification has previously been considered to be a passive process resulting from oversaturation of plasma with Ca2+ and phosphate, but subsequently it has been reported to involve dedifferentiation and reprogramming of vascular smooth muscle cells into an osteo- and chondrogenic phenotype promoting vascular calcification (12). Thus, vascular calcification is an active process (5). Elevated extracellular phosphate concentrations stimulate the reprogramming of vascular cells to promote vascular calcification (10). Compelling evidence points to an essential role of the type III sodium-dependent phosphate transporter (PIT1, also known as SLC20A1) in phosphate-induced calcification (13), a carrier with an additional putative role in renal tubular phosphate transport (14). The osteoblastic reprogramming could be triggered by Tnf-α, inducing a cascade of procalcification signaling (15). Tnf-α requires NF-κB p65 and the transcriptional regulator Msx2, which is involved in bone development, to induce expression of the chondrogenic/osteogenic transcription factors osterix and Cbfa1 (also known as Runx2) and vascular calcification (16). Cbfa1 is essential for induction of vascular calcification (17). Tnf-α promotes Msx2 expression and thereby mediates vascular calcification via Wnt signaling (18). Wnt3a and Wnt7a in turn mediate osteogenic differentiation of vascular cells via β-catenin and activation of alkaline phosphatase (ALP) (19). Wnt signaling, an important effector of Msx2 induced vascular calcification, is augmented in kl/kl mice (19, 20). Wnt3a further stimulates ALP activity via p38 MAPK phosphorylation (21). Both, osterix and Cbfa1 are upregulated in vessels of dialysis patients, indicative of osteogenic remodeling in these patients (22). Klotho is capable of reducing the vascular effects of Tnf-α (23), while aldosterone was shown to upregulate vascular Tnfa (24). Klotho itself also plays a role in maintaining vascular smooth muscle cell homeostasis in response to phosphate (6). Klotho is expressed in vascular smooth muscle cells and mediates the vasoprotective effects of FGF23, but uremic serum downregulates vascular klotho and causes resistance to FGF23 in vessels of patients with CKD (25). Indicators of active vascular remodeling reminiscent of CKD were described in calcified tissue of kl/kl mice, with increased osteogenic programming, including increased Pit1 transcription (6, 26).
kl/kl mice suffer from hyperaldosteronism (27), which also resembles human CKD (28). Aldosterone fosters cardiac fibrosis (29) and endothelial dysfunction (30), cardiovascular disorders commonly observed in CKD (4, 5, 31, 32). Aldosterone increases Tnfa expression and subsequent NF-kB activation (24, 30). Vascular smooth muscle cells express the aldosterone-sensitive mineralocorticoid (MR) receptor (33), and MR receptor activation stimulates vascular calcification (34).
This study explored the role of aldosterone in the induction of vascular calcification in kl/kl mice and human aortic smooth muscle cells (HAoSMCs). To this end, vascular calcification and osteoinductive signaling were analyzed with or without treatment with the MR receptor antagonist spironolactone.
Serum calcium and phosphate concentrations were significantly higher in klotho-deficient (kl/kl) mice than in WT mice, a difference not significantly affected by life-long treatment with the MR receptor antagonist spironolactone (Figure (Figure1,1, A and B). Serum FGF23 levels were significantly higher in kl/kl mice and insensitive to spironolactone treatment (Figure (Figure1C).1C). Similarly, the serum levels of 1,25(OH)2D3 were significantly higher in kl/kl mice than in WT mice, a difference again not significantly modified by spironolactone treatment (Figure (Figure1D).1D). As illustrated in Figure Figure1E,1E, body weight of kl/kl mice was significantly lower than body weight of WT mice. Despite a tendency toward increased body weight following spironolactone treatment, no significant difference was observed between spironolactone-treated and untreated kl/kl mice. Blood pressure was slightly reduced in the kl/kl mice but was not significantly affected by the spironolactone treatment (Figure (Figure1F).1F). The elevated plasma urea nitrogen levels in kl/kl mice were reduced by the spironolactone treatment (Figure (Figure1G),1G), but plasma cystatin C levels were elevated by the spironolactone treatment (Figure (Figure11H).
Even though spironolactone treatment did not significantly modify hypercalcemia, hyperphosphatemia, or excessive 1,25(OH)2D3 and FGF23 plasma concentrations, and even though spironolactone treatment did not appreciably modify the growth deficit of kl/kl mice, spironolactone treatment was followed by a slight but statistically significant advantage in survival of kl/kl mice (Figure (Figure11I).
In search of the underlying mechanisms contributing to or accounting for the effect of spironolactone on the life span of kl/kl mice, animals were subjected to histological evaluation. As illustrated in Figure Figure2A,2A, extensive soft tissue calcifications were observed in lungs and kidneys of kl/kl mice but not of WT mice. The calcifications in kl/kl mice were substantially decreased following spironolactone treatment. As von Kossa–positive staining was most abundant in vascular tissue of the organ sections, additional histology was used to analyze calcification in aortic tissue. As a result, calcification in aorta was significantly less pronounced in spironolactone-treated kl/kl mice than in control-treated kl/kl mice. No calcification was found in WT mice (Figure (Figure2,2, B and C).
As spironolactone treatment reduced calcification in kl/kl mice without affecting serum phosphate levels, the effect of spironolactone may have been the result of an inhibitory effect on aldosterone-dependent active procalcification reprogramming of vascular tissue. As described earlier, kl/kl mice express high levels of Pit1, which is considered essential in procalcification reprogramming (6). As shown for aortic tissue (Figure (Figure3),3), Pit1 transcript levels were significantly higher in kl/kl mice than in WT mice. The increased Pit1 transcript levels were significantly decreased following spironolactone treatment of kl/kl mice (Figure (Figure3A).3A). Similarly, the transcript levels of Tnfa, an important initiator of osteoblastic differentiation, were significantly higher in aortic tissue of kl/kl mice than in WT mice, a difference again significantly blunted by spironolactone treatment (Figure (Figure3B).3B). Moreover, the mRNA levels of alkaline phosphatase (Alpl) were significantly higher in kl/kl mice than in WT mice, a difference again blunted following treatment with spironolactone (Figure (Figure3C).3C). Further experiments addressed Tnf-α–dependent signaling. In aortic tissue (Figure (Figure4A),4A), Msx2 mRNA levels were increased in kl/kl mice as compared with those in WT mice, a difference significantly blunted by spironolactone treatment. As shown in Figure Figure4,4, B and C, the mRNA expression of both the chondrogenic/osteogenic Cbfa1 and the osteogenic osterix (Osx) transcription factors was upregulated in kl/kl mice as compared with WT mice, a difference again blunted by spironolactone treatment. A similar regulation of the osteogenic proteins was found in immunostaining with subsequent confocal microscopy of aortic tissue, showing increased expression of Msx2, Cbfa1, and osterix in kl/kl mice, which was reduced by spironolactone treatment. In addition, the reduced expression of endothelial nitric oxide synthase in aortas of kl/kl mice was mitigated by spironolactone treatment (Supplemental Figure 1A; supplemental material available online with this article; doi: 10.1172/JCI64093DS1). This finding was accompanied by a reduction of Pai1 expression in the kl/kl mice following treatment with spironolactone (Supplemental Figure 1B).
In view of the strong calcification in kidney and lung tissue of kl/kl mice (Figure (Figure2A),2A), osteoinductive signaling was further analyzed in those tissues. Similar to what has been observed in aortic tissue, renal Tnfa transcript levels were elevated in kl/kl mice as compared with those in WT mice, a difference again significantly blunted by spironolactone treatment (Figure (Figure5A).5A). Similarly, renal Msx2, Cbfa1, and Osx gene transcript levels and Cbfa1 and osterix protein abundance were increased in kl/kl mice as compared with WT mice, a difference again partially prevented by spironolactone treatment (Figure (Figure5,5, B–E). As shown in Supplemental Figure 2, NF-κB p65, as Tnf-α effector, and Wnt signaling, as effector of Msx2 procalcification signaling, were both upregulated in kl/kl mice and reduced by spironolactone treatment.
Similar observations were made in lung tissue. As shown in Supplemental Figure 3A. Pit1 expression was increased in lung tissue from kl/kl mice. Again, Pit1 expression was significantly reduced by spironolactone treatment. Furthermore, mRNA expression of Tnfa and Alpl (Supplemental Figure 3, B and C) as well as Msx2, Cbfa1, and Osx (Supplemental Figure 4, A–C) was significantly higher in kl/kl mice as compared with WT mice, a difference again significantly blunted by spironolactone treatment. These findings were also reflected by an increased protein abundance of Msx2, Cbfa1, and osterix in lung tissue of kl/kl mice, which was reduced by spironolactone treatment (Supplemental Figure 4D).
In order to further define causal relationships in osteoinductive signaling, primary HAoSMCs were treated for 24 hours with aldosterone and with the MR antagonist spironolactone. To avoid potential effects of endogenous ligands in the medium, the experiments were performed using charcoal-stripped FBS media. In a concentration-dependent manner, aldosterone induced the transcription of type III sodium-dependent phosphate transporter PIT1 (Figure (Figure6).6). At the concentration of 100 nM, aldosterone significantly increased PIT1 transcript levels. At concentrations as low as 0.1 nM, aldosterone increased PIT1 mRNA expression (statistically significant in t test as compared with control, P < 0.05). Aldosterone-induced PIT1 mRNA expression was significantly suppressed by cotreatment with 10 μM spironolactone. As illustrated in Figure Figure7,7, aldosterone (100 nM) significantly increased the mRNA expression of TNFA, MSX2, CBFA1, and ALPL in HAoSMCs, an effect abrogated by cotreatment with spironolactone (10 μM). Moreover, aldosterone treatment significantly enhanced ALP activity in HAoSMCs, an effect abrogated by spironolactone cotreatment (Figure (Figure77E).
Further experiments addressed the role of aldosterone and the protective effects of spironolactone on HAoSMCs at high phosphate concentrations (Figure (Figure8,8, A and B). Treatment of HAoSMCs with 2 mM β-glycerophosphate increased PIT1 and CBFA1 mRNA expression. Addition of aldosterone to the high phosphate medium significantly increased the expression of PIT1 and CBFA1 as compared with high phosphate medium alone. Interestingly, spironolactone exerted a profound effect on PIT1 and CBFA1 expression induced by high phosphate medium beyond counteracting the effects of added aldosterone.
Additional experiments addressed the role of FGF23 in aldosterone-induced osteoblastic differentiation. To this end, HAoSMCs were treated with 100 nM aldosterone and/or 5 ng/ml human FGF23 with or without silencing of klotho (Figure (Figure8,8, C–F). Treatment of HAoSMCs with FGF23 blunted the effects of aldosterone treatment on PIT1 and CBFA1 mRNA expression. The protective effects of FGF23 were abrogated by silencing of klotho in HAoSMCs.
Additional experiments addressed the role of PIT1 in aldosterone-induced osteoblastic differentiation. To this end, RNA interference was used to suppress endogenous PIT1 mRNA levels in HAoSMCs. To confirm the effects of silencing on HAoSMCs, PIT1 expression levels were examined by quantitative RT-PCR. As shown in Figure Figure9,9, PIT1 mRNA levels were significantly reduced in HAoSMCs silenced with PIT1 siRNA but not in HAoSMCs transfected with the negative control siRNA. Treatment with 100 nM aldosterone significantly upregulated the transcript levels of TNFA, MSX2, CBFA1, and ALPL in HAoSMCs pretreated with negative control siRNA. In contrast, TNFA, MSX2, CBFA1, and ALPL mRNA levels were not increased in response to aldosterone in the HAoSMCs silenced with PIT1 siRNA (Figure (Figure9,9, C–F). These results suggest that PIT1 contributed to or even accounted for induction of osteogenic gene expression in HAoSMCs by aldosterone. Moreover, ALP activity was increased by aldosterone, an effect again abrogated in HAoSMCs silenced with PIT1 siRNA (Figure (Figure99G).
Similar to patients with CKD, kl/kl mice develop severe MBD, with extensive vascular calcification (6). The present observations reveal that vascular calcification of kl/kl mice can be mitigated by spironolactone treatment. According to the present observations, aldosterone stimulates the expression of chondrogenic/osteogenic transcription factors and of ALP in vitro and in vivo. The blockage of aldosterone by the MR receptor antagonist spironolactone mitigates the effects of aldosterone and reduces the procalcification signaling in vitro and in vivo.
Similar to human CKD, the kl/kl mouse shows elevated aldosterone levels (27, 28). Vascular smooth muscle cells possess the MR receptor, and aldosterone is known to promote vascular calcification (33–35). Aldosterone further increases Tnfa expression (36) and upregulates Bmp2, which does, however, not seem to be required for the procalcifying properties of aldosterone (34). The present observations provide further insight into the spironolactone-sensitive signaling leading to vascular calcification. The results showing aldosterone effects on the HAoSMCs point to a causal role of SLC20A1, which has emerged as a key factor in vascular calcification (37, 38). Aldosterone dose-dependently upregulates PIT1 expression and potentiates the effects of phosphate on PIT1 expression. The profound protective effects of spironolactone indicate an intrinsic activation of the MR at high extracellular phosphate concentration. More importantly, silencing of PIT1 completely abrogated all effects of aldosterone on osteoinductive signaling. The exact mechanism of how PIT1 mediates vascular calcification is still elusive (37). PIT1 may not be primarily effective by mediating cellular phosphate uptake (39). PIT1 mainly localizes to the sarcoplasmic reticulum, and its cell surface expression is not the key to vascular calcification (39). As reported earlier (38, 39), PIT1 expression is insensitive to TNF-α. We show that conversely TNFA expression is sensitive to PIT1, as PIT1 silencing decreases TNFA expression induced by aldosterone, indicating that in vascular smooth muscle cells PIT1 may be upstream instead of downstream of TNFA expression. Ample evidence underscores the importance of TNF-α and the TNF-α–sensitive signaling leading to initiation of vascular smooth muscle cell osteoblastic differentiation (5). According to the present observations, aldosterone increases expression of PIT1, which is in turn required for expression of TNFA and chondrogenic/osteogenic transcription factors, MSX2 and CBFA1, and ALPL as well as ALP activity. It is tempting to speculate that PIT1 transcription is regulated directly by the aldosterone-MR complex, as the promoter sequence of the PIT1 gene contains putative MR response elements MRE/GRE.
Nevertheless, other factors beside aldosterone regulate PIT1 (38, 39). The expression of PIT1 is decreased in a klotho-overexpressing mouse line, pointing to an additional inhibitory effect of klotho on PIT1 expression (6). Klotho is expressed in vascular smooth muscle cells and is required for the vasculoprotective effects of FGF23 signaling (25). In accordance, FGF23 mitigates the effects of aldosterone on PIT1 expression and subsequent chondrogenic/osteogenic signaling, as determined by CBFA1 expression in HAoSMCs. The in vitro findings of PIT1 mediating the effects of aldosterone do not rule out other effects of spironolactone treatment. Endothelial cells are involved in the induction of vascular calcification, and aldosterone has detrimental effects on the endothelium and the vasculature (40, 41). Aldosterone downregulates eNos, an effect reversed by spironolactone (30). Nitric oxide interferes with vascular calcification by regulating Pai1 (42). Enhanced Pai1 expression has similarly been observed in the kl/kl mice (43).
However, the phenotype of the kl/kl mice and the FGF23 knockout mice results from excessive formation of 1,25(OH)2D3 and subsequent hyperphosphatemia, as it is reversed by vitamin D–deficient or low phosphate diet (27, 44–46). In CKD, 1,25(OH)2D3 formation is reduced and the vascular calcification results from hyperphosphatemia due to impaired renal phosphate elimination, although the use of phosphate binders was recently questioned (4, 10, 11, 47). Paradoxically, 1,25(OH)2D3 agonists were shown to actually decrease vascular calcification and exert beneficial effects in vascular tissues (48). Thus, 1,25(OH)2D3 may play a dual role in tissue calcification. Although 1,25(OH)2D3 increases plasma Ca2+ and phosphate concentrations, it suppresses NF-κB and TNF-α (49), which in turn are involved in the stimulation of vascular calcification (50–52). This could also be influenced by the induction of klotho expression by 1,25(OH)2D3, which enables FGF23 binding and subsequent protective signaling (25). FGF23 exerts profound protective effects on the vasculature in high phosphate conditions; however, this effect requires klotho as a cofactor. In patients with CKD, klotho expression could be stimulated by 1,25(OH)2D3, an effect blunted or lacking in the kl/kl mice. The extremely high serum levels of FGF23 in kl/kl mice are therefore most likely unable to exert vasculoprotective effects, a condition similar to human patients with CKD.
There may be a crosstalk between klotho and the renin-angiotensin-aldosterone system, as vascular cells express Cyp11b2 and are capable of producing aldosterone (53–57). Aldosterone may further promote the osteochondrogenic remodeling of vascular smooth muscle cells by downregulating klotho and thereby mediating FGF23 resistance (6, 57), nonetheless, following aldosterone treatment, HAoSMCs still respond to FGF23 treatment, which counteracts the effects of aldosterone.
The importance of other factors beside aldosterone involved in vascular calcification is reflected by the finding that spironolactone treatment could not abrogate, but only reduce the calcification-prone phenotype of kl/kl mice, despite profound protective effects in vitro. The study is further limited by other possible effects of spironolactone in vivo. Although in vitro experiments with aldosterone suggest an important role of MR activation in vascular calcification, the beneficial effects of spironolactone in vivo may only partially be due to MR inhibition. Spironolactone inhibits also other receptors, most notably the androgen receptor, and prevents bone loss in hyperandrogenic women, whereas eplerenone is much more selective for the MR receptor and has fewer antiandrogenic side effects (58, 59). The androgen receptor is similarly associated with vascular calcification, although its exact role in vascular calcification is still incompletely understood (60, 61). Spironolactone treatment further decreased plasma urea nitrogen levels but increased plasma cystatin C levels. Despite the observed effects of spironolactone on osteoinductive signaling, the effects of spironolactone treatment on survival were only moderate. Thus, additional mechanisms compromise renal function and limit the life span of kl/kl mice.
MBD with vascular calcification is a determinant of the mortality in CKD (2, 3). Patients with CKD also suffer from severe hyperphosphatemia, with soft tissue calcifications and arteriosclerosis, resulting in dramatically increased cardiovascular mortality, the most common death of dialysis patients (31). The expression of klotho is strongly reduced in these patients and a sensitive marker of CKD (6). Along those lines, klotho substitution significantly improved the outcome in a CKD model (62). Patients with CKD and kl/kl mice share the phosphate overloading and klotho deficiency with resistance to FGF23, which then exerts detrimental effects on the vasculature (7, 63). The kl/kl mouse is therefore an established animal model mimicking the pathophysiology of CKD and MBD. The extensive vascular and soft tissue calcification paralleled by induction of a procalcification programming in kl/kl mice mimics excessive calcifications in patients with CKD with similar osteoinductive signaling (22, 64).
In view of the present observations, aldosterone blockage by spironolactone may reduce vascular calcification and may be considered a therapeutic option in patients with CKD. Spironolactone treatment bears the risk of hyperkalemia but is otherwise well tolerated in patients with early to moderate CKD (65). Thus, even in patients with CKD, the benefits may outweigh the risks of spironolactone treatment.
Further information can be found in Supplemental Methods.
The origin of the mice, breeding, and genotyping were described previously (8). As klotho-deficient mice show severe calcifications at 3 weeks of age (66, 67), life-long treatment with spironolactone was maintained in this study. The klotho WT (WT) and kl/kl mice had access to vehicle drinking water without or with addition of 80 mg/l spironolactone (Sigma-Aldrich) and rodent chow ad libitum (68, 69). Blood was collected by retroorbital puncture, and the plasma concentrations of blood urea nitrogen, phosphate, and Ca2+ were measured by a photometric method (FUJI FDC 3500i). An ELISA Kit was used to determine plasma concentrations of 1,25(OH)2D3 (Immunodiagnostic Systems), FGF23 (Immutopics), or cystatin C (Biovendor) according to manufacturer’s instructions. Blood pressure measurements were performed by left ventricular apical stab technique under isoflurane anesthesia with a pressure transducer (World Precision Instruments). Mice were then sacrificed, and aortic, lung, and kidney tissues were collected for further experiments at approximately 8 to 9 weeks of age.
Primary HAoSMCs (70, 71) (provided by Dorothea Siegel-Axel, Medical Clinic IV, Department of Endocrinology, Diabetology, Angiology, Nephrology and Clinical Chemistry, University of Tübingen) were routinely cultured in Waymouth’s MB 752/1 medium and Ham’s F-12 nutrient mixture (1:1, Gibco, Life Technologies) supplemented with 10% FBS (Gibco, Life Technologies) and 100 U/ml penicillin and 100 μg/ml streptomycin (Gibco, Life Technologies). HAoSMCs were grown to confluency and used in all experiments from passages 4 to 10. The media was changed to 10% charcoal-stripped FBS media (Gibco, Life Technologies) 24 hours prior to each experiment to reduce the effects of endogenous ligands. Unless indicated otherwise, cells were treated for 24 hours with aldosterone and/or spironolactone (Sigma-Aldrich) dissolved in DMSO with 2 mM β-glycerophosphate (Sigma-Aldrich) or with 5 ng/ml of human FGF23 (R&D Systems). Equal amounts of vehicle were used as a control.
For silencing of PIT1 and KLOTHO, HAoSMCs were cultured on 6-well plates (2 × 105 cells per well). The cells were subsequently transfected with 10 nM validated PIT1 siRNA (ID no. s13087, Ambion, Life Technologies) with 10 nM KLOTHO siRNA (ID no. s225119, Ambion, Life Technologies) or with 10 nM negative control siRNA (ID no. 4390843, Ambion, Life Technologies) using siPORT amine transfection agent (Ambion, Life Technologies) according to the manufacturer’s protocol. The cells were used 48 hours after transfection. The efficiency of silencing was verified by quantitative RT-PCR.
HAoSMCs were cultured on 24-well plates (4 × 104 cells per well) in 10% charcoal-stripped FBS media. Where indicated, 1 day after seeding, cells were silenced using 10 nM PIT1 siRNA or 10 nM negative control siRNA, as described previously. HAoSMCs were treated for 7 days with vehicle, aldosterone, and/or spironolactone at the concentrations indicated in the figure legends. Fresh media with agents were added every 2 to 3 days. For determination of cellular ALP activity, cells were washed 3 times with PBS and assayed for ALP activity using the ALP Colorimetric Assay Kit (Abcam) according to the manufacturer’s protocol. ALP activity was normalized to total protein concentration, as assessed by the Bradford assay (Bio-Rad Laboratories).
Quantitative RT-PCR was performed as described previously (72). Briefly, after sacrificing the animals, tissues were immediately snap frozen in liquid nitrogen. Total RNA was isolated from mouse tissues by using Trifast Reagent (Peqlab) according to the manufacturer’s instructions. HAoSMCs were washed with PBS, and total RNA was isolated using Trifast Reagent (Peqlab) according to the manufacturer’s instructions. Reverse transcription of 2 μg RNA was performed using oligo(dT)12–18 primers (Invitrogen) and SuperScript III Reverse Transcriptase (Invitrogen). cDNA samples were treated with RNaseH (Invitrogen). Quantitative real-time PCR was performed with the iCycler iQ Real-Time PCR Detection System (Bio-Rad Laboratories) and iQ Sybr Green Supermix (Bio-Rad Laboratories) according to the manufacturer’s instructions. Further information about primer sequences can be found in the Supplemental Methods. The specificity of the PCR products was confirmed by analysis of the melting curves and in addition by agarose gel electrophoresis. All PCRs were performed in duplicate, and mRNA fold changes were calculated by the 2–ΔΔCt method using GAPDH as internal reference.
For histological evaluation, thoracic aortic tissue and lung and kidney tissues from kl/kl and WT mice, without or with treatment with spironolactone, were fixed with 4% paraformaldehyde, embedded in paraffin, cut in 2- to 3-μm sections, and stained with H&E and von Kossa (73). For quantification, 2 random von Kossa–stained sections from the thoracic aortic tissues were digitized. The surface of the aorta was manually defined as the region of interest, and the surface affected by calcification was manually measured with Adobe Photoshop software (Adobe). The calcified area was calculated as calcified aortic surface/total aortic surface (pixels/pixels).
For immunohistochemistry, paraformaldehyde-fixed thoracic aortic tissue and lung and kidney tissue were cryoprotected in 30% sucrose, frozen in mounting medium (Tissue-Tek, Sakura Finetek), and sectioned at a thickness of 8 μm on coated slides. To reduce nonspecific background staining, slides were incubated with 5% normal goat serum or with 5% BSA in PBS/ 0.1% TritonX for 1 hour at room temperature. Sections were incubated overnight at 4°C with the following primary antibodies: rabbit polyclonal anti-Sp7/osterix (diluted 1:75, Abcam), rabbit polyclonal anti-Cbfa1 (diluted 1:50, Santa Cruz Biotechnology Inc.), or goat polyclonal anti-Msx2 (diluted 1:50, Santa Cruz Biotechnology Inc.). Binding of primary antibodies was visualized using goat anti-rabbit Alexa Fluor 488–conjugated antibody (diluted 1:1,000, Invitrogen) or donkey anti-goat Alexa Fluor 488–conjugated antibody (diluted 1:1,000, Invitrogen) incubated for 1 hour at room temperature. Nuclei were stained using DRAQ-5 dye (diluted 1:1,000, Biostatus) and actin using Rhodamine Phalloidin (diluted 1:100, Invitrogen). The slides were mounted with Prolong Gold antifade reagent (Invitrogen). Images were collected with a confocal laser-scanning microscope (LSM 510, Carl Zeiss MicroImaging GmbH) using a water immersion A-Plan ×40/1.2W DICIII. Confocal images are representative for 3 mice per group. Negative controls were carried out simultaneously with all experiments by omitting incubation with primary antibodies.
Data are provided as mean ± SEM; n represents the number of independent experiments. All data were tested for significance using ANOVA following post-hoc analysis with SPSS software or unpaired, 2-tailed t test where indicated. Four groups were compared: WT mice treated either with spironolactone or with control solution and kl/kl mice treated either with spironolactone or with control solution. Two random sections of aortic tissue from untreated and treated kl/kl mice were quantified for von Kossa–positive staining. Survival outcome was investigated by Kaplan-Meier plot and tested with log-rank test statistics. In all tests, P values of less than 0.05 were considered statistically significant.
All animal experiments were conducted according to the guidelines of the American Physiological Society as well as the German law for the welfare of animals and were approved by the respective authority (Regierungspräsidium Tübingen, Germany). Human aortas were obtained from organ donors after obtaining informed consent (approved by the “Clinical Ethics Committee at the University Hospital Tübingen,” Tübingen, Germany).
The authors gratefully acknowledge the outstanding technical assistance of Klaudia Kloß, Dennis Thiele, Elfriede Faber, and Julia Spilcke-Liss and the meticulous preparation of the manuscript by Tanja Loch, Sari Ruebe, and Lejla Subasic. This study was supported by the Deutsche Forschungsgemeinschaft.
Conflict of interest: The authors have declared that no conflict of interest exists.
Citation for this article: J Clin Invest. 2013;123(2):812–822. doi:10.1172/JCI64093.
See the related Commentary beginning on page 542.