Cardiomyocyte-specific overexpression of syndecan-4 in mice results in activation of calcineurin-NFAT signalling and exacerbated cardiac hypertrophy

Abstract

Background

Cardiomyocyte hypertrophy is a hallmark of cardiac dysfunction in patients with aortic stenosis (AS), and can be triggered by left ventricular (LV) pressure overload in mice by aortic banding (AB). Syndecan-4 is a transmembrane heparan sulphate proteoglycan which is found increased in the myocardium of AS patients and AB mice. The role of syndecan-4 in cardiomyocyte hypertrophy is not well understood.

Purpose of the study

We developed mice with cardiomyocyte-specific overexpression of syndecan-4 (Sdc4-Tg) and subjected these to AB to examine the role of syndecan-4 in hypertrophy and activation of the pro-hypertrophic calcineurin-NFAT signalling pathway.

Methods and results

Sdc4-Tg mice showed exacerbated cardiac remodelling upon AB compared to wild type (WT). At 2–6 weeks post-AB, Sdc4-Tg and WT mice showed similar hypertrophic growth, while at 20 weeks post-AB, exacerbated hypertrophy and dysfunction were evident in Sdc4-Tg mice. After cross-breeding of Sdc4-Tg mice with NFAT-luciferase reporter mice, we found increased NFAT activation in Sdc4-Tg hearts after AB. Immunoprecipitation showed that calcineurin bound to syndecan-4 in Sdc4-Tg hearts. Isolated cardiomyocytes from Sdc4-Tg mice showed alterations in Ca²⁺ fluxes, suggesting that syndecan-4 regulated Ca²⁺ levels, and thereby, activating the syndecan-4-calcineurin complex resulting in NFAT activation and hypertrophic growth. Similarly, primary cardiomyocyte cultures from neonatal rats showed increased calcineurin-NFAT-dependent hypertrophic growth upon viral Sdc4 overexpression.

Conclusion

Our study of mice with cardiomyocyte-specific overexpression of Sdc4 have revealed that syndecan-4 is important for activation of the Ca²⁺-dependent calcineurin-NFAT signalling pathway, hypertrophic remodelling and dysfunction in cardiomyocytes in response to pressure overload.

Supplementary Information

The online version contains supplementary material available at 10.1007/s11033-022-07985-y.

Introduction

Heart failure carries high morbidity, mortality and societal costs [1–3]. Cardiac hypertrophy, inflammation and fibrosis are central remodelling processes leading to cardiac dysfunction and failure [4], and can be triggered by left ventricular (LV) pressure overload in patients with hypertension or aortic stenosis (AS).

Proteoglycans, proteins substituted with covalently attached glycosaminoglycan (GAG) chains [5], are believed to play important roles during cardiac remodelling and failure [6–9]. Syndecan-4 is a transmembrane heparan sulphate proteoglycan consisting of an ectodomain with GAG chains extending into the extracellular matrix (ECM), a transmembrane domain, and a short cytoplasmic tail involved in signalling and binding to the cytoskeleton [5, 9–17]. The GAG-substituted ectodomain can be shed from the cell surface [18]. Syndecan-4 levels are elevated in hearts of AS patients and mice subjected to aortic banding (AB) [13, 19–23]. We have shown that the Ca²⁺-activated phosphatase calcineurin binds directly to the cytoplasmic domain of syndecan-4 [13], activating downstream nuclear factor of activated T-cell (NFAT) transcription factors, i.e., a central pathway directing pathological cardiomyocyte remodelling [24–27]. These data suggest that syndecan-4 regulates hypertrophy through calcineurin-NFAT signalling.

Syndecan-4 localizes to the costamere and Z-disc of cardiomyocytes [28], areas linking the cytoskeleton to the ECM that are believed to be important for sensing mechanical stress. Cardiomyocyte syndecan-4 expression is increased in response to mechanical stress and inflammatory stimuli [21]. Studies of constitutive syndecan-4 knock-out (Sdc4-KO) mice suggest that syndecan-4 regulates cardiac hypertrophy [13, 19–22], however, its specific role in cardiomyocyte remodelling has been difficult to tease out. Syndecan-4 is expressed at comparable levels in cardiac myocytes and fibroblasts [19], and while it is clear that syndecan-4 is important for fibroblast function, formation of focal adhesions, fibrosis and immune cell infiltration [7–9, 21, 29], its role in cardiomyocytes remains incompletely understood.

Here, we developed a mouse line with cardiomyocyte-specific overexpression of syndecan-4 (Sdc4-Tg) and subjected these to AB to examine the role of syndecan-4 in cardiomyocytes specifically.

Results

Generation of mice with cardiomyocyte-specific overexpression of syndecan-4

To generate mice with cardiomyocyte-specific syndecan-4 overexpression, we inserted mouse Sdc4 cDNA (NP_035651) under control of the mouse Myh6 promoter [encoding α-myosin heavy chain (α-MHC)], followed by the simian virus (SV) 40 splice acceptor site and polyadenylation signal sequence (Fig. 1A). A 110 bp SV40 fragment was used to genotype the Sdc4-Tg mice (Fig. 1B). A C57BL/6J mouse line with stable, germline transmission of the Sdc4-Tg allele was established. Sdc4-Tg male and female mice had similar appearance, behaviour and fertility compared to wild type (WT) littermates. Overexpression of Sdc4 mRNA in hearts of Sdc4-Tg mice was confirmed, i.e., 90-fold higher in the LV, 75-fold higher in the right ventricle (RV), and 139-fold higher in atria vs. WT (Fig. 1C). As expected from Myh6-driven overexpression, which is cardiomyocyte-specific, we found no difference in Sdc4 mRNA levels in other tissues investigated, i.e., fat, intestine, liver, lung, spleen, kidney, brain or skeletal muscle. We did not observe alterations in expression of the three other syndecans in the heart (Sdc1-3; Fig. 1D).

Fig. 1.

Generation of mice with cardiomyocyte-specific overexpression of syndecan-4. A Mice with cardiomyocyte-specific overexpression of syndecan-4 (Sdc4-Tg) were generated by inserting mouse Sdc4 cDNA upstream of the mouse Myh6 promoter, followed by the simian virus (SV40) splice acceptor site and polyadenylation signal sequence (schematic shown). A C57BL/6J mouse line with stable, germline transmission of the Sdc4-Tg allele was established. See Table 1 for baseline characteristics. B Representative genotyping gel of DNA from mice at weaning age, showing a 110 bp SV40 fragment used to identify Sdc4-Tg mice. A control fragment was amplified in all mice. C Relative mRNA expression of Sdc4 in the left ventricle (LV), right ventricle (RV), atria, fat, intestine, lung, liver, kidney, spleen, brain and skeletal muscle (gastrocnemius) of Sdc4-Tg and WT mice (n = 3), normalized to Gapdh. D Relative mRNA expression of Sdc1-3 in the LV, normalized to Gapdh. Data are mean ± SEM. Statistical differences (C, D) were tested using t-test vs. respective control tissue; **p < 0.01, ***p < 0.001. E, F Representative immunoblots of syndecan-4 in LV protein lysates (E; vinculin was used for loading control), and methanol-precipitated and heparan sulphate (HS)-digested lysates (F) from Sdc4-Tg and WT mice (n = 3–5), showing increased levels of syndecan-4 full-length (FL) and cellular fragment (CF) in hearts of Sdc4-Tg mice, the latter in line with increased syndecan-4 shedding. See Fig. S1 for syndecan-4 antibody validation. Overexpression of hemagglutinin (HA)-tagged syndecan-4 in HEK293 cells was used as positive control

While the core syndecan-4 protein is 24 kDa, syndecan-4 substituted with heparan sulphate GAGs appears in gels as bands of different sizes, in addition to variants too big to enter the gel. We have previously developed a custom made syndecan-4 antibody detecting a cytoplasmatic epitope (antibody validation in previous reports [13, 21, 23] and Fig. S1) which was used here. Immunoblotting of heart lysates showed increased levels of syndecan-4-specific protein bands including full-length (FL) syndecan-4 protein in Sdc4-Tg hearts vs. WT (Fig. 1E). Increased FL syndecan-4 protein was confirmed using methanol precipitation of heart lysates prior to treatment with heparan sulphate (HS)-degrading enzymes, and immunoblotting using an antibody recognizing the HS stubs [21, 23, 30] (Fig. 1F). Of note, although it is known to be expressed, syndecan-4 protein in WT hearts appeared nearly non-detectable when immunoblotted side-by-side with Sdc4-Tg hearts due to relatively high syndecan-4 levels in Sdc4-Tg.

When the extracellular domain of syndecan-4 is shed from the cell surface, the shed ectodomain (SE) is separated from the cellular fragment (CF), consisting of the transmembrane and cytoplasmic parts. The custom made syndecan-4 antibody with the cytoplasmatic epitope also detects the 10–15 kDa CF which was used to estimate syndecan-4 shedding levels (Fig. S1). Sdc4 overexpression resulted in constitutive shedding, evident from the increased levels of the CF in Sdc4-Tg hearts (Fig. 1E). Thus, syndecan-4 mRNA, FL protein and shed levels were increased in hearts of Sdc4-Tg mice, without alterations in expression of the other three syndecan family members, and without altered syndecan-4 expression in other tissues investigated.

Sdc4-Tg mice show no overt cardiac phenotype at baseline or during ageing

The cardiac phenotype of Sdc4-Tg mice was examined at 6–8, 30 and 60 weeks of age. We found no differences in LV weight (LVW) or lung weight (LW), or echocardiographic cardiac dimensions or function compared to WT littermates, in line with no overt cardiac phenotype of Sdc4-Tg at baseline or during ageing (Table 1). To investigate the molecular profiles of these hearts, expression of signature molecules of heart failure (Nppa and Nppb encoding atrial and brain natriuretic peptides (ANP and BNP), respectively), NFAT activation (Rcan1-4 encoding the Regulator of calcineurin (RCAN) 1–4, a gene whose transcription is under the direct control of calcineurin-NFAT [31, 32]), and fibrosis, i.e., structural collagens I and III (encoded by Col1a2 and Col3a1, respectively), was measured. Sdc4-Tg mice showed 2.6-fold increased Nppa and 2.0-fold increased Nppb expression at baseline, and 1.6-fold increased Nppb during aging (Fig. S2A, B, respectively), perhaps indicating a low level, pro-hypertrophic state. We found no differences in expression of Rcan1-4 (Fig. S2C), or collagens (Fig. S2D, E).

Table 1.

Characteristics of Sdc4-Tg mice at baseline and during ageing

	WT 6-8w	Sdc4-Tg 6-8w	WT 30w	Sdc4-Tg 30w	WT 60w	Sdc4-Tg 60w
Sex	M	M	M	M	M	M
N	13	16	10	4	10	5
BW (g)	23.35  ± 0.53	23.53  ± 0.47	32.84  ± 0.63	32.70  ± 1.55	39.77  ± 2.13	36.56  ± 1.68
LVW/BW (mg/g)	3.38  ± 0.06	3.30  ± 0.05	3.15  ± 0.08	3.19  ± 0.20	3.02  ± 0.15	2.94  ± 0.11
LW/BW (mg/g)	6.14  ± 0.46	5.82  ± 0.13	5.00  ± 0.13	5.56  ± 0.56	4.72  ± 0.22	4.80  ± 0.12
N	8	10	7	7	5	5
LAD (mm)	1.81  ± 0.06	1.80  ± 0.05	1.94  ± 0.08	1.88  ± 0.06	1.94  ± 0.03	2.03  ± 0.02
LVPWd (mm)	0.70  ± 0.02	0.70  ± 0.02	0.73  ± 0.01	0.70  ± 0.02	0.76  ± 0.03	0.74  ± 0.01
IVSd (mm)	0.72  ± 0.02	0.70  ± 0.02	0.75  ± 0.01	0.71  ± 0.01	0.76  ± 0.02	0.76  ± 0.01
LVIDd (mm)	4.10  ± 0.11	4.15  ± 0.06	4.36  ± 0.10	4.41  ± 0.15	4.54  ± 0.08	4.50  ± 0.14
FS (%)	21.66  ± 2.25	21.22  ± 1.08	22.61  ± 1.05	25.62  ± 1.12	22.59  ± 1.69	19.72  ± 1.51
Calc. LV mass (mg)	108.60  ± 4.72	108.60  ± 3.78	127.10  ± 5.18	122.40  ± 8.83	140.80  ± 6.51	136.10  ± 7.44

M-mode echocardiography data and post-mortem organ weights (mean ± SEM) of Sdc4-Tg and littermate wild-type (WT) male mice at 6–8, 30 and 60 weeks of age

Unpaired t-test Sdc4-Tg vs. WT at 6-8w, 30w and 60w, respectively

BW body weight, LVW left ventricular weight, LW lung weight, LAD left atrial diameter, IVSd interventricular septum thickness in diastole, LVPWd left ventricular posterior wall thickness in diastole, LVIDd left ventricular internal diameter in diastole, FS fractional shortening

Sdc4-Tg mice show exacerbated cardiac remodelling with faster heart failure progression upon pressure overload

To understand the role of syndecan-4 in cardiac hypertrophy, mice were subjected to AB or sham control operation. The cardiac phenotype was examined by standard echocardiography at 2, 6, 12 (Table SI) and 20 weeks (Table 2), with more extensive examination at termination 20 weeks post-AB, including organ weights, Doppler echocardiography and magnetic resonance imaging (MRI; Table 2 and Fig. 2A). We observed no difference in mortality between Sdc4-Tg to WT mice over the 20 weeks (Fig. S3A).

Table 2.

Characteristics of Sdc4-Tg mice after AB

	20 weeks
	Sham WT	Sham Sdc4-Tg	AB WT	AB Sdc4-Tg
Biometric data
N	9	9	11	14
BW (g)	32.12  ± 0.67	33.09  ± 0.93	31.58  ± 0.94	29.91  ± 0.50
HW/BW (mg/g)	4.69  ± 0.29	4.38  ± 0.22	7.30  ± 0.44**	9.41  ± 0.72***,#
LVW/BW (mg/g)	3.13  ± 0.32	2.86  ± 0.29	5.16  ± 0.31***	6.13  ± 0.22***,#
RVW/BW (mg/g)	1.26  ± 0.43	1.25  ± 0.48	0.97  ± 0.07	1.12  ± 0.13
LW/BW (mg/g)	4.79  ± 0.15	4.81  ± 0.08	7.69  ± 0.63**	8.93  ± 0.64***
M-mode echocardiography
N	9	9	11	14
LAD (mm)	1.66  ± 0.03	1.70  ± 0.03	2.26  ± 0.16**	2.54  ± 0.12***
LVPWd (mm)	0.73  ± 0.02	0.74  ± 0.02	0.99  ± 0.05***	1.02  ± 0.05***
IVSd (mm)	0.73  ± 0.02	0.75  ± 0.01	1.00  ± 0.04***	0.99  ± 0.03***
LVIDd (mm)	4.11  ± 0.08	4.12  ± 0.11	4.44  ± 0.13	4.96  ± 0.17***,#
FS (%)	31.27  ± 2.61	29.45  ± 1.98	18.77  ± 2.11***	14.88  ± 1.95***
Calc. LV mass (mg)	112.90  ± 5.43	115.30  ± 3.91	191.60  ± 11.48***	236.30  ± 14.45***,#
Doppler flow echocardiography
N	9	9	7–11	5–13
Heart rate (BPM)	478.20  ± 16.38	487.70  ± 17.67	481.00  ± 13.65	495.80  ± 9.63
Peak mitral velocity (m/s)	624.10  ± 31.63	609.30  ± 35.48	688.90  ± 37.58	648.20  ± 61.03
Mitral deceleration (m/s)	2418  ± 159	2606  ± 198	3936  ± 333**	4121  ± 414**
CO in LVOT (ml/min)	63.33  ± 4.54	51.00  ± 2.73	57.73  ± 6.03	40.62  ± 3.58**,#
Peak RVOT velocity (m/s)	602  ± 23.09	666.20  ± 15.58	698.90  ± 43.21	551.20  ± 50.31#
Tissue Doppler echocardiography
N	9	8	11	14
Systolic velocity (mm/s)	26.56  ± 1.80	25.00  ± 0.93	17.85  ± 1.78***	15.06  ± 0.83***
Diastolic velocity (mm/s)	25.56  ± 1.28	23.50  ± 1.38	19.63  ± 1.91*	15.94  ± 0.94***
MRI
N	3	4	4	8
Calc. LV mass (mg)	126.30  ± 12.70	129.10  ± 3.85	187.50  ± 8.13***	232.70  ± 8.24***,##
LV EDV (μl)	52.92  ± 4.08	60.33  ± 3.65	102.00  ± 8.45*	121.60  ± 10.60**
LV ESV (μl)	26.64  ± 6.46	30.20  ± 1.45	52.11  ± 12.24	82.75  ± 13.91*
LV EF (%)	50.63  ± 8.44	49.77  ± 1.72	50.56  ± 6.90	35.02  ± 6.03

Biometric data, M-mode, flow Doppler and tissue Doppler echocardiography, and magnetic resonance imaging (MRI) data (mean ± SEM) of male Sdc4-Tg and wild-type (WT) littermate control mice 20 weeks after aortic banding (AB) or sham operation. See Table SI for animal characteristics 2, 6 and 12 weeks after AB or sham operation. Blood flow over the stenosis was measured 24 h after AB: WT 3.94 ± 0.07 m/s and Sdc4-Tg 3.86 ± 0.08 m/s, and was not statistically different between the groups

BW body weight, LVW left ventricular weight, LW lung weight, LAD left atrial diameter, IVSd interventricular septum thickness in diastole, LVPWd left ventricular posterior wall thickness in diastole, LVIDd left ventricular internal diameter in diastole, FS fractional shortening, CO cardiac output, LVOT left ventricular outflow tract, RVOT right ventricular outflow tract, LV left ventricle, EDV end-diastolic volume, ESV end-systolic volume, EF ejection fraction, BPM beats per minute

One-way ANOVA with Dunnett´s post-test vs. WT sham; *p < 0.05; **p < 0.01; ***p < 0.001, and vs. WT AB; #p < 0.05

Fig. 2.

Sdc4-Tg mice show exacerbated cardiac remodelling upon pressure overload. A Representative magnetic resonance imaging (MRI), mid-ventricular, short-axis view, of Sdc4-Tg and wild-type (WT) mice subjected to aortic banding (AB) or sham operation for 20 weeks (20w). See Tables 2 and SI for characteristics post-AB or sham at 2, 6, 12 and 20w. Relative mRNA levels of signature molecules of heart failure, Nppa and Nppb [B, C; encoding atrial and brain natriuretic peptides (ANP and BNP, respectively)] in left ventricle (LV), right ventricle (RV) and atria of Sdc4-Tg and WT at 20w post-AB or sham (n = 7–9). Relative mRNA levels of markers of pathological cardiomyocyte remodelling, Myh6 and Myh7 [D, E; encoding α- and β-myosin heavy chain (MHC), respectively] in the LV of Sdc4-Tg and WT mice after 20w of AB or sham. Gene expression was normalized to Gapdh. Data are mean ± SEM. Statistical differences were tested using one-way ANOVA with Dunnett’s post-testing vs. respective WT sham, *p < 0.05, **p < 0.01, ***p < 0.001; or vs. WT AB20w, ^#p < 0.05

At 2 or 6 weeks post-AB, both genotypes developed comparable hypertrophic remodelling, evidenced by increased thickness of the LV posterior wall (LVPWd) and the interventricular septum (IVSd) in diastole, and calculated LV mass compared to sham controls (Table SI).

Interestingly, at 12 weeks post-AB, Sdc4-Tg mice showed increased calculated LV mass compared to WT (Table SI). Fractional shortening (FS) was reduced at 12 weeks post-AB in the Sdc4-Tg mice compared to WT, suggesting contractile dysfunction.

Importantly, at 20 weeks post-AB, exacerbated hypertrophy, remodelling and dysfunction in Sdc4-Tg mice vs. WT was evident from cardiac phenotyping (Table 2). Firstly, Sdc4-Tg mice showed increased heart weight (HW; 29% increase vs. WT), LVW (19% increase vs. WT) and LW (17% increase vs. WT). The increased HW and LVW were supported by estimations of LV mass from echocardiography (24% increase vs. WT) and MRI (25% increase vs. WT) (Table 2). Echocardiography showed that while LVPWd and IVSd were increased to a similar extent in Sdc4-Tg and WT 20 weeks post-AB, Sdc4-Tg mice displayed increased LV internal diameter in diastole (LVIDd) compared to WT AB, i.e., exacerbated dilatation (Fig. 2A). Both Sdc4-Tg and WT mice showed impaired function 20 weeks post-AB, based on reduced FS and tissue Doppler showing reduced systolic and diastolic velocities (Table 2). These measurements tended to show exacerbated dysfunction in Sdc4-Tg, without reaching statistical significance. As expected from heart failure signature molecules ANP and BNP, after 20 weeks of AB, Nppa was increased in the LV (Fig. 2B), and Nppb in the LV, right ventricle (RV) and atria (Fig. 2C) of both genotypes vs. sham. Supporting exacerbated heart failure, there was increased expression of Nppa in the LV and RV of Sdc4-Tg mice compared to WT after AB (Fig. 2B), and increased expression of Nppb in the RV (Fig. 2C). The signature molecular change of pathological cardiomyocyte remodelling, with reduced expression of Myh6 (encoding α- MHC) and increased expression of Myh7 (encoding β-MHC), was present in both genotypes after AB (Fig. 2D, E, respectively). Altogether, cardiac phenotyping showed that cardiomyocyte-specific overexpression of Sdc4 in vivo resulted in a faster progression towards dysfunction and failure after pressure overload.

Sdc4-Tg mice show increased cardiac NFAT activation

To examine whether cardiomyocyte-specific overexpression of Sdc4 affected NFAT activation in vivo, Sdc4-Tg mice were crossed with FVB/N NFAT-luciferase (NFAT-luc) reporter mice. NFAT activity was assessed in LV samples after 2 weeks of pressure overload of Sdc4-Tg-NFAT-luc and NFAT-luc littermates. At baseline, we found no difference in NFAT activation between Sdc4-Tg-NFAT-luc and NFAT-luc mice (Fig. 3A). Upon AB, we observed no difference in mortality in Sdc4-Tg-NFAT-luc mice vs. NFAT-luc control mice (Fig. S3B). Sdc4-Tg-NFAT-luc mice showed increased LV and LW weights upon pressure overload compared to NFAT-luc controls (Table SII), suggesting exacerbated congestive heart failure after AB in mice with Sdc4 overexpression.

Fig. 3.

Sdc4-Tg mice show increased NFAT activation upon pressure overload. A Relative NFAT-luciferase (luc) activity in whole left ventricle (LV) of Sdc4-Tg -NFAT-luc and NFAT-luc mice at baseline (6–8 weeks of age, n = 8), and after two weeks of aortic banding (AB) or sham operation (n = 6–15). See Table SII for mouse characteristics. Relative mRNA levels of calcineurin (encoded by Ppp3cb; B) and nuclear factor of activated T-cells c4 (NFATc4, encoded by Nfatc4; C) in the LV of Sdc4-Tg and WT mice after 20 weeks of AB. Gene expression was normalized to Gapdh. Data are mean ± SEM. Statistical differences were tested using t-test (baseline), or one-way ANOVA with Dunnett´s post-testing vs. NFAT-luc sham, *p < 0.05; and vs. NFAT-luc AB2w, ^#p < 0.05 (A), or using one-way ANOVA with Dunnett´s post-testing vs. respective WT sham, ***p < 0.001; and vs. WT AB20w. D Immunoprecipitation of full-length (FL) syndecan-4 from LVs of Sdc4-Tg mice, using an antibody detecting an extracellular epitope (see Fig. S1 for syndecan-4 antibody validation), or rat IgG as control. Representative immunoblots of syndecan-4 and calcineurin (n = 3). As positive controls for the calcineurin antibody, mouse brain lysate and recombinant calcineurin (130 kDa) was used. As positive control for the syndecan-4 antibody, overexpression of hemagglutinin (HA)-tagged syndecan-4 in HEK293 cells was used as positive control

Importantly, NFAT activation was increased 8.23-fold in Sdc4-Tg-NFAT-luc mice after AB compared to controls; significantly more than in NFAT-luc after AB. Thus, mice with cardiomyocyte-specific overexpression of Sdc4 show increased calcineurin-NFAT activation after AB.

We found no differences in mRNA expression of calcineurin (encoded by Ppp3cb) or NFATc4 (encoded by Nfatc4) between Sdc4-Tg vs. WT mice after AB (Fig. 3B, C, respectively). Immunoprecipitation of FL syndecan-4 in LVs from Sdc4-Tg mice was performed using an antibody detecting an extracellular epitope on syndecan-4 (see Fig. S1 for antibody validation), showing that calcineurin complexed with syndecan-4 to a similar degree in sham- and AB-operated mice (Fig. 3D). Thus, it was likely not increased levels of calcineurin-NFAT or calcineurin-syndecan-4 complexing that was the underlying cause of increased NFAT activation in Sdc4-Tg hearts after AB.

Cardiomyocytes from adult Sdc4-Tg mice show increased diastolic Ca²⁺ levels

To address whether the increased calcineurin-NFAT activation in Sdc4-Tg hearts was associated with altered cardiomyocyte Ca²⁺ transients, cytosolic and nuclear Ca²⁺ transients were measured in cardiomyocytes from adult Sdc4-Tg and WT mice, paced at 0.5 Hz and 2 Hz (Fig. 4). In cytosol (Fig. 4A–D), the diastolic Ca²⁺ levels (F0) were higher in Sdc4-Tg vs. WT at both 0.5 Hz and 2 Hz. Systolic Ca²⁺ levels (F) were not different at 0.5 Hz, but were higher in Sdc4-Tg compared to WT at 2 Hz. We found no differences in cytosolic Ca²⁺ transient amplitude (F/F0) or Ca²⁺ extrusion rate (tau) at 0.5 or 2 Hz. In the nucleus (Fig. 4A–C and E), the diastolic Ca²⁺ levels (F0) were higher in Sdc4-Tg vs. WT at both 0.5 Hz and 2 Hz. Systolic Ca²⁺ levels (F) were not different at 0.5 Hz, and showed a tendency towards higher Ca²⁺ levels in Sdc4-Tg at 2 Hz (p = 0.08). The nuclear Ca²⁺ transient amplitude (F/F0) was reduced in Sdc4-Tg at both 0.5 Hz and 2 Hz, with a slower Ca²⁺ extrusion rate (tau) at 0.5 Hz and 2 Hz. These experiments suggest that in cardiomyocytes from Sdc4-Tg mice, diastolic Ca²⁺ fluxes were altered, which likely influences calcineurin-NFAT signalling. Since transient receptor potential channels (TRPCs) 1, 3 and 6 regulate Ca²⁺-dependent calcineurin-NFAT activation in cardiomyocytes [33], we measured Trpc 1, 3 and 6 expression in Sdc4-Tg hearts. However, we found no differences in their expression levels vs. WT hearts (Fig. S4A–C, respectively).

Fig. 4.

Cardiomyocytes from adult Sdc4-Tg mice show increased diastolic Ca²⁺ levels. A Representative fluorescence confocal microscopy images of cardiomyocytes isolated from adult Sdc4-Tg and wild-type (WT) mice, loaded with the fluorescence-labelled Ca²⁺ indicator Fluo 4-AM. Representative tracings of cells paced at 0.5 Hz (baseline condition; B) and 2 Hz (stressed condition; C). D, E Ca²⁺ transient characteristics of n = 16–19 cells from n = 3 WT and Sdc4-Tg mice, paced at 0.5 Hz and 2 Hz. Data are mean ± SEM. Statistical differences were tested using an unpaired t-test vs. respective WT control, *p < 0.05, **p < 0.01

Sdc4-Tg mice did not show differences in cardiac fibrosis or immune cell infiltration upon pressure overload

To test whether overexpression of Sdc4 in cardiomyocytes in vivo affected cardiac fibrosis, expression of Col1a2, Col3a1, the collagen cross-linking enzyme lysyl oxidase (encoded by Lox), connective tissue growth factor (encoded by Ctgf), and periostin (encoded by Postn) was assessed in LV, RV and atria of Sdc4-Tg and WT mice 20 weeks post-AB (Fig. S5A–E, respectively). Altogether, the comparable increase in these genes post-AB vs. sham suggested no difference in fibrosis in Sdc4-Tg hearts post-AB.

Expression of the myofibroblast signature gene Acta2 (encoding α-smooth muscle actin) was increased to a similar extent in Sdc4-Tg and WT mice post-AB vs. sham (Fig. S5F), indicating no differences in myofibroblast differentiation in hearts with increased cardiomyocyte expression of syndecan-4.

To test whether overexpression of Sdc4 in cardiomyocytes in vivo affected T-cell infiltration, expression of Cd3 (cluster of differentiation 3), a transmembrane receptor expressed on T-cells, was assessed as in LV, RV and atria of Sdc4-Tg and WT mice 20 weeks post-AB. Cd3 was increased to a comparable extent in Sdc4-Tg and WT hearts post-AB vs. sham (Fig. S6), suggesting similar extent of T-cell infiltration. These results indicated that overexpression of Sdc4 in cardiomyocytes in vivo did not affect cardiac T-cell infiltration after pressure overload.

Viral Sdc4 overexpression in cultured cardiomyocytes results in increased calcineurin-dependent hypertrophic growth and NFAT activation

To test whether overexpression of syndecan-4 induced a direct hypertrophic response in cardiomyocytes, primary cultures were prepared from neonatal rats. Neonatal cardiomyocytes (NCM) were transduced with an adenovirus encoding Sdc4 (AdSdc4) in vitro, resulting in increased Sdc4 mRNA (Fig. 5A) and protein (Fig. 5B) levels, both syndecan-4 FL and shedding (i.e., increased levels of syndecan-4 CF). Importantly, compared to NCM transduced with control virus (AdNull), NCM transduced with AdSdc4 showed increased protein synthesis measured by radioactive H³-leucine incorporation, in line with increased hypertrophic growth in vitro (Fig. 5C). The increased protein synthesis resulting from Sdc4 overexpression was attenuated when cells were co-treated with the calcineurin inhibitor Cyclosporine A (CsA), suggesting that the Sdc4-induced protein synthesis in NCM was calcineurin-dependent (Fig. 5C). Increased mRNA expression of Nppa (Fig. 5D) and Nppb (Fig. 5E) supported the finding of increased hypertrophic growth, and increased Rcan1-4 levels (Fig. 5F) indicated increased cardiomyocyte calcineurin-NFAT signalling.

Fig. 5.

Cultured neonatal cardiomyocytes overexpressing Sdc4 show increased calcineurin-dependent hypertrophic growth and NFAT activation. A Relative mRNA level of Sdc4 in neonatal cardiomyocytes (NCM) from rats transduced with an adenovirus encoding Sdc4 (AdSdc4) or control (AdNull), n = 11–12. B Representative immunoblot (n = 3) showing increased full-length (FL) syndecan-4 protein and shedding, i.e., increased levels of the cellular fragment (CF) remaining in cells after shedding of the ectodomain, in NCM protein lysates. Vinculin was used for loading control. C Radioactive H³-leucine incorporation, used to estimate protein synthesis and hypertrophic growth in vitro, in NCM transduced with AdSDC4 or AdNull (n = 8), or co-treated with Cyclosporine A (CsA, n = 5–6), an inhibitor of calcineurin. Serum-treated cells served as positive control of growth (n = 3). Relative expression of signature molecules of heart failure, Nppa and Nppb [D, E; encoding atrial and brain natriuretic peptides (ANP and BNP, respectively)], and the nuclear factor of activated T-cells (NFAT)-responsive gene Rcan1-4 (F) in NCM transduced with AdSdc4 or AdNull, n = 11–12. Data are mean ± SEM. Gene expression was normalized to Rpl4 (A and C–E). Statistical differences were tested using one-way ANOVA with Tukey´s multiple comparison test (C), or an unpaired t-test vs. AdNull (A and D–F), **p < 0.01, ***p < 0.001

Finally, we tested whether shed syndecan-4 ectodomains (SE) affected cardiomyocyte growth and NFAT signalling in vitro. Syndecan-4 SE was produced in human embryonic kidney (HEK) 293 cells transfected with a plasmid encoding HA-tagged Sdc4, which results in constitutive shedding evidenced by increased levels of CF in cell lysates (Fig. S1A) and SE in the medium (Fig. S1B). Cultured NCM were treated with conditioned medium from the HEK293 cells. Comparing NCM treated with shed syndecan-4 to NCM treated with vehicle control conditioned media, we found no differences in expression of Nppa, Nppb or Rcan1-4 (Fig. S7A–C, respectively). Thus, the observed effects of Sdc4 overexpression on cardiomyocyte hypertrophy and NFAT signalling were likely mediated through the FL syndecan-4 protein, and not shed syndecan-4 ectodomains.

Discussion

To examine the role of syndecan-4 in cardiomyocyte hypertrophy and activation of the Ca²⁺-dependent calcineurin-NFAT pathway, we developed a mouse line with cardiomyocyte-specific Sdc4 overexpression. Sdc4-Tg mice showed no overt cardiac phenotype without stress. Importantly, Sdc4-Tg mice showed exacerbated cardiac remodelling upon pressure overload. At 2–6 weeks post-AB, Sdc4-Tg and WT mice developed comparable hypertrophic remodelling, however, at 12 weeks, Sdc4-Tg showed worse contractile dysfunction. At 20 weeks post-AB, exacerbated hypertrophy, remodelling and dysfunction in Sdc4-Tg mice was evident from post-mortem organ weights, echocardiography and MRI. Using NFAT-luciferase reporter mice, we found that NFAT activation was increased in Sdc4-Tg hearts after AB. Immunoprecipitation showed that calcineurin bound to syndecan-4 to a similar degree in sham- and AB-operated Sdc4-Tg mice. Isolated cardiomyocytes from adult Sdc4-Tg mice showed increased diastolic Ca²⁺ levels, suggesting that syndecan-4 regulates Ca²⁺ levels, and that elevated Ca²⁺ levels activate the syndecan-4-calcineurin complex, resulting in NFAT activation and hypertrophic growth. Primary cardiomyocyte cultures from neonatal rats showed increased calcineurin-NFAT-dependent hypertrophic growth upon viral Sdc4 overexpression. Taken together, cardiomyocyte-specific overexpression of Sdc4 results in hypertrophic remodelling with activation of Ca²⁺-dependent calcineurin-NFAT signalling, resulting in a faster progression towards dysfunction after pressure overload.

Syndecan-4 localizes to the costamere and Z-disc of cardiomyocytes [28], areas linking the cytoskeleton to the ECM, that are believed to be important for sensing mechanical stress. Syndecan-4 mRNA and protein levels are elevated in hypertrophic and failing hearts of patients with AS and mice after AB [13, 19–23]. We have shown that in AS patients, shed syndecan-4 is detected at higher levels in the coronary sinus than in peripheral blood [23], suggesting it is shed from the hypertrophic human heart. Serum syndecan-4 levels are elevated in patients with heart failure [34, 35], increase in proportion with LV mass, and correlate with LV geometrical parameters [35], suggesting it could have value as a blood biomarker. Mimicking the elevated syndecan-4 mRNA, protein and shedding in the myocardium of AS patients, syndecan-4 mRNA, protein and shedding was elevated in Sdc4-Tg hearts. Syndecans are involved in a variety of functions [5, 10, 12], and our understanding of syndecan-4 in cardiac remodelling has mainly come from studies of constitutive Sdc4-KO mice [13, 14, 19–22]. As syndecan-4 is expressed at comparable levels in cardiac myocytes and fibroblasts [19], its specific role in cardiomyocytes has remained incompletely understood. To tease this out, we developed Sdc4-Tg mice with cardiomyocyte-specific syndecan-4 overexpression. Bearing in mind that these mice have relatively high cardiomyocyte syndecan-4 expression, mice with cardiomyocyte-specific KO should be developed in the future.

The Sdc4-Tg mice gave us the novel insight that syndecan-4 directs Ca²⁺-dependent calcineurin-NFAT activation and hypertrophic remodelling after pressure overload in cardiomyocytes in vivo. NFAT activation was increased in Sdc4-Tg hearts, which is in line with reduced NFAT activation and hypertrophic remodelling in hearts of Sdc4-KO mice [13]. In cultured cardiomyocytes, we found that viral overexpression of syndecan-4 resulted in NFAT activation and hypertrophic growth. This is in line with reduced NFAT activation and hypertrophic growth in cardiomyocytes from Sdc4-KO mice and increased NFAT activation in WT cardiomyocytes treated with a syndecan-4 peptide [13], however it contrasts a study of cultured cardiomyocytes with reduced syndecan-4 expression, where NFAT activation was increased [14]. Altogether, we believe that syndecan-4 is an activator of cardiomyocyte NFAT signalling.

NFAT transcription factors are activated specifically by dephosphorylation by the Ca²⁺-activated phosphatase calcineurin [26]. We have identified that calcineurin binds directly to the cytoplasmic domain of syndecan-4 though its autoinhibitory domain, a domain regulating calcineurin activity, and that this binding is elevated in WT mice after AB [13]. We here confirmed that calcineurin binds to syndecan-4 in cardiomyocytes. That level of binding was comparable in sham- and AB-treated mice could be due to the relatively high syndecan-4 levels in Sdc4-Tg mice, however, this also implies that the binding itself is not sufficient for calcineurin activation by syndecan-4. We have previously identified that the Ca²⁺-binding co-activator calmodulin (CaM) is localized to the syndecan-4-calcineurin complex in mouse hearts [13], suggesting that the syndecan-4-mediated calcineurin activation is Ca²⁺-dependent. We here found increased diastolic levels of Ca²⁺ in cardiomyocytes from Sdc4-Tg hearts. Ca²⁺ binds to calmodulin, resulting in calmodulin modifying its interactions with target proteins, e.g., calcineurin. Calcineurin avoids activation by cardiac cycle beat-to-beat Ca²⁺ oscillations, but is activated by cytosolic levels elevated beyond a threshold, typically found in heart failure [36]. Thus, we believe that elevated Ca²⁺ levels found in cardiomyocytes with high syndecan-4 levels, likely through calmodulin binding, is a probable mechanism for NFAT activation, both through syndecan-4-bound and non-syndecan-4-bound calcineurin.

Although care should be taken when interpreting these results, the increased Ca²⁺ levels in Sdc4-Tg cardiomyocytes could be a result of direct effects of syndecan-4 on cardiomyocyte Ca²⁺ channels. Syndecan-4 has been linked to regulation of cellular Ca²⁺ levels through transient receptor potential channels (TRPCs) [37]. Although we found no differences in expression of Trpc 1, 3 and 6 in Sdc4-Tg hearts, more detailed studies are needed to elucidate whether syndecan-4 regulates Ca²⁺ fluxes through these or other ion channels in cardiomyocytes, and thereby, cardiomyocyte calcineurin-NFAT activation.

Since we and others have established that syndecan-4 is important for fibroblast function, formation of focal adhesions, fibrosis and immune cell infiltration [7–9, 21, 29], we could not rule out from studies of full-body Sdc4-KO mice that cardiomyocyte effects were not secondary to fibroblast-mediated changes or inflammation. Syndecan-4 is located to focal adhesions in fibroblasts, linking the cytoskeleton to the ECM [7, 8, 29, 38], and regulates cardiac myofibroblast transdifferentiation and production of ECM constituents, including collagens, and collagen cross-linking [19, 20]. Syndecan-4 also regulates infiltration of immune cells to the heart [21, 23, 39]. Our results from cardiomyocyte-specific syndecan-4 overexpression suggest that syndecan-4-mediated fibrosis is a direct effect of increased levels in fibroblasts, and that immune cell infiltration likely is not directed by increased levels in cardiomyocytes.

In conclusion, we here developed mice with cardiomyocyte-specific overexpression of the transmembrane heparan sulphate proteoglycan syndecan-4, and identified that syndecan-4 is important for activation of Ca²⁺-dependent calcineurin-NFAT signalling, hypertrophic remodelling and dysfunction in cardiomyocytes in response to pressure overload. These findings extend our understanding of the important role that syndecan-4 plays in the failing heart.

Methods

Ethics

Animal protocols were reviewed and approved by the Norwegian National Animal Research Committee (protocol IDs 4216, 8617 and IV 1-17U) and conformed to the NIH Guide for the Care and Use of Laboratory Animals (NIH publication no. 85-23, revised 2011). Reporting of procedures and results was in accordance with the Animal Research: Reporting of In Vivo Experiments (ARRIVE) guidelines [40].

Mouse lines

A DNA fragment encoding the entire open reading frame of mouse Sdc4 cDNA (NP_035651) was inserted into a pBluescript plasmid vector downstream of the mouse Myh6 promoter, and upstream of the SV40 splice acceptor site and polyadenylation signal sequence. Correct Sdc4 insert was confirmed by sequencing, and expression in HEK293 cells was confirmed after transferal to a pCMV-SPORT6.1 backbone (Addgene, MA), with transfection using Lipofectamine2000 (Invitrogen, UK). Embryo injection of the Myh6-Sdc4 construct was performed at the Karolinska Institutet Mouse Models (KIMM) facility, Karolinska Institutet, Stockholm, Sweden, yielding two transgenic mice confirmed by genotyping. Upon breeding with C57BL/6JBomTac (Taconic, Skensved, Denmark), a C57BL/6J mouse line with stable, germline transmission of the Sdc4-Tg allele was established. Heterozygous Sdc4-Tg and WT littermates from F2 generation and onwards were used for experiments. Genotyping was performed at weaning age with DNA isolated from ear biopsies, amplifying a 110 bp SV40 fragment by polymerase chain reaction (PCR) to identify Sdc4-Tg mice (primers: F1_5′- CAGTGGTGGAATGCCTTTAATGA-3′, R1_5′- AGGAGTAGAATGTTGAGAGTCAGCAGTA-3′), and a 200 bp control fragment in the Fabpi gene present in all mice (primers: F2_5′-TGGACAGGACTGGACCTCTGCTTTCTTAGA– 3′, R2_5′-TAGAGCTTTGCCACATCACAGGTCATTCAG-3′). To confirm specific syndecan-4 expression in the heart, LV, RV, atria, intestine, spleen, skeletal muscle (gastrocnemius muscle), lung, liver, brain and kidney were harvested from male mice. NFAT-luciferase (NFAT-luc) reporter mice (FVB/N) [27] were kindly provided by Professor Jeffery D. Molkentin (Cincinnati Children’s Hospital Medical Center, Cincinnati, OH). These mice carry nine copies of NFAT-binding sites from the IL-4 promoter upstream of the luciferase reporter gene. Homozygous NFAT-luc mice were crossed with heterozygous Sdc4-Tg mice to generate heterozygous Sdc4-Tg-NFAT-luc mice and NFAT-luc littermate controls on mixed background. Male mice were used.

Aortic banding

Banding of the ascending aorta of 6–8 week old male Sdc4-Tg, WT, Sdc4-Tg-NFAT-luc and NFAT-luc mice was performed by an experienced researcher blinded to genotype, as described [21, 41, 42]. Sham-operation consisted of the same procedure without tightening of the suture. During surgery, mice were intubated and ventilated with a mixture of 98% oxygen and 2% isoflurane. Animals received post-operative analgesia by subcutaneous injection of 0.02 ml buprenorphine (0.3 mg/ml).

Cardiac phenotyping

Echocardiography of mice breathing 1.75% isoflurane on a mask was performed using the VEVO 2100 system (VisualSonics, Toronto, Canada) by an experienced researcher blinded to genotype, as described [21, 23, 42]. Sdc4-Tg and WT mice were examined by echocardiography at baseline (6–8 weeks of age) and during aging (30 and 60 weeks of age). Echocardiography with Doppler flow 24 h after AB was used to include mice with a maximal flow velocity over the stenosis (Vmax) of 3.5–4.5 m/s. Sdc4-Tg and WT mice were followed with serial echocardiography at 2, 6, 12 and 20 weeks post-AB. LVPWd, IVSd, LVIDd and systole (LVIDs) were obtained from M-mode recordings. LV mass and FS were calculated from M-mode images: 1.05*(IVSd + LVPWd + LVIDd)³ −  (LVIDd³), and 100*((LVIDd-LVIDs)/LVIDd), respectively. Left atrial diameter (LAD) was measured in atrial diastole. Tissue Doppler echocardiography was used to obtain maximal systolic and diastolic tissue velocities, and Doppler flow echocardiography was used to examine peak mitral velocity, mitral deceleration, peak RV outlet tract (RVOT) velocity. Cardiac output (CO) in LV outlet tract (LVOT) was calculated from heart rate, LVOT velocity time integral (VTI) and LVOT diameter.

MRI was performed using a 9.4T preclinical MR system (Agilent Technologies Inc., CA) in a randomly selected subset of Sdc4-Tg and WT 20 weeks after sham or AB, by an experienced researcher blinded to genotype, as described [43, 44]. Mice were sedated and mask ventilated 1.0–1.5% isoflurane, and body temperature was maintained by heated air guided by continuous body temperature recoding. Apical-to-basal LV short-axis slices (7–10 slices of thickness 1.0 mm) were acquired, and LV mass calculated as the sum of LV wall thicknesses from all slices *1.05, from slices obtained both in systole and diastole. End-diastolic volume (EDV) and end-systolic volume (ESV) were calculated as the sum of lumen diameter from all slices, from slices obtained in diastole and systole, respectively. Ejection fraction (EF) was calculated by the following formula: (100*(EDV − ESV)/EDV).

Mice were sacrificed by cervical dislocation under deep anaesthesia. Tissues were rapidly excised, rinsed in 1X phosphate-buffered saline (PBS) and blotted dry, snap-frozen in liquid nitrogen and stored at -70 °C. Atria, RV and LV were rapidly dissected and snap-frozen for molecular analyses. No tissue was prepared for histology. LVW, RV weight (RVW) and LW were normalized to body weight (BW).

Left ventricular NFAT-luciferase activity

Frozen, whole LVs from Sdc4-Tg-NFAT-luc and NFAT-luc mice were homogenized twice at 30 Hz for 100 s using 5 mm stainless steel beads and the TissueLyser II (Qiagen), according to the Luciferase Assay System protocol (Promega, WI). Samples were kept on ice, vortexed and centrifuged at 12 000×g for 30 s. Luminescence from was quantified on the Hidex Sense Microplate Reader (Finland).

Ca²⁺ transients in isolated adult ventricular cardiomyocytes

Cardiomyocytes from adult male Sdc4-Tg and WT mice were isolated as described [45]. Mice were anaesthetized in 4% isoflurane, 65% N₂O and 31% O₂, and intubated and ventilated with 2% isoflurane, 66% N₂O and 32% O₂. The heart was excised and immediately cooled in buffer A (Hepes 25 mM, NaCl 130 mM, KCl 5.4 mM, NaH₂PO₄ 0.4 mM, MgCl₂ 0.5 mM, D-glucose 22 mM, pH 7.4) at 4 °C. Cardiomyocytes were isolated by direct needle perfusion of the LV for 20–25 min with buffer A containing collagenase II (Worthington Biochemical Corporation, US). Following sedimentation of cardiomyocytes, the cells were washed twice in buffer A containing (1) 0.1% bovine serum albumin (BSA) and 0.1 mmol/L CaCl₂, and (2) 0.1% BSA and 0.2 mmol/L CaCl₂.

Cells were loaded with 5 uM Fluo 4-AM for 30 min, before superfused with a solution containing (in mmol/L): NaCl 140, Hepes 5, KCl 5.4, CaCl₂ 1, MgCl₂ 0.5, D-glucose 5.5 and NaH₂PO₄ 0.4. pH, adjusted to 7.4 with NaOH. All experiments were performed at room temperature. Cytosolic and nuclear Ca²⁺ transients were obtained simultaneously in field-stimulated cells at 0.5 and 2 Hz using a line scan on a confocal microscope. Cardiomyocytes were scanned every 1.5 ms by an LSM 7 Live scanning system (Zeiss, Germany), with a 512 pixel line drawn along the longitudinal axis of the cell, including the nucleus and cytosol, as previously described [46]. All settings, including gain, were kept stable between experiments. Ca²⁺ transients were analysed in ImageJ (NIH, MD), and the rate constant was calculated from tau values obtained using Clampfit 10.4 monoexponential fitting of the Ca²⁺ extrusion phase (Axon instruments, Union City, CA).

HEK293 cell cultures and transfection

HEK 293 cells were cultured and transfected using Lipofectamine 2000 (Invitrogen) with human influenza hemagglutinin (HA)-tagged mouse Sdc4 (NP_035651; HA-Sdc4) in a pcDNA3.1 plasmid (Invitrogen; custom made by Genscript Corporation, NJ), as described [13, 21, 23]. Transfection with empty pcDNA3.1 plasmid (vehicle) and non-transfected cells served as controls. HEK293 cells were harvested 24 h after transfection, and samples stored at − 70 °C. Cell protein lysates and medium were used as positive controls and for antibody validation by immunoblotting. Conditioned medium from transfected HEK293 cells was also used to treat cultured cardiomyocytes from neonatal rats to study effects of shed syndecan-4 fragments. The conditioned medium was cleared by centrifugation at 5000×g.

Neonatal cardiomyocyte cultures

Ventricular cardiomyocyte cultures were prepared from hearts of neonatal (1–3 days old) Wistar rats (Taconic), as described [21, 23, 47]. Hearts were trimmed of atrial tissue and digested mechanically in a collagenase/pancreatin solution, and transferred to uncoated culture flasks with serum-containing medium for 20 min, allowing fibroblasts to attach. Unattached cells, i.e., cardiomyocytes, were transferred to 6-well dishes coated with gelatin/fibronectin at a density of 3.75 × 10⁵/ml medium. Cells were kept in a 37 °C, 5% CO₂ humidified incubator. The purity of similar cultures has been confirmed by an 800-fold higher expression of cardiac troponin I (TnnI) in cardiomyocytes compared to fibroblasts [21]. Cells from three separate cell culture isolations were used.

NCM were transduced with a human adenovirus type 5 encoding mouse Sdc4 under control of the CMV promoter (Ad-mSDC4, ADV-271493) or empty vector control (Ad-CMV-Null, #1300), both from Vector Biolabs, for 48 h, with serum deprivation during the final 24 h, as described [42]. Virus titer was 5 × 10⁶ plaque forming units (PFU)/ml medium. Cells were co-treated with the calcineurin inhibitor Cyclosporine A (CsA). Cells were harvested and mRNA and protein stored at − 70 °C.

In a separate set of experiments, following 24 h of serum deprivation, NCM were treated for 24 h with 2 ml conditioned medium (diluted 2:1 in fresh medium) from HA-Sdc4 or vehicle-expressing HEK293 cells, containing shed syndecan-4 ectodomains or control, respectively, as described [23]. A limitation to these experiments is that the glycosylation of syndecan-4 may differ between human embryonic kidney and NCM. Cardiomyocytes were harvested and mRNA stored at − 70 °C.

Neonatal cardiomyocyte protein synthesis assay

The radioactive [³H] leucine incorporation protein synthesis assay was performed as described [42, 48]. NCM were virally transduced in serum-containing medium for 24 h prior to culturing in serum-deprived medium containing 1.25 µCi/ml [³H] leucine (American Radiolabel Chemicals, MO) for 72 h. At harvest, cardiomyocytes were washed in 95% ethanol and lysed in 0.2 M NaOH. Lysates were diluted in Pico-Fluor 40 (PerkinElmer) and [³H] leucine incorporation quantified as counts per minute (CPM) using the Wallac Winspectral 1414 liquid scintillation counter (PerkinElmer, MA). Samples were measured in duplicates, and serum was used as positive control.

RNA isolation and quantitative real-time PCR

RNA was extracted from frozen LV tissue or cultured cardiomyocytes using the RNeasy Mini Kit (Qiagen). Reverse transcription of 2 μg RNA was performed using the iScript cDNA Synthesis Kit (BIO-RAD). Pre-designed TaqMan assays (Applied Biosystems, CA) were used to determine gene expression (Table SIII). Results were detected on a 7900HT Fast Real Time PCR System, and data analysed using Sequence Detection Software 2.3 (Applied Biosystems).

Protein isolation, immunoprecipitation and immunoblotting

Protein lysates were prepared from frozen LV tissue or cultured cardiomyocytes with ice cold 1X PBS-based lysis buffer (1% Triton X-100 (Sigma, MI), 0.1% Tween-20 (Sigma), protease (Complete EDTA-free tablets) and phosphatase inhibitors (PhosSTOP; both from Roche Diagnostics, Germany). Tissue samples were homogenized twice at 30 Hz for 100 s using 5 mm stainless steel beads and the TissueLyser II, left on ice for 30 min and centrifuged at 20 000×g for 10 min at 4 °C.

Analysis of syndecan-4 protein after precipitation of proteoglycans and GAG digestion was performed as described [21, 23, 30]. Proteoglycans were precipitated from 100 μg LV protein lysates or 40 μg cell protein lysates in methanol overnight at − 20 °C, and the pellet was resuspended in heparitinase buffer with haparitinase I–III and chondroitinase cABC (Amsbio, UK). Samples were incubated twice for 2 h at 37 °C, with addition of second and third aliquots of enzymes.

Immunoprecipitation from LV protein lysates was performed using Dynabeads, according to protocol (14311D, Thermo Fischer Scientific), using 7 μg of a syndecan-4 antibody (BD550351, BD Biosciences) detecting an extracellular epitope (see Fig. S1) or rat IgG (sc-2026, Santa Cruz Biotechnology) as negative control. Immunoprecipitates were analysed by immunoblotting.

SDS-PAGE and blotting was performed according to the Criterion protocol (BIO-RAD), as described [13, 48]. Blots were blocked in 8% dry-milk (BIO-RAD), 5% BSA (BIO-RAD) or 1% casein (Roche Diagnostics) and incubated with antibodies diluted in 2% dry-milk/5% BSA/1% casein. Blots were developed using ECL Plus Western Blotting Detection System (GE Healthcare, UK) in the Las-4000 mini (Fujifilm, Japan), stripped (Restore Western Blot Stripping Buffer, Thermo Scientific) and reprobed. Quantification and processing were performed using Image J (NIH) and Adobe Photoshop CC 2019. Primary antibodies used are found in Table SIII. Syndecan-4 antibodies were validated in cell lysates and medium from HEK293 cells overexpressing syndecan-4 (Fig. S1). A custom made antibody recognizing the cytoplasmic epitope of syndecan-4 [13, 21, 23] was used to detect FL syndecan-4 and the transmembrane plus cytoplasmic part of syndecan-4 (10–15 kDa) remaining in cells after shedding of its ectodomain, the latter used to estimate shedding in cell or LV lysates. HRP-conjugated secondary antibodies (Southern Biotechnology, AL) were applied to all blots.

Statistics

Data are expressed as group means ± standard error of the mean (SEM). Graphs were made and statistical differences tested in GraphPad Prism 9, with p < 0.05 was considered significant. The specific statistical tests used are described in the figure legends.

Supplementary Information

Below is the link to the electronic supplementary material.

Abbreviations

AB

Aortic banding

AS

Aortic stenosis

ARRIVE

Animal research: reporting of in vivo experiments

ANP

Atrial natriuretic peptide

BW

Body weight

BSA

Bovine serum albumin

BNP

Brain natriuretic peptide

CO

Cardiac output

CF

Cellular fragment

CPM

Counts per minute

CsA

Cyclosporine A

EF

Ejection fraction

EDV

End-diastolic volume

ESV

End-systolic volume

ECM

Extracellular matrix

FS

Fractional shortening

FL

Full-length

GAG

Glycosaminoglycan

HA

Hemagglutinin

HW

Heart weight

HS

Heparan sulphate

HEK

Human embryonic kidney

IVS

Interventricular septal thickness

KO

Knock-out

LAD

Left atrial diameter

LV

Left ventricle

LVID

Left ventricular internal diameter

LVOT

Left ventricular outflow tract

LVPW

Left ventricular posterior wall thickness

LVW

Left ventricular weight

LW

Lung weight

luc

luciferase

MRI

Magnetic resonance imaging

MHC

Myosin heavy chain

NCM

Neonatal cardiomyocyte

NFAT

Nuclear factor of activated T-cell

PBS

Phosphate-buffered saline

PCR

Polymerase chain reaction

RCAN

Regulator of calcineurin

RV

Right ventricle

RVOT

Right ventricular outflow tract

SV

Simian virus

SE

Shed ectodomain

VTI

Velocity time integral

Author contributions

All authors contributed to the study conception and design. Material preparation, data collection and analysis were performed by IGL, JMA, AOM, MES, JS, BAB, MSA and IS. The first draft of the manuscript was written by IGL and all authors commented on the manuscript. All authors read and approved the final manuscript.

Funding

Open access funding provided by University of Oslo (incl Oslo University Hospital). This work was supported by the Research Council of Norway, Anders Jahre’s Fund for the Promotion of Science, the South-Eastern Regional Health Authority, the Kristian Gerhard Jebsen Foundation, and the Olav Raagholt and Gerd Meidel Raagholt`s Fund for Science, Norway.

Declarations

Conflict of interest

The authors have no relevant financial or non-financial interests to disclose.