Background
Barth syndrome (BTHS) is a rare genetic disorder that affects multiple organs. The mutated gene causing BTHS is
(TAZ), which encodes a mitochondrial transacylase tafazzin, a key enzyme in the cardiolipin (CL) remodeling pathway. Mutations in the
TAZ result in CL deficiency, and increase the monolysocardiolipin (MLCL) to cardiolipin ratio (MLCL/CL) accompanied by structural and functional defects in mitochondria of affected individuals and
Taz knockdown (TazKD) mice [
1,
2]. This mitochondrial CL deficiency destabilizes the integrity and activity of electron transfer chain (ETC.) complexes [
3‐
5]. The human phenotype includes dilated cardiomyopathy, underdeveloped skeletal musculature, and intermittent neutropenia [
6]. Inactivation of
Taz with doxycycline-inducible (tet-on) shRNA-mediated gene silencing in mice results in the LV dilation and systolic dysfunction after 6 months of age [
1,
7]. In addition, previous studies also reported the embryonic lethality in TazKD mice when knockdown was initiated with doxycycline at high dose [
8].
Current therapies for BTHS are limited and have variable efficacy. These include antioxidants, a diet supplemented with specific amino acids, and granulocyte colony stimulating factor (GCSF) to treat neutropenia. Patients with BTHS may develop progressive heart failure and require mechanical circulatory support and cardiac transplantation [
9]. An acute decline in health from a stable status to a life-threatening crisis can occur with little warning so that patients and their families live in a constant state of anxiety. Developing effective therapies for BTHS continues to be a challenge, especially because of the limited number of patients, extraordinary phenotypic variability, and unpredictable clinical course [
9‐
11].
Energy limitation plays a major role in heart failure [
12]. The replenishment of energy supply in cardiac cells by metabolic therapy is an expanding opportunity in the treatment of heart failure. Due to a central role in energy metabolism and mitochondrial bioenergetics, peroxisome proliferator-activated receptors (PPARs) may be potential therapeutic targets for metabolic targeted therapy to ameliorate cardiac dysfunction induced by
Taz deficiency. Indeed, beneficial effects of activation of the PPAR/PGC1α axis have been demonstrated in various mitochondrial disorders. Pharmacological activation of PPARα facilitates post-ischemic functional recovery in hypertrophied neonatal rabbit hearts [
13] and slows down the progression of the left ventricular dysfunction in the porcine model of tachycardia-induced cardiomyopathy [
14]. In patients with metabolic syndrome, BF reduces the incidence of myocardial infarction and lowers cardiac mortality risk [
15]. Treatment with BF provided beneficial effects in patients with carnitine palmitoyltransferase-II (CPT-II) deficiency [
16], although other studies reported conflicting results [
17,
18]. Here, we report the results of experimental treatment with BF in a mouse model of BTHS, with an shRNA-mediated knockdown of
Taz expression (TazKD) that exhibits age-dependent cardiomyopathy [
1,
7].
Methods
Animals
All animal studies were approved by the Institutional Animal Care and Use Committee of Cincinnati Children’s Hospital Medical Center. Animals were housed in micro-isolator cages at 25
o C under a 14/10 h light/dark cycle with free access to drinking water and food. Doxycycline-inducible shRNA-mediated TazKD mice have been described previously [
1,
4,
7].
Taz knockdown was induced prior to conception by feeding females doxycycline-containing rodent chow (625 mg/kg) 3 days before mating. This approach allows 85–95% silencing of
Taz in heart and skeletal muscle [
1]. In the ensuing offspring, after 3 months of age, the doxycycline administration route was switched to drinking water (0.1% doxycycline, 10% sugar). Both WT and TazKD mice were continuously maintained on doxycycline-containing water for the duration of the study. Male mice with C57BL/6 background were used in experiments.
Micro-osmotic pumps (Alzet model 1002) were used to deliver controlled amounts (0.25 μL/h) of isoproterenol (Iso), a β-adrenergic agonist, to mice for 14 days. Pumps were loaded with a dose of Iso consistent with 30 mg/kg/day. All aseptic procedures were performed in a rodent surgical suite. Mice were anesthetized with 1.75% isoflurane. A small incision of approximately 3–5 mm was made at the nape of the neck. The pump was inserted and CV-22 biodegradable suture was used to close the wound. Then the mice were returned to their original cages for recovery.
At 3 months of age, mice were given specifically formulated pelleted rodent chow that contained either no or 0.5% bezafibrate (TestDiet, St. Louis, MO) provided at libitum for 2 or 4 months. At the same time, the doxycycline administration route was changed for all animals from rodent chow to drinking water with 0.1% of doxycycline and 10% sucrose since manufacturing and sterilizing the rodent chow that contained both bezafibrate and doxycycline was technically difficult.
Echocardiography
Two-dimensional and M-mode transthoracic echocardiography were performed under isoflurane anesthesia as previously described using a Vevo 2100 Micro-Imaging system (VisualSonics, Inc.) and a 40 MHz transducer [
1]. Off-line analyses were performed by investigators blinded to genotype.
Quantitative PCR
Quantitative PCR- based assay was used to determine mitochondrial DNA (mtDNA) copy numbers relative to the diploid chromosomal DNA content. Fragment of mtDNA was amplified using ACTATCCCCTTCCCCATTTG and GCTACCCCCAAGTTTAATGG primer pair. Fragment of chromosomal DNA was amplified with ACAAAGCAAAGGAGCTGGAG and TCATTGCCACTGCTGAGAAC primers. Taz expression was analyzed with quantitative RT-PCR using murine Taz-specific primers ATGCCCCTCCATGTGAAGTG and TGGTTGGAGACGGTGATAAGG. Results are expressed relative to β-actin mRNA content, that was determined using following primer set: AAGAGCTATGAGCTGCCTGA and ACGGATGTCAACGTCACACT. Quantitative PCR was performed using a Realplex Mastercycler (Eppendorf) and SYBR Green RT-PCR reagent (Bio-Rad). PCR conditions were 30 s at 95 °C, 30 s at 55 °C, and 30 s at 68 °C for 35 cycles.
Western blot analysis
Western immunoblot analyses were done by standard techniques using NuPAGE Novex Bis-Tris pre-cast gels (Life Technologies, Carlsbad, CA). Tissues were homogenized in ice-cold buffer composed of 0.1 M KH2PO4, 2 mM EDTA, 2% Triton X-100 and protease inhibitor cocktail (Roche, Basel, Switzerland). Homogenates were centrifuged at 12 000 × g at 4o C and protein concentrations in supernatants were determined with the BCA assay (BioRad, Hercules, CA). After electrophoresis, proteins were transferred to nitrocellulose membranes. Membranes were blocked with 5% BSA overnight. Protein levels of ETC. complexes were detected with a cocktail of mouse monoclonal antibodies specific to selected subunits of the complexes (Life Technologies). Custom-made antibodies specific to mitochondrial malate dehydrogenase (mMDH) were used for the loading control. Secondary IRDye antibodies were used for imaging (Licor Biosciences, Lincoln, NE). Membranes were scanned with an Odyssey CLx scanner. Band intensity analysis and data quantification were done with Image Studio software.
Cardiolipin analysis
Tissue homogenates were made in Milli-Q water in a Qiagen Tissuelyser II using stainless steel beads of 5 mm for two times 30 s at 30 rev/s. The protein concentration of the homogenates was determined with the BCA assay. Phospholipids were extracted using a single-phase extraction. An internal standard (CL(14:0)4 was added to all samples containing 1 mg of protein followed by 1.5 mL of chloroform/methanol (1:1, v/v). Subsequently, the mixtures were sonicated in the water bath for 5 min, followed by centrifugation at 16,000 × g for 5 min. The supernatants (organic layer) were then transferred to the glass vials and evaporated under a nitrogen stream at 45 °C. Subsequently, the residues were dissolved in 150 μL of chloroform/methanol (9:1, v/v), and 10 μL of the solution was injected into the HPLC-MS system.
The HPLC system consisted of an Ultimate 3000 binary (U) HPLC pump, a vacuum degasser, a column temperature controller, and an autosampler (Thermo Scientific, Waltham, MA, USA). The column temperature was maintained at 25 °C. The lipid extracts were injected onto a LiChrospher 2* 250-mm silica-60 column, 5 μm particle diameter (Merck, Darmstadt, Germany). The phospholipids were separated from interfering compounds by a linear gradient between solution B (chloroform/methanol, 97:3, v/v) and solution A (methanol/water, 85:15, v/v). Solutions A and B contained 5 and 0.2 ml of 25% (v/v) aqueous ammonia per liter of eluent, respectively. The gradient (0.3 ml/min) was as follows: 0–1 min 10%A, 1–4 min, 10%A–20%A, 4–12 min 20%A–85% A; 12–12.1 min, 85%A–100% A; 12.1–14.0 min, 100% A, 14–14.1 min, 100%A–10%A and 14.1–15 min, equilibration with 10% A. All gradient steps were linear, and the total analysis time, including the equilibration, was 15 min. A Q Exactive Plus MS (Thermo Scientific) was used in the negative and positive electrospray ionization mode. Nitrogen was used as the nebulizing gas. The source collision-induced dissociation collision energy was set at 0 V. The spray voltage was 2500 V, and the capillary temperature was 256 °C. In both negative and positive modes, mass spectra of phospholipid molecular species were obtained by continuous scanning from m/z 150 to m/z 2000 with a resolution of 280.000 (FMWH at m/z 200).
For bioinformatic analysis of the data, the raw HPLC/MS data were converted to an mzXML format using msConvert for the Negative Scan data and ReAdW for the Positive Scan data. The data set was processed using a semi-automated metabolomics pipeline written in the R programming language [
http://www.r-project.org]. In brief, it consisted of the following five steps: (1) pre-processing, (2) identification of metabolites, (3) isotope correction, (4) normalization and scaling and (5) statistical analysis, using the XCMS R package.
Isolation of mitochondria and analysis of ETC complex I-III activity
Cardiac mitochondria were isolated and enzymatic activities of complex I-III segment and citrate synthase were measured spectrophotometrically, as previously described [
4].
Statistical analysis
Statistical analysis, reported as means ± standard deviations, was performed with one-way ANOVA. Post-hoc analyses of echocardiographic indices were performed using the Mann-Whitney non-parametric test. For statistical comparison of cardiolipin content between the groups, one-way ANOVA with post-hoc Bonferroni correction was used. A probability value of 0.05 or lower was considered significant.
Discussion
In humans with mutations in energy metabolism genes, physiological stressors, such as fasting, cold exposure, exercise, or infections can rapidly induce life-threatening events in otherwise stable and asymptomatic patients [
20‐
22]. This is certainly the situation in BTHS. Similarly, mouse models of energy metabolism disorders often require additional physiological stressors, e.g. fasting, cold-exposure, β-adrenergic stimulation or a high-fat diet, to evoke a cardiac phenotype [
23‐
26]. Isoproterenol, a β-adrenergic agonist, acts as a specific pathological stressor to exacerbate cardiac phenotypes and has become a useful tool to study cardiac disorders in animal models [
27].
Cardiomyopathy in humans with BTHS may present earlier; prenatally or early postnatally. In mice, despite the same genotype, two distinct phenotypes have been reported. Prior reports of this model demonstrated that cardiomyopathy develops only in adult mice, when knockdown is induced with relatively low dose of doxycycline (25–80 mg/kg/daily) [
1,
7]. In contrast, fetal cardiac defects and embryonic or early postnatal lethality were observed when Taz knockdown was initiated
in utero with higher dose of doxycycline (~300 mg/kg/daily) [
8]. A plausible cause of distinct phenotypes of these two models with the same genotype is the dose of doxycycline. Seibler et al. showed that the dose of doxycycline influenced the speed with which the knockdown achieved a steady-state level [
8,
28].
In this study, we show that β-adrenergic stimulation resulted in LV systolic dysfunction in TazKD mice at 4.5 months of age, while in those not receiving a β-adrenergic challenge, the cardiac phenotype becomes apparent after 7 months of age. These results suggest that Taz deficiency in adult mice is better compensated than in humans and additional external stressors are necessary to elicit the cardiac phenotype.
Bezafibrate is a pan-activator of PPAR signaling and promotes transcriptional activation of genes involved in oxidative metabolism [
29]. BF activates PPAR-PGC1α signaling and mitochondrial biogenesis in brain, ameliorating Huntington’s disease, mitochondrial encephalopathy and tau pathology phenotypes in mice [
30‐
32]. BF improves substrate metabolism and reduces right ventricular hypertrophy in congestive heart failure model [
33]. Fibrates slow down the progression of the LV dysfunction in tachycardia-induced cardiomyopathy [
14]. Interestingly, overexpression of PGC1α induced mitochondrial biogenesis in the skeletal muscles of cytochrome c oxidase (complex IV) deficient mice. However, BF failed to induce mitochondrial biogenesis and even showed adverse effects on the skeletal muscles of mice with various mitochondrial myopathies [
34‐
36]. Published reports suggest that BF may evoke distinct responses in different tissues: BF rescues mitochondrial defects in liver, skin, spleen and heart inducing mitochondrial biogenesis in these tissues [
13,
16,
36]. However, BF has no beneficial effects, or even could be detrimental to glycolytic skeletal muscles [
17,
34,
37].
BF is commonly prescribed to patients with dyslipidemia and diabetes. In humans, BF is used at 10 mg/kg daily dose. At this dosage, BF is undetectable in plasma and reportedly ineffective for PPAR activation in rodents. The pharmacological effect on lipogenesis is achieved by transcriptional down-regulation of sterol regulatory element-binding protein 1c in liver tissue via a PPAR-independent mechanism. Low-dose BF (10 mg/kg/day) failed to have any significant impact on the expression of PPARα, PGC1α and fatty acid oxidation genes in the liver [
29]. In rodents, BF is commonly administered via a chow diet containing 0.5% of the drug that corresponds to 600–800 mg/kg/daily dose. This dose is approximately 60–80 times higher than the usual dose for humans for the treatment of dyslipidemia [
30,
31,
34‐
36,
38]. At dosage of 0.5%, BF is well tolerated by rodents. These observations prompted us to use BF in the same dosage.
BF effectively ameliorated cardiac phenotypes in Iso-treated TazKD mice. These experiments strongly suggest that the PPAR/PGC1α signaling system is a promising therapeutic target for cardiomyopathy in patients with BTHS. However, Iso evokes complex responses in cardiomyocytes at high dosage (100 mg/kg) and may be toxic to cells, promoting oxidative stress and apoptosis [
39]. We wanted to show that the observed therapeutic effect of BF on Iso-pretreated TazKD mice was not mediated by the protection of the heart from β-adrenergic stress. Thus, in the separate set of experiments, we administered BF to mice without Iso pretreatment. In this series, we administered BF for a prolonged period between 3 and 7 months of age. BF markedly improved contractile function in TazKD mice at 7 months of age, showing that therapeutic action of BF is not mediated by the protection of the heart from β-adrenergic stress.
Taz knockdown caused a significant increase of mtDNA content and showed a tendency of increased citrate synthase activity in cardiomyocytes. These observations are indicative of adaptive mitochondrial proliferation in TazKD cardiac muscle in response to energy deficiency and are consistent with previous observations [
1]. However, mitochondrial proliferation in hearts of untreated TazKD mice was accompanied by reduction of electron flow through CI-III segment of ETC. and diminished content of several subunits of ETC. complexes. These observations are consistent with previously reported proteomic studies on TazKD mice [
3]. BF further increased mitochondrial DNA content, citrate synthase activity, partially augmented electron flow through the CI-CIII segment of ETC. and demonstrated a tendency to increase expression of ETC. proteins in TazKD mice. Interestingly, an increase of the CI-III activity occurred despite the deterioration of CL content in the mitochondria. It is plausible that an increased turnover rates of individual subunits or chaperones of ETC. complexes I and III compensate for enzyme deficiency, even if CL is depleted in the mitochondria.
Although BF had no effect on
Taz expression, it caused notable changes in molecular speciation of cardiolipin. BF significantly reduced content of tetralinoleoyl CL and increased content of MLCLs in cardiac muscle. In WT group, BF increased content of minor CL species with (76:12) – (76:10) acyl groups corresponding to C19 odd chain polyunsaturated fatty acids (Fig.
3e). However, in TazKD group, there was an opposite shift towards to CL species with shorter and less-saturated side chains. The physiological significance of these shifts is unclear.
Acknowledgements
Not applicable.