Data supporting the angiotensin II activates MEL18 to deSUMOylate HSF2 for hypertension-related heart failure

In association with the published article “Inhibition of HSF2 SUMOylation via MEL18 upregulates IGF-IIR and leads to hypertension-induced cardiac hypertrophy” (Huang et al., 2017) [1], this data article contains information about deSUMOylation of HSF2 on lysine 82 on angiotensin II (ANG II) -induced cardiac hypertrophy, which is mediated by MEL18. Isolated adult human whole heart tissue showed MEL18-mediated HSF2-IGF-IIR pathway is upregulated in hypertension human heart, compared to health human heart.


a b s t r a c t
In association with the published article "Inhibition of HSF2 SUMOylation via MEL18 upregulates IGF-IIR and leads to hypertension-induced cardiac hypertrophy"   [1], this data article contains information about deSUMOylation of HSF2 on lysine 82 on angiotensin II (ANG II) -induced cardiac hypertrophy, which is mediated by MEL18. Isolated adult human whole heart tissue showed MEL18-mediated HSF2-IGF-IIR pathway is upregulated in hypertension human heart, compared to health human heart.  SUMOylation of HSF2 at K82 is analyzed by immunoprecipitation and immunoblotting, compared in myocytes expressing HSF2 that substitutes lysine to arginine at Lys 82. The Fig. 1 shows SUMOylation of HSF2 is observed in myocytes expressing wild-type HSF2, not HSF2 K82R . Fig. 2 shows that deSUMOylation of HSF2 by ANGII-mediated MEL18 activation leads to cardiac hypertrophy. Fig. 3 represents that angiotensin II receptor blockers (ARBs) alleviates the cardiac dysfunction in spontaneous hypertensive rats (SHRs). Fig. 4 shows that MEL18-mediated HSF2-IGF-IIR pathway is upregulated in hypertension human heart, compared to health human heart. Data source location

Taichung, Taiwan
Data accessibility Data is available with this article

Value of the data
The data provide information about SUMOylation of HSF2 at lysine 82 residues by SUMO-1 in cardiomyocyte can be deSUMOylated by ANG II-mediated MEL18 activation.
The data presents ANG II mediated MEL18 to deSUMOylate HSF2, leading to cardiac hypertrophy.
The data provide information about the deSUMOylation HSF2 by MEL18 for cardiac hypertrophy is significant in adult hypertensive human heart, compared to adult healthy human heart.

Data
Result of immunoblotting is presented which residue that SUMO-1 conjugating with HSF2 in NRVMs is shown in Fig. 1. Assessment of cardiomyocyte size by wheat germ agglutinin (WGA) fluorescence dye is shown in Fig. 2. Left ventricular fractional shortening (FS%), ejection fraction (EF%), left ventricular internal diameter end systole (LVIDs) and left ventricular mass (LV mass) of WKY and SHR are displayed in Fig. 3 and Table 1 [1]. Result of immunoblotting on adult whole heart tissue from isolated healthy and hypertension human subject is presented in Fig. 4. Spontaneously hypertensive rats (SHR) and normotensive control Wistar Kyoto rats (WKY) were used in our experiments [2]. The rats were housed at a constant temperature (22°C) on a 12-h light/ dark cycle with food and tap water. The animals were arranged into three groups: WKY rats, SHR rats, and SHR rats treated with irbesartan (SHR/ARB). Each group contained five female 12-weeks old NRVMs transfected with HSF2 WT and HSF2 K82R for 24 h, and then treated with 100 nM ANG II for 24 h. Cells were incubated with 5.0 μg/mL WGA for 10 min at 37°C, and then fixed with 4% paraformaldehyde for 15 min. Cells were washed with PBS for observation by fluorescent microscopy. B. NRVMs transfected with siRNA against MEL18 for 24 h, and then treated with 100 nM ANG II for 24 h. Cells were incubated with 5.0 μg/mL WGA for 10 min at 37°C, and then fixed with 4% paraformaldehyde for 15 min. Cells were washed with PBS for observation by fluorescent microscopy. *Po 0.05, **P o0.01 and ***Po 0.001 represent significant differences (n¼3). Data are presented as the mean 7 SD. All presented micrographs are representative of three sets of independent experiments. animals. The angiotensin II receptor blocker (ARB) drug irbesartan (40 mg/kg/d; Merck, Brazil) was placed in the drinking water.

Neonatal rat ventricular myocyte (NRVM) primary culture
NRVMs were prepared and cultured using a Neonatal Rat/Mouse Cardiomyocyte Isolation Kit (Cellutron Life Technology, Baltimore, MD). The hearts from 1-to 3-d-old Sprague Dawley rats were dissected and transferred to a sterile beaker. Each heart was digested in the beaker with stirring at 37°C for 12 min. The supernatant was then transferred to a new sterile tube and spun at 1,200 rpm for 1 min. The cell pellets were then resuspended in D3 buffer and preplated for 1 h by seeding on an uncoated plate at 37°C in a CO 2 incubator to select cardiac fibroblasts. The unattached cells were transferred to plates that were precoated with NS medium (supplemented with 10% fetal bovine serum). After overnight culture, the NS medium was replaced with serum-free NW medium. The cardiomyocyte cultures were ready for experiments 48 h after the initial plating. Fig. 3. The cardiac functions are evaluated by echocardiographic analysis. Consecutively administered the angiotensin II receptor blocker (ARB) irbesartan to 12-week-old spontaneously hypertensive rats (SHRs) for 6 weeks. The cardiac functions were evaluated by echocardiographic analysis. Heart function was rescued when the rats were administered the ARB. *Po 0.05 and **Po 0.01 represent significant differences (n¼ 5). Data are presented as the mean7 SD.

Expression plasmids and gene construction
Flag-HSF2 was a gift from Dr. Ying-Lei Miao (Department of Gastroenterology, the First Affiliated Hospital of Kunming Medical University, Yunnan, China). The Flag-HSF2 K82R was generated by the QuickChange II site-direct mutagenesis kit (Agilent Technologies, CA, USA) [1]. The siRNA against rat MEL-18 (SASI_Rn02_00213006, sequence start 208) were purchased from Sigma (St. Louis, MO, USA).

Western blot analysis and immunoprecipitation
For these analyses, 30 μg of the total lysates or 10 μg of the subcellular fractions was separated through 6-12% SDS-polyacrylamide gel electrophoresis, then transferred to a PVDF membrane (GE Healthcare, Amersham, UK). The membranes were blocked using 5% non-fat milk and blotted with specific antibodies overnight at 4°C. Then, the protein signals were measured using horseradish peroxidase-conjugated secondary antibodies (1:10,000, GE Healthcare, Amersham, UK) and the Immobilon Western Chemiluminescent HRP Substrate (Millipore, MA, USA). Densitometric analysis of the immunoblots was performed with the AlphaImager2200 digital imaging system (Digital Imaging System, CA, USA). The digital images were processed in Adobe Photoshop 7.0. Each blot was stripped using Restore Western Blot Stripping Buffer (Pierce, IO, USA) and incubated with other antibodies. The results were analyzed and quantified using Image J software (NIH, MD, USA).
Immunoprecipitation was performed from NRVM lysates using the PureProteome™ Protein G Magnetic Bead System (Millipore, MA, USA) according to the manufacturer's instructions [3]. First, 300 μg of the cell lysate was prepared. The lysate was then combined and allowed to interact with 2 μg of a specific primary antibody, and the mixture was incubated on a rotator at 4°C overnight.
Immunoprecipitated proteins were eluted from the magnetic beads at 95°C for 5 min and separated by SDS-PAGE. The proteins were transferred to a PVDF membrane and probed with specific antibodies. Fig. 4. The representative blot showed the MEL18-HSF2-IGF-IIR signaling pathway was significantly upregulated in adult human whole hypertensive heart tissue.

Assessment of cardiomyocyte size in vitro
Neonatal rat ventricular cardiac myocytes were grown on slides for 24 h. After 24 h attachments, cells were transfected with indicated siRNA or construct for 24 h, and then treated with ANG II for 24 h. Then, cells were fixed with 4% paraformaldehyde and stained for the WGA (5 μg/mL, Molecular Probe, CA, USA). Images were analyzed to determine cell surface area [4]. Cell images from at least ten randomly chosen fields (×40 objective) of 60 cardiomyocytes were measured in three separate experiments using NIH image software.

Statistical analysis
All experiments were performed at least 3 times. Statistical analysis was performed using GraphPad Prism5 statistical software (San Diego, CA). Statistical significance was set at P o 0.05. Multiple comparisons of the data were analyzed through ANOVA assays. Tukey's Honestly Significant Difference tests (Tukey HSD) for post hoc comparison were used with a significance level of 5%. All results were quantified using Image J (NIH, MA, USA) and processed using Adobe Photoshop.