Decrease of Pdzrn3 is required for heart maturation and protects against heart failure

Figures

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  Figure 1. Physiological PDZRN3 expression around birth. Results of Pdzrn3 overexpression. (a) Representative Western blot demonstrates levels of PDZRN3 in the embryo at E11.5, 12.5 and 15.5 days; and after birth (0.5, 4, 7 and 14 days). αtubulin was used as the loading control. (b) Schematic of Pdzrn3 overexpression (OE) in the heart. Control mice were (MHC-tTA, Pdzrn3 OE mice were pTRE-Pdzrn3; αMHC-tTA. (c) Representative Western blot demonstrates levels of endogenous PDZRN as well as overexpression from 0.5 to 14 days and at 8 weeks after birth. αtubulin was used as the loading control. (d) The ratio is quantified and calibrated to the average of 0.5 d control mice. Data are expressed as mean ± s.e.m. (n = 6–13).

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  Figure 2. Myocardial reactivation of Pdzrn3 induces eccentric cardiac hypertrophy. (a) LVEF was quantified from 3 to 8 weeks of age (control, n = 4; Pdzrn3 OE, n = 7). (b) Kaplan–Meier curve showing survival rate of control and Pdzrn3 OE mice from birth until 40 weeks of age (control and Pdzrn3 OE groups, n = 9). (c) Representative images of hematoxylin and eosin (H&E) stained sections of control and Pdzrn3 OE hearts at 6 weeks, demonstrate that Pdzrn3 OE mice have enlarged hearts. (d) Increased LV internal cross section (control, n = 3; Pdzrn3 OE, n = 5). (e) Increased heart weight (HW) to body weight (BW) ratio (control, n = 5; Pdzrn3 OE, n = 5). (f) Increase of the mRNA levels of atrial (Nppa) and brain (Nppb) natriuretic peptide in Pdzrn3 OE versus control mice over time. mRNA levels were normalized to cyclophiline and are expressed as a relative expression/fold increase over levels found in control mice at 1 week (n = 3–7 mice per group). (g) In hearts from Pdzrn3 OE mice, quantification of total collagen deposition on picrosirius red staining revealing an increase in fibrosis and CD45 immunolabeling, and an increase of inflammatory cells at 6 and 4 weeks of age, respectively (n = 4…

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  Figure 3. Cardiac specific overexpression of Pdzrn3 impairs cardiomyocyte elongation. (a) The sphericity index was determined by measuring the area (A) and the circumference (P) of myocytes. The ratio of an “ideal” round cell is close to 1, whereas that of an elongated cell is closer to 0. Cardiomyocytes that were in the longitudinal plane were selected for quantification of the sphericity index. (b) Representative images of control and Pdzrn3 OE heart sections stained with wheat germ agglutinin (WGA)-FITC (scale bars represent 20 μm) at 3 W. Quantification of myocyte cross-sectional sphericity of control and Pdzrn3 OE heart sections. Data are represented as mean ± sem. Significance vs control **P < 0.01 by one way ANOVA plus bonferroni test (control vs. Pdzrn3 OE group, n = 4 at 2 weeks, n = 3 at 3 weeks and n = 5 at 4 weeks). (c) Representative electron micrographs showing morphological disorganization of cardiomyocytes of control and Pdzrn3 OE heart at 8 weeks of age (scale bars represent 1 μm). (d) Quantitative F-actin/G-actin ratios in heart lysates from 2-week-old mice were measured with actin polymerization in vivo assay kit. Western blot analysis of G-actin (G) and F-actin (F)…

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  Figure 4. Myocardial reactivation of Pdzrn3 alters postnatal cardiomyocyte maturation. (a) Electron micrographs of part of an intercalated disk between two cardiac of control and Pdzrn3 OE heart at 8 weeks of age (scale bars represent 2 μm) and in right part, schema of ID distribution. (b) Immunolabeling of Cx43, ZO1, β catenin and α actinin in hearts from control and Pdzrn3 OE mice at 2 weeks. Scale bars represent 10 μm. (c) Western blot analysis of indicated proteins in heart tissues retrieved from control and Pdzrn3 OE mice at 1 and 2 weeks (W) of age. Relative expression of Cx43, from Western blots. Significance vs. control *P < 0.05; ***P < 0.001 by unpaired t-test (at 1 week, n = 4 mice per group; at 2 weeks, n = 6 mice per group).

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  Figure 5. Altered subcellular distribution of junction proteins in cell–cell membrane under Pdzrn3 induced signaling. (a) Western blot analysis of indicated proteins in plasma membrane fraction only of heart tissues retrieved from control and Pdzrn3 OE mice at 2 Weeks of age. Relative expression of Dsg2, from Western blots. Significance vs. control *P < 0.05; 1 by unpaired t-test (n = 5 mice per group). (b) Representative confocal microscopy images of primary cardiomyocytes from control and Pdzrn3 OE neonates stained with antibodies against Dsg2, Cx43, WGA-Fitc and ZO1. (c) After immunostaining of HeLa cells depleted of Pdzrn3 (si Pdzrn3) or not (si control) for Dsg2 (green), fluorescence intensity profile curve were plotted. Data are represented as mean ± sem from three independent experiments. (d) Western blot analysis of indicated proteins in triton-X-100 soluble and insoluble fractions from HeLa depleted either of Pdzrn3 (si Pdzrn3) or flotillin-2 (si flotillin 2).

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  Figure 6. Postnatal time window for cardiac cell differentiation. (a, b) Schematic study timeline of doxycline treatment administration (Dox), tissue collection and echocardiography follow up. (c, e) Immunolabeling of Cx43 and ZO1 in hearts from control and Pdzrn3 OE mice following doxycycline treatment. Scale bars represent 50 μm. (d, f) LVEF quantification under doxycycline treatment in control and Pdzrn3 OE mice in d protocol, respectively n = 6 vs. 8; in h protocol, respectively n = 6 vs. 4 mice.

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  Figure 7. Depletion of Pdzrn3 protects against decompensated cardiac hypertrophy. (a) Schematic study plan showing timeline of tamoxifen administration (Tmx), Ang II pump implantation, echocardiography (Echo.) follow up and tissue collection. (b) Western blot reporting levels of PDZRN3 in the adult mice under sham condition (Veh) and after AngII treatment. αtubulin was used as the loading control. (c) PDZRN3 ratio is quantified in veh and AngII groups and calibrated to the average of veh mice. Data are expressed as mean ± SD. Significance vs. control **P < 0.001 by unpaired t-test (n = 4 in veh- and n = 6 in AngII treated-groups). (d) Schematic of Pdzrn3 deletion in cardiac cells. Control mice were Pdzrn3f/f. MCM-Pdzrn3 KO mice were MHC-MerCreMer; Pdzrn3f/f. (e) Representative Western blot demonstrates conditional depletion of Pdzrn3 in MCM-Pdzrn3f/f mice compared to Pdzrn3f/f control mice. αtubulin was used as the loading control. (f) The ratio is quantified and calibrated to the average of Pdzrn3f/f control mice. Data are expressed as mean ± s.d. Significance vs. control *P < 0.05 by unpaired t-test (n = 3 per group). (g) Ratio of heart weight (HW) to body weight (BW). (h) Quantification…