Cardiac fibroblast‐specific p38α MAP kinase promotes cardiac hypertrophy via a putative paracrine interleukin‐6 signaling mechanism

Figure 1. Inducible fibroblast-specific deletion of p38α in mouse heart. A) Schematic diagram of the deletion strategy, combining Col1a2-Cre-ER(T) mice with floxed Mapk14 mice. Deletion of exons 2–3 occurs after tamoxifen injection, which activates Cre-ER(T). Red arrowheads denote position of genotyping primers X, Y, and Z (see Materials and Methods). B) Genotyping PCR showing effective exon 2/3 deletion in ear notch samples from tamoxifen-injected, experimental Cre-positive Mapk14fl/fl mice (E1–2) compared with control Cre-negative Mapk14fl/fl mice (C1–3). Top: Cre primers (Cre = 408 bp). Bottom: Mapk14 exon 2/3 floxed/deletion primers. Deletion (Z + Y) = 411 bp; floxed (X + Y) = 188 bp; and M = 100-bp ladder. C) Real-time RT-PCR analysis of Mapk14 mRNA levels in primary cultures of cardiac fibroblasts from control (Ctrl) Cre-negative Mapk14fl/fl mice (n = 6) and Cre-positive Mapk14fl/fl KO mice (n = 8) after tamoxifen injection. *P < 0.05. D) Immunoblot analysis of p38α protein in primary cultures of cardiac fibroblasts from control Cre-positive Mapk14wt/wt (C), heterozygous Cre-positive Mapk14wt/fl (Het), and experimental Cre-positive Mapk14fl/fl mice (E1–4) after tamoxifen injection.…

Figure 2. Effect of fibroblast-specific p38α KO on ISO-induced cardiac dysfunction. A) Timeline for chronic β-adrenergic receptor activation model of cardiac hypertrophy. B) Individual representative PV loops obtained from control and fibroblast-specific p38α KO mice following infusion with either saline (control, blue) or ISO (red). C) PV conductance catheter data. Individual data and means ± sem are shown. Group sizes: control saline (n = 9), control ISO (n = 8), KO saline (n = 7), and KO ISO (n = 8). EDV, end diastolic volume; CO, cardiac output; SV, stroke volume. ANOVA with Sĭdák post hoc test: *P < 0.05, ***P < 0.001. NS, not significant.

Figure 3. Effect of fibroblast-specific p38α KO on isoproterenol-induced cardiac hypertrophy. Control or Fb-p38α KO mice were injected with tamoxifen and mini-osmotic pumps implanted for delivery of saline or ISO as in Fig. 2A. Pumps were removed and heart tissue collected 1 wk later. A) Ventricular weight/tibia length ratio (cardiac weight index) from animals used in PV analysis. Group sizes: control saline (n = 9), control ISO (n = 8), KO saline (n = 7), and KO ISO (n = 8). B) Real-time RT-PCR analysis of cardiac mRNA levels for cardiomyocyte hypertrophy markers atrial natriuretic factor (Nppa) and β-myosin heavy chain (Myh7) and fibrosis markers Col1a1 and Col3a1. Group sizes: control saline (n = 11), control ISO (n = 9), KO saline (n = 8), and KO ISO (n = 11). C) Representative images of WGA-labeled heart sections used to determine myocyte cross-sectional area. D) Mean cardiomyocyte size (cross-sectional area) determined from WGA-stained images. Group sizes: control saline (n = 8), control ISO (n = 7), and KO ISO (n = 8). E) Representative images of WGA-labeled heart sections used to determine areas of interstitial fibrosis. F) Mean interstitial fibrotic area determined from…

Figure 4. Effect of fibroblast-specific p38α KO on isoproterenol-induced miRNA expression. Control or Fb-p38α KO mice were injected with tamoxifen and infused with saline or ISO as described in Figs. 2A and 3 legend. Heart tissue was collected 1 wk after removal of miniosmotic pumps and expression levels of 84 cardiovascular miRNAs determined using a real-time RT-PCR array. Group sizes: n = 4. See Supplemental Table 1 for full data set. A) miRNAs (miR) increased or decreased following ISO infusion. *P < 0.05, **P < 0.01 for effect of ISO (unpaired Student’s t test). B) miRNAs modulated by fibroblast-specific p38α KO. *P < 0.05, **P < 0.01, ***P < 0.001 (ANOVA with Šidák post hoc test). NS, not significant, compared with control saline group. #P < 0.05, compared with control ISO group. Data expressed relative to array-normalization controls.

Figure 5. Effects of isoproterenol and cardiac DAMPs on p38α activation and expression of hypertrophy-inducing factors in cultured cardiac fibroblasts. A) Western blotting of phosphorylated (activated) p38α and total p38α expression showing time of response to 5 μM ISO, concentration response to 0.1–10 μM ISO after 15 min, and time of response to cardiac DAMPs. Blots are representative of 3 separate experiments. B) Real-time RT-PCR data showing effect of ISO (5 μM, 6 h, n = 8) or cardiac DAMPs (6 h, n = 12) on mRNA expression of Fgf2, Il6, Tgfb1 and Igf1. Data expressed as percentage Gapdh mRNA levels. **P < 0.01, ***P < 0.001. NS, not significant (paired-ratio Student’s t test).

Figure 6. Role of p38α in DAMPs-modulated expression of hypertrophy-inducing genes in cardiac fibroblasts. A) Real-time RT-PCR showing time of effect of DAMPs on mRNA expression of Il6, Tgfb1, and Igf1. *P < 0.05, **P < 0.01 (n = 3). B) ELISA showing time of IL-6 secretion from cardiac fibroblasts stimulated with cardiac DAMPs. Red filled circles represent DAMP-stimulated IL-6 secretion, and black-filled squares represent basal secretion without addition of DAMPs (measured up to 6 h only). *P < 0.05 compared with time 0 (n = 3). C) Real-time RT-PCR data showing effect of 10 μM SB203580 or DMSO vehicle control on DAMP-induced expression of hypertrophy-inducing genes after 6 h (n = 9). *P < 0.05, **P < 0.01, ***P < 0.001 (ANOVA with Šidák post hoc test). NS, not significant. Data normalized to Gapdh mRNA levels and expressed relative to the control. D) ELISA showing effect of 10 μM SB203580 or DMSO vehicle control on DAMP-induced IL-6 secretion after 6 h (n = 9). ANOVA with Sĭdák post hoc test. *P < 0.05; NS, not significant. E) Western blot showing DAMP-induced phosphorylation (p-) of HSP27 and p38α after 20 min and inhibition by 10 μM SB203580. Total p38α expression was included as the…