TLR4 deficiency significantly attenuated the increase in heart weight/body weight ratio (10.0% vs 33.9%) and cell size (11.8% vs 68.4%) following aortic banding compared to wild-type mice.
Does TLR4 deficiency reduce cardiac hypertrophy following pressure overload in mice?
TLR4 is a novel receptor contributing to the development of cardiac hypertrophy in vivo, involving both TLR4-mediated and PI3K/Akt/mTOR signaling pathways.
Absolute Event Rate: 10% vs 33.9%
OBJECTIVE: We have previously demonstrated that nuclear factor kappa B (NFkappaB) activation is needed for the development of cardiac hypertrophy in vivo. NFkappaB is a downstream transcription factor in the Toll-like receptor (TLR)-mediated signaling pathway; therefore, we investigated a role of TLR4 in cardiac hypertrophy in vivo. METHODS: TLR4-deficient mice (C.C3H-Tlr4(lps-d), n = 6), wild-type (WT) genetic background mice (BALB/c, n = 6), TLR4-deleted strain (C57BL/10ScCr, n = 8), and WT controls (C57BL/10ScSn, n = 8) were subjected to aortic banding for 2 weeks. Age-matched surgically operated mice served as controls. In a separate experiment, rapamycin (2 mg/kg, daily) was administered to TLR4-deficient mice and WT mice immediately following aortic banding. The ratio of heart weight/body weight (HW/BW) was calculated, and cardiac myocyte size was examined by FITC-labeled wheat germ agglutinin staining of membranes. NFkappaB binding activity and the levels of phospho-p70S6K in the myocardium were also examined. RESULTS: Aortic banding significantly increased the ratio of HW/BW by 33.9% (0.601 +/- 0.026 vs. 0.449 +/- 0.004) and cell size by 68.4% in WT mice and by 10.00% (0.543 +/- 0.011 vs. 0.495 +/- 0.005) and by 11.8% in TLR4-deficient mice, respectively, compared with respective sham controls. NFkappaB binding activity and phospho-p70S6K levels were increased by 182.6% and 115.2% in aortic-banded WT mice and by 78.0% and 162.0% in aortic-banded TLR4-deficient mice compared with respective sham controls. In rapamycin-treated aortic-banded mice, the ratio of HW/BW was increased by 18.0% in WT mice and by 3.5% in TLR4-deficient mice compared with respective sham controls. CONCLUSION: Our results demonstrate that TLR4 is a novel receptor contributing to the development of cardiac hypertrophy in vivo and that both the TLR4-mediated pathway and PI3K/Akt/mTOR signaling are involved in the development of cardiac hypertrophy in vivo.
Ha et al. (Tue,) conducted a other in Cardiac hypertrophy (n=28). TLR4 deficiency (and rapamycin) vs. Wild-type mice and sham controls was evaluated on Ratio of heart weight/body weight (HW/BW) increase. TLR4 deficiency significantly attenuated the increase in heart weight/body weight ratio (10.0% vs 33.9%) and cell size (11.8% vs 68.4%) following aortic banding compared to wild-type mice.
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