Research Paper Volume 2, Issue 1 pp 43—62

Local IGF-1 isoform protects cardiomyocytes from hypertrophic and oxidative stresses via SirT1 activity

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Figure 4. mIGF-1 prevents Ang II- and IGF-1-induced cell hypertrophy ([3H]-leucine incorporation) in HL-1 cardiomyocytes and in mouse neonatal primary cardiomyocytes. (A) HL-1 cardiomyocytes were transfected with the indicated plasmids, or treated with 20 ng/ml IGF-1 for 24 h, or exposed to Ang II (1 μM for 24 h). Untransfected cells were used as control (CTL). Together with Ang II, HL-1 cells were also incubated with 1μCi/ml of [3H]-labeled leucine (24 h). (B) Neonatal primary cardiomyocytes from wild type or mIGF-1 Tg mice were treated with SirT1 inhibitors (sirtinol, 100 μM; EX-527, 1 μM), or treated with 20 ng/ml IGF-1 for 24 h, or exposed to Ang II (1 μM for 24 h); concomitantly to Ang II addition, cells were incubated with 1mCi/ml of [3H]-labeled leucine (24 h). (A, B) [3H]-leucine incorporation values were normalized to total protein content and expressed as % of control. Results are means ± SE of 3 independent experiments (**,***p versus unstimulated control cells or untreated WT cardiomyocytes).