Graduate Institute of Basic Medical Science, China Medical University, Taichung, Taiwan.
J Cell Physiol. 2012 Jan;227(1):259-68. doi: 10.1002/jcp.22728.
The IGF-II/mannose 6-phosphate receptor (IGF-IIR/Man-6-P) up-regulation correlates with heart disease progression and its signaling cascades directly trigger pathological cardiac hypertrophy, fibrosis, and cardiomyocytes apoptosis. IGF-IIR gene expression/ suppression is able to prevent myocardial remodeling. However, the regulating mechanisms for the IGF-IIR gene remain unclear. This study performed reverse transcriptase PCR (RT-PCR) and methylation-specific PCR (MS-PCR) to detect expression and DNA methylation of CpG islands within the IGF-IIR genomic DNA region. Our finding revealed that the IGF-IIR gene was up-regulated both in H9c2 cells treated with tumor necrosis factor-alpha (TNF-α), lipopolysaccharide (LPS), angiotensin II (ANGII) and inomycin, and age-dependently in spontaneously hypertensive rat (SHR) heart. For the DNA methylation study, although there were four CpG islands within IGF-IIR genomic regions, the DNA methylation distribution showed no change either in cells treated with ANGII or in the SHR heart. Using chemical inhibitors to individually block histone acetyltransferase (HAT) and histone deacetylase (HDAC) activity, we found that histone acetylation was essential for ANGII-induced IGF-IIR gene expression using RT-PCR and luciferase assay. The Chromatin immuno-precipitation assay indicated that acetyl-Histone H3 and acetyl-Histone H4 associated with the IGF-IIR promoter increased in the presence of ANGII, otherwise methyl-CpG binding domain protein 2 (MeCP2) is disassociated with this. Taken together, this study demonstrates that histone acetylation plays a critical role in IGF-IIR up-regulation during pathological cardiac diseases and might provide a targeting gene in transcriptional therapies for the failing heart.
IGF-II/mannose 6-phosphate 受体(IGF-IIR/Man-6-P)的上调与心脏病进展相关,其信号级联直接触发病理性心肌肥大、纤维化和心肌细胞凋亡。IGF-IIR 基因表达/抑制能够预防心肌重构。然而,IGF-IIR 基因的调节机制尚不清楚。本研究通过逆转录 PCR(RT-PCR)和甲基化特异性 PCR(MS-PCR)检测 IGF-IIR 基因组 DNA 区域内 CpG 岛的表达和 DNA 甲基化。我们的发现表明,在 TNF-α、脂多糖(LPS)、血管紧张素 II(ANGII)和肌苷霉素处理的 H9c2 细胞以及自发性高血压大鼠(SHR)心脏中,IGF-IIR 基因均上调。对于 DNA 甲基化研究,尽管 IGF-IIR 基因组区域内有四个 CpG 岛,但在 ANGII 处理的细胞或 SHR 心脏中,DNA 甲基化分布没有变化。使用化学抑制剂分别阻断组蛋白乙酰转移酶(HAT)和组蛋白去乙酰化酶(HDAC)的活性,我们发现 RT-PCR 和荧光素酶测定表明,组蛋白乙酰化对于 ANGII 诱导的 IGF-IIR 基因表达是必需的。染色质免疫沉淀分析表明,在存在 ANGII 的情况下,与 IGF-IIR 启动子结合的乙酰化组蛋白 H3 和乙酰化组蛋白 H4 增加,否则甲基化 CpG 结合域蛋白 2(MeCP2)与此分离。总之,这项研究表明,组蛋白乙酰化在病理性心脏疾病中 IGF-IIR 上调中起关键作用,并且可能为衰竭心脏的转录治疗提供靶向基因。