Department of Biochemistry, Showa University School of Medicine, Shinagawa-ku, Tokyo, Japan.
J Atheroscler Thromb. 2012;19(7):601-7. doi: 10.5551/jat.10736. Epub 2012 May 4.
Hydrogen peroxide-inducible clone-5 (Hic-5) is a focal adhesion scaffold protein primarily expressed in vascular and visceral smooth muscle cells. We recently generated mice lacking Hic-5, which grew with no apparent abnormality (Kim-Kaneyama J, et al. J Mol Cell Cardiol. 2011;50(1):77-86). However, we discovered that recovery of arterial media following vascular injury is delayed significantly in Hic-5 knockout mice consequent to enhanced apoptosis of cultured vascular smooth muscle cells after mechanical stress; thus, Hic-5 is regarded as a novel factor in vascular remodeling. The Hic-5 gene is also induced by transforming growth factor-β, a well-known accelerator in fibrosis. Hic-5 involvement in various fibrotic disorders, e.g., scar formation, keloid formation and glomerulosclerosis, has been proposed. siRNA silencing of Hic-5 in a breast cancer cell line reduces its invasiveness; moreover, Hic-5 serves as a steroid hormone co-activator and likely participates in endometriosis and prostate cancer. Thus, functional characterization of Hic-5 in various pathophysiological conditions may afford novel mechanistic insights into a wide variety of diseases.
过氧化氢诱导克隆-5(Hic-5)是一种主要在血管和内脏平滑肌细胞中表达的黏着斑支架蛋白。我们最近生成了缺乏 Hic-5 的小鼠,这些小鼠生长时没有明显的异常(Kim-Kaneyama J,等人。J Mol Cell Cardiol。2011;50(1):77-86)。然而,我们发现,在 Hic-5 基因敲除小鼠中,血管损伤后动脉中膜的恢复明显延迟,这是由于机械应激后培养的血管平滑肌细胞凋亡增强所致;因此,Hic-5 被认为是血管重构的一个新的因素。Hic-5 基因也被转化生长因子-β诱导,转化生长因子-β是纤维化的一个众所周知的促进因子。已经提出 Hic-5 参与各种纤维性疾病,例如瘢痕形成、瘢痕疙瘩形成和肾小球硬化症。在乳腺癌细胞系中用 siRNA 沉默 Hic-5 可降低其侵袭性;此外,Hic-5 作为甾体激素共激活因子,可能参与子宫内膜异位症和前列腺癌。因此,在各种病理生理条件下对 Hic-5 的功能进行特征分析可能为各种疾病提供新的机制见解。