Jamba Ariunbold, Kondo Shuji, Urushihara Maki, Nagai Takashi, Kim-Kaneyama Joo-Ri, Miyazaki Akira, Kagami Shoji
Department of Pediatrics, Institute of Health Bioscience, The University of Tokushima Graduate School, Tokushima, Japan.
Department of Biochemistry, Showa University School of Medicine, Tokyo, Japan.
PLoS One. 2015 Apr 2;10(4):e0122773. doi: 10.1371/journal.pone.0122773. eCollection 2015.
Hydrogen peroxide-inducible clone-5 (Hic-5) is a transforming growth factor (TGF)-β1-inducible focal adhesion protein. We previously demonstrated that Hic-5 was localized in mesangial cells and its expression was associated with glomerular cell proliferation and matrix expansion in human and rat glomerulonephritis (GN). In the present study, we first assessed the role of Hic-5 in mesangioproliferative GN by injecting Habu venom into heminephrectomized wild type (Hic-5+/+) and Hic-5-deficient (Hic-5-/-) mice. Hic-5+/+ GN mice exhibited glomerular cell proliferation on day 7. Surprisingly, glomerular cell number and Ki-67-positive cells in Hic-5-/- GN mice were significantly greater than those in Hic-5+/+ GN mice on day 7, although the number of glomerular apoptotic cells and the expression of growth factors (platelet-derived growth factor-BB and TGF-β1) and their receptors were similarly increased in both Hic-5+/+ and Hic-5-/- GN mice. In culture experiments, proliferation assays showed that platelet-derived growth factor-BB and TGF-β1 enhanced the proliferation of Hic-5-/- mesangial cells compared with Hic-5+/+ mesangial cells. In addition, mitogenic regulation by Hic-5 was associated with altered and coordinated expression of cell cycle-related proteins including cyclin D1 and p21. The present results suggest that Hic-5 might regulate mesangial cell proliferation in proliferative GN in mice. In conclusion, modulation of Hic-5 expression might have a potential to prevent mesangial cell proliferation in the acute mitogenic phase of glomerulonephritis.
过氧化氢诱导克隆-5(Hic-5)是一种转化生长因子(TGF)-β1诱导的粘着斑蛋白。我们先前证明Hic-5定位于系膜细胞,其表达与人类和大鼠肾小球肾炎(GN)中的肾小球细胞增殖和基质扩张有关。在本研究中,我们首先通过向半肾切除的野生型(Hic-5+/+)和Hic-5缺陷型(Hic-5-/-)小鼠注射哈布蛇毒来评估Hic-5在系膜增生性GN中的作用。Hic-5+/+ GN小鼠在第7天出现肾小球细胞增殖。令人惊讶的是,尽管在Hic-5+/+和Hic-5-/- GN小鼠中肾小球凋亡细胞数量以及生长因子(血小板衍生生长因子-BB和TGF-β1)及其受体的表达同样增加,但在第7天,Hic-5-/- GN小鼠中的肾小球细胞数量和Ki-67阳性细胞显著多于Hic-5+/+ GN小鼠。在培养实验中,增殖分析表明,与Hic-5+/+系膜细胞相比,血小板衍生生长因子-BB和TGF-β1增强了Hic-5-/-系膜细胞的增殖。此外,Hic-5的促有丝分裂调节与包括细胞周期蛋白D1和p21在内的细胞周期相关蛋白的表达改变和协调有关。目前的结果表明,Hic-5可能调节小鼠增殖性GN中的系膜细胞增殖。总之,调节Hic-5表达可能具有预防肾小球肾炎急性有丝分裂期系膜细胞增殖的潜力。