Yamamoto Tomoko, Kato Yoichiro, Shibata Noriyuki, Sawada Tatsuo, Osawa Makiko, Kobayashi Makio
Department of Pathology, Tokyo Women's Medical University, Shinjuku-ku, Tokyo, Japan.
Int J Exp Pathol. 2008 Oct;89(5):332-41. doi: 10.1111/j.1365-2613.2008.00599.x.
Fukutin, a gene responsible for Fukuyama type congenital muscular dystrophy (FCMD), is presumably related to the glycosylation of alpha-dystroglycan (alpha-DG), involved in basement membrane formation. Hypoglycosylation of alpha-DG plays a key role for the pathogenesis of FCMD. On the other hand, fukutin and alpha-DG are also expressed in various non-neuromuscular tissues. Recently, a role of alpha-DG as a cancer suppressor has been proposed, because of a decrease of glycosylated alpha-DG in cancers. In this study, function of fukutin was investigated in two cancer cell lines, focusing on whether fukutin is involved in the glycosylation of alpha-DG in cancer cells and has any possible roles related to a cancer suppressor. Localization of fukutin and a result of laminin-binding assay after RNA interference suggest that fukutin may be involved in the glycosylation of alpha-DG in a small portion in these cancer cell lines. In Western blotting and immuno-electron microscopy, localization of fukutin in the nucleus was suggested in addition to the Golgi apparatus and/or endoplasmic reticulum. Immunohistochemically, there were more Ki-67-positive cells and more nuclear staining of phosphorylated c-jun after knockdown of fukutin in two cell lines. Fukutin appears to suppress cell proliferation through a system involving c-jun, although it is unclear this process is related to alpha-DG or not at present. The result may propose a possibility of another function of fukutin in addition to the glycosylation of alpha-DG in cancer cells.
福库亭是一种与福山型先天性肌营养不良症(FCMD)相关的基因,可能与α- dystroglycan(α-DG)的糖基化有关,α-DG参与基底膜的形成。α-DG的低糖基化在FCMD的发病机制中起关键作用。另一方面,福库亭和α-DG也在各种非神经肌肉组织中表达。最近,由于癌症中糖基化α-DG的减少,有人提出α-DG具有抑癌作用。在本研究中,我们在两种癌细胞系中研究了福库亭的功能,重点关注福库亭是否参与癌细胞中α-DG的糖基化以及是否具有与抑癌相关的任何可能作用。RNA干扰后福库亭的定位和层粘连蛋白结合试验结果表明,福库亭可能在这些癌细胞系的一小部分中参与α-DG的糖基化。在蛋白质印迹法和免疫电子显微镜检查中,除了高尔基体和/或内质网外,还提示福库亭在细胞核中定位。免疫组织化学显示,在两种细胞系中敲低福库亭后,Ki-67阳性细胞更多,磷酸化c-jun的核染色更多。福库亭似乎通过涉及c-jun的系统抑制细胞增殖,尽管目前尚不清楚该过程是否与α-DG有关。该结果可能提示福库亭在癌细胞中除了α-DG糖基化之外还有其他功能的可能性。