Lallemand D, Manent J, Couvelard A, Watilliaux A, Siena M, Chareyre F, Lampin A, Niwa-Kawakita M, Kalamarides M, Giovannini M
INSERM, U674, Paris, France.
Oncogene. 2009 Feb 12;28(6):854-65. doi: 10.1038/onc.2008.427. Epub 2008 Nov 24.
The NF2 gene product, merlin/schwannomin, is a cytoskeleton organizer with unique growth-inhibiting activity in specific cell types. A narrow spectrum of tumors is associated with NF2 deficiency, mainly schwannomas and meningiomas, suggesting cell-specific mechanisms of growth control. We have investigated merlin function in mouse Schwann cells (SCs). We found that merlin regulates contact inhibition of proliferation by limiting the delivery of several growth factor receptors at the plasma membrane of primary SCs. Notably, upon cell-to-cell contact, merlin downregulates the membrane levels of ErbB2 and ErbB3, thus inhibiting the activity of the downstream mitogenic signaling pathways protein kinase B and mitogen-activated protein kinase. Consequently, loss of merlin activity is associated with elevated levels of ErbB receptors in primary SCs. We also observed accumulation of growth factor receptors such as ErbB2 and 3, insulin-like growth factor 1 receptor and platelet-derived growth factor receptor in peripheral nerves of Nf2-mutant mice and in human NF2 schwannomas, suggesting that this mechanism could play an important role in tumorigenesis.
神经纤维瘤病2型(NF2)基因产物默林/施万诺明是一种细胞骨架组织者,在特定细胞类型中具有独特的生长抑制活性。与NF2缺陷相关的肿瘤谱较窄,主要是神经鞘瘤和脑膜瘤,提示存在细胞特异性生长控制机制。我们研究了默林在小鼠雪旺细胞(SCs)中的功能。我们发现,默林通过限制几种生长因子受体向原代SCs质膜的转运来调节增殖的接触抑制。值得注意的是,细胞间接触时,默林会下调ErbB2和ErbB3的膜水平,从而抑制下游促有丝分裂信号通路蛋白激酶B和丝裂原活化蛋白激酶的活性。因此,默林活性的丧失与原代SCs中ErbB受体水平的升高有关。我们还在Nf2突变小鼠的外周神经和人类NF2神经鞘瘤中观察到生长因子受体如ErbB2和3、胰岛素样生长因子1受体和血小板衍生生长因子受体的积累,表明该机制可能在肿瘤发生中起重要作用。