Ventura Elisa, Weller Michael, Burghardt Isabel
Laboratory of Molecular Neuro-Oncology, Department of Neurology, University Hospital Zurich and University of Zurich, Zurich 8091, Switzerland.
Laboratory of Molecular Neuro-Oncology, Department of Neurology, University Hospital Zurich and University of Zurich, Zurich 8091, Switzerland
J Immunol. 2017 Jun 15;198(12):4569-4574. doi: 10.4049/jimmunol.1601176. Epub 2017 May 8.
Glioblastoma is the most common and aggressive intrinsic brain tumor in adults. Self-renewing, highly tumorigenic glioma-initiating cells (GIC) have been linked to glioma invasive properties, immunomodulation, and increased angiogenesis, leading to resistance to therapy. TGF-β signaling has been associated with the tumorigenic activity of GIC. TGF-β is synthesized as a precursor molecule and proteolytically processed to the mature form by members of the family of the proprotein convertases subtilisin/kexin. In this study we report that furin is unique among the proprotein convertases subtilisin/kexin in being highly expressed in human GIC. Furin cleaves and promotes activation of pro-TGF-β1 and pro-TGF-β2, and TGF-β2 in turn increases furin levels. Notably, TGF-β2 controls furin activity in an ALK-5-dependent manner involving the ERK/MAPK pathway. We thus uncover a role of ERK1 in the regulation of furin activity by supporting a self-sustaining loop for high TGF-β activity in GIC.
胶质母细胞瘤是成人中最常见且侵袭性最强的原发性脑肿瘤。具有自我更新能力、高度致瘤性的胶质瘤起始细胞(GIC)与胶质瘤的侵袭特性、免疫调节及血管生成增加有关,从而导致对治疗产生抗性。转化生长因子-β(TGF-β)信号传导与GIC的致瘤活性相关。TGF-β作为前体分子合成,并由枯草杆菌蛋白酶/克新蛋白原转化酶家族成员进行蛋白水解加工成成熟形式。在本研究中,我们报告弗林蛋白酶在枯草杆菌蛋白酶/克新蛋白原转化酶中是独特的,它在人GIC中高表达。弗林蛋白酶切割并促进前TGF-β1和前TGF-β2的激活,而TGF-β2反过来又增加弗林蛋白酶水平。值得注意的是,TGF-β2以依赖ALK-5的方式控制弗林蛋白酶活性,涉及ERK/MAPK途径。因此,我们揭示了ERK1通过支持GIC中高TGF-β活性的自我维持环在调节弗林蛋白酶活性中的作用。