Department of Anatomy, University of Kiel, D-24098 Kiel, Germany.
Biol Chem. 2011 Mar;392(3):199-207. doi: 10.1515/BC.2010.119.
Seprase or fibroblast activation protein-α (FAP-α) is a cell-surface serine protease that was previously described nearly exclusively on reactive and tumor stromal fibroblasts and thought to be involved in tissue remodeling. We investigated the expression and significance of FAP-α in astrocytomas/glioblastomas. As shown by quantitative reverse transcription polymerase chain reaction (RT-PCR) and immunohistochemistry, FAP-α was elevated in whole glioblastoma tissues and in particular in most glioma cells in situ and in vitro. In glioma stem-like cells (gliospheres), FAP-α was detected at low levels; however, FAP-α was considerably induced upon differentiation with 10% fetal calf serum. To explore its functional role, FAP-α was silenced by siRNA transfection. In Boyden chamber assays, FAP-α silenced cells migrated similar as control cells through non-coated or Matrigel (basal lamina)-coated porous membranes, but significantly slower through membranes coated with gelatin or brevican, a major component of brain extracellular matrix. Furthermore, FAP-α-silenced glioma cells migrated through murine brain slices much slower under the conditions tested than differentially fluorescent-labeled control cells. Thus, FAP-α is highly expressed on the surface of glioma cells and contributes to diffuse glioma invasion through extracellular matrix components.
Seprase 或成纤维细胞激活蛋白-α(FAP-α)是一种细胞表面丝氨酸蛋白酶,以前主要在反应性和肿瘤基质成纤维细胞上描述,被认为参与组织重塑。我们研究了 FAP-α在星形细胞瘤/胶质母细胞瘤中的表达和意义。定量逆转录聚合酶链反应(RT-PCR)和免疫组织化学显示,FAP-α在整个胶质母细胞瘤组织中升高,特别是在原位和体外的大多数胶质瘤细胞中升高。在神经胶质瘤干细胞(神经球)中,FAP-α的水平较低;然而,在 10%胎牛血清分化时,FAP-α被显著诱导。为了探索其功能作用,我们通过 siRNA 转染沉默了 FAP-α。在 Boyden 室测定中,与对照细胞相比,FAP-α 沉默细胞通过未涂层或 Matrigel(基底膜)涂层的多孔膜迁移相似,但通过涂层有明胶或 brevician(大脑细胞外基质的主要成分)的膜迁移明显较慢。此外,在测试条件下,与荧光差异标记的对照细胞相比,FAP-α 沉默的神经胶质瘤细胞通过鼠脑切片的迁移速度要慢得多。因此,FAP-α在胶质瘤细胞表面高度表达,并通过细胞外基质成分促进弥漫性胶质瘤浸润。