Translational Research Laboratory, Catalan Institute of Oncology-IDIBELL, L'Hospitalet de Llobregat, Spain.
Thromb Haemost. 2011 May;105(5):873-82. doi: 10.1160/TH10-10-0630. Epub 2011 Mar 8.
The GAS6/ProS-TAM system is composed of two vitamin K-dependent ligands (GAS6 and protein S) and their three protein tyrosine kinase receptors TYRO3, AXL and MERTK, known as the TAM receptors. The system plays a prominent role in conditions of injury, inflammation and repair. In murine models of atherosclerotic plaque formation, mutations in its components affect atherosclerosis severity. Here we used Taqman low-density arrays and immunoblotting to study mRNA and protein expression of GAS6, ProS and the TAM receptors in human carotid arteries with different degrees of atherosclerosis. The results show a clear down-regulation of the expression of AXL in atheroma plaques with respect to normal carotids that is matched by decreased abundance of AXL in protein extracts detected by immunoblotting. A similar decrease was observed in PROS1 mRNA expression in atherosclerotic carotids compared to the normal ones, but in this case protein S (ProS) was clearly increased in protein extracts of carotid arteries with increasing grade of atherosclerosis, suggesting that ProS is carried into the plaque. MERTK was also increased in atherosclerotic carotid arteries with respect to the normal ones, suggesting that the ProS-MERTK axis is functional in advanced human atherosclerotic plaques. MERTK was expressed in macrophages, frequently in association with ProS, while ProS was abundant also in the necrotic core. Our data suggest that the ProS-MERTK ligand-receptor pair was active in advanced stages of atherosclerosis, while AXL signalling is probably down-regulated.
GAS6/ProS-TAM 系统由两种维生素 K 依赖性配体(GAS6 和蛋白 S)及其三个蛋白酪氨酸激酶受体 TYRO3、AXL 和 MERTK 组成,称为 TAM 受体。该系统在损伤、炎症和修复等情况下发挥重要作用。在动脉粥样硬化斑块形成的小鼠模型中,其成分的突变会影响动脉粥样硬化的严重程度。在这里,我们使用 Taqman 低密度基因芯片和免疫印迹技术研究了不同程度动脉粥样硬化的人颈动脉中 GAS6、ProS 和 TAM 受体的 mRNA 和蛋白表达。结果表明,与正常颈动脉相比,在动脉粥样硬化斑块中 AXL 的表达明显下调,这与免疫印迹检测到的 AXL 蛋白提取物丰度降低相匹配。与正常颈动脉相比,PROS1 mRNA 在动脉粥样硬化颈动脉中的表达也明显下降,但在这种情况下,随着动脉粥样硬化程度的增加,蛋白 S(ProS)在颈动脉蛋白提取物中明显增加,表明 ProS 被带入斑块。MERTK 在动脉粥样硬化颈动脉中也高于正常颈动脉,表明 ProS-MERTK 轴在人类晚期动脉粥样硬化斑块中具有功能。MERTK 在巨噬细胞中表达,常与 ProS 相关,而 ProS 在坏死核心中也很丰富。我们的数据表明,在动脉粥样硬化的晚期阶段,ProS-MERTK 配体-受体对是活跃的,而 AXL 信号可能被下调。