Basque Julie, Martel Marc, Leduc Richard, Cantin André M
Pulmonary Research Unit, Faculty of Medicine and Health Sciences, Universite de Sherbrooke, Sherbrooke, Canada.
Can J Physiol Pharmacol. 2008 Sep;86(9):606-12. doi: 10.1139/y08-063.
Transforming growth factor-beta (TGFbeta) is synthesized as a precursor protein, pro-TGFbeta, that must be cleaved by a furin-like proteinase before it becomes biologically active. We hypothesized that alkalinization of the trans-Golgi network (TGN)/endosome system may suppress pro-TGFbeta processing and decrease TGFbeta secretion. This hypothesis was tested in human A549 alveolar epithelial and T98G glioblastoma cell lines and in C57BL/6 mice. Inhibition of furin-like activity with decanoyl-RVKR chloromethylketone suppressed pro-TGFbeta processing, thereby significantly reducing the levels of secreted TGFbeta. Brefeldin A, bafilomycin A1, ammonium chloride, and monensin also prevented pro-TGFbeta processing. The alkalinizing lysosomotropic drugs chloroquine, hydroxychloroquine, amodiaquine, and azithromycin had a similar effect on the overall production of mature bioactive TGFbeta. Reduced levels of secreted TGFbeta were also associated with a decrease in Smad2 signaling. Mice treated with chloroquine showed a decrease in bronchoalveolar lavage fluid TGFbeta. We conclude that alkalinizing lysosomotropic drugs inhibit pro-TGFbeta processing.
转化生长因子-β(TGFβ)以前体蛋白即前TGFβ的形式合成,在其具有生物活性之前必须被一种类弗林蛋白酶切割。我们推测,反式高尔基体网络(TGN)/内体系统的碱化可能会抑制前TGFβ的加工并减少TGFβ的分泌。该假设在人A549肺泡上皮细胞和T98G胶质母细胞瘤细胞系以及C57BL/6小鼠中进行了验证。用癸酰-RVKR氯甲基酮抑制类弗林蛋白酶活性可抑制前TGFβ的加工,从而显著降低分泌型TGFβ的水平。布雷菲德菌素A、巴弗洛霉素A1、氯化铵和莫能菌素也可阻止前TGFβ的加工。碱化溶酶体药物氯喹、羟氯喹、阿莫地喹和阿奇霉素对成熟生物活性TGFβ的总体产生具有类似作用。分泌型TGFβ水平的降低也与Smad2信号传导的减少有关。用氯喹处理的小鼠支气管肺泡灌洗液中的TGFβ减少。我们得出结论,碱化溶酶体药物可抑制前TGFβ的加工。