Department of Dermatology, Peking University First Hospital, Research Center for Medical Mycology, Peking University, Beijing 100034, China.
Chin Med J (Engl). 2013 Jan;126(2):220-5.
Invasive aspergillosis (IA), which is mainly caused by Aspergillus fumigatus (A. fumigatus), is a major cause of morbidity and mortality in immunocompromised patients. Despite considerable progress in currently available antifungals the mortality still remains high in critically ill patients. U0126 which is a highly selective inhibitor of MEK1 and MEK2 in the RAF/MEK/ERK pathway in mammalian cells has been demonstrated to have an anti-proliferative role in cancer cells. The purpose of this study was to explore the role of U0126 on growth inhibition and activation of mitogen-activated protein kinases (MAPKs) in A. fumigatus.
Germination percentage and hyphae growth in A. fumigatus treated with U0126 were observed and compared with untreated controls. Western blotting analysis was used to detect changes in activation of SakA, MpkA and MpkB.
U0126 inhibited germination and hyphae growth in A. fumigatus and enhanced the phosphorylation of SakA and MpkA under oxidative stress. U0126 at 10 µmol/L did not block the activation of MpkB during nitrogen starvation stress.
U0126 shows promise as an antifungal candidate and the MAPK pathway may be a possible antifungal drug target for A. fumigatus.
侵袭性曲霉病(IA)主要由烟曲霉(A. fumigatus)引起,是免疫功能低下患者发病率和死亡率的主要原因。尽管目前可用的抗真菌药物有了相当大的进展,但重症患者的死亡率仍然很高。U0126 是哺乳动物细胞 RAF/MEK/ERK 通路中 MEK1 和 MEK2 的高度选择性抑制剂,已被证明在癌细胞中具有抗增殖作用。本研究旨在探讨 U0126 对烟曲霉生长抑制和丝裂原激活蛋白激酶(MAPKs)激活的作用。
观察并比较了 U0126 处理前后烟曲霉的发芽率和菌丝生长情况。采用 Western blot 分析检测 SakA、MpkA 和 MpkB 激活的变化。
U0126 抑制烟曲霉的发芽和菌丝生长,并在氧化应激下增强 SakA 和 MpkA 的磷酸化。在氮饥饿应激下,10µmol/L 的 U0126 并未阻断 MpkB 的激活。
U0126 有望成为一种抗真菌候选药物,MAPK 通路可能是烟曲霉抗真菌药物的潜在靶点。