Departments of Medicine, Surgery, and Cell Biology, Duke University Medical Center, Durham, NC 27710, USA.
Proc Natl Acad Sci U S A. 2010 May 18;107(20):9323-8. doi: 10.1073/pnas.0910712107. Epub 2010 May 3.
Regenerative medicine holds the promise of replacing damaged tissues largely by stem cell activation. Hedgehog signaling through the plasma membrane receptor Smoothened (Smo) is an important process for regulating stem cell proliferation. The development of Hedgehog-related therapies has been impeded by a lack of US Food and Drug Administration (FDA)-approved Smo agonists. Using a high-content screen with cells expressing Smo receptors and a beta-arrestin2-GFP reporter, we identified four FDA-approved drugs, halcinonide, fluticasone, clobetasol, and fluocinonide, as Smo agonists that activate Hedgehog signaling. These drugs demonstrated an ability to bind Smo, promote Smo internalization, activate Gli, and stimulate the proliferation of primary neuronal precursor cells alone and synergistically in the presence of Sonic Hedgehog protein. Halcinonide, fluticasone, clobetasol, and fluocinonide provide an unprecedented opportunity to develop unique clinical strategies to treat Hedgehog-dependent illnesses.
再生医学有望通过激活干细胞来替代受损组织。通过质膜受体 Smoothened(Smo)进行 Hedgehog 信号传导是调节干细胞增殖的重要过程。由于缺乏美国食品和药物管理局 (FDA) 批准的 Smo 激动剂,Hedgehog 相关疗法的发展受到了阻碍。我们使用表达 Smo 受体和β-arrestin2-GFP 报告基因的细胞进行高内涵筛选,鉴定出四种 FDA 批准的药物,即卤倍他索、氟替卡松、氯倍他索和氟轻松,它们是激活 Hedgehog 信号的 Smo 激动剂。这些药物具有结合 Smo、促进 Smo 内化、激活 Gli 和刺激原代神经元前体细胞增殖的能力,并且在存在 Sonic Hedgehog 蛋白时具有协同作用。卤倍他索、氟替卡松、氯倍他索和氟轻松为开发治疗 Hedgehog 依赖性疾病的独特临床策略提供了前所未有的机会。