靶向肺泡II型细胞脂质代谢蛋白FASN和GPAM可减少肺转移
Targeting the lipid metabolism proteins FASN and GPAM in alveolar type II cells decreases lung metastasis
作者信息Xiao-Zheng Liu, Yulia Panina, Weigang Cai, Juan Fernández-García, Yiming Peng-Winkler, Jiadong Mao, Alina Dahlhaus, Hui-Chao Zhou, Ming Liu, Melanie Planque, Johannes Ceuppens, Sebastian Igelmann, Xander Spotbeen, Jakub Idkowiak, Jonas Dehairs, Janine Theile, Konstantinos Axarlis, Kristien Borremans, Josephine Van Cauwenberge, Avinash Ghanate, Josep Tarragó-Celada, Alejandro Suárez-Bonnet, Richard Mitter, Vincen Wu, Paolo Inglese, James S McKenzie, Rory T Steven, Alex Dexter, Bin Yan, Jean-Luc Vorng, Zoltán Takáts, Josephine Bunch, Ian S Gilmore, Peter Carmeliet, Christine Desmedt, Ilaria Malanchi, Johannes V Swinnen, Patricia Altea-Manzano, Kim-Anh Lê Cao, Johannes Meiser, Mariia Yuneva, Sarah-Maria Fendt
在肺中定植的癌细胞通常需要肺泡Ⅱ型(AT2)细胞产生的脂质。然而,显性转移灶是否依赖AT2细胞来源的脂质,以及能否通过靶向AT2细胞来抑制转移瘤生长,目前尚不清楚。通过空间分析,我们发现小鼠和患者的乳腺癌肺转移灶会刺激其周围AT2细胞增殖,并将其重编程为脂质供给细胞。机制上,转移瘤分泌组激活AT2细胞中的转录因子甾醇调节元件结合转录因子1(SREBP-1),从而增强包括脂肪酸合酶(FASN)和甘油-3-磷酸酰基转移酶1(GPAM)在内的关键从头脂质合成基因的表达。特异性敲除AT2细胞中的Fasn或系统性靶向FASN与GPAM,能显著抑制小鼠肺转移瘤的生长。总之,我们发现显性转移灶可重编程AT2细胞,而靶向AT2细胞的脂质代谢可抑制转移瘤生长。