Immunoregulation Section, Laboratory of Molecular Biology and Immunology, National Institute on Aging, Baltimore, MD 21224, USA.
J Immunol. 2013 Mar 15;190(6):2575-84. doi: 10.4049/jimmunol.1201920. Epub 2013 Feb 13.
Breast cancer cells facilitate distant metastasis through the induction of immunosuppressive regulatory B cells, designated tBregs. We report in this study that, to do this, breast cancer cells produce metabolites of the 5-lipoxygenase pathway such as leukotriene B4 to activate the peroxisome proliferator-activated receptor α (PPARα) in B cells. Inactivation of leukotriene B4 signaling or genetic deficiency of PPARα in B cells blocks the generation of tBregs and thereby abrogates lung metastasis in mice with established breast cancer. Thus, in addition to eliciting fatty acid oxidation and metabolic signals, PPARα initiates programs required for differentiation of tBregs. We propose that PPARα in B cells and/or tumor 5-lipoxygenase pathways represents new targets for pharmacological control of tBreg-mediated cancer escape.
乳腺癌细胞通过诱导免疫抑制性调节 B 细胞(称为 tBregs)促进远处转移。在本研究中我们报告,为了做到这一点,乳腺癌细胞产生 5-脂氧合酶途径的代谢产物,如白三烯 B4,以激活 B 细胞中的过氧化物酶体增殖物激活受体 α(PPARα)。白三烯 B4 信号的失活或 B 细胞中 PPARα 的基因缺失会阻止 tBregs 的产生,从而阻断已建立乳腺癌小鼠的肺转移。因此,除了引发脂肪酸氧化和代谢信号外,PPARα 还启动了 tBreg 分化所需的程序。我们提出,B 细胞中的 PPARα 和/或肿瘤 5-脂氧合酶途径代表了用于药物控制 tBreg 介导的癌症逃逸的新靶点。