Lunardi Andrea, Gaboli Mirella, Giorgio Marco, Rivi Roberta, Bygrave Anne, Antoniou Michael, Drabek Dubravka, Dzierzak Elaine, Fagioli Marta, Salmena Leonardo, Botto Marina, Cordon-Cardo Carlos, Luzzatto Lucio, Pelicci Pier Giuseppe, Grosveld Frank, Pandolfi Pier Paolo
Cancer Genetics Program, Beth Israel Deaconess Cancer Center, Department of Medicine and Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
Genes Cancer. 2011 Jan;2(1):10-9. doi: 10.1177/1947601911402682.
The promyelocytic leukemia gene (PML) of acute promyelocytic leukemia is an established tumor suppressor gene with critical functions in growth suppression, induction of apoptosis, and cellular senescence. Interestingly, although less studied, PML seems to play a key role also in immune response to viral infection. Herein, we report that Pml(-/-) mice spontaneously develop an atypical invasive and lethal granulomatous lesion known as botryomycosis (BTM). In Pml(-/-) mice, BTM is the result of impaired function of macrophages, whereby they fail to become activated and are thus unable to clear pathogenic microorganisms. Accordingly, Pml(-/-) mice are resistant to lipopolysaccharide (LPS)-induced septic shock as a result of an ineffective production of cytokines and chemokines, suggesting a role for PML in the innate immune Toll-like receptor (TLR)/NF-κB prosurvival pathway. These results not only shed light on a new fundamental function of PML in innate immunity, but they also point to a proto-oncogenic role for PML in certain cellular and pathological contexts.
急性早幼粒细胞白血病的早幼粒细胞白血病基因(PML)是一种公认的肿瘤抑制基因,在生长抑制、诱导细胞凋亡和细胞衰老方面具有关键作用。有趣的是,尽管研究较少,但PML似乎在对病毒感染的免疫反应中也起着关键作用。在此,我们报告Pml(-/-)小鼠会自发发展出一种非典型的侵袭性致死性肉芽肿病变,称为葡萄球菌病(BTM)。在Pml(-/-)小鼠中,BTM是巨噬细胞功能受损的结果,即巨噬细胞无法被激活,因此无法清除致病微生物。相应地,由于细胞因子和趋化因子产生无效,Pml(-/-)小鼠对脂多糖(LPS)诱导的脓毒症休克具有抗性,这表明PML在先天性免疫Toll样受体(TLR)/NF-κB促生存途径中发挥作用。这些结果不仅揭示了PML在先天性免疫中的一项新的基本功能,还指出了PML在某些细胞和病理背景下的原癌基因作用。