Institute of Biology III at the Faculty of Biology, Albert-Ludwigs-University of Freiburg, Schänzlestr. 1, 79104 Freiburg, Germany.
Institute for Clinical Chemistry and Pathobiochemistry, Klinikum Rechts der Isar, School of Medicine, Technical University Munich, Ismaningerstr. 22, 81675 Munich, Germany; TranslaTUM, Center for Translational Cancer Research, Technical University Munich, Einsteinstr.25, 81675 Munich, Germany.
Curr Opin Immunol. 2021 Aug;71:69-74. doi: 10.1016/j.coi.2021.05.011. Epub 2021 Jun 23.
BAFF is an essential cytokine primarily known for its role in maintaining B cell homeostasis via induction of a pro-survival gene expression profile. Additionally, recent evidence suggests that BAFF induced signaling also drives a metabolic program that is needed for homeostatic cell mass maintenance in resting B cells and which increases the cells' capacity to divide. Many components of the signaling cascades initiated by BAFF, the alternative NFκB pathway and the PI3K/AKT/mTOR pathway, are active in roles beyond their classically assigned function. These components can directly or indirectly impact metabolic reprogramming. Further exploration of the role BAFF signaling plays in B cell metabolism could help to identify metabolic vulnerabilities of hyperactive B cells in the context of autoimmunity.
BAFF 是一种重要的细胞因子,主要通过诱导抗生存基因表达谱来维持 B 细胞的内稳态。此外,最近的证据表明,BAFF 诱导的信号也驱动了一个代谢程序,该程序对于静息 B 细胞中维持细胞质量的内稳态是必需的,并且增加了细胞分裂的能力。BAFF 启动的信号级联的许多成分、替代 NFκB 途径和 PI3K/AKT/mTOR 途径,在其经典功能之外的作用中是活跃的。这些成分可以直接或间接地影响代谢重编程。进一步探索 BAFF 信号在 B 细胞代谢中的作用,可以帮助识别自身免疫中过度活跃的 B 细胞的代谢脆弱性。