Sanford-Burnham-Prebys Medical Discovery Institute, Orlando, Florida, USA.
Department of Biochemistry and Molecular Biology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Immunity. 2018 Oct 16;49(4):615-626.e6. doi: 10.1016/j.immuni.2018.09.005.
Macrophages polarize into distinct phenotypes in response to complex environmental cues. We found that the nuclear receptor PPARγ drove robust phenotypic changes in macrophages upon repeated stimulation with interleukin (IL)-4. The functions of PPARγ on macrophage polarization in this setting were independent of ligand binding. Ligand-insensitive PPARγ bound DNA and recruited the coactivator P300 and the architectural protein RAD21. This established a permissive chromatin environment that conferred transcriptional memory by facilitating the binding of the transcriptional regulator STAT6 and RNA polymerase II, leading to robust production of enhancer and mRNAs upon IL-4 re-stimulation. Ligand-insensitive PPARγ binding controlled the expression of an extracellular matrix remodeling-related gene network in macrophages. Expression of these genes increased during muscle regeneration in a mouse model of injury, and this increase coincided with the detection of IL-4 and PPARγ in the affected tissue. Thus, a predominantly ligand-insensitive PPARγ:RXR cistrome regulates progressive and/or reinforcing macrophage polarization.
巨噬细胞在复杂的环境信号刺激下会极化成为不同的表型。我们发现,核受体 PPARγ 在反复受到白细胞介素(IL)-4 刺激时,会使巨噬细胞发生显著的表型变化。在这种情况下,PPARγ 对巨噬细胞极化的作用不依赖于配体结合。配体不敏感的 PPARγ 与 DNA 结合,并招募共激活因子 P300 和结构蛋白 RAD21。这建立了一个允许性染色质环境,通过促进转录调节因子 STAT6 和 RNA 聚合酶 II 的结合,为转录记忆提供条件,导致在 IL-4 再刺激时增强子和 mRNA 的大量产生。配体不敏感的 PPARγ 结合控制了巨噬细胞中细胞外基质重塑相关基因网络的表达。在损伤小鼠模型的肌肉再生过程中,这些基因的表达增加,并且这种增加与受影响组织中 IL-4 和 PPARγ 的检测同时发生。因此,主要是配体不敏感的 PPARγ:RXR 顺式作用元件调节进行性和/或强化的巨噬细胞极化。