Inhibition of LXR controls the polarization of human inflammatory macrophages through upregulation of MAFB.
Arturo González de la AlejaCristina HerreroMónica Torres-TorresanoMaría Teresa SchiaffinoAlejandro Del CastilloBárbara AlonsoMiguel A VegaAmaya Puig-KrögerAntonio CastrilloÁngel L CorbiPublished in: Cellular and molecular life sciences : CMLS (2023)
Monocyte-derived macrophages contribute to pathogenesis in inflammatory diseases and their effector functions greatly depend on the prevailing extracellular milieu. Whereas M-CSF primes macrophages for acquisition of an anti-inflammatory profile, GM-CSF drives the generation of T cell-stimulatory and pro-inflammatory macrophages. Liver X Receptors (LXRα and LXRβ) are nuclear receptors that control cholesterol metabolism and regulate differentiation of tissue-resident macrophages. Macrophages from rheumatoid arthritis and other inflammatory pathologies exhibit an enriched LXR pathway, and recent reports have shown that LXR activation raises pro-inflammatory effects and impairs the acquisition of the anti-Inflammatory profile of M-CSF-dependent monocyte-derived macrophages (M-MØ). We now report that LXR inhibition prompts the acquisition of an anti-inflammatory gene and functional profile of macrophages generated within a pathological environment (synovial fluid from Rheumatoid Arthritis patients) as well as during the GM-CSF-dependent differentiation of human monocyte-derived macrophages (GM-MØ). Mechanistically, inhibition of LXR results in macrophages with higher expression of the v-Maf Avian Musculoaponeurotic Fibrosarcoma Oncogene Homolog B (MAFB) transcription factor, which governs the macrophage anti-inflammatory profile, as well as over-expression of MAFB-regulated genes. Indeed, gene silencing experiments on human macrophages evidenced that MAFB is required for the LXR inhibitor to enhance the anti-inflammatory nature of human macrophages. As a whole, our results demonstrate that LXR inhibition prompts the acquisition of an anti-inflammatory transcriptional and functional profile of human macrophages in a MAFB-dependent manner, and propose the use of LXR antagonists as potential therapeutic alternatives in macrophage re-programming strategies during inflammatory responses.
Keyphrases
- anti inflammatory
- endothelial cells
- rheumatoid arthritis
- transcription factor
- dendritic cells
- poor prognosis
- induced pluripotent stem cells
- oxidative stress
- pluripotent stem cells
- genome wide
- dna methylation
- cell proliferation
- binding protein
- peripheral blood
- signaling pathway
- quality improvement
- drug induced
- genome wide identification