NFAT5-regulated macrophage polarization supports the proinflammatory function of macrophages and T Lymphocytes
| Autor: | Sonia Tejedor, Jose Aramburu, Maria Buxadé, Cristina López-Rodríguez, Mónica Tellechea |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2018 |
| Předmět: |
0301 basic medicine
Nfat5 protein Adipose tissue macrophages medicine.medical_treatment Immunology Macrophage polarization Biology Proinflammatory cytokine 03 medical and health sciences Carcinoma Lewis Lung Mice 0302 clinical medicine Th2 Cells medicine Transcription factors Immunology and Allergy Cytotoxic T cell Macrophage Animals Homeostasis Retnla protein Tissue homeostasis Inflammation Mice Knockout Arginase Macrophages Cell Differentiation Inflammation mediators Neoplasms Experimental Th1 Cells Cd8-Positive t-lymphocytes Interleukin-12 Cell biology Up-Regulation Mice Inbred C57BL 030104 developmental biology Cytokine 030220 oncology & carcinogenesis Interleukin 12 Intercellular Signaling Peptides and Proteins |
| Zdroj: | Recercat. Dipósit de la Recerca de Catalunya instname |
| Popis: | Macrophages are exquisite sensors of tissue homeostasis that can rapidly switch between pro- and anti-inflammatory or regulatory modes to respond to perturbations in their microenvironment. This functional plasticity involves a precise orchestration of gene expression patterns whose transcriptional regulators have not been fully characterized. We had previously identified the transcription factor NFAT5 as an activator of TLR-induced responses, and in this study we explore its contribution to macrophage functions in different polarization settings. We found that both in classically and alternatively polarized macrophages, NFAT5 enhanced functions associated with a proinflammatory profile such as bactericidal capacity and the ability to promote Th1 polarization over Th2 responses. In this regard, NFAT5 upregulated the Th1-stimulatory cytokine IL-12 in classically activated macrophages, whereas in alternatively polarized ones it enhanced the expression of the pro-Th1 mediators Fizz-1 and arginase 1, indicating that it could promote proinflammatory readiness by regulating independent genes in differently polarized macrophages. Finally, adoptive transfer assays in vivo revealed a reduced antitumor capacity in NFAT5-deficient macrophages against syngeneic Lewis lung carcinoma and ID8 ovarian carcinoma cells, a defect that in the ID8 model was associated with a reduced accumulation of effector CD8 T cells at the tumor site. Altogether, detailed analysis of the effect of NFAT5 in pro- and anti-inflammatory macrophages uncovered its ability to regulate distinct genes under both polarization modes and revealed its predominant role in promoting proinflammatory macrophage functions. This work was supported by grants from the Spanish Ministry of Economy and Competitiveness and Fondo Europeo de Desarrollo Regional/European Fund for Regional Development (SAF2012-36535, and SAF2015-71363-R) and Fundació la Marató TV3 (1225-30 and 201619-30). We also acknowledge funding support from Generalitat de Catalunya (Grant 2014SGR1153) and the Spanish Ministry of Economy and Competitiveness through the María de Maeztu Program for Units of Excellence in Research and Development (Grant MDM-2014-0370). M.T. was supported by fellowships from Fundació Catalunya-La Pedrera (2011) and Generalitat de Catalunya (Formació Investigadors-Direcció General de Recerca program 2013). S.T. was supported by a predoctoral fellowship of the Spanish Ministry of Economy and Competitiveness (Grant BES-2013-062670). C.L.-R. is a recipient of an Institució Catalana de Recerca i Estudis Avançats (Generalitat de Catalunya) Acadèmia Award. |
| Databáze: | OpenAIRE |
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