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Updated: Sep 11, 2025

Reprograming Model of Human Monocyte-derived Macrophages for In-vitro Assays
Published on: April 18, 2025
mTOR Signaling in Macrophages: All Depends on the Context
Angelika Fedor1, Krzysztof Bryniarski1, Katarzyna Nazimek1
1Department of Immunology, Jagiellonian University Medical College, Czysta 18, 31-121 Kraków, Poland.
Abstract:
Macrophages are undoubtedly one of the most widely studied cells of the immune system, among other reasons, because they are involved in a wide variety of biological processes. Deregulation of their activity is observed in a number of different disorders, including autoimmune diseases. At the same time, mammalian target of rapamycin (mTOR) is attracting increasing research attention because the pathways dependent on this kinase are activated by a variety of signals, including cytokines and proinflammatory mediators, mediate essential processes for cell survival and metabolism, and can be regulated epigenetically via microRNAs. Therefore, our narrative review aimed to summarize and discuss recent advances in the knowledge of the activation of mTOR signaling in macrophages, with a special focus on autoimmune disorders and the possibility of mTOR control by microRNAs. The summarized research observations allowed us to conclude that the effects of activity and/or inhibition of individual mTOR complexes in macrophages are largely context dependent, and therefore, these broad immunological contexts and other specific conditions should always be taken into account when attempting to modulate these pathways for therapeutic purposes.
Insights
Mammalian target of rapamycin (mTOR) signaling in macrophages is crucial for immune responses and metabolism. Its modulation for autoimmune diseases requires careful consideration of context-dependent effects and microRNA regulation.
Area of Science:
- Immunology
- Cell Biology
- Molecular Biology
Background:
- Macrophages are key immune cells involved in numerous biological processes.
- Dysregulated macrophage activity is linked to various disorders, notably autoimmune diseases.
- Mammalian target of rapamycin (mTOR) signaling pathways are activated by inflammatory signals and regulate cell survival and metabolism.
Purpose of the Study:
- To review recent advances in understanding mTOR signaling activation in macrophages.
- To focus on the role of mTOR in autoimmune disorders.
- To explore the potential for microRNA-mediated control of mTOR in macrophages.
Main Methods:
- Narrative review of existing research.
- Synthesis of studies on mTOR signaling, macrophages, and autoimmune diseases.
- Analysis of microRNA regulation of mTOR pathways.
Main Results:
- mTOR signaling is activated by cytokines and inflammatory mediators.
- MicroRNAs can epigenetically regulate mTOR pathways.
- The effects of mTOR modulation in macrophages are highly context-dependent.
Conclusions:
- Modulating mTOR pathways in macrophages for therapeutic purposes requires careful consideration of the specific immunological context.
- Understanding the interplay between mTOR, macrophages, and microRNAs is critical for developing treatments for autoimmune diseases.
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