Signaling Pathways Leading to mTOR Activation Downstream Cytokine Receptors in Lymphocytes in Health and Disease.

Int J Mol Sci

CIRI-Centre International de Recherche en Infectiologie (Team Lyacts), Inserm, U1111, Université Claude Bernard Lyon 1, CNRS, UMR5308, ENS de Lyon, F-69007 Lyon, France.

Published: August 2023

AI Article Synopsis

  • - CD8+ T cells and Natural Killer (NK) cells are crucial for fighting off viral infections and cancer, and their effectiveness relies on various signals from their environment, including cytokines and nutrients.
  • - The mechanistic target of rapamycin (mTOR) serves as a central regulator of cellular growth and metabolism, playing a key role in the maturation of these immune cells.
  • - Recent research is focusing on how mTOR is activated in primary immune cells (instead of cell lines) and how understanding this signaling can enhance immunotherapy strategies for treating cancer.

Article Abstract

CD8+ T cells and Natural Killer (NK) cells are cytotoxic lymphocytes important in the response to intracellular pathogens and cancer. Their activity depends on the integration of a large set of intracellular and environmental cues, including antigenic signals, cytokine stimulation and nutrient availability. This integration is achieved by signaling hubs, such as the mechanistic target of rapamycin (mTOR). mTOR is a conserved protein kinase that controls cellular growth and metabolism in eukaryotic cells and, therefore, is essential for lymphocyte development and maturation. However, our current understanding of mTOR signaling comes mostly from studies performed in transformed cell lines, which constitute a poor model for comprehending metabolic pathway regulation. Therefore, it is only quite recently that the regulation of mTOR in primary cells has been assessed. Here, we review the signaling pathways leading to mTOR activation in CD8+ T and NK cells, focusing on activation by cytokines. We also discuss how this knowledge can contribute to immunotherapy development, particularly for cancer treatment.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10454121PMC
http://dx.doi.org/10.3390/ijms241612736DOI Listing

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