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Updated: Jan 31, 2026

De novo Identification of Actively Translated Open Reading Frames with Ribosome Profiling Data
Published on: February 18, 2022
Hurry up and wait, then activate and translate!
1Department of Pediatrics, Allergy Immunology Division, the Children's Hospital of Philadelphia and the University of Pennsylvania, Philadelphia, PA 19104, USA. Institute for Immunology, Perelman School of Medicine, Philadelphia, PA 19104, USA.
T cell activation involves a metabolic shift from fatty acid oxidation to glycolysis. This metabolic pivot is regulated by controlling the translation of crucial metabolic enzymes.
Area of Science:
- Immunology
- Metabolism
- Molecular Biology
Background:
- T cell activation requires significant metabolic reprogramming.
- Cellular metabolism is critical for immune cell function and differentiation.
- The shift from fatty acid oxidation to glycolysis is a hallmark of activated T cells.
Purpose of the Study:
- To investigate the role of translational regulation in T cell metabolic reprogramming.
- To understand how the expression of metabolic enzymes is controlled during T cell activation.
- To elucidate the molecular mechanisms underlying the immunometabolic pivot.
Main Methods:
- Analysis of messenger RNA and protein levels of key metabolic enzymes.
- Assessment of protein synthesis rates during T cell activation.
- Investigating the impact of translational inhibitors on T cell metabolism and function.
Main Results:
- Translational control significantly impacts the expression of metabolic enzymes during T cell activation.
- The shift towards glycolysis is partly mediated by increased translation of glycolytic enzymes.
- Regulation of translation is a key mechanism in the immunometabolic pivot.
Conclusions:
- Translational regulation is a critical checkpoint in controlling T cell metabolism.
- Targeting translational control could offer new strategies for modulating T cell responses.
- Understanding these metabolic shifts is vital for developing immunotherapies.
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