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Updated: May 15, 2026

Measuring Mitochondrial Function of Naïve and Effector CD8 T Cells
Published on: March 28, 2025
T-cell activation induces selective changes of cellular lipidome
Tapio Lonnberg1, Laxman Yetukuri, Tuulikki Seppanen-Laakso
1Turku Centre for Biotechnology, University of Turku and Abo Akademi University, Turku, Finland.
Insights
T-cell activation involves metabolic shifts, altering cellular lipid composition. Human umbilical cord blood T-cells showed changes in phosphatidylcholines and phosphatidylethanolamines, indicating de novo fatty acid synthesis during early activation.
Area of Science:
- Immunology
- Cellular Metabolism
- Lipidomics
Background:
- Naïve T helper cell activation initiates complex signaling pathways.
- This activation requires significant metabolic changes for proliferation and effector function.
Purpose of the Study:
- To investigate alterations in cellular lipid composition during T-cell activation.
- To understand the metabolic reprogramming of T-cells post-activation.
Main Methods:
- Human umbilical cord blood T-cells were activated via T-cell receptor stimulation.
- Ultra-performance liquid chromatography mass spectrometry (UPLC-MS) was used to analyze lipid profiles.
- Transcriptomics data were integrated with lipidomic findings.
Main Results:
- Significant changes in cellular lipid concentrations were observed within 72 hours of T-cell activation, correlating with cell division.
- Phosphatidylcholines and phosphatidylethanolamines shifted towards shorter and more saturated molecular species.
- Evidence suggested de novo fatty acid synthesis and incorporation into cellular membranes.
Conclusions:
- T-cell activation induces substantial remodeling of the cellular lipidome.
- Endogenous fatty acid synthesis plays a key role in adapting T-cells for effector functions.
- Lipidomic changes reflect metabolic reprogramming essential for T-cell proliferation and differentiation.
Abstract:
Activation of naïve T helper cells by presentation of cognate antigen initiates a complex intracellular signaling process leading to development of functionally active effector cell population. The switch from quiescent naïve state to activated state involves a profound change of cellular metabolism, required for completion of multiple rounds of proliferation. Using ultra performance liquid chromatography mass spectrometry, we analyzed how this change is reflected on the cellular lipid composition in human umbilical cord blood T-cells. We found that considerable concentration changes take place during the first 72 hours after T-cell receptor activation, correlating with first rounds of activation-induced cell division. Most importantly, composition of phosphatidylcholines and phosphatidylethanolamines exhibited consistent trend towards shorter and more saturated molecular species. Together with related transcriptomics data, the results clearly suggested induction of de novofatty acid synthesis and accumulation of endogenously synthesized fatty acids into the cellular membranes, leading to partial remodeling of the cellular lipidome in the newly developed effector cell population.
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