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Quantification of Endothelial Fatty Acid Uptake using Fluorescent Fatty Acid Analogs
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Fatty Acid Uptake in T Cell Subsets Using a Quantum Dot Fatty Acid Conjugate
Megan E Muroski1, Jason Miska1, Alan L Chang2
1Department of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, USA.
Scientific Reports
|July 21, 2017
Summary
Researchers developed a novel fluorescent probe to measure fatty acid (FA) uptake in T cells within tumors. This tool reveals how T cell location and activation impact FA metabolism, crucial for understanding tumor immunosuppression.
Area of Science:
- Immunology
- Cell Biology
- Biochemistry
Background:
- Fatty acid (FA) metabolism is critical for T cell function in the tumor microenvironment.
- Understanding FA uptake by T cell subsets is key to addressing tumor immunosuppression.
Purpose of the Study:
- To develop and validate a novel fluorescent probe for measuring T cell FA uptake.
- To investigate the impact of T cell location and activation status on FA uptake.
- To analyze FA uptake differences between T cell subsets, particularly regulatory T cells (Tregs).
Main Methods:
- Generation of a novel FA-Qdot 605 dye conjugate.
- In vitro and in vivo assessment of the probe's specificity for T cell FA uptake.
- Flow cytometric analysis of T cells from tumor microenvironments.
- Simultaneous detection of glucose and FA uptake within tumors.
Main Results:
- The novel FA-Qdot 605 probe accurately measures T cell FA uptake in vitro and in vivo.
- T cell FA uptake is influenced by their location and activation status.
- Regulatory T cells (Tregs) exhibit higher FA uptake compared to effector T cells.
- Simultaneous detection of glucose and FA uptake in the tumor microenvironment is feasible.
Conclusions:
- The developed fluorescent probe is a sensitive and specific tool for studying T cell FA metabolism in vivo.
- This probe offers new insights into the role of FA metabolism in T cell function and tumor immunosuppression.
- The findings support the importance of FA metabolism in Treg function and provide a method to study it.

