T cell cholesterol transport links intestinal immune responses to dietary lipid absorption

The intrinsic pathways that control membrane organization in immune cells and their impact on cellular functions are poorly defined. We found that the nonvesicular cholesterol transporter Aster-A linked plasma membrane (PM) cholesterol availability in CD4 T cells to systemic metabolism. Aster-A was recruited to the PM during T cell receptor (TCR) activation, where it facilitated the removal of accessible cholesterol. Loss of Aster-A increased cholesterol accumulation in the PM, which enhanced TCR nanoclustering and signaling. Aster-A associated with stromal interaction molecule 1 (STIM1) and negatively regulated calcium (Ca<sup>2+</sup>) flux. Aster-A deficiency promoted CD4 T cells to acquire a T helper 17 (T<sub>H</sub>17) phenotype and stimulated interleukin-22 production, which reduced intestinal fat absorption and conferred resistance to diet-induced obesity. These findings delineate how immune cell membrane homeostasis links to systemic physiology.

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Publication Details

Journal
Science
Published
2025-10-09
DOI
https://doi.org/10.1126/science.adt4169
Citations
6
Primary Topic
Immune Cell Function and Interaction
Type
article
Field-Weighted Citation Impact
4.78
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article

T cell cholesterol transport links intestinal immune responses to dietary lipid absorption

Thomas A. Weston, Yousang Gwack, Alexander H. Bedard, John P. Kennelly et al.
6 citations
Science
Immune Cell Function and Interaction
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article

T cell cholesterol transport links intestinal immune responses to dietary lipid absorption

Thomas A. Weston, Yousang Gwack, Alexander H. Bedard, John P. Kennelly, Peter Tontonoz, Alessandra Ferrari, Lauren F. Uchiyama, Sonal Srikanth, Julia J. Mack, Steven J. Bensinger, Whitaker Cohn, Emily Whang, Julian P. Whitelegge, Yajing Gao, Stephen G. Young, Min Sub Lee, Xiao Xu, Alexander Nguyen, D Cho
article en
6 citations

Abstract

The intrinsic pathways that control membrane organization in immune cells and their impact on cellular functions are poorly defined. We found that the nonvesicular cholesterol transporter Aster-A linked plasma membrane (PM) cholesterol availability in CD4 T cells to systemic metabolism. Aster-A was recruited to the PM during T cell receptor (TCR) activation, where it facilitated the removal of accessible cholesterol. Loss of Aster-A increased cholesterol accumulation in the PM, which enhanced TCR nanoclustering and signaling. Aster-A associated with stromal interaction molecule 1 (STIM1) and negatively regulated calcium (Ca<sup>2+</sup>) flux. Aster-A deficiency promoted CD4 T cells to acquire a T helper 17 (T<sub>H</sub>17) phenotype and stimulated interleukin-22 production, which reduced intestinal fat absorption and conferred resistance to diet-induced obesity. These findings delineate how immune cell membrane homeostasis links to systemic physiology.

ScienceVol. 390(6769)
University of California, Los Angeles (US)
Openalex Percentile: Top 4%
Immune Cell Function and Interaction
4.78
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