ATF4 drives regulatory T cell functional specification in homeostasis and obesity

Regulatory T cells (T<sub>regs</sub>) have diverse functional specification in homeostasis and disease. However, how liver T<sub>regs</sub> function and are transcriptionally regulated in obesity is not well understood. Here, we identified that effector T<sub>regs</sub> expressing activating transcription factor 4 (ATF4) were enriched in the livers of obese mice. ATF4 was critical for driving an effector T<sub>reg</sub> transcriptional program, and ATF4-expressing T<sub>regs</sub> promoted the development of obesity-induced liver fibrosis by enhancing transforming growth factor-β activation via integrin αvβ8. T<sub>reg</sub>-specific deletion of <i>Atf4</i> resulted in reduced liver T<sub>regs</sub> and attenuation of obesity-induced liver abnormalities. Furthermore, ATF4 was required to promote the differentiation of nonlymphoid tissue T<sub>reg</sub> precursors under steady state. These findings demonstrate that ATF4 is important for regulating T<sub>reg</sub> functional specification in homeostasis and obesity.

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Publication Details

Journal
Science Immunology
Published
2025-03-14
DOI
https://doi.org/10.1126/sciimmunol.adp7193
Citations
9
Primary Topic
Immune Cell Function and Interaction
Type
article
Field-Weighted Citation Impact
7.18
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article

ATF4 drives regulatory T cell functional specification in homeostasis and obesity

Amha Atakilit, Dean Sheppard, Zixuan Zeng, Li‐Fan Lu et al.
9 citations
Science Immunology
Immune Cell Function and Interaction
7.18
article

ATF4 drives regulatory T cell functional specification in homeostasis and obesity

Amha Atakilit, Dean Sheppard, Zixuan Zeng, Li‐Fan Lu, Enchen Zhou, Dinghong Zhang, Gaowei Wang, Karina Cunha e Rocha, Wei Ying, Chunyu Jin, Kailun Zhou, Houji Qin, Andrea Farrell, Ke Wang
article en
9 citations

Abstract

Regulatory T cells (T<sub>regs</sub>) have diverse functional specification in homeostasis and disease. However, how liver T<sub>regs</sub> function and are transcriptionally regulated in obesity is not well understood. Here, we identified that effector T<sub>regs</sub> expressing activating transcription factor 4 (ATF4) were enriched in the livers of obese mice. ATF4 was critical for driving an effector T<sub>reg</sub> transcriptional program, and ATF4-expressing T<sub>regs</sub> promoted the development of obesity-induced liver fibrosis by enhancing transforming growth factor-β activation via integrin αvβ8. T<sub>reg</sub>-specific deletion of <i>Atf4</i> resulted in reduced liver T<sub>regs</sub> and attenuation of obesity-induced liver abnormalities. Furthermore, ATF4 was required to promote the differentiation of nonlymphoid tissue T<sub>reg</sub> precursors under steady state. These findings demonstrate that ATF4 is important for regulating T<sub>reg</sub> functional specification in homeostasis and obesity.

Science ImmunologyVol. 10(105)
University of California, San Francisco (US), University of California San Diego (US), Nanjing University (CN)
Good health and well-being
Openalex Percentile: Top 3%
Immune Cell Function and Interaction
7.18
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