Thymic stromal lymphopoietin promotes abdominal aortic aneurysm formation by regulating macrophage polarization

Background: The inflammatory cytokine thymic stromal lymphopoietin (TSLP) has pleiotropic roles in immune response and tissue homeostasis, yet its function in abdominal aortic aneurysm (AAA) remains entirely unexplored. Methods: . Underlying mechanisms were probed by bulk RNA sequencing. Results: , TSLP directly induced M1 while inhibited M2 macrophage polarization. Transcriptomics identified that TSLP upregulated pro-inflammatory pathways in macrophages, including positive regulation of cytokine production, regulation of immune effector process, cytokine-cytokine receptor interaction and chemokine signaling pathway. Conclusions: Our integrated multi-level analysis has identified TSLP as a novel pathogenic driver of AAA, which promotes disease progression by reprogramming macrophage polarization. These findings nominate TSLP signaling as a mechanistically grounded and therapeutically promising target for AAA.

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Publication Details

Journal
Frontiers in Immunology
Published
2026-04-07
DOI
https://doi.org/10.3389/fimmu.2026.1767913
Primary Topic
Dermatology and Skin Diseases
Type
article
Field-Weighted Citation Impact
0.00
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article

Thymic stromal lymphopoietin promotes abdominal aortic aneurysm formation by regulating macrophage polarization

Mingkai Huang, JingYong Li, X.-F. Wang, Mingyi Li et al.
Frontiers in Immunology
Dermatology and Skin Diseases
article

Thymic stromal lymphopoietin promotes abdominal aortic aneurysm formation by regulating macrophage polarization

Mingkai Huang, JingYong Li, X.-F. Wang, Mingyi Li, Qinlin Li, Zheng Huang, Xuzhe Zhang, Wangling Hu, XingLin Chen, Lingfeng Zha, Ni Xia, Fen Yang, Jiao Jiao, Qi Zheng, Xiang Cheng, Tingting Tang
article en

Abstract

Background: The inflammatory cytokine thymic stromal lymphopoietin (TSLP) has pleiotropic roles in immune response and tissue homeostasis, yet its function in abdominal aortic aneurysm (AAA) remains entirely unexplored. Methods: . Underlying mechanisms were probed by bulk RNA sequencing. Results: , TSLP directly induced M1 while inhibited M2 macrophage polarization. Transcriptomics identified that TSLP upregulated pro-inflammatory pathways in macrophages, including positive regulation of cytokine production, regulation of immune effector process, cytokine-cytokine receptor interaction and chemokine signaling pathway. Conclusions: Our integrated multi-level analysis has identified TSLP as a novel pathogenic driver of AAA, which promotes disease progression by reprogramming macrophage polarization. These findings nominate TSLP signaling as a mechanistically grounded and therapeutically promising target for AAA.

Frontiers in ImmunologyVol. 17
Target (United States) (US), Huazhong University of Science and Technology (CN)
Good health and well-being
Openalex Percentile: Top 27%
Dermatology and Skin Diseases
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