A placental and fetal liver TGFβ signaling axis drives fetal immunosuppression in maternal obesity

Maternal obesity (MO) impairs immunological development in the offspring with poorly defined mechanisms. By integrating single-cell RNA sequencing datasets from placentas and fetal livers of diet-induced obese mice, data showed that MO markedly enhances inflammatory and immune activation within the placenta but induces immunosuppression in fetal liver. Inter-organ cell-cell communication analysis further revealed that placental Spp1 signaling sent by macrophage potentiates TGFβ/Smad signaling in fetal liver immune cells, which promotes Rbl2 upregulation and induces a G1 phase arrest in T cells and basophils. Finally, T cell function is inhibited by MO. Totally, this study identifies a potential placental-fetal liver Spp1-TGFβ-Rbl2 axis associated with fetal immunosuppression due to MO.

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Publication Details

Journal
iScience
Published
2026-08-21
DOI
https://doi.org/10.1016/j.isci.2026.117295
Primary Topic
Gestational Diabetes Research and Management
Type
article
Field-Weighted Citation Impact
0.00

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article

A placental and fetal liver TGFβ signaling axis drives fetal immunosuppression in maternal obesity

Qiaorong Cui, Chaeyoung Shin, Xinrui Li, Zhongyun Kou et al.
iScience
Gestational Diabetes Research and Management
article

A placental and fetal liver TGFβ signaling axis drives fetal immunosuppression in maternal obesity

Qiaorong Cui, Chaeyoung Shin, Xinrui Li, Zhongyun Kou, Li-Wei Chen, Md Nazmul Hossain, Sharmeen Islam, Min Du, Jeanene Marie de Avila, Mei-Jun Zhu
article en

Abstract

Maternal obesity (MO) impairs immunological development in the offspring with poorly defined mechanisms. By integrating single-cell RNA sequencing datasets from placentas and fetal livers of diet-induced obese mice, data showed that MO markedly enhances inflammatory and immune activation within the placenta but induces immunosuppression in fetal liver. Inter-organ cell-cell communication analysis further revealed that placental Spp1 signaling sent by macrophage potentiates TGFβ/Smad signaling in fetal liver immune cells, which promotes Rbl2 upregulation and induces a G1 phase arrest in T cells and basophils. Finally, T cell function is inhibited by MO. Totally, this study identifies a potential placental-fetal liver Spp1-TGFβ-Rbl2 axis associated with fetal immunosuppression due to MO.

iScienceVol. 29(9)
Washington State University (US)
Eunice Kennedy Shriver National Institute of Child Health and Human Development
Good health and well-being
Openalex Percentile: Top 8%
Gestational Diabetes Research and Management
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