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.
Authors
- Qiaorong Cui
- Chaeyoung Shin (ORCID: https://orcid.org/0000-0002-9030-1362)
- Xinrui Li (ORCID: https://orcid.org/0000-0002-6324-7794)
- Zhongyun Kou (ORCID: https://orcid.org/0000-0003-2369-049X)
- Li-Wei Chen
- Md Nazmul Hossain
- Sharmeen Islam
- Min Du
- Jeanene Marie de Avila
- Mei-Jun Zhu
Institutions
- Washington State University (US)
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
Funders
- Eunice Kennedy Shriver National Institute of Child Health and Human Development