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Shu Biu William Yeung
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Professor
Research Interests
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Recent Grants
Grant: Close
微RNA let-7對小鼠囊胚形成的作用
Open Date: 2018-01-01
Close Date: 2020-12-31
Grant: Close
精子與輸卵管上皮細胞的相互作用對人類精子受精能力和選擇優質精子的作用
Open Date: 2018-01-01
Close Date: 2020-12-31
Grant: Close
理解子宫内膜细胞对子宫内膜间质干细胞样细胞活性在月经期间的调节机制
Open Date: 2017-01-01
Close Date: 2020-06-30
Grant: Close
子宮肌層細胞對子宮內膜幹細胞活性的調節
Open Date: 2016-01-01
Close Date: 2018-12-31
Grant: Close
雙酚A 類似物:在胚胎種植和子宮內膜容受性中的機制
Open Date: 2016-01-01
Close Date: 2018-12-31
Articles (5)
Year:
2026
Year:
2026
Year:
2025
BACKGROUND: Preeclampsia is a serious disease of pregnancy that lacks early diagnosis methods or effective treatment, except delivery. Dysregulated uterine immune cells and spiral arteries are implicated in preeclampsia, but the mechanistic link remains unclear. METHODS: Single-cell RNA sequencing and spatial transcriptomics were used to identify immune cell subsets associated with preeclampsia. Cell-based studies and animal models including conditional knockout mice and a new preeclampsia mouse model induced by recombinant mouse galectin-9 were applied to validate the pathogenic role of a CD11c high subpopulation of decidual macrophages (dMφ) and to determine its underlying regulatory mechanisms in preeclampsia. A retrospective preeclampsia cohort study was performed to determine the value of circulating galectin-9 in predicting preeclampsia. RESULTS: We discovered a distinct CD11c high dMφ subset that inhibits spiral artery remodeling in preeclampsia. The proinflammatory CD11c high dMφ exhibits perivascular enrichment in the decidua from patients with preeclampsia. We also showed that trophoblast-derived galectin-9 activates CD11c high dMφ by means of CD44 binding to suppress spiral artery remodeling. In 3 independent preeclampsia mouse models, placental and plasma galectin-9 levels were elevated. Galectin-9 administration in mice induces preeclampsia-like phenotypes with increased CD11c high dMφ and defective spiral arteries, whereas galectin-9 blockade or macrophage-specific CD44 deletion prevents such phenotypes. In pregnant women, increased circulating galectin-9 levels in the first trimester and at 16 to 20 gestational weeks can predict subsequent preeclampsia onset. CONCLUSIONS: These findings highlight a key role of a distinct perivascular inflammatory CD11c high dMφ subpopulation in the pathogenesis of preeclampsia. CD11c high dMφ activated by increased galectin-9 from trophoblasts suppresses uterine spiral artery remodeling, contributing to preeclampsia. Increased circulating galectin-9 may be a biomarker for preeclampsia prediction and intervention.
Year:
2024
Year:
2024
Collaborators (6)
Rachel Chan
The University of Hong Kong
Chi Ngong Philip Chiu
Associate Professor
The University of Hong Kong
Cheuk Lun Lee
Assistant Professor
The Hong Kong Polytechnic University
Ernest Ng
The University of Hong Kong
Hannu Koistinen
University of Helsinki
Meirong Du
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