A Galectin-9-Driven CD11c high Decidual Macrophage Subset Suppresses Uterine Vascular Remodeling in Preeclampsia

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. Single-cell RNA sequencing and spatial transcript...

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Veröffentlicht in:Circulation (New York, N.Y.) N.Y.), 2024-05, Vol.149 (21), p.1670-1688
Hauptverfasser: Li, Yanhong, Sang, Yifei, Chang, Yunjian, Xu, Chunfang, Lin, Yikong, Zhang, Yao, Chiu, Philip C N, Yeung, William S B, Zhou, Haisheng, Dong, Ningzheng, Xu, Ling, Chen, Jiajia, Zhao, Weijie, Liu, Lu, Yu, Di, Zang, Xingxing, Ye, Jiangfeng, Yang, Jinying, Wu, Qingyu, Li, Dajin, Wu, Ligang, Du, Meirong
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container_end_page 1688
container_issue 21
container_start_page 1670
container_title Circulation (New York, N.Y.)
container_volume 149
creator Li, Yanhong
Sang, Yifei
Chang, Yunjian
Xu, Chunfang
Lin, Yikong
Zhang, Yao
Chiu, Philip C N
Yeung, William S B
Zhou, Haisheng
Dong, Ningzheng
Xu, Ling
Chen, Jiajia
Zhao, Weijie
Liu, Lu
Yu, Di
Zang, Xingxing
Ye, Jiangfeng
Yang, Jinying
Wu, Qingyu
Li, Dajin
Wu, Ligang
Du, Meirong
description 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. 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 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. We discovered a distinct CD11c dMφ subset that inhibits spiral artery remodeling in preeclampsia. The proinflammatory CD11c dMφ exhibits perivascular enrichment in the decidua from patients with preeclampsia. We also showed that trophoblast-derived galectin-9 activates CD11c 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 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. These findings highlight a key role of a distinct perivascular inflammatory CD11c dMφ subpopulation in the pathogenesis of preeclampsia. CD11c 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.
doi_str_mv 10.1161/CIRCULATIONAHA.123.064391
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Dysregulated uterine immune cells and spiral arteries are implicated in preeclampsia, but the mechanistic link remains unclear. 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 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. We discovered a distinct CD11c dMφ subset that inhibits spiral artery remodeling in preeclampsia. The proinflammatory CD11c dMφ exhibits perivascular enrichment in the decidua from patients with preeclampsia. We also showed that trophoblast-derived galectin-9 activates CD11c 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 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. These findings highlight a key role of a distinct perivascular inflammatory CD11c dMφ subpopulation in the pathogenesis of preeclampsia. CD11c dMφ activated by increased galectin-9 from trophoblasts suppresses uterine spiral artery remodeling, contributing to preeclampsia. 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Dysregulated uterine immune cells and spiral arteries are implicated in preeclampsia, but the mechanistic link remains unclear. 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 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. We discovered a distinct CD11c dMφ subset that inhibits spiral artery remodeling in preeclampsia. The proinflammatory CD11c dMφ exhibits perivascular enrichment in the decidua from patients with preeclampsia. We also showed that trophoblast-derived galectin-9 activates CD11c 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 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. These findings highlight a key role of a distinct perivascular inflammatory CD11c dMφ subpopulation in the pathogenesis of preeclampsia. CD11c dMφ activated by increased galectin-9 from trophoblasts suppresses uterine spiral artery remodeling, contributing to preeclampsia. 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We also showed that trophoblast-derived galectin-9 activates CD11c 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 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. These findings highlight a key role of a distinct perivascular inflammatory CD11c dMφ subpopulation in the pathogenesis of preeclampsia. CD11c dMφ activated by increased galectin-9 from trophoblasts suppresses uterine spiral artery remodeling, contributing to preeclampsia. 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source MEDLINE; American Heart Association; Journals@Ovid Complete
subjects Animals
CD11 Antigens
Decidua - metabolism
Decidua - pathology
Disease Models, Animal
Female
Galectins - metabolism
Humans
Hyaluronan Receptors - genetics
Hyaluronan Receptors - metabolism
Macrophages - immunology
Macrophages - metabolism
Macrophages - pathology
Mice
Mice, Inbred C57BL
Mice, Knockout
Pre-Eclampsia - immunology
Pre-Eclampsia - metabolism
Pregnancy
Retrospective Studies
Uterus - blood supply
Uterus - metabolism
Vascular Remodeling
title A Galectin-9-Driven CD11c high Decidual Macrophage Subset Suppresses Uterine Vascular Remodeling in Preeclampsia
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