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 |
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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 |
format | Article |
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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.</description><identifier>ISSN: 0009-7322</identifier><identifier>EISSN: 1524-4539</identifier><identifier>DOI: 10.1161/CIRCULATIONAHA.123.064391</identifier><identifier>PMID: 38314577</identifier><language>eng</language><publisher>United States</publisher><subject>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</subject><ispartof>Circulation (New York, N.Y.), 2024-05, Vol.149 (21), p.1670-1688</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1241-3d25efe3f5d8c7c6d4485491f3498f462720c269a0ab8620bb6c5f763b3238a33</cites><orcidid>0000-0002-6201-2109 ; 0000-0002-6202-7159 ; 0000-0002-9021-8825 ; 0000-0002-5307-6784 ; 0000-0002-2999-5844 ; 0000-0003-0561-9315 ; 0000-0003-2280-9727 ; 0000-0003-0670-0879 ; 0000-0003-1721-8922 ; 0000-0001-5380-1942</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3674,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38314577$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Yanhong</creatorcontrib><creatorcontrib>Sang, Yifei</creatorcontrib><creatorcontrib>Chang, Yunjian</creatorcontrib><creatorcontrib>Xu, Chunfang</creatorcontrib><creatorcontrib>Lin, Yikong</creatorcontrib><creatorcontrib>Zhang, Yao</creatorcontrib><creatorcontrib>Chiu, Philip C N</creatorcontrib><creatorcontrib>Yeung, William S B</creatorcontrib><creatorcontrib>Zhou, Haisheng</creatorcontrib><creatorcontrib>Dong, Ningzheng</creatorcontrib><creatorcontrib>Xu, Ling</creatorcontrib><creatorcontrib>Chen, Jiajia</creatorcontrib><creatorcontrib>Zhao, Weijie</creatorcontrib><creatorcontrib>Liu, Lu</creatorcontrib><creatorcontrib>Yu, Di</creatorcontrib><creatorcontrib>Zang, Xingxing</creatorcontrib><creatorcontrib>Ye, Jiangfeng</creatorcontrib><creatorcontrib>Yang, Jinying</creatorcontrib><creatorcontrib>Wu, Qingyu</creatorcontrib><creatorcontrib>Li, Dajin</creatorcontrib><creatorcontrib>Wu, Ligang</creatorcontrib><creatorcontrib>Du, Meirong</creatorcontrib><title>A Galectin-9-Driven CD11c high Decidual Macrophage Subset Suppresses Uterine Vascular Remodeling in Preeclampsia</title><title>Circulation (New York, N.Y.)</title><addtitle>Circulation</addtitle><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.</description><subject>Animals</subject><subject>CD11 Antigens</subject><subject>Decidua - metabolism</subject><subject>Decidua - pathology</subject><subject>Disease Models, Animal</subject><subject>Female</subject><subject>Galectins - metabolism</subject><subject>Humans</subject><subject>Hyaluronan Receptors - genetics</subject><subject>Hyaluronan Receptors - metabolism</subject><subject>Macrophages - immunology</subject><subject>Macrophages - metabolism</subject><subject>Macrophages - pathology</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Pre-Eclampsia - immunology</subject><subject>Pre-Eclampsia - metabolism</subject><subject>Pregnancy</subject><subject>Retrospective Studies</subject><subject>Uterus - blood supply</subject><subject>Uterus - metabolism</subject><subject>Vascular Remodeling</subject><issn>0009-7322</issn><issn>1524-4539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkN9OwjAchRujEURfwdQHGPb_1stlKJCgGARvl677DWrGWFpm4ts7g5p4dXIuvpOTD6E7SsaUKnqfzVfZZpGu58vndJaOKeNjogTX9AwNqWQiEpLrczQkhOgo5owN0FUI731VPJaXaMATToWM4yFqUzw1NdijayIdTbz7gAZnE0ot3rntDk_AurIzNX4y1h_andkCfu2KAMc-2tZDCBDw5gjeNYDfTLBdbTxewf5QQu2aLXYNfvEAtjb7NjhzjS4qUwe4-ckR2jw-rLNZtFhO51m6iCxlgka8ZBIq4JUsExtbVQqRSKFpxYVOKqFYzIhlShtiikQxUhTKyipWvOCMJ4bzEdKn3f52CB6qvPVub_xnTkn-bTH_bzHvLeYniz17e2LbrthD-Uf-auNf4JtvSQ</recordid><startdate>20240521</startdate><enddate>20240521</enddate><creator>Li, Yanhong</creator><creator>Sang, Yifei</creator><creator>Chang, Yunjian</creator><creator>Xu, Chunfang</creator><creator>Lin, Yikong</creator><creator>Zhang, Yao</creator><creator>Chiu, Philip C N</creator><creator>Yeung, William S B</creator><creator>Zhou, Haisheng</creator><creator>Dong, Ningzheng</creator><creator>Xu, Ling</creator><creator>Chen, Jiajia</creator><creator>Zhao, Weijie</creator><creator>Liu, Lu</creator><creator>Yu, Di</creator><creator>Zang, Xingxing</creator><creator>Ye, Jiangfeng</creator><creator>Yang, Jinying</creator><creator>Wu, Qingyu</creator><creator>Li, Dajin</creator><creator>Wu, Ligang</creator><creator>Du, Meirong</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-6201-2109</orcidid><orcidid>https://orcid.org/0000-0002-6202-7159</orcidid><orcidid>https://orcid.org/0000-0002-9021-8825</orcidid><orcidid>https://orcid.org/0000-0002-5307-6784</orcidid><orcidid>https://orcid.org/0000-0002-2999-5844</orcidid><orcidid>https://orcid.org/0000-0003-0561-9315</orcidid><orcidid>https://orcid.org/0000-0003-2280-9727</orcidid><orcidid>https://orcid.org/0000-0003-0670-0879</orcidid><orcidid>https://orcid.org/0000-0003-1721-8922</orcidid><orcidid>https://orcid.org/0000-0001-5380-1942</orcidid></search><sort><creationdate>20240521</creationdate><title>A Galectin-9-Driven CD11c high Decidual Macrophage Subset Suppresses Uterine Vascular Remodeling in Preeclampsia</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1241-3d25efe3f5d8c7c6d4485491f3498f462720c269a0ab8620bb6c5f763b3238a33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Animals</topic><topic>CD11 Antigens</topic><topic>Decidua - metabolism</topic><topic>Decidua - pathology</topic><topic>Disease Models, Animal</topic><topic>Female</topic><topic>Galectins - metabolism</topic><topic>Humans</topic><topic>Hyaluronan Receptors - genetics</topic><topic>Hyaluronan Receptors - metabolism</topic><topic>Macrophages - immunology</topic><topic>Macrophages - metabolism</topic><topic>Macrophages - pathology</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Pre-Eclampsia - immunology</topic><topic>Pre-Eclampsia - metabolism</topic><topic>Pregnancy</topic><topic>Retrospective Studies</topic><topic>Uterus - blood supply</topic><topic>Uterus - metabolism</topic><topic>Vascular Remodeling</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Yanhong</creatorcontrib><creatorcontrib>Sang, Yifei</creatorcontrib><creatorcontrib>Chang, Yunjian</creatorcontrib><creatorcontrib>Xu, Chunfang</creatorcontrib><creatorcontrib>Lin, Yikong</creatorcontrib><creatorcontrib>Zhang, Yao</creatorcontrib><creatorcontrib>Chiu, Philip C N</creatorcontrib><creatorcontrib>Yeung, William S B</creatorcontrib><creatorcontrib>Zhou, Haisheng</creatorcontrib><creatorcontrib>Dong, Ningzheng</creatorcontrib><creatorcontrib>Xu, Ling</creatorcontrib><creatorcontrib>Chen, Jiajia</creatorcontrib><creatorcontrib>Zhao, Weijie</creatorcontrib><creatorcontrib>Liu, Lu</creatorcontrib><creatorcontrib>Yu, Di</creatorcontrib><creatorcontrib>Zang, Xingxing</creatorcontrib><creatorcontrib>Ye, Jiangfeng</creatorcontrib><creatorcontrib>Yang, Jinying</creatorcontrib><creatorcontrib>Wu, Qingyu</creatorcontrib><creatorcontrib>Li, Dajin</creatorcontrib><creatorcontrib>Wu, Ligang</creatorcontrib><creatorcontrib>Du, Meirong</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Circulation (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Yanhong</au><au>Sang, Yifei</au><au>Chang, Yunjian</au><au>Xu, Chunfang</au><au>Lin, Yikong</au><au>Zhang, Yao</au><au>Chiu, Philip C N</au><au>Yeung, William S B</au><au>Zhou, Haisheng</au><au>Dong, Ningzheng</au><au>Xu, Ling</au><au>Chen, Jiajia</au><au>Zhao, Weijie</au><au>Liu, Lu</au><au>Yu, Di</au><au>Zang, Xingxing</au><au>Ye, Jiangfeng</au><au>Yang, Jinying</au><au>Wu, Qingyu</au><au>Li, Dajin</au><au>Wu, Ligang</au><au>Du, Meirong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Galectin-9-Driven CD11c high Decidual Macrophage Subset Suppresses Uterine Vascular Remodeling in Preeclampsia</atitle><jtitle>Circulation (New York, N.Y.)</jtitle><addtitle>Circulation</addtitle><date>2024-05-21</date><risdate>2024</risdate><volume>149</volume><issue>21</issue><spage>1670</spage><epage>1688</epage><pages>1670-1688</pages><issn>0009-7322</issn><eissn>1524-4539</eissn><abstract>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.</abstract><cop>United States</cop><pmid>38314577</pmid><doi>10.1161/CIRCULATIONAHA.123.064391</doi><tpages>19</tpages><orcidid>https://orcid.org/0000-0002-6201-2109</orcidid><orcidid>https://orcid.org/0000-0002-6202-7159</orcidid><orcidid>https://orcid.org/0000-0002-9021-8825</orcidid><orcidid>https://orcid.org/0000-0002-5307-6784</orcidid><orcidid>https://orcid.org/0000-0002-2999-5844</orcidid><orcidid>https://orcid.org/0000-0003-0561-9315</orcidid><orcidid>https://orcid.org/0000-0003-2280-9727</orcidid><orcidid>https://orcid.org/0000-0003-0670-0879</orcidid><orcidid>https://orcid.org/0000-0003-1721-8922</orcidid><orcidid>https://orcid.org/0000-0001-5380-1942</orcidid><oa>free_for_read</oa></addata></record> |
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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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