Evidence map›Paper›PMID 35220880›Full record

ArticleAutophagy2022

A defective lysophosphatidic acid-autophagy axis increases miscarriage risk by restricting decidual macrophage residence.

Hui-Li Yang, Zhen-Zhen Lai, Jia-Wei Shi, Wen-Jie Zhou, Jie Mei, Jiang-Feng Ye, Tao Zhang, Jian Wang, Jian-Yuan Zhao, Da-Jin Li and 1 more

Open access · greenAbstract read
In one paragraph

Article in Autophagy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
6.6field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

53 citing papers in PubMed, 78 citations in OpenAlex.

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  14. Immune activation induced by FOLR2Frontiers in immunology · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 3 countries.

Hui-Li YangLaboratory for Reproductive Immunology, NHC Key Lab of Reproduction Regulation (Shanghai Institute for Biomedical and Pharmaceutical Technologies), Hospital of Obstetrics and Gynecology, Shanghai Medical School, Fudan University, Shanghai, 200080 People's Republic of China.
Zhen-Zhen LaiLaboratory for Reproductive Immunology, NHC Key Lab of Reproduction Regulation (Shanghai Institute for Biomedical and Pharmaceutical Technologies), Hospital of Obstetrics and Gynecology, Shanghai Medical School, Fudan University, Shanghai, 200080 People's Republic of China.
Jia-Wei ShiLaboratory for Reproductive Immunology, NHC Key Lab of Reproduction Regulation (Shanghai Institute for Biomedical and Pharmaceutical Technologies), Hospital of Obstetrics and Gynecology, Shanghai Medical School, Fudan University, Shanghai, 200080 People's Republic of China.
Wen-Jie ZhouCenter of Reproductive Medicine of Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, People's Republic of China.
Jie MeiReproductive Medicine Center, Department of Obstetrics and Gynecology, Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medicine School, Nanjing, 210000, People's Republic of China.
Jiang-Feng YeDivision of Obstetrics and Gynecology, KK Women's and Children's Hospital, 229899, Singapore.
Tao ZhangAssisted Reproductive Technology Unit, Department of Obstetrics and Gynecology, Faculty of Medicine, Chinese University of Hong Kong, Hong Kong, People's Republic of China.
Jian WangLaboratory for Reproductive Immunology, NHC Key Lab of Reproduction Regulation (Shanghai Institute for Biomedical and Pharmaceutical Technologies), Hospital of Obstetrics and Gynecology, Shanghai Medical School, Fudan University, Shanghai, 200080 People's Republic of China.
Jian-Yuan ZhaoState Key Laboratory of Genetic Engineering, Collaborative Innovation Center for Genetics and Development, School of Life Sciences, Fudan University, Shanghai 200433, People's Republic of China.
Da-Jin LiLaboratory for Reproductive Immunology, NHC Key Lab of Reproduction Regulation (Shanghai Institute for Biomedical and Pharmaceutical Technologies), Hospital of Obstetrics and Gynecology, Shanghai Medical School, Fudan University, Shanghai, 200080 People's Republic of China.
Ming-Qing LiLaboratory for Reproductive Immunology, NHC Key Lab of Reproduction Regulation (Shanghai Institute for Biomedical and Pharmaceutical Technologies), Hospital of Obstetrics and Gynecology, Shanghai Medical School, Fudan University, Shanghai, 200080 People's Republic of China.ORCID 0000-0002-9276-0722
Fudan University · CNChinese University of Hong Kong · HKKK Women's and Children's Hospital · SGNanjing Drum Tower Hospital · CNShanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Massive infiltrated and enriched decidual macrophages (dMφ) have been widely regarded as important regulators of maternal-fetal immune tolerance and trophoblast invasion, contributing to normal pregnancy. However, the characteristics of metabolic profile and the underlying mechanism of dMφ residence remain largely unknown. Here, we observe that dMφ display an active glycerophospholipid metabolism. The activation of ENPP2-lysophosphatidic acid (LPA) facilitates the adhesion and retention, and M2 differentiation of dMφ during normal pregnancy. Mechanistically, this process is mediated through activation of the LPA receptors (LPAR1 and PPARG/PPARγ)-DDIT4-macroautophagy/autophagy axis, and further upregulation of multiple adhesion factors (e.g., cadherins and selectins) in a CLDN7 (claudin 7)-dependent manner. Additionally, poor trophoblast invasion and placenta development, and a high ratio of embryo loss are observed in

Indexed as

Abortion, SpontaneousAutophagyActinsAcyltransferasesAnimalsBeclin-1CadherinsChemokine CXCL10ClaudinsEpithelial Cell Adhesion MoleculeEstersFemaleFibroblast Growth Factor 2GlycerophospholipidsGranulocyte-Macrophage Colony-Stimulating FactorGroup IV Phospholipases A2ActinsAcyltransferasesBeclin-1CadherinsChemokine CXCL10ClaudinsCLDN7 protein, humanEpithelial Cell Adhesion MoleculeEstersFibroblast Growth Factor 2GlycerophospholipidsGPCPD1 protein, humanGranulocyte-Macrophage Colony-Stimulating FactorGroup IV Phospholipases A2Hepatocyte Nuclear Factor 4Hypoxia-Inducible Factor 1IntegrinsKeratin-7LigandsLypla1 protein, mouselysophosphatidic acidLysophospholipaseLysophospholipidsMacrophage Colony-Stimulating FactorMARVELD2 protein, humanMARVEL Domain Containing 2 ProteinMechanistic Target of Rapamycin Complex 1Microtubule-Associated ProteinsMonoacylglycerol LipasesMuramidasePhospholipasesPhospholipases A1Phosphoric Diester HydrolasesPhosphoric Monoester HydrolasesPlatelet-Derived Growth FactorPPAR gammaPyrophosphatasesReceptors, Lysophosphatidic AcidReceptors, NK Cell Lectin-LikeSelectinsSequestosome-1 ProteinSirolimusThiolester HydrolasesTOR Serine-Threonine KinasesVascular Cell Adhesion Molecule-1Zonula Occludens-1 ProteinAbortionCLDN7DDIT4decidual macrophageENPP2LPAR1lysophosphatidic acidtrophoblast invasion

Identifiers

PMID35220880
PMCPMC9542369
OpenAlexW4214690923

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.