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Isolation of Leukocytes from the Human Maternal-fetal Interface
Published on: May 21, 2015
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Dysregulated low-density granulocyte contributes to early spontaneous abortion
Hongxia Ye1,2,3, Lan Li4, Yajun Dong1
1Department of Reproductive Immunology, Chengdu Xi'nan Gynecology Hospital, Chengdu, Sichuan, China.
Frontiers in Immunology
|March 13, 2023
Summary
Low-density granulocytes (LDG) play a role in maintaining early pregnancy. Dysregulation of LDG contributes to spontaneous abortion (SA), offering new therapeutic targets for this common pregnancy complication.
Area of Science:
- Immunology
- Reproductive Medicine
- Cell Biology
Background:
- Spontaneous abortion (SA) is a common adverse pregnancy outcome with poorly understood pathogenesis.
- Immunological factors are implicated in SA, but the role of low-density granulocytes (LDG) remains under-investigated.
Purpose of the Study:
- To investigate the characteristics and contribution of LDG and their subpopulations in early pregnancy and spontaneous abortion.
- To explore the role of LDG in the pathogenesis of early SA.
Main Methods:
- Recruitment of non-pregnant, normally pregnant, and SA women.
- Isolation and analysis of LDG from peripheral blood and decidua using flow cytometry.
- Assessment of LDG phenotype, subpopulations, and Neutrophil Extracellular Trap (NET) formation via immunofluorescence and immunohistochemistry.
Main Results:
- LDG percentages in peripheral blood and decidua differed between pregnant and non-pregnant states, with altered patterns in SA.
- Specific LDG subpopulations (CD16int/- and CD16hi) showed distinct changes in SA.
- Decidual LDG exhibited higher activation potential, and increased NET formation was observed in SA decidua.
Conclusions:
- LDG are involved in early pregnancy maintenance.
- Dysregulated LDG function and increased decidual NET formation are associated with spontaneous abortion.
- LDG represent potential therapeutic targets for managing early SA.
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