Loading…
Elevated inflammatory mediators from the maternal-fetal interface to fetal circulation during labor
•Inflammatory mediators up regulated in maternal-fetal interface during labor.•Maternal-fetal interface should also include the uterine and fetal circulation.•Elevated maternal inflammatory factors could enter the fetal circulation during labor. Elevated cytokines, like IL-1βand IL-6, are known to c...
Saved in:
Published in: | Cytokine (Philadelphia, Pa.) Pa.), 2021-12, Vol.148, p.155707-155707, Article 155707 |
---|---|
Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | •Inflammatory mediators up regulated in maternal-fetal interface during labor.•Maternal-fetal interface should also include the uterine and fetal circulation.•Elevated maternal inflammatory factors could enter the fetal circulation during labor.
Elevated cytokines, like IL-1βand IL-6, are known to contribute to the pathogenesis of labor. However, the change of inflammatory mediators in maternal-fetal interface to fetal circulation is obscure.
Study design and methods: We investigated the changes of inflammatory cytokines, chemokines and macrophage in maternal-fetal interface tissues and fetal circulation of women in labor vs. non-labor. Human myometrium, placenta, decidua, fetal membrane and umbilical blood were obtained from in-labor and non-in-labor women who eventually delivered live, singleton infants at term (>37 weeks gestation) by elective caesarean section. Luminex was used to measure the level of cytokines (TNF-α, IL-1β, IL-6, IL-8) and chemokines (MCP-1, GM-CSF, MIP-1α, MIP-1β) in each sample (tissue and umbilical blood). Macrophage infiltration was demonstrated by immunohistochemistry.
During labor, the level of cytokines TNF-α, IL-1β, IL-6 and IL-8 and chemokine MCP-1 and MIP-1β in myometrium is significantly higher (p |
---|---|
ISSN: | 1043-4666 1096-0023 |
DOI: | 10.1016/j.cyto.2021.155707 |