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Updated: Mar 23, 2026

Ex vivo Culture of Human Placental Explants for the Study of Viral Transmission Across the Maternal-Fetal Interface
Published on: December 30, 2025
Inflammatory Response of Human Gestational Membranes to Ureaplasma parvum Using a Novel Dual-Chamber Tissue Explant
Lauren C Potts1, Liping Feng1, Patrick C Seed2
1Department of Obstetrics and Gynecology, Duke University, Durham, North Carolina.
Abstract:
Preterm premature rupture of membranes (PPROM) is often associated with intra-amniotic inflammation and infection. Current understanding of the pathogenesis of PPROM includes activation of pro-inflammatory cytokines and proteolytic enzymes leading to compromise of membrane integrity. The impact of exposure to bacterial pathogens, including Ureaplasma parvum, on gestational membranes is poorly understood. Our objective was to develop a dual-chamber system to characterize the inflammatory response of gestational membranes to U. parvum in a directional nature. Full-thickness human gestational membrane explants, with either choriodecidua or amnion oriented superiorly, were suspended between two washers in a cylindrical device, creating two distinct compartments. Brilliant green dye was introduced into the top chamber to assess the integrity of the system. Tissue viability was evaluated after 72 h using a colorimetric cell proliferation assay. Choriodecidua or amnion was exposed to three doses of U. parvum and incubated for 24 h. Following treatment, media from each compartment were used for quantification of U. parvum (quantitative PCR), interleukin (IL)-8 (enzyme-linked immunosorbent assay), and matrix metalloproteinase (MMP)-2 and MMP-9 activity (zymography). We observed that system integrity and explant viability were maintained over 72 h. Dose-dependent increases in recovered U. parvum, IL-8 concentration, and MMP-2 activity were detected in both compartments. Significant differences in IL-8 concentration and MMP-9 activity were found between the choriodecidua and amnion. This tissue explant system can be used to investigate the inflammatory consequences of directional bacterial exposure for gestational membranes and provides insight into the pathogenesis of PPROM and infectious complications of pregnancy.
Insights
This study developed a dual-chamber system to investigate how Ureaplasma parvum affects gestational membranes, revealing dose-dependent inflammatory responses and differences between membrane layers in preterm premature rupture of membranes (PPROM).
Area of Science:
- Reproductive biology
- Infectious disease
- Inflammation research
Background:
- Preterm premature rupture of membranes (PPROM) is linked to intra-amniotic inflammation and infection.
- The role of bacterial pathogens like Ureaplasma parvum in PPROM pathogenesis is not fully understood.
- Gestational membrane integrity is compromised by inflammatory cytokines and enzymes.
Purpose of the Study:
- To create a dual-chamber system for studying directional inflammatory responses of gestational membranes.
- To characterize the impact of Ureaplasma parvum exposure on human gestational membrane explants.
- To investigate the differential inflammatory and proteolytic responses of choriodecidua and amnion.
Main Methods:
- Developed a dual-chamber explant system using full-thickness human gestational membranes.
- Assessed system integrity and tissue viability over 72 hours.
- Exposed membrane explants to Ureaplasma parvum and measured bacterial load, IL-8, and MMP-2/MMP-9 activity.
Main Results:
- The dual-chamber system maintained tissue integrity and viability.
- Ureaplasma parvum exposure led to dose-dependent increases in bacteria, IL-8, and MMP-2 in both compartments.
- Significant differences in IL-8 and MMP-9 levels were observed between choriodecidua and amnion layers.
Conclusions:
- The developed system effectively models directional bacterial exposure to gestational membranes.
- Ureaplasma parvum induces inflammation and matrix metalloproteinase activity in a dose-dependent manner.
- This model provides insights into PPROM pathogenesis and pregnancy-related infectious complications.

