Decidual stromal cell‐derived PGE2 regulates macrophage responses to microbial threat. (7th August 2018)

• Record Type: Journal Article
• Authors: Rogers, Lisa M.; Anders, Anjali P.; Doster, Ryan S.; Gill, Elizabeth A.; Gnecco, Juan S.; Holley, Jacob M.; Randis, Tara M.; Ratner, Adam J.; Gaddy, Jennifer A.; Osteen, Kevin; Aronoff, David M.
• Is Part Of: American journal of reproductive immunology. Volume 80:Number 4(2018)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2018-08-07
• Subjects: chorioamnionitis -- fetal membranes -- infection -- microfluidics -- pregnancy -- prostaglandins; Human reproduction -- Immunological aspects -- Periodicals; 616.69206
• DOI: 10.1111/aji.13032
• Languages: English
• ISSNs: 1046-7408

Abstract

Abstract : Problem: Bacterial chorioamnionitis causes adverse pregnancy outcomes, yet host‐microbial interactions are not well characterized within gestational membranes. The decidua, the outermost region of the membranes, is a potential point of entry for bacteria ascending from the vagina to cause chorioamnionitis. We sought to determine whether paracrine communication between decidual stromal cells and macrophages shaped immune responses to microbial sensing. Method of study: Decidual cell‐macrophage interactions were modeled in vitro utilizing decidualized, telomerase‐immortalized human endometrial stromal cells (dTHESCs) and phorbol ester‐differentiated THP‐1 macrophage‐like cells. The production of inflammatory mediators in response to LPS was monitored by ELISA for both cell types, while phagocytosis of bacterial pathogens ( Escherichia coli and Group B Streptococcus (GBS)) was measured in THP‐1 cells or primary human placental macrophages. Diclofenac, a non‐selective cyclooxygenase inhibitor, and prostaglandin E2 (PGE2 ) were utilized to interrogate prostaglandins as decidual cell‐derived paracrine immunomodulators. A mouse model of ascending chorioamnionitis caused by GBS was utilized to assess the colocalization of bacteria and macrophages in vivo and assess PGE2 production. Results: In response to LPS, dTHESC and THP‐1 coculture demonstrated enhancement of most inflammatory mediators, but a potent suppression of macrophage TNF‐α generation was observed. This appeared to reflect a paracrine‐mediated effect of decidual cell‐derived PGE2 . In mice with GBS chorioamnionitis, macrophages accumulated at sites of bacterial invasion with increased PGE2 in amniotic fluid, suggesting such paracrine effects might hold relevance in vivo. Conclusion: These data suggest key roles for decidual stromal cells in modulating tissue responses to microbial threat through release of PGE2 .