Arunmani Mani, John W. Hotra, Sean C Blackwell, Laura Goetzl, J. Refuerzo
{"title":"Mesenchymal stem cells suppress inflammatory cytokines in lipopolysaccharide exposed preterm and term human pregnant myometrial cells.","authors":"Arunmani Mani, John W. Hotra, Sean C Blackwell, Laura Goetzl, J. Refuerzo","doi":"10.1055/a-2216-9194","DOIUrl":null,"url":null,"abstract":"Objective The objective of this study was to determine the cytokine response in human pregnant preterm and term myometrial cells exposed to lipopolysaccharide (LPS) and co-cultured with mesenchymal stem cells (MSCs). Study design Myometrium was obtained at cesarean delivery in term and preterm patients. Human myometrial cells were exposed to 5 μg/ml LPS for 4 hours (h) followed by 1 μg/ml LPS for 24 h and were co-cultured with MSCs for 24 h. Culture supernatants were collected at 24h and expression of cytokines, including IL-1β, IL-6, IL-8, TNF-α, TGF-β and IL-10, was quantified by ELISA. Results There was significantly increased expression of the pro-inflammatory cytokines IL-1β, IL-6, IL-8 and TNF-α in preterm myometrial cells treated with LPS compared to untreated preterm myometrial cells. Co-culture with MSCs significantly suppressed the pro-inflammatory cytokine levels in LPS treated preterm vs. treated term myometrial cells. Moreover, MSC co-cultured preterm myometrial cells expressed increased levels of the anti-inflammatory cytokines TGF-β and IL-10 compared to treated term myometrial cells. Conclusion MSCs ameliorate LPS-mediated inflammation in preterm human myometrial cells compared to term myometrial cells. Immunomodulatory effects of MSCs mediated through anti-inflammatory cytokine regulation suggest a potential cell-based therapy for preterm birth.","PeriodicalId":368060,"journal":{"name":"American Journal of Perinatology Reports","volume":"33 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-11-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Perinatology Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1055/a-2216-9194","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Objective The objective of this study was to determine the cytokine response in human pregnant preterm and term myometrial cells exposed to lipopolysaccharide (LPS) and co-cultured with mesenchymal stem cells (MSCs). Study design Myometrium was obtained at cesarean delivery in term and preterm patients. Human myometrial cells were exposed to 5 μg/ml LPS for 4 hours (h) followed by 1 μg/ml LPS for 24 h and were co-cultured with MSCs for 24 h. Culture supernatants were collected at 24h and expression of cytokines, including IL-1β, IL-6, IL-8, TNF-α, TGF-β and IL-10, was quantified by ELISA. Results There was significantly increased expression of the pro-inflammatory cytokines IL-1β, IL-6, IL-8 and TNF-α in preterm myometrial cells treated with LPS compared to untreated preterm myometrial cells. Co-culture with MSCs significantly suppressed the pro-inflammatory cytokine levels in LPS treated preterm vs. treated term myometrial cells. Moreover, MSC co-cultured preterm myometrial cells expressed increased levels of the anti-inflammatory cytokines TGF-β and IL-10 compared to treated term myometrial cells. Conclusion MSCs ameliorate LPS-mediated inflammation in preterm human myometrial cells compared to term myometrial cells. Immunomodulatory effects of MSCs mediated through anti-inflammatory cytokine regulation suggest a potential cell-based therapy for preterm birth.