Cargando…

A role for the NLRC4 inflammasome in premature rupture of membrane

PROM is one of the common complications of perinatal period, which seriously threatens the mother and newborn. The purpose of this study was to identify the role of NLRC4 inflammasomes in this process and their underlying mechanisms. We performed high-throughput RNA sequencing of fetal membrane tiss...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhu, Jinming, Ma, Chunling, Zhu, Lina, Li, Juan, Peng, Fengyun, Huang, Lei, Luan, Xiaomei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7446792/
https://www.ncbi.nlm.nih.gov/pubmed/32833985
http://dx.doi.org/10.1371/journal.pone.0237847
_version_ 1783574187488575488
author Zhu, Jinming
Ma, Chunling
Zhu, Lina
Li, Juan
Peng, Fengyun
Huang, Lei
Luan, Xiaomei
author_facet Zhu, Jinming
Ma, Chunling
Zhu, Lina
Li, Juan
Peng, Fengyun
Huang, Lei
Luan, Xiaomei
author_sort Zhu, Jinming
collection PubMed
description PROM is one of the common complications of perinatal period, which seriously threatens the mother and newborn. The purpose of this study was to identify the role of NLRC4 inflammasomes in this process and their underlying mechanisms. We performed high-throughput RNA sequencing of fetal membrane tissue from 3 normal pregnant women and 3 term-premature rupture of fetal membrane (TPROM) patients who met the inclusion criteria, and found that NLRC4 was significantly up-regulated in TPROM patients. An observational study of TPROM patients (PROM group, n = 30) and normal pregnant women (control group, n = 30) was performed at the Xuzhou Maternal and Child Health Hospital affiliated to Xuzhou Medical University from May 2018 to May 2019. The expression of genes involved in inflammasome complex including NLRC1, NLRC3, AIM2, NLRC4, ASC, caspase-1, IL-6, IL-18 and IL-1βwas determined via real-time PCR, immunohistochemistry and immunofluorescence. Measurement of NLRC4 level in serum was conducted by ELISA assay. The results showed that the NLRC4, ASC, caspase-1, IL-1β and IL-18 levels in fetal membrane, placental tissues and maternal serum were markedly higher in the PROM group than that in the control group. In conclusion, NLRC4 is a markedly up-regulated gene in TPROM fetal membrane tissue, suggesting that NLRC4 is involved in the occurrence and development of TPROM; NLRC4 levels in maternal blood serum are closely related to TPROM and have the potential to assist doctors in predicting and diagnosing PROM.
format Online
Article
Text
id pubmed-7446792
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-74467922020-08-26 A role for the NLRC4 inflammasome in premature rupture of membrane Zhu, Jinming Ma, Chunling Zhu, Lina Li, Juan Peng, Fengyun Huang, Lei Luan, Xiaomei PLoS One Research Article PROM is one of the common complications of perinatal period, which seriously threatens the mother and newborn. The purpose of this study was to identify the role of NLRC4 inflammasomes in this process and their underlying mechanisms. We performed high-throughput RNA sequencing of fetal membrane tissue from 3 normal pregnant women and 3 term-premature rupture of fetal membrane (TPROM) patients who met the inclusion criteria, and found that NLRC4 was significantly up-regulated in TPROM patients. An observational study of TPROM patients (PROM group, n = 30) and normal pregnant women (control group, n = 30) was performed at the Xuzhou Maternal and Child Health Hospital affiliated to Xuzhou Medical University from May 2018 to May 2019. The expression of genes involved in inflammasome complex including NLRC1, NLRC3, AIM2, NLRC4, ASC, caspase-1, IL-6, IL-18 and IL-1βwas determined via real-time PCR, immunohistochemistry and immunofluorescence. Measurement of NLRC4 level in serum was conducted by ELISA assay. The results showed that the NLRC4, ASC, caspase-1, IL-1β and IL-18 levels in fetal membrane, placental tissues and maternal serum were markedly higher in the PROM group than that in the control group. In conclusion, NLRC4 is a markedly up-regulated gene in TPROM fetal membrane tissue, suggesting that NLRC4 is involved in the occurrence and development of TPROM; NLRC4 levels in maternal blood serum are closely related to TPROM and have the potential to assist doctors in predicting and diagnosing PROM. Public Library of Science 2020-08-24 /pmc/articles/PMC7446792/ /pubmed/32833985 http://dx.doi.org/10.1371/journal.pone.0237847 Text en © 2020 Zhu et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Zhu, Jinming
Ma, Chunling
Zhu, Lina
Li, Juan
Peng, Fengyun
Huang, Lei
Luan, Xiaomei
A role for the NLRC4 inflammasome in premature rupture of membrane
title A role for the NLRC4 inflammasome in premature rupture of membrane
title_full A role for the NLRC4 inflammasome in premature rupture of membrane
title_fullStr A role for the NLRC4 inflammasome in premature rupture of membrane
title_full_unstemmed A role for the NLRC4 inflammasome in premature rupture of membrane
title_short A role for the NLRC4 inflammasome in premature rupture of membrane
title_sort role for the nlrc4 inflammasome in premature rupture of membrane
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7446792/
https://www.ncbi.nlm.nih.gov/pubmed/32833985
http://dx.doi.org/10.1371/journal.pone.0237847
work_keys_str_mv AT zhujinming aroleforthenlrc4inflammasomeinprematureruptureofmembrane
AT machunling aroleforthenlrc4inflammasomeinprematureruptureofmembrane
AT zhulina aroleforthenlrc4inflammasomeinprematureruptureofmembrane
AT lijuan aroleforthenlrc4inflammasomeinprematureruptureofmembrane
AT pengfengyun aroleforthenlrc4inflammasomeinprematureruptureofmembrane
AT huanglei aroleforthenlrc4inflammasomeinprematureruptureofmembrane
AT luanxiaomei aroleforthenlrc4inflammasomeinprematureruptureofmembrane
AT zhujinming roleforthenlrc4inflammasomeinprematureruptureofmembrane
AT machunling roleforthenlrc4inflammasomeinprematureruptureofmembrane
AT zhulina roleforthenlrc4inflammasomeinprematureruptureofmembrane
AT lijuan roleforthenlrc4inflammasomeinprematureruptureofmembrane
AT pengfengyun roleforthenlrc4inflammasomeinprematureruptureofmembrane
AT huanglei roleforthenlrc4inflammasomeinprematureruptureofmembrane
AT luanxiaomei roleforthenlrc4inflammasomeinprematureruptureofmembrane