Abnormal processing of IL-1β in NLRP7-mutated monocytes in hydatidiform mole patients.
CLINICAL AND EXPERIMENTAL IMMUNOLOGY(2020)
Abstract
NOD-like receptor pyrin 7 (NLRP7) has been identified as the major gene responsible for the recurrent hydatidiform mole (RHM). The immunological role of NLRP7 mutation in HM patients has not been conclusively demonstrated. Hence, we aim to demonstrate this role in our study. We followed 12 new patients with NLRP7 non-synonymous variations (NSVs) from date to date. Peripheral blood mononuclear cells (PBMCs) were collected separately from patients with and without NLRP7 mutation. Super-natant interleukin (IL)-1 beta secretion, intracellular pro-IL-1 beta and mature IL-1 beta expressions were measured after 24 h lipopolysaccharide (LPS) stimulation. Plasmids with corresponding NSVs were generated to evaluate the ability of processing pro-IL-1 beta into mature IL-1 beta in vitro. Homozygous or compound heterozygous NLRP7 mutations secreted less IL-1 beta in roots of abnormal intracellular pro-IL-1 beta or mature IL-1 beta, according to different domains. Plasmids with NSVs could also affect processing or/and trafficking together with caspase-1 and apoptosis-associated speck-like protein (ASC). Inflammasome-related NLRP7 mutation is a potential mechanism of RHM.
MoreTranslated text
Key words
hydatidiform mole,IL-1 beta,NLRP7
AI Read Science
Must-Reading Tree
Example
![](https://originalfileserver.aminer.cn/sys/aminer/pubs/mrt_preview.jpeg)
Generate MRT to find the research sequence of this paper
Chat Paper
Summary is being generated by the instructions you defined