HMGB1 promotes immune abnormalities in preeclampsia by recruiting monocyte/decidual macrophages and inducing M1 polarization†.

Preeclampsia (PE) is a severe pregnancy complication, characterized by immune dysregulation and placental hypoxia. Decidua macrophages (dMφ) are essential at maternal-fetal interface, involves aberrant activation of dMφ toward the M1 phenotype in PE. High mobility group box 1 (HMGB1), released from necrotic cells after injury, accumulates in the placenta and peripheral blood of patients with PE. This study aims to investigate the interaction between macrophages and trophoblasts, exploring how HMGB1 affects macrophage functions and its potential involvement in the pathophysiology of PE. Decidua tissue was obtained from 37 women, comprising women with severe PE, PE, and normal pregnancies. HMGB1 levels in decidua were evaluated by immunohistochemistry, western blot, and quantitative reverse transcriptase-polymerase chain reaction (RT-qPCR). Additionally, primary dMφ and peripheral blood monocytes (pMo) were isolated to develop a co-culture model simulating the maternal-fetal interface cell model of PE. Flow cytometric analysis and in vitro cell migration assay investigated the interaction between macrophages and HMGB1. This study identified elevated HMGB1 expression in PE patients, located in trophoblast, decidual stromal cells, and the extracellular matrix. Furthermore, hypoxia induced trophoblast to express and secrete HMGB1, promoting pMo and dMφ migration. Additionally, HMGB1 recruited monocyte-induced macrophages (pMφ) and dMφ, while driving M1 macrophage polarization. This study offers insights into the suppressive effects of the crosstalk between dMφ and trophoblasts at the maternal-fetal interface, lending credence to macrophage-targeted interventions of PE as a potential therapeutic strategy.