Laboratory for Reproductive Immunology, Hospital of Obstetrics and Gynecology, Fudan University, Shanghai, China.
Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou, China.
Am J Reprod Immunol. 2018 Jun;79(6):e12836. doi: 10.1111/aji.12836. Epub 2018 Mar 3.
To explore whether IL-33/ST2 axis modulates the polarization and efferocytosis of decidual macrophages (dMφs).
The phenotype characteristics of dMφs from both normal pregnant women and recurrent spontaneous abortion (RSA) patients were determined by real-time polymerase chain reaction (RT-PCR) and flow cytometry (FCM). Then, the efferocytosis and expression of IL-33 and its receptor (ST2) in dMφs were analyzed by FCM. Finally, the effects of sST2, a decoy receptor for IL-33 that inhibits the IL-33/ST2 signaling pathway, on the polarization and efferocytosis of dMφs and human macrophage cell line U937 were investigated.
Compared with normal pregnancy, dMφs from RSA patients presented a M1 phenotype with high secretion of IL-33, whereas the expression of ST2 decreased. However, dMφs from RSA patients possessed a more powerful efferocytosis ability to clear the apoptotic decidual stromal cells (DSCs) compared with dMφs from normal pregnancy patients. Treatment with recombinant human sST2 led to the up-regulation of M1 bias and efferocytosis ability of both normal dMφs and U937.
This study indicates that IL-33 secreted by dMφs promotes M2 bias at the feto-maternal interface, and as a result, RSA might attribute to the disturbance of IL-33/ST2 axis and the enhancement of efferocytosis of dMφs subsequently.
探讨白细胞介素 33/ST2 轴是否调节蜕膜巨噬细胞(dMφs)的极化和吞噬作用。
通过实时聚合酶链反应(RT-PCR)和流式细胞术(FCM)测定正常妊娠妇女和复发性自然流产(RSA)患者的 dMφs 的表型特征。然后,通过 FCM 分析 dMφs 中的吞噬作用和白细胞介素 33 及其受体(ST2)的表达。最后,研究了白细胞介素 33 的诱饵受体 sST2(抑制白细胞介素 33/ST2 信号通路)对 dMφs 和人巨噬细胞系 U937 的极化和吞噬作用的影响。
与正常妊娠相比,RSA 患者的 dMφs 表现出 M1 表型,IL-33 分泌增加,而 ST2 的表达降低。然而,与正常妊娠患者的 dMφs 相比,RSA 患者的 dMφs 具有更强的吞噬作用能力,能够清除凋亡的蜕膜基质细胞(DSCs)。用重组人 sST2 处理会导致正常 dMφs 和 U937 的 M1 偏倚和吞噬作用能力上调。
本研究表明,dMφs 分泌的白细胞介素 33 促进了胎母界面的 M2 偏向,因此,RSA 可能归因于白细胞介素 33/ST2 轴的紊乱以及随后 dMφs 的吞噬作用增强。