4.5 Article

M2 macrophage-derived G-CSF promotes trophoblasts EMT, invasion and migration via activating PI3K/Akt/Erk1/2 pathway to mediate normal pregnancy

Journal

JOURNAL OF CELLULAR AND MOLECULAR MEDICINE
Volume 25, Issue 4, Pages 2136-2147

Publisher

WILEY
DOI: 10.1111/jcmm.16191

Keywords

EMT; G‐ CSF; invasion; macrophages; migration; trophoblasts

Funding

  1. National Key Research and Development Program of China [2018YFC1002804, 2016YFC1000600]
  2. National Natural Science Foundation of China [81771662, 81971356, 81801540]

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Macrophages were found to promote epithelial-to-mesenchymal transition (EMT) of trophoblasts, enhancing their migrative and invasive abilities. The key factor G-CSF derived from M2 macrophages was shown to activate the PI3K/Akt/Erk1/2 signaling pathway, promoting EMT, migration, and invasion of trophoblasts. High expression of G-CSF in placental villous tissues of normal pregnancy patients compared to those with recurrent spontaneous abortion suggests its important role in regulating trophoblasts EMT, migration, and invasion.
Trophoblasts are important parts of the placenta and exert vital roles in the maternal-foetal crosstalk, and sufficient trophoblasts migration and invasion is critical for embryo implantation and normal pregnancy. Macrophages, as the major components of decidual microenvironment at maternal-foetal interface, can interact with trophoblasts to participate in the regulation of normal pregnancy. Previously, our group have demonstrated that trophoblasts could induce macrophages polarization to M2 subtype by secreting interleukin-6 (IL-6); however, the understanding of macrophages regulating the migration and invasion of trophoblasts is limited. In the present study, we used the co-cultured model to further investigate the effects of macrophages on trophoblasts migration and invasion. Our results showed that co-culture with macrophages promoted epithelial-to-mesenchymal transition (EMT) of trophoblasts, thereby enhancing their migrative and invasive abilities. Further experiments revealed that M2 macrophage-derived G-CSF was a key factor, which promoted the EMT, migration and invasion of trophoblasts via activating PI3K/Akt/Erk1/2 signalling pathway. Clinically, G-CSF was highly expressed in placental villous tissues of normal pregnancy patients compared to patients with recurrent spontaneous abortion, and its expression level was significantly correlation with EMT markers. Taken together, these findings indicate the important role of M2 macrophages in regulating trophoblasts EMT, migration and invasion, contributing to a new insight in concerning the crosstalk between macrophages and trophoblasts in the establishment and maintenance of normal pregnancy.

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