Decidual stromal cells maintain decidual macrophage homeostasis by secreting IL-24 in early pregnancy

妊娠早期蜕膜基质细胞通过分泌 IL-24 维持蜕膜巨噬细胞稳态

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作者:Hui-Li Yang, Cheng-Jie Wang, Zhen-Zhen Lai, Shao-Liang Yang, Zi-Meng Zheng, Jia-Wei Shi, Ming-Qing Li, Jun Shao

Conclusion

IL-24 secreted by DSCs promotes the renewal and homeostasis of decidual macrophages possibly via down-regulating the ratio of Bcl-2/Bax and up-regulating of the expression of Ki-67 in early pregnancy.

Results

The growth of DSCs was not affected obviously only by IL-24 knockdown while the growth of knockdown DSCs was inhibited significantly after co-cultured with decidual macrophages. The levels of IL-24 receptors (IL-20R1 and IL-22R1) were moderately to highly expressed on decidual macrophages and human macrophage cell line U937. The differentiation of decidual macrophages treated by rhIL-24 or co-cultured with IL-24 knockdown DSCs was not affected. Both apoptosis and viability of U937 cells were promoted by rhIL-24. The ratio of Bcl-2/Bax was down-regulated and Ki-67 was up-regulated by IL-24 treatment. The expression of Bcl-2/Bax was up-regulated while Ki-67 was down-regulated in U937 cells after co-cultured by IL-24 knockdown DSCs.

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