Endometrial autophagy is essential for embryo implantation during early pregnancy

ATG5型 ATG12 子宫内膜 蜕膜 男科 胚胎 怀孕 下调和上调 生物 自噬 医学 蜕膜化 细胞生物学 内科学 内分泌学 胎儿 细胞凋亡 胎盘 生物化学 遗传学 基因
作者
Yan Su,Juanjuan Zhang,Junlin He,Xueqing Liu,Xuemei Chen,Yubin Ding,Chao Tong,Chuan Peng,Yanqing Geng,Yingxiong Wang,Rufei Gao
出处
期刊:Journal of Molecular Medicine [Springer Science+Business Media]
卷期号:98 (4): 555-567 被引量:19
标识
DOI:10.1007/s00109-019-01849-y
摘要

Embryo implantation is an essential and complex process in mammalian reproduction. However, little evidence has indicated the involvement of autophagy during embryo implantation. To determine the possible role of autophagy in uterine of pregnant mice during the peri-implantation stage, we first examined the expression of autophagy-related markers ATG5 and LC3 on day 4, 5, and 6 of pregnancy (D4, D5, and D6, respectively). Compared with expression on D4, downregulation of the autophagy-related markers was observed on D5 and D6, the days after the embryo attached to the receptivity endometrium. Further examination showed that autophagy-related markers ATG5, ATG12, LC3, cathepsin B, and P62 at the implantation site were significantly decreased when comparing with the inter-implantation site. Fewer number of autophagosomes at the implantation site were also observed by transmission electron microscopy. To confirm the functional role of autophagy during embryo implantation in mice, we administered the autophagy inhibitor 3-methyladenine and chloroquine to mice. After treated with 3-methyladenine, the expression of decidual markers HOXA10 and progesterone receptor were significantly reduced. Furthermore, a reduction in implantation sites and increase in the HOXA10 and PR protein levels were observed in response to chloroquine treatment. In addition, impaired uterine decidualization and dysregulation of the PR and HOXA10 protein levels was observed after autophagy inhibited by 3-methyladenine and chloroquine in in vivo artificial decidualization mouse model. In the last, LC3 and P62 were also observed in normal human proliferative, secretory, and decidua tissues. In conclusion, endometrial autophagy may be essential for embryo implantation, and it may be associated with endometrial decidualization during early pregnancy. KEY MESSAGE: • Autophagy-related markers were significantly decreased at implantation site. • Autophagy inhibition results in abnormal decidualization. • Autophagy is essential for embryo implantation.

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