Endometrial autophagy is essential for embryo implantation during early pregnancy.


Journal

Journal of molecular medicine (Berlin, Germany)
ISSN: 1432-1440
Titre abrégé: J Mol Med (Berl)
Pays: Germany
ID NLM: 9504370

Informations de publication

Date de publication:
04 2020
Historique:
received: 26 03 2019
accepted: 25 10 2019
revised: 16 10 2019
pubmed: 20 2 2020
medline: 16 6 2021
entrez: 20 2 2020
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 32072231
doi: 10.1007/s00109-019-01849-y
pii: 10.1007/s00109-019-01849-y
doi:

Substances chimiques

Autophagy-Related Protein 5 0
Biomarkers 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

555-567

Auteurs

Yan Su (Y)

Laboratory of Reproductive Biology, School of Public Health, Chongqing Medical University, Chongqing, 400016, China.
Joint International Research Laboratory of Reproduction&Development, Chongqing, 400016, China.

Juan-Juan Zhang (JJ)

Laboratory of Reproductive Biology, School of Public Health, Chongqing Medical University, Chongqing, 400016, China.
Reproductive Medicine Centre, Taihe Hospital, Hubei University of Medicine, 32 South Renmin Road, Shiyan, 442000, Hubei, China.

Jun-Lin He (JL)

Laboratory of Reproductive Biology, School of Public Health, Chongqing Medical University, Chongqing, 400016, China.
Joint International Research Laboratory of Reproduction&Development, Chongqing, 400016, China.

Xue-Qing Liu (XQ)

Laboratory of Reproductive Biology, School of Public Health, Chongqing Medical University, Chongqing, 400016, China.
Joint International Research Laboratory of Reproduction&Development, Chongqing, 400016, China.

Xue-Mei Chen (XM)

Laboratory of Reproductive Biology, School of Public Health, Chongqing Medical University, Chongqing, 400016, China.
Joint International Research Laboratory of Reproduction&Development, Chongqing, 400016, China.

Yu-Bin Ding (YB)

Laboratory of Reproductive Biology, School of Public Health, Chongqing Medical University, Chongqing, 400016, China.
Joint International Research Laboratory of Reproduction&Development, Chongqing, 400016, China.

Chao Tong (C)

Joint International Research Laboratory of Reproduction&Development, Chongqing, 400016, China.
Department of Obstetrics, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, China.

Chuan Peng (C)

Joint International Research Laboratory of Reproduction&Development, Chongqing, 400016, China.
The Chongqing Key Laboratory of Translational Medicine in Major Metabolic Diseases, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, China.

Yan-Qing Geng (YQ)

Laboratory of Reproductive Biology, School of Public Health, Chongqing Medical University, Chongqing, 400016, China.
Joint International Research Laboratory of Reproduction&Development, Chongqing, 400016, China.

Ying-Xiong Wang (YX)

Laboratory of Reproductive Biology, School of Public Health, Chongqing Medical University, Chongqing, 400016, China. yxwang@cqmu.edu.cn.
Joint International Research Laboratory of Reproduction&Development, Chongqing, 400016, China. yxwang@cqmu.edu.cn.

Ru-Fei Gao (RF)

Laboratory of Reproductive Biology, School of Public Health, Chongqing Medical University, Chongqing, 400016, China. gao_ru_fei@cqmu.edu.cn.
Joint International Research Laboratory of Reproduction&Development, Chongqing, 400016, China. gao_ru_fei@cqmu.edu.cn.

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Classifications MeSH