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Vertebrate reproductive science and technology
REVIEW

Society for Reproductive Biology Founders’ Lecture 2009. Preparing fertile soil: the importance of endometrial receptivity

Lois A. Salamonsen A B , Guiying Nie A , Natalie J. Hannan A and Evdokia Dimitriadis A
+ Author Affiliations
- Author Affiliations

A Prince Henry’s Institute of Medical Research, PO Box 5152, Clayton, Vic. 3168, Australia.

B Corresponding author. Email: lois.salamonsen@princehenrys.org

Reproduction, Fertility and Development 21(7) 923-934 https://doi.org/10.1071/RD09145
Submitted: 16 June 2009  Accepted: 3 August 2009   Published: 24 August 2009

Abstract

The human endometrium is receptive for implantation of a blastocyst for only 4–5 days in each menstrual cycle. Failure of implantation is a major reason for infertility in women and the inability to achieve endometrial receptivity is responsible for much of the failure of reproductive technologies. Endometrial receptivity requires changes in the uterine luminal and glandular cells, particularly in terms of their secretory capacity and altered expression of adhesion molecules. In parallel with these changes, decidualisation (differentiation) of the endometrial stroma is initiated in women during the receptive phase, regardless of the presence of a blastocyst. Increased leucocyte numbers are also important. The microenvironments provided by the endometrium during the receptive phase and that support implantation are highly complex and constantly changing as implantation progresses. The present review provides a comprehensive overview of the cellular and molecular events of human implantation. It also summarises work from our laboratories emphasising the functional importance of proprotein convertase 6, along with key cytokines (interleukin-11, leukaemia inhibitory factor, activin A) and chemokines (including CX3CL1 and CCL14), during implantation. Of particular importance is how these mediators contribute to receptivity and how they are disturbed in infertile women. Factors that are critical for uterine receptivity may also be manipulated to provide new contraceptive strategies for women.


Acknowledgements

Work in the authors’ laboratories is currently supported by the National Health and Medical Research Council of Australia through a program grant (494802), fellowships (388901 to L.A.S.; 494808 to G.N.), a career development grant (550905 to E.D.) and project grants (441117 and 388916), as well as by Contraceptive Research and Development/Consortium for Industrial Collaboration in Contraceptive Research. The authors thank Sue Panckridge for assistance with the figures. In particular, thanks are due to the patients and their doctors who generously contribute endometrial tissue for our research.


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