Skip to main content Accessibility help
×
Hostname: page-component-78c5997874-lj6df Total loading time: 0 Render date: 2024-11-14T19:26:28.558Z Has data issue: false hasContentIssue false

7 - Embryo interactions in human implantation

from SECTION 1 - PREPARATION FOR IMPLANTATION – THE UTERINE ENVIRONMENT

Published online by Cambridge University Press:  05 June 2014

Francisco Domínguez
Affiliation:
Fundacion Instituto Valenciano de Infertilidad, Spain
Jose A Horcajadas
Affiliation:
Fundacion Instituto Valenciano de Infertilidad, Spain
Ana Cervero
Affiliation:
Fundacion Instituto Valenciano de Infertilidad, Spain
Antonio Pellicer
Affiliation:
Instituto Valenciano de Infertilidad, Spain
Carlos Simón
Affiliation:
Fundacion Instituto Valenciano de Infertilidad, Spain
Hilary Critchley
Affiliation:
University of Edinburgh
Iain Cameron
Affiliation:
University of Southampton
Stephen Smith
Affiliation:
Lee Kong Chian School of Medicine
Get access

Summary

Introduction

Embryonic implantation, the process by which the human embryo orientates towards, attaches to and finally invades the underlying maternal endometrial tissue, requires a receptive endometrium, a functionally normal blastocyst and adequate cross-communication between endometrium and blastocyst. During apposition, human blastocysts find a location in which to implant, while they are guided to a specific area in the maternal endometrium. In the adhesion phase, which occurs six to seven days after ovulation, within the ‘implantation window’, direct contact occurs between the endometrial epithelium and the trophectoderm. Finally, in the invasion phase, the embryonic trophoblast traverses the basement membrane and passes the endometrial stroma to reach the uterine vessels.

Many molecules (hormones, cytokines, integrins, enzymes, etc.) take part in the dialogue between the human blastocyst and the maternal endometrium to achieve implantation. We present here our published data on the embryonic regulation of endometrial epithelial molecules such as chemokine receptors, the leptin system and the relaxin receptor LGR7. A final section on gene profiling is also included.

Chemokine receptors at the maternal-embryonic interface

Chemokines, a family of small polypeptides with molecular weights in the range 8—12 kDa, attract specific leucocyte subsets by binding to cell-surface receptors. In reproductive biology, these molecules have been implicated in crucial processes such as ovulation, menstruation and parturition, and in pathological processes such as preterm delivery, HIV infection, endometriosis and ovarian hyperstimulation syndrome, as well as in embryo implantation.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2005

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×