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6 - Tissue remodelling the fetal-maternal interface: the regulation of matrix metalloproteinase 9 transcription

from SECTION 1 - PREPARATION FOR IMPLANTATION – THE UTERINE ENVIRONMENT

Published online by Cambridge University Press:  05 June 2014

Marie Cohen
Affiliation:
University of Geneva
Paul Bischof
Affiliation:
University of Geneva
Hilary Critchley
Affiliation:
University of Edinburgh
Iain Cameron
Affiliation:
University of Southampton
Stephen Smith
Affiliation:
Lee Kong Chian School of Medicine
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Summary

Introduction

As life moved out of the oceans, new reproductive strategies developed to account for the loss of nutrients and oxygen normally provided by the water environment. Despite the fact that many examples of viviparity exist in invertebrates, fish, amphibians and reptiles, placentation is a relatively new acquisition in evolution. The establishment of an intimate trophic connection between mother and embryo is a characteristic of mammals. Implantation and the ensuing placentation are thus new strategies in reproduction, which allow the development of a small number of fetuses in the protective maternal organism. As the mammals evolved from small rodent-like creatures with short gestational periods to larger animals with prolonged gestations, the placenta had to adapt to the increasing needs of the growing fetus.

Orchestrating the blastocyst—endometrial summit requires perfect synchronisation between embryonic development and endometrial maturation. This synchronisation does not only involve the embryo and the endometrium but also the maternal pituitary and the ovary. As a result of ovarian oestradiol and progesterone secretions, the endometrium proliferates and differentiates. During the mid-luteal phase (days 22—24 of a 28-day cycle) decidualisation starts around the endometrial spiral arteries and extends to the whole endometrium within a few days. The endometrial extracellular matrix (ECM) becomes distended because water is attracted, possibly owing to the decidual secretion of hygroscopic molecules such as heparan sulphate proteoglycans.

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Publisher: Cambridge University Press
Print publication year: 2005

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