» Articles » PMID: 25023682

Embryonic Diapause: Development on Hold

Overview
Journal Int J Dev Biol
Date 2014 Jul 16
PMID 25023682
Citations 51
Authors
Affiliations
Soon will be listed here.
Abstract

Embryonic diapause, the temporary suspension of development of the embryo, is a fascinating reproductive strategy that has been frequently exploited across the animal kingdom. It is characterized by an arrest in development that occurs at the blastocyst stage in over 130 species of mammals. Its presumed function is to uncouple mating from parturition, to ensure that both occur at the most propitious moment for survival of the species. Diapause can be facultative, i.e. induced by physiological conditions, or obligate, i.e. present in every gestation of a species. In the latter case, the proximal signals for regulation are related to photoperiod. Three diverse models, the mouse, the mustelid carnivores and the wallaby have been studied in detail. From these studies it can be discerned that, although the endocrine cues responsible for induction of diapause and re-initiation of development vary widely between species, there are a number of commonalities. Evidence to date indicates that the uterus exercises the proximal regulatory influence over whether an embryo enters into and when it exits from diapause. Some factors have been identified that appear crucial to this regulation, in particular, the polyamines. Recent studies indicate that diapause can be induced in species where it does not exist in nature. This suggests that the potential for diapause in mammals to be due to a single evolutionary event, to which control mechanisms adapted when the trait was beneficial to reproductive success. Further work at the molecular, cellular and organismic levels will be required before the physiological basis of diapause is resolved.

Citing Articles

Prolactin drives cortical neuron maturation and dendritic development during murine embryonic stem cell differentiation.

Martinez-Alarcon O, Colin-Lagos D, Ramirez-Meza X, Castilla A, Hernandez-Montes G, Flores-Garza E Front Cell Dev Biol. 2025; 13:1551090.

PMID: 40078368 PMC: 11897521. DOI: 10.3389/fcell.2025.1551090.


Oxytocin induces embryonic diapause.

Minder J, Winokur S, Stephens J, Tong J, Cassel N, Schuster L Sci Adv. 2025; 11(10):eadt1763.

PMID: 40043121 PMC: 11881891. DOI: 10.1126/sciadv.adt1763.


Transcriptional Regulatory Network of the Embryonic Diapause Termination Process in .

Wang B, He Z, Zhang M, Zhang R, Song Z, Li A Genes (Basel). 2025; 16(2).

PMID: 40004504 PMC: 11855619. DOI: 10.3390/genes16020175.


Molecular and cellular regulators of embryo implantation and their application in improving the implantation potential of IVF-derived blastocysts.

Liu C, Fukui E, Matsumoto H Reprod Med Biol. 2025; 24(1):e12633.

PMID: 39866379 PMC: 11759885. DOI: 10.1002/rmb2.12633.


The role of serendipity in our investigation of embryo implantation.

Sutherland A Dev Biol. 2025; 520:135-140.

PMID: 39826766 PMC: 11830518. DOI: 10.1016/j.ydbio.2025.01.010.