Placental adaptations to the maternal-fetal environment: implications for fetal growth and developmental programming
- PMID: 22560117
- DOI: 10.1016/j.rbmo.2012.03.017
Placental adaptations to the maternal-fetal environment: implications for fetal growth and developmental programming
Abstract
The placenta is a transient organ found in eutherian mammals that evolved primarily to provide nutrients for the developing fetus. The placenta exchanges a wide array of nutrients, endocrine signals, cytokines and growth factors with the mother and the fetus, thereby regulating intrauterine development. Recent studies show that the placenta is not just a passive organ mediating maternal-fetal exchange. It can adapt its capacity to supply nutrients in response to intrinsic and extrinsic variations in the maternal-fetal environment. These dynamic adaptations are thought to occur to maximize fetal growth and viability at birth in the prevailing conditions in utero. However, some of these adaptations may also affect the development of individual fetal tissues, with patho-physiological consequences long after birth. Here, this review summarizes current knowledge on the causes, possible mechanisms and consequences of placental adaptive responses, with a focus on the regulation of transporter-mediated processes for nutrients. This review also highlights the emerging roles that imprinted genes and epigenetic mechanisms of gene regulation may play in placental adaptations to the maternal-fetal environment.
Copyright © 2012 Reproductive Healthcare Ltd. Published by Elsevier Ltd. All rights reserved.
Similar articles
-
Regulation of supply and demand for maternal nutrients in mammals by imprinted genes.J Physiol. 2003 Feb 15;547(Pt 1):35-44. doi: 10.1113/jphysiol.2002.033274. Epub 2003 Jan 24. J Physiol. 2003. PMID: 12562908 Free PMC article. Review.
-
Placental adaptive responses and fetal programming.J Physiol. 2006 Apr 1;572(Pt 1):25-30. doi: 10.1113/jphysiol.2006.104968. Epub 2006 Feb 9. J Physiol. 2006. PMID: 16469781 Free PMC article. Review.
-
Review: Adaptation in placental nutrient supply to meet fetal growth demand: implications for programming.Placenta. 2010 Mar;31 Suppl:S70-4. doi: 10.1016/j.placenta.2009.12.020. Epub 2010 Jan 12. Placenta. 2010. PMID: 20060581 Review.
-
Role of the placenta in fetal programming: underlying mechanisms and potential interventional approaches.Clin Sci (Lond). 2007 Jul;113(1):1-13. doi: 10.1042/CS20060339. Clin Sci (Lond). 2007. PMID: 17536998 Review.
-
Imprinted genes, placental development and fetal growth.Horm Res. 2006;65 Suppl 3:50-8. doi: 10.1159/000091506. Epub 2006 Apr 10. Horm Res. 2006. PMID: 16612114 Review.
Cited by
-
Modeling Normal Mouse Uterine Contraction and Placental Perfusion with Non-invasive Longitudinal Dynamic Contrast Enhancement MRI.bioRxiv [Preprint]. 2024 Feb 4:2024.01.31.577398. doi: 10.1101/2024.01.31.577398. bioRxiv. 2024. Update in: PLoS One. 2024 Jul 1;19(7):e0303957. doi: 10.1371/journal.pone.0303957 PMID: 38352563 Free PMC article. Updated. Preprint.
-
Mechanistic Target of Rapamycin Complex 2 Regulation of the Primary Human Trophoblast Cell Transcriptome.Front Cell Dev Biol. 2021 Nov 4;9:670980. doi: 10.3389/fcell.2021.670980. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 34805133 Free PMC article.
-
Placental Microarray Profiling Reveals Common mRNA and lncRNA Expression Patterns in Preeclampsia and Intrauterine Growth Restriction.Int J Mol Sci. 2020 May 20;21(10):3597. doi: 10.3390/ijms21103597. Int J Mol Sci. 2020. PMID: 32443673 Free PMC article.
-
Regulation of feto-maternal barrier by matriptase- and PAR-2-mediated signaling is required for placental morphogenesis and mouse embryonic survival.PLoS Genet. 2014 Jul 31;10(7):e1004470. doi: 10.1371/journal.pgen.1004470. eCollection 2014 Jul. PLoS Genet. 2014. PMID: 25078604 Free PMC article.
-
Prenatal and postnatal stress and asthma in children: Temporal- and sex-specific associations.J Allergy Clin Immunol. 2016 Sep;138(3):740-747.e3. doi: 10.1016/j.jaci.2016.01.014. Epub 2016 Mar 4. J Allergy Clin Immunol. 2016. PMID: 26953156 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical