Document Detail


Distinct actions of insulin-like growth factors (IGFs) on placental development and fetal growth: lessons from mice and guinea pigs.
MedLine Citation:
PMID:  18191196     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Placental insufficiency is thought to be a key factor in many cases of intrauterine growth restriction which complicates about 6% of pregnancies in western countries. Understanding the molecular control of placental and fetal growth is essential to identifying diagnostic and therapeutic targets to improve pregnancy success. Insulin-like growth factor (IGF)-I and IGF-II gene ablation or maternal food restriction reduce tissue and circulating IGF abundance in the fetus, placenta and mother and are associated with both placental and fetal growth restriction. Conversely, in vivo treatment of the pregnant guinea pig with IGF-I or IGF-II from early to mid pregnancy increases fetal weight and enhances placental transport near term. IGF-II, and an IGF2R specific analogue, enhanced placental structural differentiation, whereas IGF-I altered maternal body composition. These outcomes demonstrate endocrine roles within the mother for both IGFs, as well as autocrine/paracrine effects of IGF-II in enhancing placentation and pregnancy success. Therefore, factors that alter placental expression of IGF-II, or maternal circulating IGF-I or IGF-II in early pregnancy may affect placental exchange function late in gestation when the demands of the fetus escalate. IGF-II within the fetus may also signal its nutrient demands to the placenta to improve its function to suit. Therefore each IGF of endocrine and local origin has important, but distinct, roles in placental development and function.
Authors:
C T Roberts; J A Owens; A N Sferruzzi-Perri
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Review     Date:  2008-01-11
Journal Detail:
Title:  Placenta     Volume:  29 Suppl A     ISSN:  0143-4004     ISO Abbreviation:  Placenta     Publication Date:  2008 Mar 
Date Detail:
Created Date:  2008-03-14     Completed Date:  2008-07-17     Revised Date:  2009-11-19    
Medline Journal Info:
Nlm Unique ID:  8006349     Medline TA:  Placenta     Country:  England    
Other Details:
Languages:  eng     Pagination:  S42-7     Citation Subset:  IM    
Affiliation:
Discipline of Obstetrics and Gynaecology, University of Adelaide, Adelaide, S.A. 5005, Australia. claire.roberts@adelaide.edu.au
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MeSH Terms
Descriptor/Qualifier:
Animals
Female
Fetal Development / physiology*
Guinea Pigs
Humans
Insulin-Like Growth Factor I / physiology*
Insulin-Like Growth Factor II / physiology*
Mice
Placenta / physiology*
Pregnancy
Receptor, IGF Type 1 / physiology
Receptor, IGF Type 2 / physiology
Chemical
Reg. No./Substance:
0/Receptor, IGF Type 2; 67763-96-6/Insulin-Like Growth Factor I; 67763-97-7/Insulin-Like Growth Factor II; EC 2.7.10.1/Receptor, IGF Type 1

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