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Maternal Factors Are Associated with the Expression of Placental Genes Involved in Amino Acid Metabolism and Transport

INTRODUCTION: Maternal environment and lifestyle factors may modify placental function to match the mother’s capacity to support the demands of fetal growth. Much remains to be understood about maternal influences on placental metabolic and amino acid transporter gene expression. We investigated the...

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Autores principales: Day, Pricilla E., Ntani, Georgia, Crozier, Sarah R., Mahon, Pam A., Inskip, Hazel M., Cooper, Cyrus, Harvey, Nicholas C., Godfrey, Keith M., Hanson, Mark A., Lewis, Rohan M., Cleal, Jane K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4682815/
https://www.ncbi.nlm.nih.gov/pubmed/26657885
http://dx.doi.org/10.1371/journal.pone.0143653
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author Day, Pricilla E.
Ntani, Georgia
Crozier, Sarah R.
Mahon, Pam A.
Inskip, Hazel M.
Cooper, Cyrus
Harvey, Nicholas C.
Godfrey, Keith M.
Hanson, Mark A.
Lewis, Rohan M.
Cleal, Jane K.
author_facet Day, Pricilla E.
Ntani, Georgia
Crozier, Sarah R.
Mahon, Pam A.
Inskip, Hazel M.
Cooper, Cyrus
Harvey, Nicholas C.
Godfrey, Keith M.
Hanson, Mark A.
Lewis, Rohan M.
Cleal, Jane K.
author_sort Day, Pricilla E.
collection PubMed
description INTRODUCTION: Maternal environment and lifestyle factors may modify placental function to match the mother’s capacity to support the demands of fetal growth. Much remains to be understood about maternal influences on placental metabolic and amino acid transporter gene expression. We investigated the influences of maternal lifestyle and body composition (e.g. fat and muscle content) on a selection of metabolic and amino acid transporter genes and their associations with fetal growth. METHODS: RNA was extracted from 102 term Southampton Women’s Survey placental samples. Expression of nine metabolic, seven exchange, eight accumulative and three facilitated transporter genes was analyzed using quantitative real-time PCR. RESULTS: Increased placental LAT2 (p = 0.01), y (+) LAT2 (p = 0.03), aspartate aminotransferase 2 (p = 0.02) and decreased aspartate aminotransferase 1 (p = 0.04) mRNA expression associated with pre-pregnancy maternal smoking. Placental mRNA expression of TAT1 (p = 0.01), ASCT1 (p = 0.03), mitochondrial branched chain aminotransferase (p = 0.02) and glutamine synthetase (p = 0.05) was positively associated with maternal strenuous exercise. Increased glutamine synthetase mRNA expression (r = 0.20, p = 0.05) associated with higher maternal diet quality (prudent dietary pattern) pre-pregnancy. Lower LAT4 (r = -0.25, p = 0.05) and aspartate aminotransferase 2 mRNA expression (r = -0.28, p = 0.01) associated with higher early pregnancy diet quality. Lower placental ASCT1 mRNA expression associated with measures of increased maternal fat mass, including pre-pregnancy BMI (r = -0.26, p = 0.01). Lower placental mRNA expression of alanine aminotransferase 2 associated with greater neonatal adiposity, for example neonatal subscapular skinfold thickness (r = -0.33, p = 0.001). CONCLUSION: A number of maternal influences have been linked with outcomes in childhood, independently of neonatal size; our finding of associations between placental expression of transporter and metabolic genes and maternal smoking, physical activity and diet raises the possibility that their effects are mediated in part through alterations in placental function. The observed changes in placental gene expression in relation to modifiable maternal factors are important as they could form part of interventions aimed at maintaining a healthy lifestyle for the mother and for optimal fetal development.
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spelling pubmed-46828152015-12-31 Maternal Factors Are Associated with the Expression of Placental Genes Involved in Amino Acid Metabolism and Transport Day, Pricilla E. Ntani, Georgia Crozier, Sarah R. Mahon, Pam A. Inskip, Hazel M. Cooper, Cyrus Harvey, Nicholas C. Godfrey, Keith M. Hanson, Mark A. Lewis, Rohan M. Cleal, Jane K. PLoS One Research Article INTRODUCTION: Maternal environment and lifestyle factors may modify placental function to match the mother’s capacity to support the demands of fetal growth. Much remains to be understood about maternal influences on placental metabolic and amino acid transporter gene expression. We investigated the influences of maternal lifestyle and body composition (e.g. fat and muscle content) on a selection of metabolic and amino acid transporter genes and their associations with fetal growth. METHODS: RNA was extracted from 102 term Southampton Women’s Survey placental samples. Expression of nine metabolic, seven exchange, eight accumulative and three facilitated transporter genes was analyzed using quantitative real-time PCR. RESULTS: Increased placental LAT2 (p = 0.01), y (+) LAT2 (p = 0.03), aspartate aminotransferase 2 (p = 0.02) and decreased aspartate aminotransferase 1 (p = 0.04) mRNA expression associated with pre-pregnancy maternal smoking. Placental mRNA expression of TAT1 (p = 0.01), ASCT1 (p = 0.03), mitochondrial branched chain aminotransferase (p = 0.02) and glutamine synthetase (p = 0.05) was positively associated with maternal strenuous exercise. Increased glutamine synthetase mRNA expression (r = 0.20, p = 0.05) associated with higher maternal diet quality (prudent dietary pattern) pre-pregnancy. Lower LAT4 (r = -0.25, p = 0.05) and aspartate aminotransferase 2 mRNA expression (r = -0.28, p = 0.01) associated with higher early pregnancy diet quality. Lower placental ASCT1 mRNA expression associated with measures of increased maternal fat mass, including pre-pregnancy BMI (r = -0.26, p = 0.01). Lower placental mRNA expression of alanine aminotransferase 2 associated with greater neonatal adiposity, for example neonatal subscapular skinfold thickness (r = -0.33, p = 0.001). CONCLUSION: A number of maternal influences have been linked with outcomes in childhood, independently of neonatal size; our finding of associations between placental expression of transporter and metabolic genes and maternal smoking, physical activity and diet raises the possibility that their effects are mediated in part through alterations in placental function. The observed changes in placental gene expression in relation to modifiable maternal factors are important as they could form part of interventions aimed at maintaining a healthy lifestyle for the mother and for optimal fetal development. Public Library of Science 2015-12-14 /pmc/articles/PMC4682815/ /pubmed/26657885 http://dx.doi.org/10.1371/journal.pone.0143653 Text en © 2015 Day et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Day, Pricilla E.
Ntani, Georgia
Crozier, Sarah R.
Mahon, Pam A.
Inskip, Hazel M.
Cooper, Cyrus
Harvey, Nicholas C.
Godfrey, Keith M.
Hanson, Mark A.
Lewis, Rohan M.
Cleal, Jane K.
Maternal Factors Are Associated with the Expression of Placental Genes Involved in Amino Acid Metabolism and Transport
title Maternal Factors Are Associated with the Expression of Placental Genes Involved in Amino Acid Metabolism and Transport
title_full Maternal Factors Are Associated with the Expression of Placental Genes Involved in Amino Acid Metabolism and Transport
title_fullStr Maternal Factors Are Associated with the Expression of Placental Genes Involved in Amino Acid Metabolism and Transport
title_full_unstemmed Maternal Factors Are Associated with the Expression of Placental Genes Involved in Amino Acid Metabolism and Transport
title_short Maternal Factors Are Associated with the Expression of Placental Genes Involved in Amino Acid Metabolism and Transport
title_sort maternal factors are associated with the expression of placental genes involved in amino acid metabolism and transport
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4682815/
https://www.ncbi.nlm.nih.gov/pubmed/26657885
http://dx.doi.org/10.1371/journal.pone.0143653
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