4.6 Article

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

Journal

PLOS ONE
Volume 10, Issue 12, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0143653

Keywords

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Funding

  1. Medical Research Council [MC_US_A620_0033]
  2. Wessex Medical Research
  3. Arthritis Research UK
  4. National Osteoporosis Society
  5. International Osteoporosis Foundation
  6. Cohen Trust
  7. NIHR Southampton Biomedical Research Centre
  8. University of Southampton
  9. University Hospital Southampton NHS Foundation Trust
  10. NIHR Musculoskeletal Biomedical Research Unit
  11. University of Oxford
  12. Dunhill Medical Trust
  13. Gerald Kerkut Charitable Trust
  14. National Institute for Health Research through the NIHR Southampton Biomedical Research Centre
  15. European Union [289346]
  16. MRC [MC_U147585819, G0400491, MC_UU_12011/4, MC_UP_A620_1017, MC_U147585827] Funding Source: UKRI
  17. British Heart Foundation [RG/07/009/23120] Funding Source: researchfish
  18. Medical Research Council [MC_UP_A620_1017, MC_U147585827, U1475000001, MC_U147585819, MC_UP_A620_1014, MC_UU_12011/1, MC_U147585824, MC_UU_12011/4, G0400491] Funding Source: researchfish
  19. National Institute for Health Research [NF-SI-0508-10082, NF-SI-0513-10085] Funding Source: researchfish
  20. Versus Arthritis [17702] Funding Source: researchfish

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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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