Regulation of ADRP expression by long-chain polyunsaturated fatty acids in BeWo cells, a human placental choriocarcinoma cell line

J Lipid Res. 2006 Apr;47(4):815-23. doi: 10.1194/jlr.M500527-JLR200. Epub 2006 Jan 3.

Abstract

Transplacental transfer of maternal fatty acids is critical for fetal growth and development. In the placenta, a preferential uptake of fatty acids toward long-chain polyunsaturated fatty acids (LCPUFAs) has been demonstrated. Adipose differentiation-related protein (ADRP) is a lipid droplet-associated protein that has been ascribed a role in cellular fatty acid uptake and storage. However, its role in placenta is not known. We demonstrate that ADRP mRNA and protein are regulated by fatty acids in a human placental choriocarcinoma cell line (BeWo) and in primary human trophoblasts. LCPUFAs of the n-3 and n-6 series [arachidonic acid (20:4n-6), docosahexaenoic acid (22:6n-3), and eicosapentaenoic acid (20:5n-3)] were more efficient than shorter fatty acids at stimulating ADRP mRNA expression. The fatty acid-mediated increase in ADRP mRNA expression was not related to the differentiation state of the cells. Synthetic peroxisome proliferator-activated receptor and retinoic X receptor agonists increased ADRP mRNA level but had no effect on ADRP protein level in undifferentiated BeWo cells. Furthermore, we show that incubation of BeWo cells with LCPUFAs, but not synthetic agonists, increased the cellular content of radiolabeled oleic acid, coinciding with the increase in ADRP mRNA and protein level. These studies provide new information on the regulation of ADRP in placental trophoblasts and suggest that LCPUFA-dependent regulation of ADRP could be involved in the metabolism of lipids in the placenta.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Differentiation
  • Cell Line, Tumor
  • Choriocarcinoma / metabolism*
  • Choriocarcinoma / pathology
  • Dose-Response Relationship, Drug
  • Fatty Acids, Unsaturated* / chemistry
  • Fatty Acids, Unsaturated* / metabolism
  • Fatty Acids, Unsaturated* / pharmacology
  • Female
  • Humans
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Perilipin-2
  • Placenta / pathology*
  • Pregnancy
  • RNA, Messenger / metabolism
  • Trophoblasts / drug effects
  • Trophoblasts / metabolism*

Substances

  • Fatty Acids, Unsaturated
  • Membrane Proteins
  • PLIN2 protein, human
  • Perilipin-2
  • RNA, Messenger