Expression profile and thyroid hormone responsiveness of transporters and deiodinases in early embryonic chicken brain development

Mol Cell Endocrinol. 2012 Feb 26;349(2):289-97. doi: 10.1016/j.mce.2011.11.012. Epub 2011 Nov 22.

Abstract

We used the chick embryo to study the mechanisms regulating intracellular TH availability in developing brain. TH-transporters OATP1C1 and MCT8, and deiodinases D1, D2, and D3 were expressed in a region-specific way, well before the onset of endogenous TH secretion. Between day 4 and 10 of development MCT8 and D2 mRNA levels increased, while OATP1C1 and D3 mRNA levels decreased. D2 and D3 mRNAs were translated into active protein, while no D1 activity was detectable. Injection of THs into the yolk 24h before sampling increased TH levels in the brain and resulted in decreased OATP1C1 and increased MCT8 expression in 4-day-old embryos. A compensatory response in deiodinase activity was only observed at day 8. We conclude that THs are active in the early embryonic brain and TH-transporters and deiodinases can regulate their availability. However, the absence of clear compensatory mechanisms at day 4 makes the brain more vulnerable for changes in maternal TH supply.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain / drug effects
  • Brain / embryology
  • Brain / metabolism*
  • Chick Embryo
  • Chickens
  • Embryonic Development
  • Gene Expression Regulation, Developmental
  • Iodide Peroxidase / genetics
  • Iodide Peroxidase / metabolism*
  • Membrane Transport Proteins / genetics
  • Membrane Transport Proteins / metabolism*
  • Organ Specificity
  • Polymerase Chain Reaction
  • RNA, Messenger / analysis
  • RNA, Messenger / biosynthesis
  • Thyroid Gland / embryology
  • Thyroid Gland / metabolism*
  • Thyroxine / metabolism*
  • Thyroxine / pharmacology
  • Time Factors
  • Triiodothyronine / metabolism*
  • Triiodothyronine / pharmacology

Substances

  • Membrane Transport Proteins
  • RNA, Messenger
  • Triiodothyronine
  • Iodide Peroxidase
  • Thyroxine