Distinct modulation of a gene expression of the type 1 and 2 IP(3) receptors by retinoic acid in brain areas

Neurochem Int. 2005 Jun;46(7):559-64. doi: 10.1016/j.neuint.2005.01.003.

Abstract

Inositol 1,4,5-trisphosphate (IP(3)) receptors belong to the intracellular calcium channels that release calcium from the intracellular stores after binding IP(3). Three types of IP(3) receptors occurred in a tissue specific manner and different promoters direct their gene expression. Thus, understanding of the transcriptional regulation is the first step towards comprehension of the function of these receptors. Since the retinoic acid activates RARE and AP2 transcription factors, the present study focuses on determination of whether or not expression of type 1 and 2 IP(3) receptors is modulated by retinoic acid in selected brain areas. We have found that mRNA levels of the type 1 IP(3) receptors were decreased significantly in cerebellum and hypothalamus, but not in the brain stem of rats treated with retinoic acid, compared to untreated littermates. The mRNA levels of the type 2 IP(3) receptor were significantly decreased in all tested tissues, cerebellum, hypothalamus, and also in brain stem after the treatment with retinoic acid. These results show that gene expression of both type 1 and 2 IP(3) receptors is regulated by retinoic acid, although the effect of retinoic acid on mRNA levels of the type 1 IP(3) receptors is dependent on brain area.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antineoplastic Agents / metabolism
  • Antineoplastic Agents / pharmacology
  • Brain / drug effects
  • Brain / metabolism*
  • Brain Stem / drug effects
  • Brain Stem / metabolism
  • Calcium Channels / drug effects
  • Calcium Channels / genetics*
  • Calcium Channels / metabolism
  • Calcium Signaling / drug effects
  • Calcium Signaling / physiology
  • Cerebellum / drug effects
  • Cerebellum / metabolism
  • Gene Expression Regulation / drug effects
  • Gene Expression Regulation / physiology*
  • Hypothalamus / drug effects
  • Hypothalamus / metabolism
  • Inositol 1,4,5-Trisphosphate Receptors
  • Male
  • Membrane Glycoproteins / genetics*
  • Neurons / drug effects
  • Neurons / metabolism*
  • RNA, Messenger / drug effects
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Wistar
  • Receptors, Cytoplasmic and Nuclear / drug effects
  • Receptors, Cytoplasmic and Nuclear / genetics*
  • Receptors, Cytoplasmic and Nuclear / metabolism
  • Tretinoin / metabolism*
  • Tretinoin / pharmacology

Substances

  • Antineoplastic Agents
  • Calcium Channels
  • Inositol 1,4,5-Trisphosphate Receptors
  • Itpr1 protein, rat
  • Membrane Glycoproteins
  • RNA, Messenger
  • Receptors, Cytoplasmic and Nuclear
  • Tretinoin