Roles of retinoic acid signaling in normal and abnormal development of the palate and tongue

Congenit Anom (Kyoto). 2014 May;54(2):69-76. doi: 10.1111/cga.12049.

Abstract

Palatogenesis involves various developmental events such as growth, elevation, elongation and fusion of opposing palatal shelves. Extrinsic factors such as mouth opening and subsequent tongue withdrawal are also needed for the horizontal elevation of palate shelves. Failure of any of these steps can lead to cleft palate, one of the most common birth defects in humans. It has been shown that retinoic acid (RA) plays important roles during palate development, but excess RA causes cleft palate in fetuses of both rodents and humans. Thus, the coordinated regulation of retinoid metabolism is essential for normal palatogenesis. The endogenous RA level is determined by the balance of RA-synthesizing (retinaldehyde dehydrogenases: RALDHs) and RA-degrading enzymes (CYP26s). Cyp26b1 is a key player in normal palatogenesis. In this review, we discuss recent progress in the study of the pathogenesis of RA-induced cleft palate, with special reference to the regulation of endogenous RA levels by RA-degrading enzymes.

Keywords: Cyp26s; Raldhs; palate development; retinoic acid; tongue development.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Cleft Palate / genetics
  • Cleft Palate / pathology
  • Cytochrome P-450 Enzyme System / genetics
  • Cytochrome P-450 Enzyme System / metabolism*
  • Embryo, Mammalian / metabolism
  • Embryonic Development
  • Humans
  • Organogenesis / genetics
  • Palate / embryology
  • Palate / growth & development*
  • Palate / pathology
  • Retinal Dehydrogenase / genetics
  • Retinal Dehydrogenase / metabolism
  • Retinoic Acid 4-Hydroxylase
  • Rodentia
  • Signal Transduction / genetics
  • Tongue / embryology
  • Tongue / growth & development*
  • Tongue / pathology
  • Tretinoin / metabolism*

Substances

  • Tretinoin
  • Cytochrome P-450 Enzyme System
  • Retinoic Acid 4-Hydroxylase
  • Retinal Dehydrogenase