Retinoic acid controls expression of tissue remodeling genes Hmgn1 and Fgf18 at the digit-interdigit junction

Dev Dyn. 2010 Feb;239(2):665-71. doi: 10.1002/dvdy.22188.

Abstract

Previous studies on retinoic acid receptor (RAR) mutants suggested that retinoic acid (RA) is required for loss of interdigital mesenchyme during digit formation. Here, we report that the RA-generating enzyme retinaldehyde dehydrogenase-2 (Raldh2) is expressed in the interdigital mesenchyme whereas Cyp26b1, controlling RA degradation, is expressed in digits, limiting autopodal RA action to the interdigital zones. Embryonic day 13.5 Raldh2-/- mouse embryos lose expression of the RARE-lacZ RA-reporter transgene and matrix metalloproteinase-11 (Mmp11) throughout the interdigital mesenchyme, while expression of RARb, Fgf18, and high mobility group N1 (Hmgn1) is lost at the digit-interdigit junction. Raldh2-/- autopods exhibit reduced interdigital apoptosis associated with loss of Bmp7 expression, but Bmp2, Bmp4, Msx2, and Fgf8 were unaffected. Although interdigital expression of Hmgn1 was greatly down-regulated in Raldh2-/- autopods, complementary expression of Sox9 in digit cartilage was unaffected. Regulation of Hmgn1 and Fgf18 at the digit-interdigit junction suggests RA controls tissue remodeling as well as apoptosis.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Aldehyde Oxidoreductases / metabolism*
  • Animals
  • Apoptosis
  • Bone Morphogenetic Proteins / metabolism
  • Embryonic Development*
  • Fibroblast Growth Factors / metabolism*
  • HMGN1 Protein / metabolism*
  • Hindlimb / embryology
  • Hindlimb / metabolism
  • Matrix Metalloproteinase 11 / metabolism
  • Mice
  • Mutation
  • Receptors, Retinoic Acid / metabolism
  • SOX9 Transcription Factor / metabolism
  • Signal Transduction
  • Tretinoin / metabolism*

Substances

  • Bone Morphogenetic Proteins
  • HMGN1 Protein
  • Receptors, Retinoic Acid
  • SOX9 Transcription Factor
  • Sox9 protein, mouse
  • fibroblast growth factor 18
  • retinoic acid receptor beta
  • Tretinoin
  • Fibroblast Growth Factors
  • Aldehyde Oxidoreductases
  • RALDH2 protein, mouse
  • Matrix Metalloproteinase 11