DNA ploidy changes in rhino mouse skin induced by all-trans retinoic acid and retinol

Skin Pharmacol. 1997;10(3):135-43. doi: 10.1159/000211478.

Abstract

Objective: In order to assess the proliferative changes induced by all-trans retinoic acid (RA) and retinol (ROL), we have carried out a study of the DNA content of basal and suprabasal keratinocytes after epicutaneous application on the rhino mouse.

Study design: Skin sections were analyzed stereologically and cytophotometrically using the Feulgen technique. The diploid DNA value (2C) was obtained from hepatocyte nuclei of control animals. Whereas cells in phase G0-G1 will show a 2C content, cells during phase S and in phase G2-M will show DNA values ranging from 2C to 4C and 4C, respectively.

Results: Although epidermal thickness (ET) increased significantly in all treated animals, surface density only increased in animals treated with all-trans RA. Quantification of DNA content of basal keratinocytes showed reduction of 2C and 2C-4C populations with a commensurate increase in proportions of cells with 4C and > 4C in the animals treated with 0.025% all-trans RA and ROL. Suprabasal keratinocytes of mice treated with 0.025% all-trans showed a decrease of the 2C population and an increased proportion of cells with 4C. Whereas 0.025% all-trans RA induced an increase of both basal and suprabasal DNA indices, ROL enhanced only the basal DNA index significantly.

Conclusion: Animals treated with 0.025% ROL showed a significant increase in the basal proliferative index (PI) while the suprabasal PI remained constant; treatment with 0.025% all-trans RA produced a significant increase of both basal and suprabasal PIs and parakeratotic hyperkeratosis probably due to incomplete differentiation.

Publication types

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

MeSH terms

  • Administration, Cutaneous
  • Animals
  • Cell Cycle
  • Cell Differentiation / drug effects
  • DNA / biosynthesis*
  • Epidermis / drug effects
  • Epidermis / metabolism
  • Epidermis / pathology
  • Female
  • Hyperplasia
  • In Vitro Techniques
  • Keratinocytes / drug effects
  • Keratinocytes / metabolism
  • Keratinocytes / pathology
  • Keratolytic Agents / administration & dosage
  • Keratolytic Agents / pharmacology*
  • Mice
  • Mice, Hairless
  • Mice, Mutant Strains
  • Ploidies*
  • Skin / drug effects*
  • Skin / metabolism
  • Skin / pathology
  • Tretinoin / administration & dosage
  • Tretinoin / pharmacology*
  • Vitamin A / administration & dosage
  • Vitamin A / pharmacology*

Substances

  • Keratolytic Agents
  • Vitamin A
  • Tretinoin
  • DNA