Epigenetic Mechanisms of Epidermal Differentiation

Int J Mol Sci. 2022 Apr 28;23(9):4874. doi: 10.3390/ijms23094874.

Abstract

Keratinocyte differentiation is an essential process for epidermal stratification and stratum corneum formation. Keratinocytes proliferate in the basal layer of the epidermis and start their differentiation by changing their functional or phenotypical type; this process is regulated via induction or repression of epidermal differentiation complex (EDC) genes that play a pivotal role in epidermal development. Epidermal development and the keratinocyte differentiation program are orchestrated by several transcription factors, signaling pathways, and epigenetic regulators. The latter exhibits both activating and repressive effects on chromatin in keratinocytes via the ATP-dependent chromatin remodelers, histone demethylases, and genome organizers that promote terminal keratinocyte differentiation, and the DNA methyltransferases, histone deacetylases, and Polycomb components that stimulate proliferation of progenitor cells and inhibit premature activation of terminal differentiation-associated genes. In addition, microRNAs are involved in different processes between proliferation and differentiation during the program of epidermal development. Here, we bring together current knowledge of the mechanisms controlling gene expression during keratinocyte differentiation. An awareness of epigenetic mechanisms and their alterations in health and disease will help to bridge the gap between our current knowledge and potential applications for epigenetic regulators in clinical practice to pave the way for promising target therapies.

Keywords: ATP-dependent chromatin remodeler; DNA methyltransferases; atopic dermatitis; epidermal differentiation complex; epigenetic regulators; histone modifications; keratinocytes; microRNAs; polycomb proteins; psoriasis.

Publication types

  • Review

MeSH terms

  • Cell Differentiation / genetics
  • Chromatin / metabolism
  • Epidermis* / metabolism
  • Epigenesis, Genetic
  • Keratinocytes* / metabolism

Substances

  • Chromatin

Grants and funding

This research received no external funding.