Involvement of epigenetic modifications in thyroid hormone-dependent formation of adult intestinal stem cells during amphibian metamorphosis

Gen Comp Endocrinol. 2019 Jan 15:271:91-96. doi: 10.1016/j.ygcen.2018.11.012. Epub 2018 Nov 22.

Abstract

Amphibian metamorphosis has long been used as model to study postembryonic development in vertebrates, a period around birth in mammals when many organs/tissues mature into their adult forms and is characterized by peak levels of plasma thyroid hormone (T3). Of particular interest is the remodeling of the intestine during metamorphosis. In the highly-related anurans Xenopus laevis and Xenopus tropicalis, this remodeling process involves larval epithelial cell death and de novo formation of adult stem cells via dedifferentiation of some larval cells under the induction of T3, making it a valuable system to investigate how adult organ-specific stem cells are formed during vertebrate development. Here, we will review some studies by us and others on how T3 regulates the formation of the intestinal stem cells during metamorphosis. We will highlight the involvement of nucleosome removal and a positive feedback mechanism involving the histone methyltransferases in gene regulation by T3 receptor (TR) during this process.

Keywords: Adult stem cell; Amphibian metamorphosis; Histone acetylation; Histone methylation; Intestinal remodeling; Thyroid hormone receptor; Xenopus laevis; Xenopus tropicalis.

Publication types

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

MeSH terms

  • Adult Stem Cells / cytology
  • Adult Stem Cells / drug effects
  • Adult Stem Cells / metabolism*
  • Animals
  • Epigenesis, Genetic / drug effects*
  • Epithelial Cells / drug effects
  • Epithelial Cells / metabolism
  • Feedback, Physiological / drug effects
  • Gene Expression Regulation, Developmental / drug effects
  • Histone Methyltransferases / genetics
  • Histone Methyltransferases / metabolism
  • Intestines / cytology*
  • Larva / metabolism
  • Metamorphosis, Biological / drug effects
  • Metamorphosis, Biological / genetics*
  • Models, Biological
  • Receptors, Thyroid Hormone / metabolism
  • Triiodothyronine / pharmacology*
  • Xenopus Proteins / genetics
  • Xenopus Proteins / metabolism
  • Xenopus laevis / genetics*
  • Xenopus laevis / growth & development*

Substances

  • Receptors, Thyroid Hormone
  • Xenopus Proteins
  • Triiodothyronine
  • Histone Methyltransferases