Lamin B receptor (LBR) is involved in the induction of cellular senescence in human cells

Mech Ageing Dev. 2019 Mar:178:25-32. doi: 10.1016/j.mad.2019.01.001. Epub 2019 Jan 4.

Abstract

Cellular senescence is a phenomenon of irreversible growth arrest in mammalian somatic cells in culture. Various stresses induce cellular senescence and indeed, we have found that excess thymidine effectively induces cellular senescence in human cells. Further, many reports indicate the implication of chromatin proteins in cellular senescence. Here we analysed the role of lamin B receptor (LBR), a nuclear envelope protein that regulates heterochromatin organization, in cellular senescence induced by excess thymidine. We then found that the LBR protein was down-regulated and showed aberrant localization in cells upon induction of cellular senescence by excess thymidine. Additionally, we also found that knock-down of LBR facilitated the induction of cellular senescence by excess thymidine in cancerous HeLa cells, and importantly, it induced cellular senescence in normal human diploid fibroblast TIG-7 cells. These results suggested that decreased LBR function is involved in the induction of cellular senescence in human cells.

Keywords: Cellular senescence; Chromatin foci; LBR; Nuclear envelope; γ-H2AX ring.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bromodeoxyuridine / pharmacology
  • Cellular Senescence / genetics
  • Cellular Senescence / physiology*
  • DNA Damage / drug effects
  • DNA Replication / drug effects
  • Gene Knockdown Techniques
  • HeLa Cells
  • Heterochromatin / metabolism
  • Humans
  • Lamin B Receptor
  • Lamin Type B / metabolism
  • Nuclear Envelope / metabolism
  • Receptors, Cytoplasmic and Nuclear / genetics
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Thymidine / pharmacology

Substances

  • Heterochromatin
  • Lamin Type B
  • Receptors, Cytoplasmic and Nuclear
  • Bromodeoxyuridine
  • Thymidine