Impairment of osteoblast differentiation due to proliferation-independent telomere dysfunction in mouse models of accelerated aging

Aging Cell. 2012 Aug;11(4):704-13. doi: 10.1111/j.1474-9726.2012.00838.x. Epub 2012 Jun 11.

Abstract

We undertook genetic and nongenetic approaches to investigate the relationship between telomere maintenance and osteoblast differentiation, as well as to uncover a possible link between a known mediator of cellular aging and senile bone loss. Using mouse models of disrupted telomere maintenance molecules, including mutants in the Werner helicase (Wrn(-/-) ), telomerase (Terc(-/-) ), and Wrn(-/-) Terc(-/-) double mutants predisposed to accelerated bone loss, we measured telomere dysfunction-induced foci (TIFs) and markers of osteoblast differentiation in mesenchymal progenitor cells (MPCs). We found that telomere maintenance is directly and significantly related to osteoblast differentiation, with dysfunctional telomeres associated with impaired differentiation independent of proliferation state. Telomere-mediated defects in osteoblast differentiation are associated with increased p53/p21 expression and concomitant reduction in RUNX2. Conversely, MPCs from p53(-/-) mice do not have substantial telomere dysfunction and spontaneously differentiate into osteoblasts. These results suggest that critical telomere dysfunction may be a prominent mechanism for age-related osteoporosis and limits MPC differentiation into bone-forming cells via the p53/p21 pathway.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging, Premature / enzymology
  • Aging, Premature / genetics*
  • Aging, Premature / pathology*
  • Animals
  • Cell Differentiation / genetics
  • Cellular Senescence / genetics
  • Cellular Senescence / physiology
  • Disease Models, Animal
  • Female
  • Male
  • Mesenchymal Stem Cells / enzymology
  • Mesenchymal Stem Cells / pathology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Osteoblasts / enzymology
  • Osteoblasts / pathology*
  • Osteoporosis / enzymology
  • Osteoporosis / genetics
  • Osteoporosis / pathology
  • RecQ Helicases / deficiency
  • RecQ Helicases / genetics
  • Signal Transduction
  • Telomerase / deficiency
  • Telomerase / genetics
  • Telomere Homeostasis / genetics*
  • Werner Syndrome Helicase

Substances

  • Telomerase
  • RecQ Helicases
  • Werner Syndrome Helicase
  • Wrn protein, mouse