Notch-mediated restoration of regenerative potential to aged muscle

Science. 2003 Nov 28;302(5650):1575-7. doi: 10.1126/science.1087573.

Abstract

A hallmark of aging is diminished regenerative potential of tissues, but the mechanism of this decline is unknown. Analysis of injured muscle revealed that, with age, resident precursor cells (satellite cells) had a markedly impaired propensity to proliferate and to produce myoblasts necessary for muscle regeneration. This was due to insufficient up-regulation of the Notch ligand Delta and, thus, diminished activation of Notch in aged, regenerating muscle. Inhibition of Notch impaired regeneration of young muscle, whereas forced activation of Notch restored regenerative potential to old muscle. Thus, Notch signaling is a key determinant of muscle regenerative potential that declines with age.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aging / physiology*
  • Animals
  • Calcium-Binding Proteins
  • Cell Count
  • Cell Differentiation
  • Cell Division
  • Cell Separation
  • Culture Techniques
  • Hindlimb
  • Intercellular Signaling Peptides and Proteins
  • Intracellular Signaling Peptides and Proteins
  • Male
  • Membrane Proteins / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Muscle, Skeletal / cytology
  • Muscle, Skeletal / injuries
  • Muscle, Skeletal / physiology*
  • Myoblasts / physiology*
  • Nerve Tissue Proteins / metabolism
  • Receptor, Notch1
  • Receptors, Cell Surface*
  • Recombinant Fusion Proteins / metabolism
  • Regeneration*
  • Satellite Cells, Skeletal Muscle / physiology*
  • Serrate-Jagged Proteins
  • Signal Transduction
  • Transcription Factors*
  • Up-Regulation

Substances

  • Calcium-Binding Proteins
  • Intercellular Signaling Peptides and Proteins
  • Intracellular Signaling Peptides and Proteins
  • Membrane Proteins
  • Nerve Tissue Proteins
  • Notch1 protein, mouse
  • Numb protein, mouse
  • Receptor, Notch1
  • Receptors, Cell Surface
  • Recombinant Fusion Proteins
  • Serrate-Jagged Proteins
  • Transcription Factors
  • delta protein