The Potential Roles of Tendon Stem/Progenitor Cells in Tendon Aging

Curr Stem Cell Res Ther. 2019;14(1):34-42. doi: 10.2174/1574888X13666181017112233.

Abstract

Aging is a key dangerous factor for the occurrence and severity of tendon injury, but the exact cognition of the relationship is elusive at present. More previous studies suggest age-related changes occur at tendon mechanical properties, structure and composition, but the pathological alternations may be overlooked, which might be a cause for the structure and function variations, and even speed up the progress of age-related disorders. Recently, the presence of tendon stem/progenitor cells (TSPCs) would provide new insights for the pathogenesis of tendon aging. In this review, the tendon mechanical properties, structure and composition are presented in brief, then, the pathological changes of the aging tendon are described firstly, and the latest researches on alterations of TSPCs in the pathogenesis of tendon aging have also been analyzed. At a cellular level, the hypothetical model of altered TSPCs fate for tendon aging is also proposed. Moreover, the regulation of TSPCs as a potential way of the therapies for age-related tendon diseases is discussed. Therefore, reversing the impaired function of TSPCs and promoting the tenogenic differentiation of TSPCs could become hot spots for further study and give the opportunity to establish new treatment strategies for age-related tendon injuries.

Keywords: Tendon aging and degeneration; differentiation; mechanism; pathological alterations; tendon injury and repair; tendon stem/progenitor cells..

Publication types

  • Review

MeSH terms

  • Adult
  • Aged
  • Aging / physiology*
  • Animals
  • Calcinosis
  • Exercise Therapy
  • Female
  • Humans
  • Insulin-Like Growth Factor I / therapeutic use
  • Male
  • Matrix Metalloproteinases / metabolism
  • Metaplasia
  • Mice
  • Middle Aged
  • NIMA-Interacting Peptidylprolyl Isomerase / biosynthesis
  • Osteogenesis
  • Rats
  • Repressor Proteins / biosynthesis
  • Stem Cells / physiology*
  • Tendon Injuries / physiopathology
  • Tendon Injuries / therapy
  • Tendons / blood supply
  • Tendons / pathology
  • Tendons / physiopathology*
  • Tenocytes* / physiology
  • Trans-Activators / biosynthesis
  • Young Adult

Substances

  • CITED2 protein, human
  • NIMA-Interacting Peptidylprolyl Isomerase
  • Repressor Proteins
  • Trans-Activators
  • Insulin-Like Growth Factor I
  • Matrix Metalloproteinases