Accelerated aging phenotype in mice with conditional deficiency for mitochondrial superoxide dismutase in the connective tissue

Publikationen: Beitrag in FachzeitschriftZeitschriftenaufsätzeForschung

AutorInnen

  • Nicolai Treiber
  • Pallab Maity
  • Karmveer Singh
  • Matthias Kohn
  • Alexander F Keist
  • Florentina Ferchiu
  • Lea Sante
  • Sebastian Frese
  • Florian Kreppel
  • Stefan Kochanek
  • Anca Sindrilaru
  • Sebastian Iben
  • Josef Högel
  • Michael Ohnmacht
  • Lutz E Claes
  • Anita Ignatius
  • Jin H Chung
  • Min J Lee
  • York Kamenisch
  • Mark Berneburg
  • Thorsten Nikolaus
  • Kerstin Braunstein
  • Anne-Dorte Sperfeld
  • Albert C Ludolph
  • Karlis Briviba
  • Meinhard Wlaschek
  • Lore Florin
  • Peter Angel
  • Karin Scharffetter-Kochanek

Forschungseinrichtungen

Details

The free radical theory of aging postulates that the production of mitochondrial reactive oxygen species is the major determinant of aging and lifespan. Its role in aging of the connective tissue has not yet been established, even though the incidence of aging-related disorders in connective tissue-rich organs is high, causing major disability in the elderly. We have now addressed this question experimentally by creating mice with conditional deficiency of the mitochondrial manganese superoxide dismutase in fibroblasts and other mesenchyme-derived cells of connective tissues in all organs. Here, we have shown for the first time that the connective tissue-specific lack of superoxide anion detoxification in the mitochondria results in reduced lifespan and premature onset of aging-related phenotypes such as weight loss, skin atrophy, kyphosis (curvature of the spine), osteoporosis and muscle degeneration in mutant mice. Increase in p16(INK4a) , a robust in vivo marker for fibroblast aging, may contribute to the observed phenotype. This novel model is particularly suited to decipher the underlying mechanisms and to develop hopefully novel connective tissue-specific anti-aging strategies.

OriginalspracheEnglisch
ZeitschriftAging cell
Jahrgang10
Heft2
Seiten (von - bis)239-254
Seitenumfang16
DOIs
PublikationsstatusVeröffentlicht - 01.04.2011

ID: 66637

DOI

Beziehungsdiagramm anzeigen