Pregled bibliografske jedinice broj: 173851
A biomarker that identifies senescent human cells in culture and in aging skin in vivo
A biomarker that identifies senescent human cells in culture and in aging skin in vivo // Proceedings of the National Academy of Sciences of the United States of America, 92 (1995), 20; 9363-9367 doi:10.1073/pnas.92.20.9363 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 173851 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
A biomarker that identifies senescent human cells in culture and in aging skin in vivo
Autori
Dimri, G. P. ; Lee, X. ; Basile, G. ; Acosta, M. ; Scott, G. ; Roskelley, C. ; Medrano, E. E. ; Linskens, M. ; Rubelj, Ivica ; Pereira-Smith, Olivia M. ; Peacocke, M. ; Campisi, J.
Izvornik
Proceedings of the National Academy of Sciences of the United States of America (0027-8424) 92
(1995), 20;
9363-9367
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
senescence ; beta-galactosidase ; aging
Sažetak
Normal somatic cells invariably enter a state of irreversibly arrested growth and altered function after a finite number of divisions. This process, termed replicative senescence, is thought to be a tumor-suppressive mechanism and an underlying cause of aging. There is ample evidence that escape from senescence, or immortality, is important for malignant transformation. By contrast, the role of replicative senescence in organismic aging is controversial. Studies on cells cultured from donors of different ages, genetic backgrounds, or species suggest that senescence occurs in vivo and that organismic lifespan and cell replicative lifespan are under common genetic control. However, senescent cells cannot be distinguished from quiescent or terminally differentiated cells in tissues. Thus, evidence that senescent cells exist and accumulate with age in vivo is lacking. We show that several human cells express a beta-galactosidase, histochemically detectable at pH 6, upon senescence in culture. This marker was expressed by senescent, but not presenescent, fibroblasts and keratinocytes but was absent from quiescent fibroblasts and terminally differentiated keratinocytes. It was also absent from immortal cells but was induced by genetic manipulations that reversed immortality. In skin samples from human donors of different age, there was an age- dependent increase in this marker in dermal fibroblasts and epidermal keratinocytes. This marker provides in situ evidence that senescent cells may exist and accumulate with age in vivo.
Izvorni jezik
Engleski
Znanstvena područja
Biologija
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE
- EconLit