Erschienen in:
17.09.2018 | Invited Commentary
A novel Sudan Black B-based analogue revives lipofuscin as a biomarker for in vivo senescence
verfasst von:
Dina Tiniakos, Diana Jurk
Erschienen in:
Virchows Archiv
|
Ausgabe 6/2018
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Excerpt
Senescence is a fundamental cellular mechanism that has received increasing attention in recent years as a potentially important contributor to developmental, physiological and pathological processes including aging [
1]. The term was initially proposed by Hayflick and Moorhead in 1961 to describe the limited proliferative capacity of cultured normal human fibroblasts [
2]. After completing a finite number of divisions, these cells entered a state of permanent growth arrest without dying, termed replicative senescence (RS) [
1]. It is nowadays well-established that RS relies on telomere shortening following several cell replication events; however, various other stimuli can induce senescence. Stress-induced premature senescence (SISP) is induced independently of telomere length and occurs in response to a variety of stress signals, such as oncogene activation (oncogene-induced senescence, OIS), oxidative stress (oxidative stress-induced senescence), DNA damage, and others [
1,
3]. Irrespective of the type of stimulus, senescence is characterized by programmed cell cycle arrest, resistance to apoptosis, metabolic activity, and modified cellular function [
1,
3]. …