Cellular senescence and the senescent secretory phenotype in age-related chronic diseases

Curr Opin Clin Nutr Metab Care. 2014 Jul;17(4):324-8. doi: 10.1097/MCO.0000000000000065.

Abstract

Purpose of review: Possible mechanisms in cellular senescence and the senescence-associated secretory phenotype (SASP) that drive and promote chronic inflammation in multiple age-related chronic diseases are considered.

Recent findings: A series of studies about the SASP indicate that senescent cells may be involved in the development of chronic inflammatory diseases associated with aging.

Summary: Aging is a complex biological process accompanied by a state of chronic, low-grade, 'sterile' inflammation, which is a major contributor to the development of many age-related chronic disorders including atherosclerosis, osteoarthritis, Alzheimer's disease, type 2 diabetes, cancers, and others. It appears that cellular senescence plays a role in causing inflammation through the SASP. A better understanding of the contribution of senescent cells to the pathologies of chronic inflammatory disorders could have potentially profound diagnostic and therapeutic implications.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Aging*
  • Alzheimer Disease / physiopathology
  • Atherosclerosis / physiopathology
  • Cellular Senescence*
  • Chronic Disease
  • Diabetes Mellitus, Type 2 / physiopathology
  • Humans
  • Hypertension / physiopathology
  • Inflammation / physiopathology
  • Neoplasms / physiopathology
  • Osteoarthritis / physiopathology
  • Phenotype