Cellular Senescence: The Trojan Horse in Chronic Lung Diseases

被引:58
作者
Hamsanathan, Shruthi [1 ]
Alder, Jonathan K. [2 ,4 ]
Sellares, Jacobo [7 ,8 ]
Rojas, Mauricio [2 ,4 ,5 ]
Gurkar, Aditi U. [1 ,3 ,9 ]
Mora, Ana L. [1 ,2 ,6 ]
机构
[1] Univ Pittsburgh, Aging Inst, Pittsburgh, PA 15219 USA
[2] Univ Pittsburgh, Div Pulm Allergy & Crit Care Med, Pittsburgh, PA 15219 USA
[3] Univ Pittsburgh, Div Geriatr Med, Dept Med, Pittsburgh, PA 15219 USA
[4] Univ Pittsburgh, Dorothy P & Richard P Simmons Ctr Interstitial Lu, Pittsburgh, PA 15219 USA
[5] Univ Pittsburgh, McGowan Inst Regenerat Med, Pittsburgh, PA 15219 USA
[6] Univ Pittsburgh, Vasc Med Inst, Pittsburgh, PA 15219 USA
[7] Univ Barcelona, IDIBAPS, Hosp Clin Barcelona, Servei Pneumol,Interstitial Lung Dis Program, Barcelona, Spain
[8] Inst Salud Carlos III, Ctr Invest Biomed Red Enfermedades Resp CibeRes C, Barcelona, Spain
[9] VA Pittsburgh Healthcare Syst, Geriatr Res Educ & Clin Ctr, Pittsburgh, PA USA
基金
美国国家卫生研究院;
关键词
senescence; idiopathic pulmonary fibrosis; chronic obstructive pulmonary disease; senescence-associated secretory phenotype; lung; ONCOGENE-INDUCED SENESCENCE; PLASMINOGEN-ACTIVATOR INHIBITOR-1; IDIOPATHIC PULMONARY-FIBROSIS; DNA-DAMAGE RESPONSE; SECRETORY PHENOTYPE; OXIDATIVE STRESS; TELOMERE LENGTH; LIFE-SPAN; MITOCHONDRIAL DYSFUNCTION; TRIGGERS SENESCENCE;
D O I
10.1165/rcmb.2018-0410TR
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Senescence is a cell fate decision characterized by irreversible arrest of proliferation accompanied by a senescence-associated secretory phenotype. Traditionally, cellular senescence has been recognized as a beneficial physiological mechanism during development and wound healing and in tumor suppression. However, in recent years, evidence of negative consequences of cellular senescence has emerged, illuminating its role in several chronic pathologies. In this context, senescent cells persist or accumulate and have detrimental consequences. In this review, we discuss the possibility that in chronic obstructive pulmonary disease, persistent senescence impairs wound healing in the lung caused by secretion of proinflammatory senescence-associated secretory phenotype factors and exhaustion of progenitor cells. In contrast, in idiopathic pulmonary fibrosis, chronic senescence in alveolar epithelial cells exacerbates the accumulation of senescent fibroblasts together with production of extracellular matrix. We review how cellular senescence may contribute to lung disease pathology.
引用
收藏
页码:21 / 30
页数:10
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