Cellular Senescence in Type 2 Diabetes: A Therapeutic Opportunity

被引:312
作者
Palmer, Allyson K. [1 ,2 ]
Tchkonia, Tamara [1 ]
LeBrasseur, Nathan K. [1 ]
Chini, Eduardo N. [1 ,3 ]
Xu, Ming [1 ]
Kirkland, James L. [1 ]
机构
[1] Mayo Clin, Robert & Arlene Kogod Ctr Aging, Rochester, MN 55902 USA
[2] Mayo Clin & Mayo Grad Sch Med, Mayo Grad Sch, Mayo Med Scientist Training Program, Rochester, MN USA
[3] Mayo Clin, Department Anesthesiol, Rochester, MN USA
基金
美国国家卫生研究院;
关键词
PLASMINOGEN-ACTIVATOR INHIBITOR-1; SECRETORY PHENOTYPE; HIGH GLUCOSE; MITOCHONDRIAL DYSFUNCTION; ACCELERATED SENESCENCE; INSULIN-RESISTANCE; CRUCIAL ROLE; LIFE-SPAN; CELLS; OBESITY;
D O I
10.2337/db14-1820
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cellular senescence is a fundamental aging mechanism that has been implicated in many age-related diseases and is a significant cause of tissue dysfunction. Accumulation of senescent cells occurs during aging and is also seen in the context of obesity and diabetes. Senescent cells may play a role in type 2 diabetes pathogenesis through direct impact on pancreatic -cell function, senescence-associated secretory phenotype (SASP)-mediated tissue damage, and involvement in adipose tissue dysfunction. In turn, metabolic and signaling changes seen in diabetes, such as high circulating glucose, altered lipid metabolism, and growth hormone axis perturbations, can promote senescent cell formation. Thus, senescent cells might be part of a pathogenic loop in diabetes, as both a cause and consequence of metabolic changes and tissue damage. Therapeutic targeting of a basic aging mechanism such as cellular senescence may have a large impact on disease pathogenesis and could be more effective in preventing the progression of diabetes complications than currently available therapies that have limited impact on already existing tissue damage. Therefore, senescent cells and the SASP represent significant opportunities for advancement in the prevention and treatment of type 2 diabetes and its complications.
引用
收藏
页码:2289 / 2298
页数:10
相关论文
共 94 条
[1]   The prevalence of comorbid depression in adults with diabetes - A meta-analysis [J].
Anderson, RJ ;
Freedland, KE ;
Clouse, RE ;
Lustman, PJ .
DIABETES CARE, 2001, 24 (06) :1069-1078
[2]  
[Anonymous], 2014, NAT DIAB STAT REP ES, DOI [10.1177/1527154408322560, DOI 10.1177/1527154408322560]
[3]   Immunosenescence: emerging challenges for an ageing population [J].
Aw, Danielle ;
Silva, Alberto B. ;
Palmer, Donald B. .
IMMUNOLOGY, 2007, 120 (04) :435-446
[4]   Clearance of p16Ink4a-positive senescent cells delays ageing-associated disorders [J].
Baker, Darren J. ;
Wijshake, Tobias ;
Tchkonia, Tamar ;
LeBrasseur, Nathan K. ;
Childs, Bennett G. ;
van de Sluis, Bart ;
Kirkland, James L. ;
van Deursen, Jan M. .
NATURE, 2011, 479 (7372) :232-U112
[5]   Passage of cytokines across the blood-brain barrier [J].
Banks, WA ;
Kastin, AJ ;
Broadwell, RD .
NEUROIMMUNOMODULATION, 1995, 2 (04) :241-248
[6]   Can people with type 2 diabetes live longer than those without? A comparison of mortality in people initiated with metformin or sulphonylurea monotherapy and matched, non-diabetic controls [J].
Bannister, C. A. ;
Holden, S. E. ;
Jenkins-Jones, S. ;
Morgan, C. Ll ;
Halcox, J. P. ;
Schernthaner, G. ;
Mukherjee, J. ;
Currie, C. J. .
DIABETES OBESITY & METABOLISM, 2014, 16 (11) :1165-1173
[7]   Diabetes and atherosclerosis - Epidemiology, pathophysiology, and management [J].
Beckman, JA ;
Creager, MA ;
Libby, P .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 287 (19) :2570-2581
[8]   High glucose-induced replicative senescence: point of no return and effect of telomerase [J].
Blazer, S ;
Khankin, E ;
Segev, Y ;
Ofir, R ;
Yalon-Hacohen, M ;
Kra-Oz, Z ;
Gottfried, Y ;
Larisch, S ;
Skorecki, KL .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 296 (01) :93-101
[9]   Cellular and molecular basis of wound healing in diabetes [J].
Brem, Harold ;
Tomic-Canic, Marjana .
JOURNAL OF CLINICAL INVESTIGATION, 2007, 117 (05) :1219-1222
[10]   Senescent cells, tumor suppression, and organismal aging: Good citizens, bad neighbors [J].
Campisi, J .
CELL, 2005, 120 (04) :513-522