Senescence: a double-edged sword in beta-cell health and failure?

被引:9
作者
Varghese, Sneha S. [1 ]
Dhawan, Sangeeta [1 ]
机构
[1] City Hope Natl Med Ctr, Arthur Riggs Diabet & Metab Res Inst, Dept Translat Res & Cellular Therapeut, Duarte, CA 91010 USA
基金
美国国家卫生研究院;
关键词
beta cells; differentiation; maturation; proliferation; epigenetics; aging; senescence; diabetes; DNA-DAMAGE; PANCREAS; TYPE-1; REGENERATION; APOPTOSIS; PROLIFERATION; MECHANISM; INFLAMMATION; CONTRIBUTES; MACROPHAGES;
D O I
10.3389/fendo.2023.1196460
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cellular senescence is a complex process marked by permanent cell-cycle arrest in response to a variety of stressors, and acts as a safeguard against the proliferation of damaged cells. Senescence is not only a key process underlying aging and development of many diseases, but has also been shown to play a vital role in embryogenesis as well as tissue regeneration and repair. In context of the pancreatic beta-cells, that are essential for maintaining glucose homeostasis, replicative senescence is responsible for the age-related decline in regenerative capacity. Stress induced premature senescence is also a key early event underlying beta-cell failure in both type 1 and type 2 diabetes. Targeting senescence has therefore emerged as a promising therapeutic avenue for diabetes. However, the molecular mechanisms that mediate the induction of beta-cell senescence in response to various stressors remain unclear. Nor do we know if senescence plays any role during beta-cell growth and development. In this perspective, we discuss the significance of senescence in beta-cell homeostasis and pathology and highlight emerging directions in this area that warrant our attention.
引用
收藏
页数:9
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