RIP kinases and necroptosis in aging and aging-related diseases

Author:

Yang Yuanxin12,Li Xingyan1,Zhang Tao3,Xu Daichao1

Affiliation:

1. Interdisciplinary Research Center on Biology and Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences , Shanghai 201210 , China

2. University of Chinese Academy of Sciences , Beijing 100049 , China

3. Department of Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School , Boston, MA 02215 , United States

Abstract

Abstract Aging is a natural process that is characterized by chronic, low-grade inflammation, which represents the primary risk factor in the pathogenesis of a variety of diseases, i.e. aging-related diseases. RIP kinases, in particular RIPK1 and RIPK3, have emerged as master regulators of proinflammatory responses that act either by causing apoptosis and necroptosis or by directly regulating intracellular inflammatory signaling. While, RIPK1/3 and necroptosis are intimately linked to multiple human diseases, the relationship among RIPK1/3, necroptosis, and aging remains unclear. In this review, we discuss current evidence arguing for the involvement of RIPK1/3 and necroptosis in the progression of aging. In addition, we provide updated information and knowledge on the role of RIPK1/3 and necroptosis in aging-related diseases. Leveraging these new mechanistic insights in aging, we postulate how our improved understanding of RIPK1/3 and necroptosis in aging may support the development of therapeutics targeting RIPK1/3 and necroptosis for the modulation of aging and treatment of aging-related diseases.

Funder

National Key R&D Program of China

National Natural Science Foundation of China

Chinese Academy of Sciences

Science and Technology Commission of Shanghai Municipality

Shanghai Municipal Science and Technology Major Project

China Postdoctoral Science Foundation

Publisher

Oxford University Press (OUP)

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