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Role of sphingolipids in senescence: implication in aging and age-related diseases
Magali Trayssac, … , Yusuf A. Hannun, Lina M. Obeid
Magali Trayssac, … , Yusuf A. Hannun, Lina M. Obeid
Published July 2, 2018
Citation Information: J Clin Invest. 2018;128(7):2702-2712. https://doi.org/10.1172/JCI97949.
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Category: Review Series

Role of sphingolipids in senescence: implication in aging and age-related diseases

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Abstract

Aging is defined as the progressive deterioration of physiological function with age. Incidence of many pathologies increases with age, including neurological and cardiovascular diseases and cancer. Aging tissues become less adaptable and renewable, and cells undergo senescence, a process by which they “irreversibly” stop dividing. Senescence has been shown to serve as a tumor suppression mechanism with clear desirable effects. However, senescence also has deleterious consequences, especially for cardiovascular, metabolic, and immune systems. Sphingolipids are a major class of lipids that regulate cell biology, owing to their structural and bioactive properties and diversity. Their involvement in the regulation of aging and senescence has been demonstrated and studied in multiple organisms and cell types, especially that of ceramide and sphingosine-1-phosphate; ceramide induces cellular senescence and sphingosine-1–phosphate delays it. These discoveries could be very useful in the future to understand aging mechanisms and improve therapeutic interventions.

Authors

Magali Trayssac, Yusuf A. Hannun, Lina M. Obeid

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Figure 3

Mechanisms by which sphingolipids regulate senescence.

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Mechanisms by which sphingolipids regulate senescence.
Cer and S1P have ...
Cer and S1P have opposite effects on senescence: while Cer induces it, S1P seems to prevent it. The mechanisms by which Cer and S1P regulate senescence are very distinct. Studies on the mechanisms induced by Cer are numerous, whereas little is known about the mechanisms activated by S1P to modulate senescence. CAPP, ceramide-activated protein phosphatase.
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