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Spreading Senescent Cells' Burden and Emerging Therapeutic Targets for Frailty
Serena Marcozzi1,2, Giorgia Bigossi1, Maria Elisa Giuliani1
1Advanced Technology Center for Aging Research and Geriatric Mouse Clinic, IRCCS INRCA, 60121 Ancona, Italy.
Abstract:
The spreading of senescent cells' burden holds profound implications for frailty, prompting the exploration of novel therapeutic targets. In this perspective review, we delve into the intricate mechanisms underlying senescent cell spreading, its implications for frailty, and its therapeutic development. We have focused our attention on the emerging age-related biological factors, such as microbiome and virome alterations, elucidating their significant contribution to the loss of control over the accumulation rate of senescent cells, particularly affecting key frailty domains, the musculoskeletal system and cerebral functions. We believe that gaining an understanding of these mechanisms could not only aid in elucidating the involvement of cellular senescence in frailty but also offer diverse therapeutic possibilities, potentially advancing the future development of tailored interventions for these highly diverse patients.
Insights
Cellular senescence, the accumulation of aging cells, contributes to frailty. Understanding how senescent cells spread, influenced by factors like the microbiome, can reveal new therapeutic targets for aging.
Area of Science:
- Gerontology
- Cellular Biology
- Immunology
Background:
- Cellular senescence is a key driver of aging and age-related diseases.
- The accumulation of senescent cells contributes to tissue dysfunction and the aging phenotype.
- Frailty is a complex geriatric syndrome associated with increased vulnerability and mortality.
Purpose of the Study:
- To review the mechanisms of senescent cell spreading and its impact on frailty.
- To explore the role of age-related factors, including microbiome and virome alterations, in senescent cell accumulation.
- To discuss potential therapeutic strategies targeting cellular senescence for frailty.
Main Methods:
- This is a perspective review, synthesizing existing literature.
- Analysis of age-related biological factors influencing senescent cell burden.
- Focus on musculoskeletal and cerebral functions in the context of frailty.
Main Results:
- Senescent cell burden is implicated in the development and progression of frailty.
- Alterations in the microbiome and virome contribute to the loss of control over senescent cell accumulation.
- Musculoskeletal and cerebral functions are particularly affected by senescent cell accumulation.
Conclusions:
- Understanding senescent cell spreading mechanisms is crucial for elucidating frailty.
- Microbiome and virome alterations are significant contributors to senescent cell-related frailty.
- Targeting cellular senescence offers promising therapeutic avenues for frailty interventions.
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