Cellular Senescence and Inflammaging in the Bone: Pathways, Genetics, Anti-Aging Strategies and Interventions.
Merin LawrenceAbhishek GoyalShelly PathakPayal GangulyPublished in: International journal of molecular sciences (2024)
Advancing age is associated with several age-related diseases (ARDs), with musculoskeletal conditions impacting millions of elderly people worldwide. With orthopedic conditions contributing towards considerable number of patients, a deeper understanding of bone aging is the need of the hour. One of the underlying factors of bone aging is cellular senescence and its associated senescence associated secretory phenotype (SASP). SASP comprises of pro-inflammatory markers, cytokines and chemokines that arrest cell growth and development. The accumulation of SASP over several years leads to chronic low-grade inflammation with advancing age, also known as inflammaging. The pathways and molecular mechanisms focused on bone senescence and inflammaging are currently limited but are increasingly being explored. Most of the genes, pathways and mechanisms involved in senescence and inflammaging coincide with those associated with cancer and other ARDs like osteoarthritis (OA). Thus, exploring these pathways using techniques like sequencing, identifying these factors and combatting them with the most suitable approach are crucial for healthy aging and the early detection of ARDs. Several approaches can be used to aid regeneration and reduce senescence in the bone. These may be pharmacological, non-pharmacological and lifestyle interventions. With increasing evidence towards the intricate relationship between aging, senescence, inflammation and ARDs, these approaches may also be used as anti-aging strategies for the aging bone marrow (BM).
Keyphrases
- dna damage
- endothelial cells
- bone mineral density
- acute respiratory distress syndrome
- low grade
- stress induced
- bone marrow
- extracorporeal membrane oxygenation
- bone loss
- soft tissue
- mechanical ventilation
- physical activity
- end stage renal disease
- cardiovascular disease
- high grade
- mesenchymal stem cells
- bone regeneration
- ejection fraction
- chronic kidney disease
- squamous cell carcinoma
- knee osteoarthritis
- intensive care unit
- genome wide
- dna methylation
- cell cycle
- papillary thyroid
- cell proliferation
- young adults
- lymph node metastasis
- transcription factor
- patient reported outcomes