The connection between aging, cellular senescence and gut microbiome alterations: A comprehensive review

IF 7.8 1区 医学 Q1 Biochemistry, Genetics and Molecular Biology Aging Cell Pub Date : 2024-08-15 DOI:10.1111/acel.14315
Dong-Hyun Jang, Ji-Won Shin, Eunha Shim, Naoko Ohtani, Ok Hee Jeon
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Abstract

The intricate interplay between cellular senescence and alterations in the gut microbiome emerges as a pivotal axis in the aging process, increasingly recognized for its contribution to systemic inflammation, physiological decline, and predisposition to age-associated diseases. Cellular senescence, characterized by a cessation of cell division in response to various stressors, induces morphological and functional changes within tissues. The complexity and heterogeneity of senescent cells, alongside the secretion of senescence-associated secretory phenotype, exacerbate the aging process through pro-inflammatory pathways and influence the microenvironment and immune system. Concurrently, aging-associated changes in gut microbiome diversity and composition contribute to dysbiosis, further exacerbating systemic inflammation and undermining the integrity of various bodily functions. This review encapsulates the burgeoning research on the reciprocal relationship between cellular senescence and gut dysbiosis, highlighting their collective impact on age-related musculoskeletal diseases, including osteoporosis, sarcopenia, and osteoarthritis. It also explores the potential of modulating the gut microbiome and targeting cellular senescence as innovative strategies for healthy aging and mitigating the progression of aging-related conditions. By exploring targeted interventions, including the development of senotherapeutic drugs and probiotic therapies, this review aims to shed light on novel therapeutic avenues. These strategies leverage the connection between cellular senescence and gut microbiome alterations to advance aging research and development of interventions aimed at extending health span and improving the quality of life in the older population.

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衰老、细胞衰老与肠道微生物组改变之间的联系:综述。
细胞衰老与肠道微生物组的改变之间错综复杂的相互作用已成为衰老过程中的一个关键轴心,其对全身炎症、生理机能衰退和易患老年相关疾病的贡献日益得到认可。细胞衰老的特点是细胞在各种压力下停止分裂,从而诱发组织内的形态和功能变化。衰老细胞的复杂性和异质性,以及衰老相关分泌表型的分泌,通过促炎途径加剧了衰老过程,并影响微环境和免疫系统。与此同时,与衰老相关的肠道微生物群多样性和组成的变化会导致菌群失调,进一步加剧全身炎症并破坏各种身体功能的完整性。本综述概括了有关细胞衰老和肠道菌群失调之间相互关系的新兴研究,强调了它们对与年龄相关的肌肉骨骼疾病(包括骨质疏松症、肌肉疏松症和骨关节炎)的共同影响。报告还探讨了调节肠道微生物组和针对细胞衰老作为健康老龄化和缓解老龄相关疾病进展的创新策略的潜力。通过探讨有针对性的干预措施,包括开发衰老治疗药物和益生菌疗法,本综述旨在阐明新的治疗途径。这些策略利用细胞衰老与肠道微生物组改变之间的联系,推进老龄化研究和干预措施的开发,旨在延长老年人群的健康寿命并改善其生活质量。
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来源期刊
Aging Cell
Aging Cell 生物-老年医学
CiteScore
14.40
自引率
2.60%
发文量
212
审稿时长
8 weeks
期刊介绍: Aging Cell, an Open Access journal, delves into fundamental aspects of aging biology. It comprehensively explores geroscience, emphasizing research on the mechanisms underlying the aging process and the connections between aging and age-related diseases.
期刊最新文献
Issue Information Featured Cover Correction to ‘Increased transcriptome variation and localised DNA methylation changes in oocytes from aged mice revealed by parallel single-cell analysis’ RETRACTION: 1,25-Dihydroxyvitamin D exerts an antiaging role by activation of Nrf2-antioxidant signaling and inactivation of p16/p53-senescence signaling Issue Information
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