Division of Endocrinology and Metabolism and Kogod Center on Aging, Mayo Clinic, Rochester, MN, USA.
Bone. 2019 Apr;121:121-133. doi: 10.1016/j.bone.2019.01.015. Epub 2019 Jan 16.
Cellular senescence refers to a process induced by various types of stress that causes irreversible cell cycle arrest and distinct cellular alterations, including profound changes in gene expression, metabolism, and chromatin organization as well as activation/reinforcement of anti-apoptotic pathways and development of a pro-inflammatory secretome or senescence-associated secretory phenotype (SASP). However, because of challenges and technical limitations in identifying and characterizing senescent cells in living organisms, only recently have some of the diverse in vivo roles of these unique cells been discovered. New findings indicate that senescent cells and their SASP can have acute beneficial functions, such as in tissue regeneration and wound healing. However, in contrast, when senescent cells accumulate in excess chronically at sites of pathology or in old tissues they drive multiple age-associated chronic diseases. Senotherapeutics that selectively eliminate senescent cells ("senolytics") or inhibit their detrimental SASP ("senomorphics") have been developed and tested in aged preclinical models. These studies have established that targeting senescence is a powerful anti-aging strategy to improve "healthspan" - i.e., the healthy period of life free of chronic disease. The roles of senescence in mediating age-related bone loss have been a recent focus of rigorous investigation. Studies in mice and humans demonstrate that with aging, at least a subset of most cell types in the bone microenvironment become senescent and develop a heterogeneous SASP. Furthermore, age-related bone loss can be alleviated in old mice, with apparent advantages over anti-resorptive therapy, by reducing the senescent cell burden genetically or pharmacologically with the first class of senolytics or a senomorphic. Collectively, these findings point to targeting senescence as a transformational strategy to extend healthspan, therefore providing strong rationale for identifying and optimizing senotherapeutics to alleviate multiple chronic diseases of aging, including osteoporosis, and set the stage for translating senotherapeutics to humans, with clinical trials currently ongoing.
细胞衰老指的是各种类型的压力诱导的一种过程,会导致细胞周期不可逆地停滞,并发生明显的细胞改变,包括基因表达、代谢和染色质组织的深刻变化,以及抗凋亡途径的激活/增强和炎症分泌或衰老相关分泌表型(SASP)的发展。然而,由于在活体中鉴定和描述衰老细胞存在挑战和技术限制,直到最近才发现这些独特细胞的一些不同的体内作用。新的发现表明,衰老细胞及其 SASP 可以具有急性有益的功能,例如在组织再生和伤口愈合中。然而,相反,当衰老细胞在病理部位或老年组织中过度积累时,它们会引发多种与年龄相关的慢性疾病。已经开发和测试了选择性消除衰老细胞的衰老治疗药物(“衰老细胞清除剂”)或抑制其有害 SASP 的衰老治疗药物(“衰老模拟物”)。这些研究已经证实,靶向衰老细胞是一种强大的抗衰老策略,可以改善“健康寿命”,即没有慢性疾病的健康生活期。衰老细胞在介导与年龄相关的骨丢失中的作用是最近严格研究的焦点。在小鼠和人类中的研究表明,随着年龄的增长,骨微环境中的至少一部分大多数细胞类型都会衰老,并发展出异质的 SASP。此外,通过遗传或药理学方法用第一代衰老细胞清除剂或衰老模拟物减少衰老细胞负担,可以减轻老年小鼠的与年龄相关的骨丢失,其具有明显优于抗吸收疗法的优势。总之,这些发现表明靶向衰老细胞是一种变革性策略,可以延长健康寿命,因此为确定和优化衰老治疗药物以缓解多种与年龄相关的慢性疾病(包括骨质疏松症)提供了强有力的理由,并为将衰老治疗药物转化为人类奠定了基础,目前正在进行临床试验。