Yao Guang
Department of Molecular & Cellular Biology, University of Arizona, Tucson, AZ 85721, USA.
Arizona Cancer Center, University of Arizona, Tucson, AZ 85719, USA.
Biomedicines. 2024 Aug 13;12(8):1837. doi: 10.3390/biomedicines12081837.
Cellular senescence, traditionally viewed as a consequence of proliferating and growing cells overwhelmed by extensive stresses and damage, has long been recognized as a critical cellular aging mechanism. Recent research, however, has revealed a novel pathway termed "quiescence-origin senescence", where cells directly transition into senescence from the quiescent state, bypassing cell proliferation and growth. This opinion paper presents a framework conceptualizing a continuum between quiescence and senescence with quiescence deepening as a precursor to senescence entry. We explore the triggers and controllers of this process and discuss its biological implications. Given that the majority of cells in the human body are dormant rather than proliferative, understanding quiescence-origin senescence has significant implications for tissue homeostasis, aging, cancer, and various disease processes. The new paradigm in exploring this previously overlooked senescent cell population may reshape our intervention strategies for age-related diseases and tissue regeneration.
细胞衰老传统上被视为增殖和生长的细胞因广泛应激和损伤而不堪重负的结果,长期以来一直被认为是一种关键的细胞衰老机制。然而,最近的研究揭示了一种名为“静止起源衰老”的新途径,即细胞直接从静止状态转变为衰老状态,绕过细胞增殖和生长阶段。这篇观点论文提出了一个框架,将静止和衰老概念化为一个连续体,随着静止状态的加深,作为进入衰老的前奏。我们探讨了这一过程的触发因素和调控因素,并讨论了其生物学意义。鉴于人体中的大多数细胞处于休眠而非增殖状态,理解静止起源衰老对组织稳态、衰老、癌症及各种疾病过程具有重要意义。探索这一先前被忽视的衰老细胞群体的新范式可能会重塑我们针对与年龄相关疾病和组织再生的干预策略。