Pandey Taruna, Ma Dengke K
Cardiovascular Research Institute and Department of Physiology, University of California San Francisco, San Francisco, USA.
Innovative Genomics Institute, University of California, Berkeley, USA.
Biochemistry (Mosc). 2022 Dec;87(12):1504-1511. doi: 10.1134/S0006297922120082.
Evolution by natural selection results in biological traits that enable organismic adaptation and survival under various stressful environments. External stresses can be sometimes too severe to overcome, leading to organismic death either because of failure in adapting to such stress, or alternatively, through a regulated form of organismic death (phenoptosis). While regulated cell deaths, including apoptosis, have been extensively studied, little is known about the molecular and cellular mechanisms underlying phenoptosis and its evolutionary significance for multicellular organisms. In this article, we review documented phenomena and mechanistic evidence emerging from studies of stress-induced phenoptosis in the multicellular organism C. elegans and stress-induced deaths at cellular levels in organisms ranging from bacteria to mammals, focusing on abiotic and pathogen stresses. Genes and signaling pathways involved in phenoptosis appear to promote organismic death during severe stress and aging, while conferring fitness and immune defense during mild stress and early life, consistent with their antagonistic pleiotropy actions. As cell apoptosis during development can shape tissues and organs, stress-induced phenoptosis may also contribute to possible benefits at the population level, through mechanisms including kin selection, abortive infection, and soma-to-germline resource allocation. Current models can generate experimentally testable predictions and conceptual frameworks with implications for understanding both stress-induced phenoptosis and natural aging.
自然选择驱动的进化产生了使生物体能够在各种应激环境中适应和生存的生物学特性。外部压力有时可能过于严峻而无法克服,这会导致生物体死亡,其原因要么是无法适应这种压力,要么是通过一种受调控的生物体死亡形式(程序性死亡)。虽然包括凋亡在内的程序性细胞死亡已得到广泛研究,但对于程序性死亡背后的分子和细胞机制及其对多细胞生物的进化意义却知之甚少。在本文中,我们综述了多细胞生物秀丽隐杆线虫应激诱导程序性死亡研究以及从细菌到哺乳动物等生物体细胞水平应激诱导死亡研究中记录的现象和机制证据,重点关注非生物和病原体应激。参与程序性死亡的基因和信号通路似乎在严重应激和衰老过程中促进生物体死亡,而在轻度应激和生命早期赋予适应性和免疫防御能力,这与其拮抗多效性作用一致。由于发育过程中的细胞凋亡可以塑造组织和器官,应激诱导的程序性死亡也可能通过亲属选择、流产感染和体细胞到生殖系资源分配等机制在种群水平上带来潜在益处。当前模型可以产生可通过实验验证的预测和概念框架,有助于理解应激诱导的程序性死亡和自然衰老。