Environmental Health Sciences, University of Massachusetts, Amherst 240B Goessmann, 686 Noth Pleasant Str., Amherst, MA 01003, USA.
Ageing Res Rev. 2022 Dec;82:101770. doi: 10.1016/j.arr.2022.101770. Epub 2022 Oct 29.
Although the progress of aging research relies heavily on a theoretical framework, today there is no consensus on many critical questions in aging biology. I hypothesize that a systematic analysis of the intersection of different evolutionary mechanisms of aging with diverse resource allocation strategies in different organisms may reconcile aging hypotheses. The application of disposable soma, mutation accumulation, antagonistic pleiotropy, and life-history theory is considered across organisms with asexual reproduction, organisms with sexual reproduction and indeterminate growth in different conditions of extrinsic mortality, and organisms with determinate growth, with endotherms/homeotherms as a subgroup. This review demonstrates that different aging mechanisms are complementary to each other, and in organisms with different resource allocation strategies they form aging modalities ranging from immortality to suicidal programs. It also revamps the role of growth arrest in aging. Growth arrest evolved in many different groups of organisms as a result of resource reallocation from growth to reproduction (e.g., semelparous animals, holometabolic insects), or from growth to nutrient storage (endotherms/homeotherms). Growth arrest in different animal lineages has similar molecular mechanisms and similar consequences for longevity due to the conflict between growth-promoting and growth-suppressing programs and suppression of regenerative capacity.
尽管衰老研究的进展在很大程度上依赖于理论框架,但目前对于衰老生物学中的许多关键问题仍没有共识。我假设,对不同衰老机制与不同生物体中不同资源分配策略的交点进行系统分析,可能会调和衰老假说。可将具有无性繁殖的生物体、具有有性繁殖和在不同外源性死亡率条件下具有不定向生长的生物体、以及具有定向生长的生物体(以内温动物/恒温动物为亚组)的一次性躯体、突变积累、拮抗多效性和生活史理论的应用进行跨物种分析。本综述表明,不同的衰老机制是互补的,在具有不同资源分配策略的生物体中,它们形成了从不朽到自杀程序的衰老模式。它还重新审视了生长停滞在衰老中的作用。由于资源从生长重新分配到繁殖(例如,一次性动物、完全变态昆虫)或从生长到营养储存(内温动物/恒温动物),生长停滞在许多不同的生物体群体中进化而来。由于促进生长和抑制生长的程序之间的冲突以及对再生能力的抑制,不同动物谱系中的生长停滞具有相似的分子机制和对长寿的相似影响。