Scharf Andrea, Pohl Franziska, Egan Brian M, Kocsisova Zuzana, Kornfeld Kerry
Department of Developmental Biology, Washington University School of Medicine, St. Louis, MO, United States.
Department of Medicine, Washington University School of Medicine, St. Louis, MO, United States.
Front Cell Dev Biol. 2021 Sep 16;9:718522. doi: 10.3389/fcell.2021.718522. eCollection 2021.
Aging animals display a broad range of progressive degenerative changes, and one of the most fascinating is the decline of female reproductive function. In the model organism , hermaphrodites reach a peak of progeny production on day 2 of adulthood and then display a rapid decline; progeny production typically ends by day 8 of adulthood. Since animals typically survive until day 15 of adulthood, there is a substantial post reproductive lifespan. Here we review the molecular and cellular changes that occur during reproductive aging, including reductions in stem cell number and activity, slowing meiotic progression, diminished Notch signaling, and deterioration of germ line and oocyte morphology. Several interventions have been identified that delay reproductive aging, including mutations, drugs and environmental factors such as temperature. The detailed description of reproductive aging coupled with interventions that delay this process have made a leading model system to understand the mechanisms that drive reproductive aging. While reproductive aging has dramatic consequences for individual fertility, it also has consequences for the ecology of the population. Population dynamics are driven by birth and death, and reproductive aging is one important factor that influences birth rate. A variety of theories have been advanced to explain why reproductive aging occurs and how it has been sculpted during evolution. Here we summarize these theories and discuss the utility of for testing mechanistic and evolutionary models of reproductive aging.
衰老动物会呈现出广泛的渐进性退行性变化,其中最引人入胜的变化之一是雌性生殖功能的衰退。在该模式生物中,雌雄同体个体在成年后第2天达到后代产量的峰值,随后便迅速下降;后代产量通常在成年后第8天结束。由于动物通常能存活到成年后第15天,因此存在一段较长的生殖后寿命。在此,我们综述了生殖衰老过程中发生的分子和细胞变化,包括干细胞数量和活性的减少、减数分裂进程的减缓、Notch信号的减弱以及生殖系和卵母细胞形态的恶化。已确定了几种延缓生殖衰老的干预措施,包括突变、药物以及温度等环境因素。对生殖衰老的详细描述以及延缓这一过程的干预措施,使其成为理解驱动生殖衰老机制的领先模型系统。虽然生殖衰老对个体生育能力有巨大影响,但它对种群生态也有影响。种群动态受出生和死亡驱动,而生殖衰老是影响出生率的一个重要因素。人们提出了各种理论来解释生殖衰老为何会发生以及它在进化过程中是如何形成的。在此,我们总结这些理论,并讨论其在测试生殖衰老的机制和进化模型方面的效用。