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Lithocholic acid extends longevity of chronologically aging yeast only if added at certain critical periods of their lifespan

机译:只有在生命周期的某些关键时期添加时胆酸才能延长按时间顺序老化的酵母的寿命

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摘要

Our studies revealed that LCA (lithocholic bile acid) extends yeast chronological lifespan if added to growth medium at the time of cell inoculation. We also demonstrated that longevity in chronologically aging yeast is programmed by the level of metabolic capacity and organelle organization that they developed before entering a quiescent state and, thus, that chronological aging in yeast is likely to be the final step of a developmental program progressing through at least one checkpoint prior to entry into quiescence. Here, we investigate how LCA influences longevity and several longevity-defining cellular processes in chronologically aging yeast if added to growth medium at different periods of the lifespan. We found that LCA can extend longevity of yeast under CR (caloric restriction) conditions only if added at either of two lifespan periods. One of them includes logarithmic and diauxic growth phases, whereas the other period exists in early stationary phase. Our findings suggest a mechanism linking the ability of LCA to increase the lifespan of CR yeast only if added at either of the two periods to its differential effects on various longevity-defining processes. In this mechanism, LCA controls these processes at three checkpoints that exist in logarithmic/diauxic, post-diauxic and early stationary phases. We therefore hypothesize that a biomolecular longevity network progresses through a series of checkpoints, at each of which (1) genetic, dietary and pharmacological anti-aging interventions modulate a distinct set of longevity-defining processes comprising the network; and (2) checkpoint-specific master regulators monitor and govern the functional states of these processes.
机译:我们的研究表明,如果在细胞接种时将LCA(石胆汁胆汁酸)添加到生长培养基中,则可以延长酵母的时间寿命。我们还证明了按时间顺序老化的酵母的寿命是由它们进入静止状态之前发育的代谢能力和细胞器组织的水平来编程的,因此,按时间顺序老化的酵母很可能是发育计划进展的最后一步至少进入静止状态之前的一个检查点。在这里,我们研究了如果在生命周期的不同时期添加到生长培养基中,LCA如何在按时间顺序老化的酵母中影响寿命和确定寿命的几个细胞过程。我们发现,只有在两个寿命周期中的任何一个周期内添加LCA,LCA才能延长其在CR(热量限制)条件下的寿命。其中一个包括对数和双生生长期,而另一时期则处于早期静止期。我们的发现表明,只有在两个时期中的任何一个时期添加LCA才能增加CR酵母寿命的机制与其对各种长寿过程的不同影响有关。在这种机制下,LCA在对数/双生,双生后和早期固定阶段中存在的三个检查点控制这些过程。因此,我们假设生物分子长寿网络通过一系列检查点发展,在每个检查点上:(1)遗传,饮食和药理抗衰老干预措施调节着组成该网络的一组不同的长寿定义过程; (2)特定于检查点的主调节器监视和控制这些过程的功能状态。

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