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Pregnancy restores the regenerative capacity of the aged liver via activation of an mTORC1-controlled hyperplasia/hypertrophy switch

机译:怀孕可通过激活mTORC1控制的增生/肥大开关来恢复衰老肝脏的再生能力。

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摘要

Regenerative capacity is progressively lost with age. Here we show that pregnancy markedly improved liver regeneration in aged mice concomitantly with inducing a switch from proliferation-based liver regeneration to a regenerative process mediated by cell growth. We found that the key mediator of this switch was the Akt/mTORC1 pathway; its inhibition blocked hypertrophy, while increasing proliferation. Moreover, pharmacological activation of this pathway sufficed to induce the hypertrophy module, mimicking pregnancy. This treatment dramatically improved hepatic regenerative capacity and survival of old mice. Thus, cell growth-mediated mass reconstitution, which is relatively resistant to the detrimental effects of aging, is employed in a physiological situation and holds potential as a therapeutic strategy for ameliorating age-related functional deterioration.
机译:随着年龄的增长,再生能力逐渐丧失。在这里,我们显示怀孕显着改善了衰老小鼠的肝再生,并伴随着从基于增殖的肝再生向由细胞生长介导的再生过程的转变。我们发现此开关的关键介体是Akt / mTORC1途径。它的抑制作用阻止了肥大,同时增加了增殖。此外,该途径的药理学激活足以诱导肥大模块,模仿怀孕。这种治疗显着改善了老小鼠的肝再生能力和存活率。因此,在生理情况下采用对衰老的有害作用相对抗性的细胞生长介导的大量重建,并且其具有作为缓解年龄相关的功能恶化的治疗策略的潜力。

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