Steroid signaling mediates longevity responses to the eat-2 genetic model of dietary restriction in Caenorhabditis elegans

Q2 Medicine
Mindy Farris , Lily Fang , Arianne Aslamy , Victor Pineda
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引用次数: 2

Abstract

Dietary restriction (DR) extends lifespan in a wide range of model organisms, including Caenorhabditis elegans. It is an interesting but yet to be addressed question whether hormones serve as a systemic mechanism that mediates this longevity response. We identified a requirement for steroid signaling in lifespan extension induced by DR, by studying two members of the conserved 3β-hydroxysteroid dehydrogenase (3β-HSD) family, HSD-2 and HSD-3. Specifically, we found that lifespan extension in the eat-2 genetic model of DR is completely suppressed by a deletion mutant of hsd-2. This suppression is independent of the decreased brood size and prolonged egglay timing of eat-2, as neither was affected by hsd-2, suggesting that the hsd-2-mediated steroid signal regulates longevity without influencing reproduction. Furthermore, hsd-2 suppressed the ability of eat-2 to resist acute heat shock; stress, as measured by survival after recovery, but only later in life (day 7 and day; 13 adults). This indicates a role for hsd-2 in age-dependent responses to DR, consistent with; hsd-2 expression, which is primarily in adults. Since hsd-2 did not affect DR-induced heat shock resistance in day 1 adults, we hypothesized that hsd-3, which is only expressed in larvae, might be functioning in that role. Indeed, we found that while a deletion mutant of hsd-3 does not appear to affect eat-2 overall lifespan, it completely suppressed its ability to resist heat shock stress as day 1 adults. Therefore, although both hsd-2 and hsd-3 contribute to stress resistance in eat-2 adults, only hsd-2 impacts lifespan, as though steroid signaling in older eat-2 adults is more important for lifespan extension than steroid signaling in larvae and young adults. Taken together, our results indicate that steroid signaling through these two steroidogenic enzymes, active at distinct times during the worm lifespan, is vital for the health and longevity conferred by DR.

甾体信号介导了秀丽隐杆线虫饮食限制的eat-2遗传模型的长寿反应
饮食限制(DR)可以延长包括秀丽隐杆线虫在内的多种模式生物的寿命。这是一个有趣但仍有待解决的问题,即激素是否作为一种系统机制来调节这种长寿反应。我们通过研究保守的3β-羟基类固醇脱氢酶(3β-HSD)家族的两个成员HSD-2和HSD-3,确定了DR诱导的寿命延长需要类固醇信号传导。具体来说,我们发现DR的eat-2遗传模型中的寿命延长完全被hsd-2的缺失突变体所抑制。这种抑制与eat-2的卵量减少和产卵时间延长无关,因为两者都不受hsd-2的影响,这表明hsd-2介导的类固醇信号调节寿命而不影响繁殖。hsd-2抑制了eat-2抵抗急性热休克的能力;压力,以恢复后的存活率来衡量,但只在生命后期(第7天和第;13成年人)。这表明hsd-2在年龄依赖性DR反应中的作用,与;Hsd-2的表达,主要见于成人。由于hsd-2不影响dr诱导的第1天成虫的热休克抗性,我们假设仅在幼虫中表达的hsd-3可能起着这种作用。事实上,我们发现,虽然hsd-3的缺失突变体似乎并不影响eat-2的整体寿命,但它完全抑制了它在第1天成年时抵抗热休克应激的能力。因此,尽管hsd-2和hsd-3都有助于eat-2成虫的抗逆性,但只有hsd-2影响寿命,就像老年eat-2成虫体内的类固醇信号传导对寿命延长的作用比幼虫和年轻成虫体内的类固醇信号传导更重要一样。综上所述,我们的研究结果表明,通过这两种类固醇生成酶发出的类固醇信号,在蠕虫生命周期的不同时间活跃,对DR赋予的健康和长寿至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Translational Medicine of Aging
Translational Medicine of Aging Medicine-Geriatrics and Gerontology
CiteScore
5.30
自引率
0.00%
发文量
2
审稿时长
103 days
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