Department of Molecular and Cell Biology, University of California, Merced, CA 95343, USA.
Quantitative and Systems Biology Graduate Program, University of California, Merced, CA 95343, USA.
J Cell Sci. 2020 May 27;133(10):jcs239467. doi: 10.1242/jcs.239467.
Nutrient availability upon feeding leads to an increase in body size in the planarian However, it remains unclear how food consumption integrates with cell division at the organismal level. Here, we show that the NAD-dependent protein deacetylases sirtuins are evolutionarily conserved in planarians, and specifically demonstrate that the homolog of human sirtuin-1 (SIRT1) (encoded by ), regulates organismal growth by impairing both feeding behavior and intestinal morphology. Disruption of with RNAi or pharmacological inhibition of Sirtuin-1 leads to reduced animal growth. Conversely, enhancement of Sirtuin-1 activity with resveratrol accelerates growth. Differences in growth rates were associated with changes in the amount of time taken to locate food and overall food consumption. Furthermore, animals displayed reduced cell death and increased stem cell proliferation accompanied by impaired expression of intestinal lineage progenitors and reduced branching of the gut. Taken together, our findings indicate that Sirtuin-1 is a crucial metabolic hub capable of controlling animal behavior, tissue renewal and morphogenesis of the adult intestine.
进食时营养物质的可用性会导致扁形动物体型增大。然而,目前尚不清楚食物消耗如何与机体水平的细胞分裂相整合。在这里,我们表明,NAD 依赖性蛋白去乙酰化酶 Sirtuins 在扁形动物中是保守的,并且特别表明,人类 Sirtuin-1 的同源物(SIRT1)(由 编码)通过损害摄食行为和肠道形态来调节机体生长。用 RNAi 敲低 或药理学抑制 Sirtuin-1 会导致动物生长减少。相反,用白藜芦醇增强 Sirtuin-1 活性会加速生长。生长速度的差异与寻找食物所需的时间和整体食物消耗的变化有关。此外, 动物表现出细胞死亡减少和干细胞增殖增加,伴随着肠道谱系祖细胞表达受损和肠道分支减少。总之,我们的研究结果表明,Sirtuin-1 是一个关键的代谢枢纽,能够控制动物行为、组织更新和成年肠道的形态发生。