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进食感知而非摄取食物会导致线虫的代谢变化和不可逆转的发育停滞。

Food perception without ingestion leads to metabolic changes and irreversible developmental arrest in C. elegans.

机构信息

Department of Biology, Duke University, Box 90338, Durham, NC, 27708-0338, USA.

Department of Biology, McGill University, Montreal, QC, H3A 1B1, Canada.

出版信息

BMC Biol. 2018 Oct 8;16(1):112. doi: 10.1186/s12915-018-0579-3.

DOI:10.1186/s12915-018-0579-3
PMID:30296941
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6176503/
Abstract

BACKGROUND

Developmental physiology is very sensitive to nutrient availability. For instance, in the nematode Caenorhabditis elegans, newly hatched L1-stage larvae require food to initiate postembryonic development. In addition, larvae arrested in the dauer diapause, a non-feeding state of developmental arrest that occurs during the L3 stage, initiate recovery when exposed to food. Despite the essential role of food in C. elegans development, the contribution of food perception versus ingestion on physiology has not been delineated.

RESULTS

We used a pharmacological approach to uncouple the effects of food (bacteria) perception and ingestion in C. elegans. Perception was not sufficient to promote postembryonic development in L1-stage larvae. However, L1 larvae exposed to food without ingestion failed to develop upon return to normal culture conditions, instead displaying an irreversible arrest phenotype. Inhibition of gene expression during perception rescued subsequent development, demonstrating that the response to perception without feeding is deleterious. Perception altered DAF-16/FOXO subcellular localization, reflecting activation of insulin/IGF signaling (IIS). The insulin-like peptide daf-28 was specifically required, suggesting perception in chemosensory neurons, where it is expressed, regulates peptide synthesis and possibly secretion. However, genetic manipulation of IIS did not modify the irreversible arrest phenotype caused by food perception, revealing that wild-type function of the IIS pathway is not required to produce this phenotype and that other pathways affected by perception of food in the absence of its ingestion are likely to be involved. Gene expression and Nile red staining showed that food perception could alter lipid metabolism and storage. We found that starved larvae sense environmental polypeptides, with similar molecular and developmental effects as perception of bacteria. Environmental polypeptides also promoted recovery from dauer diapause, suggesting that perception of polypeptides plays an important role in the life history of free-living nematodes.

CONCLUSIONS

We conclude that actual ingestion of food is required to initiate postembryonic development in C. elegans. We also conclude that polypeptides are perceived as a food-associated cue in this and likely other animals, initiating a signaling and gene regulatory cascade that alters metabolism in anticipation of feeding and development, but that this response is detrimental if feeding does not occur.

摘要

背景

发育生理学对营养物质的可用性非常敏感。例如,在秀丽隐杆线虫中,刚孵化的 L1 期幼虫需要食物来启动胚胎后发育。此外,在 L3 阶段进入 dauer 休眠的幼虫,一种非进食的发育停滞状态,在暴露于食物时会开始恢复。尽管食物在秀丽隐杆线虫发育中起着至关重要的作用,但食物感知与摄入对生理学的贡献尚未被描绘。

结果

我们使用药理学方法来分离线虫中食物(细菌)感知和摄入的作用。感知本身不足以促进 L1 期幼虫的胚胎后发育。然而,暴露于食物但未摄入的 L1 幼虫在返回正常培养条件后无法发育,而是表现出不可逆的停滞表型。在感知过程中抑制基因表达可挽救随后的发育,表明没有进食的感知反应是有害的。感知改变了 DAF-16/FOXO 的亚细胞定位,反映了胰岛素/IGF 信号(IIS)的激活。胰岛素样肽 daf-28 是特异性需要的,表明在化学感觉神经元中感知,在那里它表达,调节肽的合成,可能还有分泌。然而,IIS 的遗传操作并没有改变由食物感知引起的不可逆停滞表型,这表明 IIS 途径的野生型功能不是产生这种表型所必需的,并且可能涉及到其他途径,这些途径在没有摄入食物的情况下被感知到。基因表达和尼罗红染色表明,食物感知可以改变脂质代谢和储存。我们发现饥饿的幼虫可以感知环境多肽,其具有与细菌感知相似的分子和发育作用。环境多肽也促进了 dauer 休眠的恢复,这表明多肽的感知在自由生活线虫的生活史中起着重要作用。

结论

我们得出结论,实际摄入食物是秀丽隐杆线虫启动胚胎后发育所必需的。我们还得出结论,多肽在这种情况下,可能在其他动物中也被感知为与食物相关的线索,引发信号和基因调控级联反应,改变代谢以适应进食和发育,但如果不进食,这种反应是有害的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7b7/6176503/06935d173af3/12915_2018_579_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7b7/6176503/f7f04fd1b2fd/12915_2018_579_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7b7/6176503/9352b2ebbdcb/12915_2018_579_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7b7/6176503/a35069f5affe/12915_2018_579_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7b7/6176503/f765e3954e0b/12915_2018_579_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7b7/6176503/37d6292f39e0/12915_2018_579_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7b7/6176503/06935d173af3/12915_2018_579_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7b7/6176503/f7f04fd1b2fd/12915_2018_579_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7b7/6176503/9352b2ebbdcb/12915_2018_579_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7b7/6176503/a35069f5affe/12915_2018_579_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7b7/6176503/f765e3954e0b/12915_2018_579_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7b7/6176503/37d6292f39e0/12915_2018_579_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7b7/6176503/06935d173af3/12915_2018_579_Fig6_HTML.jpg

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