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肠道酸度降低在黑腹果蝇和小鼠中诱导出肥胖样表型。

Reduced Gut Acidity Induces an Obese-Like Phenotype in Drosophila melanogaster and in Mice.

作者信息

Lin Wei-Sheng, Huang Cheng-Wen, Song You-Sheng, Yen Jui-Hung, Kuo Ping-Chang, Yeh Sheng-Rong, Lin Hung-Yu, Fu Tsai-Feng, Wu Ming-Shiang, Wang Horng-Dar, Wang Pei-Yu

机构信息

Graduate Institute of Brain and Mind Sciences, College of Medicine, National Taiwan University, Taipei, Taiwan; Department of Pediatrics, National Taiwan University Hospital Yun-Lin branch, Yun-Lin, Taiwan.

Graduate Institute of Brain and Mind Sciences, College of Medicine, National Taiwan University, Taipei, Taiwan; Institute of Biotechnology, National Tsing Hua University, HsinChu, Taiwan.

出版信息

PLoS One. 2015 Oct 5;10(10):e0139722. doi: 10.1371/journal.pone.0139722. eCollection 2015.

Abstract

In order to identify genes involved in stress and metabolic regulation, we carried out a Drosophila P-element-mediated mutagenesis screen for starvation resistance. We isolated a mutant, m2, that showed a 23% increase in survival time under starvation conditions. The P-element insertion was mapped to the region upstream of the vha16-1 gene, which encodes the c subunit of the vacuolar-type H+-ATPase. We found that vha16-1 is highly expressed in the fly midgut, and that m2 mutant flies are hypomorphic for vha16-1 and also exhibit reduced midgut acidity. This deficit is likely to induce altered metabolism and contribute to accelerated aging, since vha16-1 mutant flies are short-lived and display increases in body weight and lipid accumulation. Similar phenotypes were also induced by pharmacological treatment, through feeding normal flies and mice with a carbonic anhydrase inhibitor (acetazolamide) or proton pump inhibitor (PPI, lansoprazole) to suppress gut acid production. Our study may thus provide a useful model for investigating chronic acid suppression in patients.

摘要

为了鉴定参与应激和代谢调节的基因,我们进行了一项针对饥饿抗性的果蝇P元素介导的诱变筛选。我们分离出一个突变体m2,其在饥饿条件下的存活时间增加了23%。P元素插入位点被定位到vha16-1基因上游区域,该基因编码液泡型H⁺-ATP酶的c亚基。我们发现vha16-1在果蝇中肠高度表达,m2突变果蝇的vha16-1功能减弱,中肠酸度也降低。这种缺陷可能会导致代谢改变并加速衰老,因为vha16-1突变果蝇寿命较短,体重增加且脂肪积累增多。通过给正常果蝇和小鼠喂食碳酸酐酶抑制剂(乙酰唑胺)或质子泵抑制剂(PPI,兰索拉唑)以抑制肠道酸产生的药理学处理也诱导了类似的表型。因此,我们的研究可能为研究患者慢性酸抑制提供一个有用的模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cba2/4593636/34c00eb32b4b/pone.0139722.g001.jpg

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