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宏量营养素对 ClpB(一种 α-MSH 细菌模拟蛋白)体外生产的影响及其在饱腹感信号传导中的可能作用。

Effects of Macronutrients on the In Vitro Production of ClpB, a Bacterial Mimetic Protein of α-MSH and Its Possible Role in Satiety Signaling.

机构信息

TargEDys SA, Faculty of Medicine and Pharmacy, University of Rouen Normandy, 22, Boulevard Gambetta, Cedex 01, 76183 Rouen, France.

Nutrition, Gut and Brain Laboratory, Inserm UMR1073, University of Rouen Normandy, 76183 Rouen, France.

出版信息

Nutrients. 2019 Sep 5;11(9):2115. doi: 10.3390/nu11092115.

DOI:10.3390/nu11092115
PMID:31491982
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6769967/
Abstract

Gut microbiota can influence the feeding behavior of the host, but the underlying mechanisms are unknown. Recently, caseinolytic protease B (ClpB), a disaggregation chaperon protein of , was identified as a conformational mimetic of α-melanocyte-stimulating hormone (α-MSH), an anorexigenic neuropeptide. Importantly, ClpB was necessary for to have an anorexigenic effect in mice, suggesting that it may participate in satiety signaling. To explore this further, we determined the short-term (2 h) effects of three macronutrients: protein (bovine serum albumin), carbohydrate (D-fructose) and fat (oleic acid), on the production of ClpB by and analyzed whether ClpB can stimulate the secretion of the intestinal satiety hormone, peptide YY (PYY). Isocaloric amounts of all three macronutrients added to a continuous culture of increased ClpB immunoreactivity. However, to increase the levels of ClpB mRNA and ClpB protein in bacteria and supernatants, supplementation with protein was required. A nanomolar concentration of recombinant ClpB dose-dependently stimulated PYY secretion from the primary cell cultures of rat intestinal mucosa. Total proteins extracted from but not from ClpB-deficient strains also tended to increase PYY secretion. These data support a possible link between ClpB and protein-induced satiety signaling in the gut.

摘要

肠道微生物群可以影响宿主的进食行为,但其中的机制尚不清楚。最近,发现了一种分解蛋白酶 B(ClpB),它是一种厌食神经肽 α-促黑素细胞激素(α-MSH)的构象模拟物。重要的是,ClpB 是 发挥厌食作用所必需的,这表明它可能参与了饱腹感信号传递。为了进一步探索这一机制,我们确定了三种宏量营养素(蛋白质(牛血清白蛋白)、碳水化合物(D-果糖)和脂肪(油酸))对 产生 ClpB 的短期(2 小时)影响,并分析了 ClpB 是否可以刺激肠道饱腹感激素肽 YY(PYY)的分泌。在持续培养的 中添加三种宏量营养素的等热量,均可增加 ClpB 免疫反应性。然而,要增加细菌和上清液中 ClpB mRNA 和 ClpB 蛋白的水平,则需要补充蛋白质。重组 ClpB 的纳摩尔浓度可剂量依赖性地刺激大鼠肠黏膜原代细胞中 PYY 的分泌。从 中提取的总蛋白而不是从 ClpB 缺陷 菌株中提取的总蛋白也倾向于增加 PYY 的分泌。这些数据支持了 ClpB 与肠道中蛋白质诱导的饱腹感信号之间可能存在联系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44a5/6769967/cabdec579899/nutrients-11-02115-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44a5/6769967/629e8dd3a7d8/nutrients-11-02115-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44a5/6769967/50f0ff13c418/nutrients-11-02115-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44a5/6769967/a849f389417e/nutrients-11-02115-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44a5/6769967/cabdec579899/nutrients-11-02115-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44a5/6769967/629e8dd3a7d8/nutrients-11-02115-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44a5/6769967/50f0ff13c418/nutrients-11-02115-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44a5/6769967/a849f389417e/nutrients-11-02115-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44a5/6769967/cabdec579899/nutrients-11-02115-g004.jpg

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