Chronic Exposure to Proline Causes Aminoacidotoxicity and Impaired Beta-Cell Function: Studies In Vitro.

Q3 Medicine
Review of Diabetic Studies Pub Date : 2016-01-01 Epub Date: 2016-05-10 DOI:10.1900/RDS.2016.13.66
Zhenping Liu, Per B Jeppesen, Søren Gregersen, Lotte Bach Larsen, Kjeld Hermansen
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引用次数: 18

Abstract

Background: Pancreatic islet-cell dysfunction is a hallmark in the development of diabetes, but the reasons for the primary β-cell defect are still elusive. Elevated circulating proline levels have been found in subjects with insulin resistance, obesity, and type 2 diabetes. Therefore, we assessed β-cell function, gene expressions, and cell death after long-term exposure of pancreatic β-cells to excess proline in vitro.

Methods: Isolated mouse islets and INS-1E cells were incubated with and without excess proline. After 72 h, we examined: (1) β-cell function, including basal insulin secretion (BIS) and glucose-stimulated insulin secretion (GSIS), (2) transcription factors related to insulin gene expression and enzymes involved in the tricarboxylic acid cycle and cholesterol biogenesis, (3) cellular triglycerides (TG) and cholesterol content, (4) the death of INS-1E cells and 3H thymidine incorporation, and (5) protein expression of INS-1E cells in response to proline by proteomics.

Results: We found that high doses of proline increased BIS and decreased GSIS in both isolated mouse islets and INS-1E cells. MafA, insulin 1, and the cytochrome c oxidase subunit VIa polypeptide 2 mRNA expressions were all downregulated, indicating that proline impaired insulin gene transcription and mitochondrial oxidative phosphorylation. In contrast, mevalonate decarboxylase gene expression was upregulated, and simultaneously, cholesterol content in INS-1E cells was enhanced. Protein profiling of INS-1E cells revealed that cytosolic non-specific dipeptidase and α enolase were differentially expressed.

Conclusions: Our results indicate that proline-induced insulin transcription and mitochondrial oxidative phosphorylation impairment may contribute to the β-cell dysfunction observed in type 2 diabetes. Caution should be applied in interpreting the pathophysiological role of proline since very high proline concentrations were used in the experiments.

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慢性暴露于脯氨酸导致氨基酸毒性和β细胞功能受损:体外研究。
背景:胰岛细胞功能障碍是糖尿病发展的一个标志,但原发性β细胞缺陷的原因尚不清楚。在胰岛素抵抗、肥胖和2型糖尿病患者中发现循环脯氨酸水平升高。因此,我们评估了β细胞在体外长期暴露于过量脯氨酸的胰腺β细胞后的功能、基因表达和细胞死亡。方法:分离的小鼠胰岛细胞和INS-1E细胞用和不加过量脯氨酸孵育。72h后,我们检测了:(1)β细胞功能,包括基础胰岛素分泌(BIS)和葡萄糖刺激胰岛素分泌(GSIS),(2)胰岛素基因表达相关的转录因子和参与三羧酸循环和胆固醇生物发生的酶,(3)细胞甘油三酯(TG)和胆固醇含量,(4)INS-1E细胞死亡和3H胸苷结合,(5)蛋白质组学检测INS-1E细胞对脯氨酸反应的蛋白表达。结果:我们发现高剂量脯氨酸增加了离体小鼠胰岛细胞和INS-1E细胞的BIS,降低了GSIS。MafA、胰岛素1和细胞色素c氧化酶亚基VIa多肽2 mRNA表达均下调,表明脯氨酸损害了胰岛素基因转录和线粒体氧化磷酸化。相反,甲羟戊酸脱羧酶基因表达上调,同时INS-1E细胞胆固醇含量升高。INS-1E细胞的蛋白谱显示胞质内非特异性二肽酶和α烯醇化酶存在差异表达。结论:我们的研究结果表明脯氨酸诱导的胰岛素转录和线粒体氧化磷酸化损伤可能是2型糖尿病β细胞功能障碍的原因之一。在解释脯氨酸的病理生理作用时应谨慎,因为实验中使用了非常高的脯氨酸浓度。
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
Review of Diabetic Studies
Review of Diabetic Studies Medicine-Internal Medicine
CiteScore
1.80
自引率
0.00%
发文量
28
期刊介绍: The Review of Diabetic Studies (RDS) is the society"s peer-reviewed journal published quarterly. The purpose of The RDS is to support and encourage research in biomedical diabetes-related science including areas such as endocrinology, immunology, epidemiology, genetics, cell-based research, developmental research, bioengineering and disease management.
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