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轴下调导致葡萄糖代谢紊乱并易患代谢紊乱。

The Axis Downregulation Alters Glucose Metabolism and Predispose to Metabolic Disorders.

机构信息

Department of Molecular Carcinogenesis, Medical University of Lodz, 90-752 Lodz, Poland.

出版信息

Int J Mol Sci. 2022 Mar 19;23(6):3326. doi: 10.3390/ijms23063326.

Abstract

Recent reports indicate that the hypoxia-induced factor (HIF1α) and the Warburg effect play an initiating role in glucotoxicity, which underlies disorders in metabolic diseases. WWOX has been identified as a HIF1α regulator. downregulation leads to an increased expression of HIF1α target genes encoding glucose transporters and glycolysis' enzymes. It has been proven in the normoglycemic mice cells and in gestational diabetes patients. The aim of the study was to determine WWOX's role in glucose metabolism regulation in hyperglycemia and hypoxia to confirm its importance in the development of metabolic disorders. For this purpose, the gene was silenced in human normal fibroblasts, and then cells were cultured under different sugar and oxygen levels. Thereafter, it was investigated how silencing alters the genes and proteins expression profile of glucose transporters and glycolysis pathway enzymes, and their activity. In normoxia normoglycemia, higher glycolysis genes expression, their activity, and the lactate concentration were observed in KO fibroblasts in comparison to control cells. In normoxia hyperglycemia, it was observed a decrease of insulin-dependent glucose uptake and a further increase of lactate. It likely intensifies hyperglycemia condition, which deepen the glucose toxic effect. Then, in hypoxia hyperglycemia, KO caused weaker glucose uptake and elevated lactate production. In conclusion, the axis downregulation alters glucose metabolism and probably predispose to metabolic disorders.

摘要

最近的报告表明,缺氧诱导因子 (HIF1α) 和瓦博格效应在糖毒性中起启动作用,这是代谢疾病紊乱的基础。WWOX 已被确定为 HIF1α 的调节剂。下调会导致编码葡萄糖转运体和糖酵解酶的 HIF1α 靶基因表达增加。这在正常血糖小鼠细胞和妊娠糖尿病患者中得到了证实。本研究的目的是确定 WWOX 在高血糖和缺氧条件下对葡萄糖代谢调节的作用,以确认其在代谢紊乱发展中的重要性。为此,在人正常成纤维细胞中沉默了 基因,然后在不同糖和氧水平下培养细胞。此后,研究了沉默如何改变葡萄糖转运体和糖酵解途径酶的基因和蛋白质表达谱及其活性。在常氧正常血糖条件下,与对照细胞相比,KO 成纤维细胞中更高的糖酵解基因表达、其活性和乳酸浓度。在常氧高血糖条件下,观察到胰岛素依赖性葡萄糖摄取减少和乳酸进一步增加。这可能会加剧高血糖状态,从而加深葡萄糖毒性作用。然后,在高血糖缺氧条件下,KO 导致葡萄糖摄取减少和乳酸产量增加。总之,轴下调改变了葡萄糖代谢,可能容易导致代谢紊乱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/948d/8955937/751ced2e535f/ijms-23-03326-g001.jpg

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