Pagesy Patrick, Tachet Caroline, Mostefa-Kara Ali, Larger Etienne, Issad Tarik
Inserm, U1016, Institut Cochin, Paris, France.
Cnrs, UMR8104, Paris, France.
Exp Clin Endocrinol Diabetes. 2019 Sep;127(8):517-523. doi: 10.1055/a-0596-7337. Epub 2018 Jun 11.
O-linked-β-N-Acetylglucosaminylation (O-GlcNAcylation), a reversible post-translational modification involved in diabetic complications, is regulated by only two enzymes, O-linked N-acetylglucosamine transferase (OGT) and β-N-Acetylglucosaminidase (OGA). Increased OGA expression has been described previously in blood cells from patients with diabetes and was interpreted as an adaptative response to hyperglycemia-induced O-GlcNAcylation. OGA expression was thus proposed to have potential utility as a diagnostic marker. The present work was undertaken to determine whether determination of OGA enzymatic activity in blood cells could constitute a more rapidly accessible marker than OGA expression level measurements.Blood samples were obtained from patients with type 2 diabetes from the Department of Diabetology of the Cochin Hospital and healthy volunteers from the French blood Agency. OGA enzymatic activity and OGA mRNA expression levels were evaluated in leucocytes from patients with type 2 diabetes and from healthy donors.OGA activity was higher in leucocytes from patients with diabetes compared to control individuals. Surprisingly, OGA activity was not correlated hyperglycaemia markers (blood glucose, fructosamine, HbA) but was positively correlated with the inflammatory marker C-reactive protein. OGA mRNA levels were also increased in leucocytes from patients with diabetes and were correlated with mRNA coding for two pro-inflammatory proteins, TNFα and TxNIP.Therefore, OGA activity in leucocytes might be a more easily accessible biomarker than OGA expression levels. However, changes in OGA activity observed in patients with type 2 diabetes may reflect the inflammatory rather than the glycaemic status of these patients.
O-连接的β-N-乙酰葡糖胺化修饰(O-GlcNAcylation)是一种参与糖尿病并发症的可逆性翻译后修饰,仅由两种酶调控,即O-连接的N-乙酰葡糖胺转移酶(OGT)和β-N-乙酰葡糖胺糖苷酶(OGA)。先前已报道糖尿病患者血细胞中OGA表达增加,并被解释为对高血糖诱导的O-GlcNAcylation的适应性反应。因此,有人提出OGA表达可能具有作为诊断标志物的潜在用途。本研究旨在确定测定血细胞中OGA酶活性是否比测量OGA表达水平能构成一种更容易获得的标志物。从科钦医院糖尿病科的2型糖尿病患者和法国血液机构的健康志愿者中采集血样。评估了2型糖尿病患者和健康供者白细胞中的OGA酶活性和OGA mRNA表达水平。与对照个体相比,糖尿病患者白细胞中的OGA活性更高。令人惊讶的是,OGA活性与高血糖标志物(血糖、果糖胺、糖化血红蛋白)无关,但与炎症标志物C反应蛋白呈正相关。糖尿病患者白细胞中的OGA mRNA水平也升高,并且与编码两种促炎蛋白TNFα和TxNIP的mRNA相关。因此,白细胞中的OGA活性可能比OGA表达水平更容易作为生物标志物。然而,在2型糖尿病患者中观察到的OGA活性变化可能反映了这些患者的炎症状态而非血糖状态。