Makuch Sebastian, Kupczyk Piotr, Makarec Alicja, Chodaczek Grzegorz, Ziółkowski Piotr, Woźniak Marta
Department of Clinical and Experimental Pathology, Wroclaw Medical University, 50-368 Wroclaw, Poland,
Department of Clinical and Experimental Pathology, Wroclaw Medical University, 50-368 Wroclaw, Poland.
Cell Physiol Biochem. 2023 Mar 22;57(2):54-62. doi: 10.33594/000000615.
BACKGROUND/AIMS: Glucose metabolism has been proven as an essential process for proliferating keratinocytes, which highlights the importance of glucose transporter-1 (GLUT1) not only in the onset of psoriasis but also in the progression and severity of this inflammation-driven disease. In this study, we attempted to find a connection between proinflammatory cytokines (IL-6, IL-17, IL-23, IL-36, TNF-α), a skin inflammation inducing agent - imiquimod (IMQ) and GLUT1 expression.
Human keratinocyte HaCaT cell line was incubated with exogenous cytokines: IL-6, IL-17A, IL-23, IL-36, TNF-α at a final concentration of 100 ng/ml, or with 1 µM of IMQ, for 48 h. Following the stimulation, glucose uptake and GLUT1 expression were evaluated. The activity of GLUT1 was measured in the presence of a selective GLUT1 inhibitor, BAY-876. The expression of GLUT1 was examined by immunofluorescence and quantified by qPCR, Western blotting and densitometry.
The results from qPCR analysis showed that the administration of exogenous IL-6, IL-17, IL-23 and IL-36 to HaCaT cells resulted in upregulation of GLUT1-encoding SLC2A1 gene, while TNF-α had no significant effect. The same results were confirmed by immunofluorescence analysis, as the fluorescent intensity of GLUT1 was elevated following cytokine and IMQ stimulation. Western blot and densitometry showed that all examined cytokines, as well as IMQ, increased GLUT1 expression. HaCaT cells displayed an improved intracellular 2-deoxy-D-glucose (2-DG) uptake and GLUT1 activity after stimulation by exogenous cytokines and IMQ. The highest uptake of 2-DG was observed after IL-23 stimulation (1.93x) and the lowest after TNF-α stimulation (1.07x). BAY-876 inhibited the 2-DG uptake compared to control.
Our findings suggest that cytokines and IMQ may play a key role in regulating GLUT1 expression in HaCaT cells. We believe that GLUT1 overexpression could potentially be utilized in the targeted treatment of psoriasis.
背景/目的:葡萄糖代谢已被证明是角质形成细胞增殖的一个重要过程,这突出了葡萄糖转运蛋白1(GLUT1)不仅在银屑病发病中,而且在这种炎症驱动疾病的进展和严重程度中的重要性。在本研究中,我们试图寻找促炎细胞因子(白细胞介素-6、白细胞介素-17、白细胞介素-23、白细胞介素-36、肿瘤坏死因子-α)、一种皮肤炎症诱导剂——咪喹莫特(IMQ)与GLUT1表达之间的联系。
将人角质形成细胞HaCaT细胞系与终浓度为100 ng/ml的外源性细胞因子白细胞介素-6、白细胞介素-17A、白细胞介素-23、白细胞介素-36、肿瘤坏死因子-α,或与1 μM咪喹莫特孵育48小时。刺激后,评估葡萄糖摄取和GLUT1表达。在选择性GLUT1抑制剂BAY-876存在的情况下测量GLUT1的活性。通过免疫荧光检查GLUT1的表达,并通过qPCR、蛋白质免疫印迹法和光密度测定法定量。
qPCR分析结果表明,向HaCaT细胞中施用外源性白细胞介素-6、白细胞介素-17、白细胞介素-23和白细胞介素-36会导致编码GLUT1的SLC2A1基因上调,而肿瘤坏死因子-α没有显著影响。免疫荧光分析证实了相同的结果,因为在细胞因子和IMQ刺激后GLUT1的荧光强度升高。蛋白质免疫印迹法和光密度测定法表明,所有检测的细胞因子以及IMQ均增加了GLUT1的表达。外源性细胞因子和IMQ刺激后,HaCaT细胞的细胞内2-脱氧-D-葡萄糖(2-DG)摄取和GLUT1活性有所改善。白细胞介素-23刺激后观察到最高的2-DG摄取(1.93倍),肿瘤坏死因子-α刺激后最低(1.07倍)。与对照组相比,BAY-876抑制了2-DG摄取。
我们的研究结果表明,细胞因子和IMQ可能在调节HaCaT细胞中GLUT1的表达中起关键作用。我们认为GLUT1的过表达可能潜在地用于银屑病的靶向治疗。