TY - JOUR ID - 250703 TI - Metformin Reduces Vascular Assembly in High Glucose-Treated Human Microvascular Endothelial Cells in An AMPK-Independent Manner JO - Cell Journal (Yakhteh) JA - CELLJ LA - en SN - 2228-5806 AU - Silva, Carolina AU - Rodrigues, Ilda AU - Andrade, Sara AU - Costa, Raquel AU - Soares, Raquel AD - .Department of Biomedicine, Unit of Biochemistry, Faculty of Medicine, University of Porto, 4200-319 Porto, Portugal;.i3S, Institute of Research and Innovation in Health, University of Porto, Porto, Portugal AD - .Department of Biomedicine, Unit of Biochemistry, Faculty of Medicine, University of Porto, 4200-319 Porto, Portugal AD - .Department of Biomedicine, Unit of Biochemistry, Faculty of Medicine, University of Porto, 4200-319 Porto, Portugal;.i3S, Institute of Research and Innovation in Health, University of Porto, Porto, Portugal ;.IPATIMUP, Institute Y1 - 2021 PY - 2021 VL - 23 IS - 2 SP - 174 EP - 183 KW - AICAR KW - AMPK Signaling KW - Compound C KW - Endothelial cells KW - Metformin DO - 10.22074/cellj.2021.7212 N2 - ObjectiveThe aim is to examine the effect of metformin in human microvascular endothelial cells exposed to high glucose (HG) concentration and compare them with the effects of other 5' adenosine monophosphate-activated protein kinase (AMPK) modulators under the same condition. Materials and Methods In this experimental study, human microvascular endothelial cells (HMECs) were treated with 15 mM metformin, 1 mM 5-aminoimidazol-4-carboxamideribonucleotide (AICAR) and 10 mM compound C in the presence of 20 mM glucose (hyperglycemic condition). Migration, invasion and proliferation were evaluated as well as the capillary-like structures formation. Moreover, the expression of angiogenic genes was assessed. Results Metformin significantly inhibited vessel formation and migration, although it did not change HMECs proliferation and invasion. In addition, metformin significantly reduced collagen formation as evidenced by histological staining. Concomitantly, expression of several genes implicated in angiogenesis and fibrosis, namely TGFß2, VEGFR2, ALK1, JAG1, TIMP2, SMAD5, SMAD6 and SMAD7, was slightly upregulated. Immunostaining for proteins involved in ALK5 receptor signaling, the alternative TGFß signaling pathway, revealed significant differences in SMAD2/3 expression. Conclusion Our data showed that metformin prevents vessel assembly in HMECs, probably through an AMPK- independent mechanism. Understanding the molecular mechanisms by which this pharmacological agent affects endothelial dysfunction is of paramount importance and paves the way to its particular use in preventing development of diabetic retinopathy and nephropathy, two processes where angiogenesis is exacerbated. UR - https://www.celljournal.org/article_250703.html L1 - https://www.celljournal.org/article_250703_1b60a81ee9d155b9b0ed36e799ead5f8.pdf ER -