Abstract

Purpose The objective of this study was to determine whether diabetes mellitus (DM)-induced up-regulation of 14-3-3β (YWHAB) in endothelial cells enhances intimal hyperplasia in carotid artery-injured DM Sprague-Dawley (SD) rats. Methods YWHAB expression and rat aortic endothelial cell (RAOEC) vitality were examined using Cell Counting Kit-8 (CCK-8), quantitative reverse transcription PCR (qRT-PCR), and western blot analysis in cells treated with different glucose concentrations (5.6, 10, 15, 25, or 35 mM). For in vivo experiments, a YWHAB small interfering (si) RNA recombinant lentiviral vector (YWHAB-LV) or Mock siRNA recombinant lentiviral vector (Mock-LV) were injected into streptozotocin-induced DM SD rats via the tail vein. YWHAB expression and carotid artery morphology were assessed 7 days post injury using immunofluorescence (IF) and hematoxylin-eosin (HE) staining. The proliferation and migration of Mock-LV and YWHAB-LV-infected RAOECs treated with 25 mM glucose were examined using cell scratch tests and flow cytometry. BCL2-Associated X (BAX) distribution in RAOECs treated with 25 mM glucose was examined using IF staining and western blot analysis. Results Western blot, qRT-PCR, and CCK-8 analyses demonstrated that both YWHAB expression and cell vitality increased with increasing glucose concentration ( p < 0.05 ). YWHAB IF staining was increased in DM rats compared with the normal group ( p < 0.05 ). HE staining showed that intimal hyperplasia is alleviated in YWHAB-silenced DM rats ( p < 0.05 ). YWHAB silencing suppressed the proliferation and migration of RAOECs treated with 25 mM glucose ( p < 0.05 ). Moreover, western blot analyses and IF staining demonstrated that YWHAB silencing increased the translocation of BAX from the cytoplasm to mitochondria in RAOECs treated with 25 mM glucose ( p < 0.05 ). Conclusions Our results indicate that hyperglycemia-induced up-regulation of YWHAB in endothelial cell plays a significant role in inti