Department of Anatomy and Cell Biology, Rappaport Faculty of Medicine, Tel Aviv University, Israel.
Am J Physiol Endocrinol Metab. 2011 Apr;300(4):E613-23. doi: 10.1152/ajpendo.90484.2008. Epub 2010 Oct 5.
Skeletal growth, taking place in the cartilaginous growth plates of long bones, consumes high levels of glucose for both metabolic and anabolic purposes. We previously showed that Glut4 is present in growing bone and is decreased in diabetes. In the present study, we examined the hypothesis that in bone, GLUT4 gene expression and function are regulated via the IGF-I receptor (IGF-IR) and that Glut4 plays an important role in bone growth. Insulin and IGF-I actions on skeletal growth and glucose uptake were determined using mandibular condyle (MC) organ cultures and MC-derived primary cell cultures (MCDC). Chondrogenesis was determined by following proliferation and differentiation activities using immunohistochemical (IHC) analysis of proliferating cell nuclear antigen and type II collagen expression, respectively. Overall condylar growth was assessed morphometrically. GLUT4 mRNA and protein levels were determined using in situ hybridization and IHC, respectively. Glut4 translocation to the cell membrane was assessed using confocal microscopy analysis of GFP-Glut4 fusion-transfected cells and immunogold and electron microscopy on MC sections; glucose uptake was assayed by 2-deoxyglucose (2-DOG) uptake. Both IGF-I and insulin-stimulated glucose uptake in MCDC, with IGF-I being tenfold more potent than insulin. Blockage of IGF-IR abrogated both IGF-I- and insulin-induced chondrogenesis and glucose metabolism. IGF-I, but not insulin, induced Glut4 translocation to the plasma membrane. Additionally, insulin induced both GLUT4 and IGF-IR gene expression and improved condylar growth in insulin receptor knockout mice-derived MC. Moreover, silencing of GLUT4 gene in MCDC culture abolished both IGF-I-induced glucose uptake and chondrocytic proliferation and differentiation. In growing bone, the IGF-IR pathway stimulates Glut4 translocation and enhances glucose uptake. Moreover, intact Glut4 cellular levels and translocation machinery are essential for early skeletal growth.
骨骼生长发生在长骨的软骨生长板中,需要大量的葡萄糖来满足代谢和合成代谢的需求。我们之前已经证明,Glut4 存在于生长中的骨骼中,并在糖尿病中减少。在本研究中,我们检验了以下假说:在骨骼中,GLUT4 基因的表达和功能受 IGF-I 受体(IGF-IR)调控,Glut4 在骨骼生长中起着重要作用。使用下颌骨(MC)器官培养物和 MC 衍生的原代细胞培养物(MCDC)来确定胰岛素和 IGF-I 对骨骼生长和葡萄糖摄取的作用。通过分别用增殖细胞核抗原和 II 型胶原表达的免疫组织化学(IHC)分析来追踪增殖和分化活性,来确定软骨生成。通过形态计量学评估整体髁突生长。使用原位杂交和 IHC 分别确定 GLUT4 mRNA 和蛋白质水平。通过 GFP-Glut4 融合转染细胞的共聚焦显微镜分析和 MC 切片的免疫金和电子显微镜评估 Glut4 向细胞膜的易位;通过 2-脱氧葡萄糖(2-DOG)摄取来测定葡萄糖摄取。IGF-I 和胰岛素均刺激 MCDC 中的葡萄糖摄取,IGF-I 的作用是胰岛素的十倍。IGF-IR 阻断消除了 IGF-I 和胰岛素诱导的软骨生成和葡萄糖代谢。IGF-I 而不是胰岛素,诱导 Glut4 向质膜易位。此外,胰岛素诱导 GLUT4 和 IGF-IR 基因表达,并改善胰岛素受体敲除小鼠衍生的 MC 中的髁突生长。此外,在 MCDC 培养物中沉默 GLUT4 基因消除了 IGF-I 诱导的葡萄糖摄取以及软骨细胞增殖和分化。在生长中的骨骼中,IGF-IR 途径刺激 Glut4 易位并增强葡萄糖摄取。此外,完整的 Glut4 细胞水平和易位机制对于早期骨骼生长至关重要。