Department of Biomedical Sciences, Colorado State University, Fort Collins, CO 80523, USA.
Cell Biochem Biophys. 2012 Apr;62(3):441-50. doi: 10.1007/s12013-011-9326-x.
We have examined the association of insulin receptors (IR) and downstream signaling molecules with membrane microdomains in rat basophilic leukemia (RBL-2H3) cells following treatment with insulin or tris(2-pyridinecarbxylato)chromium(III) (Cr(pic)(3)). Single-particle tracking demonstrated that individual IR on these cells exhibited reduced lateral diffusion and increased confinement within 100 nm-scale membrane compartments after treatment with either 200 nM insulin or 10 μM Cr(pic)(3). These treatments also increased the association of native IR, phosphorylated insulin receptor substrate 1 and phosphorylated AKT with detergent-resistant membrane microdomains of characteristically high buoyancy. Confocal fluorescence microscopic imaging of Di-4-ANEPPDHQ labeled RBL-2H3 cells also showed that plasma membrane lipid order decreased following treatment with Cr(pic)(3) but was not altered by insulin treatment. Fluorescence correlation spectroscopy demonstrated that Cr(pic)(3) did not affect IR cell-surface density or compete with insulin for available binding sites. Finally, Fourier transform infrared spectroscopy indicated that Cr(pic)(3) likely associates with the lipid interface in reverse-micelle model membranes. Taken together, these results suggest that activation of IR signaling in a cellular model system by both insulin and Cr(pic)(3) involves retention of IR in specialized nanometer-scale membrane microdomains but that the insulin-like effects of Cr(pic)(3) are due to changes in membrane lipid order rather than to direct interactions with IR.
我们研究了胰岛素受体 (IR) 和下游信号分子与胰岛素或三 (2-吡啶甲羧基) 铬 (III) (Cr(pic)(3)) 处理后的大鼠嗜碱性白血病 (RBL-2H3) 细胞的膜微区的关联。单颗粒跟踪表明,在用 200 nM 胰岛素或 10 μM Cr(pic)(3)处理后,这些细胞上的单个 IR 表现出横向扩散减少和在 100nm 尺度膜隔室中的限制增加。这些处理还增加了天然 IR、磷酸化胰岛素受体底物 1 和磷酸化 AKT 与具有特征性高浮力的去污剂抗性膜微区的结合。用 Di-4-ANEPPDHQ 标记的 RBL-2H3 细胞的共聚焦荧光显微镜成像也表明,Cr(pic)(3)处理后质膜脂质有序性降低,但胰岛素处理没有改变。荧光相关光谱表明,Cr(pic)(3)不影响 IR 细胞表面密度或与胰岛素竞争可用结合位点。最后,傅里叶变换红外光谱表明,Cr(pic)(3)可能与反胶束模型膜中的脂质界面结合。总之,这些结果表明,胰岛素和 Cr(pic)(3)在细胞模型系统中激活 IR 信号都涉及将 IR 保留在专门的纳米尺度膜微区中,但 Cr(pic)(3)的胰岛素样作用是由于膜脂质有序性的变化而不是直接与 IR 相互作用所致。