Jacobs D B, Ireland M, Pickett T, Maisel H, Grunberger G
Department of Internal Medicine, Wayne State University, School of Medicine, Detroit, MI 48201.
Curr Eye Res. 1992 Dec;11(12):1137-45. doi: 10.3109/02713689208999539.
Insulin and insulin-like growth factor I (IGF-I) play a role in lens cell growth and development. The binding of these hormones to their respective receptors with its concomitant signal transduction is an important step in these cellular processes. Hormone binding to adult chicken lens insulin and IGF-I receptors, partially purified from epithelial and fiber cells, was studied to examine this activity in lens. The associated stimulation of receptor-mediated tyrosine kinase by the hormones was also studied. At an insulin concentration of 0.02 nM, specific binding was similar for epithelial and fiber receptor preparations (Epi = 0.23 +/- 0.03 fmol, Fib = 0.19 +/- 0.02 fmol). Displacement studies revealed that there was also no difference between epithelial and fiber receptor preparations in the concentration of insulin necessary for half maximal displacement of specific [125I]-insulin binding (IC50: Epi = 0.32 nM +/- 0.07 nM, Fib = 0.31 nM +/- 0.05 nM). Comparison of IGF-I (0.02 nM) binding to receptor preparations from epithelial and fiber cells demonstrated that specific binding was similar in the two preparations (Epi = 0.50 +/- 0.05 fmol, Fib = 0.42 +/- 0.05 fmol). Also, there was no difference in the concentration of IGF-I necessary for half maximal displacement of specific [125I]-IGF-I binding (IC50 = Epi: 0.27 +/- 0.05 nM, Fib: 0.28 +/- 0.04 nM). The ability of IGF-I to displace bound [125I]-insulin was also examined. The IC50 for IGF-I binding to the insulin receptors isolated from epithelial and fiber cells was 37.4 +/- 2.4 nM, and 35.4 +/- 2.8 nM, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)
胰岛素和胰岛素样生长因子I(IGF-I)在晶状体细胞的生长和发育中发挥作用。这些激素与其各自受体的结合及其伴随的信号转导是这些细胞过程中的重要步骤。研究了从成年鸡晶状体上皮细胞和纤维细胞中部分纯化的胰岛素和IGF-I受体与激素的结合情况,以检验晶状体中的这种活性。还研究了激素对受体介导的酪氨酸激酶的相关刺激作用。在胰岛素浓度为0.02 nM时,上皮细胞和纤维细胞受体制剂的特异性结合相似(上皮细胞=0.23±0.03 fmol,纤维细胞=0.19±0.02 fmol)。置换研究表明,上皮细胞和纤维细胞受体制剂在使特异性[125I] -胰岛素结合位移一半所需的胰岛素浓度方面也没有差异(IC50:上皮细胞=0.32 nM±0.07 nM,纤维细胞=0.31 nM±0.05 nM)。比较IGF-I(0.02 nM)与上皮细胞和纤维细胞受体制剂的结合情况表明,两种制剂中的特异性结合相似(上皮细胞=0.50±0.05 fmol,纤维细胞=0.42±0.05 fmol)。此外,使特异性[125I] -IGF-I结合位移一半所需的IGF-I浓度也没有差异(IC50 =上皮细胞:0.27±0.05 nM,纤维细胞:0.28±0.04 nM)。还检测了IGF-I置换结合的[125I] -胰岛素的能力。IGF-I与从上皮细胞和纤维细胞分离的胰岛素受体结合的IC50分别为37.4±2.4 nM和35.4±2.8 nM。(摘要截断于250字)