García-de Lacoba M, Alarcón C, de la Rosa E J, de Pablo F
Department of Cell and Developmental Biology, Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas, Madrid, Spain.
Endocrinology. 1999 Jan;140(1):233-43. doi: 10.1210/endo.140.1.6393.
The extensive colocalization of insulin receptor (IR) and insulin-like growth factor-I receptor (IGFR) messenger RNAs during central nervous system development, together with the effects of insulin and IGF-I in neurogenesis, raises the question of how stage- and factor-specific signaling occurs. Thus, it is necessary to characterize the receptor proteins present in vivo to start addressing this issue. Here we have studied the chick embryonic neuroretina at day 6 (E6), when it is predominantly proliferative, and at E12, when neuronal differentiation is advanced. Developmentally regulated high-affinity binding sites for both insulin and IGF-I were detected at E6 and E12. In proliferative neuroretina, typical IGFR with the highest affinity for IGF-I coexisted with separate atypical insulin binding sites, which had similar high affinity for insulin and IGF-I. Immunoprecipitation of ligand-cross-linked receptors with specific antibodies for the IR alpha-subunit, the IR beta-subunit, or the IGFR beta-subunit demonstrated the presence of IR/IGFR hybrids. They were more abundant in E6 than in E12 retina. These hybrid receptors bound most of radiolabeled insulin, but little radiolabeled IGF-I, at tracer concentrations. At E12, the specificity of the insulin binding sites changed, and it was closer to that found with IR in liver, where hybrids were undetectable. The basal autophosphorylation level of these atypical hybrid receptors was high, although insulin and, even more so, IGF-I modestly increased the phosphorylation of two IR beta-subunits of 95 and 105 kDa. The high-affinity/low-discriminative IR/IGFR hybrids predominantly found in a proliferative stage of neurogenesis can mediate the effects of proinsulin and insulin, previously demonstrated in organoculture at this stage. More importantly, this hybrid receptor may be physiologically relevant for the action of the locally produced proinsulin found in early neurogenesis.
在中枢神经系统发育过程中,胰岛素受体(IR)和胰岛素样生长因子-I受体(IGFR)信使核糖核酸广泛共定位,同时胰岛素和IGF-I在神经发生中具有作用,这就提出了阶段特异性和因子特异性信号传导如何发生的问题。因此,有必要对体内存在的受体蛋白进行表征,以便开始解决这个问题。在此,我们研究了第6天(E6)的鸡胚神经视网膜,此时它主要处于增殖状态,以及E12时的神经视网膜,此时神经元分化已进展。在E6和E12检测到了胰岛素和IGF-I的发育调控高亲和力结合位点。在增殖性神经视网膜中,对IGF-I具有最高亲和力的典型IGFR与单独的非典型胰岛素结合位点共存,这些位点对胰岛素和IGF-I具有相似的高亲和力。用针对IRα亚基、IRβ亚基或IGFRβ亚基的特异性抗体对配体交联受体进行免疫沉淀,证明存在IR/IGFR杂合体。它们在E6视网膜中比在E12视网膜中更丰富。在示踪剂浓度下,这些杂合受体结合了大部分放射性标记的胰岛素,但很少结合放射性标记的IGF-I。在E12时,胰岛素结合位点的特异性发生了变化,更接近在肝脏中与IR所发现的情况,在肝脏中未检测到杂合体。这些非典型杂合受体的基础自磷酸化水平很高,尽管胰岛素,尤其是IGF-I适度增加了95 kDa和105 kDa的两个IRβ亚基的磷酸化。主要在神经发生增殖阶段发现的高亲和力/低区分性IR/IGFR杂合体可以介导胰岛素原和胰岛素的作用,此前已在此阶段的器官培养中得到证实。更重要的是,这种杂合受体可能在生理上与早期神经发生中局部产生的胰岛素原的作用相关。