King M G, Baskin D G
Department of Biological Structure, University of Washington, Seattle.
Anat Rec. 1991 Dec;231(4):467-72. doi: 10.1002/ar.1092310409.
In order to design an approach for localizing IGF-I receptors within the intact CNS, the effect of paraformaldehyde (PAF) fixation on receptor binding was examined. Cryostat sections of rat brains, which were perfused with 0 to 10% PAF, were incubated in 125I-IGF-I and assayed for binding under equilibrium conditions. Binding was quantified from 10 brain regions, involving laminae and nuclei from median eminence, thalamus, hippocampus, choroid plexus, pyriform cortex, and cerebral cortex, by computer densitometry of film autoradiographs. The specific binding, saturation curves, Bmax and Ka, ligand specificity, and binding reversibility of IGF-I binding sites were not significantly affected by 1% or 2% PAF. However, 4% PAF elevated IGF-I receptor total binding, nonspecific binding, and Ka, and decreased Bmax, presumably by increasing the number of tissue-receptor interconnections. Only nonspecific 125I-IGF-I binding persisted when 10% PAF was used. These results indicate that tissue perfused with 2% PAF can be used for localizing IGF-I receptors by autoradiographic binding methods.
为了设计一种在完整中枢神经系统中定位胰岛素样生长因子-I(IGF-I)受体的方法,研究了多聚甲醛(PAF)固定对受体结合的影响。用0%至10%的PAF灌注大鼠脑后,制作冰冻切片,将其置于125I-IGF-I中孵育,并在平衡条件下检测结合情况。通过对放射自显影片进行计算机密度测定,从10个脑区(包括正中隆起、丘脑、海马、脉络丛、梨状皮质和大脑皮质的层和核)对结合进行定量分析。1%或2%的PAF对IGF-I结合位点的特异性结合、饱和曲线、最大结合容量(Bmax)和亲和常数(Ka)、配体特异性以及结合可逆性均无显著影响。然而,4%的PAF提高了IGF-I受体的总结合、非特异性结合和Ka,并降低了Bmax,这可能是通过增加组织-受体连接的数量实现的。当使用10%的PAF时,仅存在非特异性的125I-IGF-I结合。这些结果表明,用2%的PAF灌注的组织可用于通过放射自显影结合方法定位IGF-I受体。