Kojima I, Nishimoto I, Iiri T, Ogata E, Rosenfeld R
Fourth Department of Internal Medicine, University of Tokyo School of Medicine, Japan.
Biochem Biophys Res Commun. 1988 Jul 15;154(1):9-19. doi: 10.1016/0006-291x(88)90642-0.
In competent Balb/c 3T3 cells primed with epidermal growth factor (primed competent cells), insulin-like growth factor-II (IGF-II) stimulated calcium influx in a concentration dependent manner with the ED50 of 450 pM. When receptor-bound [125I]IGF-II was cross-linked by use of disuccinimidyl suberate, a 240 K-Da protein was radiolabeled. Excess amount of unlabeled IGF-II inhibited the affinity-labeling of the 240 K-Da protein. To further examine whether IGF-II stimulates calcium influx by acting on the type II IGF receptor, we employed polyclonal antibody raised against rat type II IGF receptor, R-II-PABl. This antibody immunoprecipitated the type II IGF receptor and inhibited IGF-II binding in Balb/c 3T3 cell membrane without affecting IGF-I binding. In primed competent cells, R-II-PABl elicited an agonistic action in stimulating [3H]thymidine incorporation. Under the same condition, R-II-PABl elicited a marked stimulation of calcium influx. These results suggest that, in Balb/c 3T3 cells, 1) relatively low concentrations of IGF-II act mainly on the type II IGF receptor; 2) the type II IGF receptor is coupled to a calcium gating system; and 3) binding of a ligand to the type II IGF receptor leads to the stimulation of DNA synthesis.
在用表皮生长因子预处理的具有增殖能力的Balb/c 3T3细胞(预处理的有增殖能力的细胞)中,胰岛素样生长因子-II(IGF-II)以浓度依赖的方式刺激钙内流,半数有效浓度(ED50)为450 pM。当用辛二酸二琥珀酰亚胺酯使受体结合的[125I]IGF-II交联时,一种240 kDa的蛋白质被放射性标记。过量的未标记IGF-II抑制了240 kDa蛋白质的亲和标记。为了进一步研究IGF-II是否通过作用于II型IGF受体来刺激钙内流,我们使用了针对大鼠II型IGF受体产生的多克隆抗体R-II-PAB1。该抗体免疫沉淀II型IGF受体,并抑制Balb/c 3T3细胞膜中的IGF-II结合,而不影响IGF-I结合。在预处理的有增殖能力的细胞中,R-II-PAB1在刺激[3H]胸腺嘧啶核苷掺入方面引发了激动作用。在相同条件下,R-II-PAB1引发了钙内流的显著刺激。这些结果表明,在Balb/c 3T3细胞中,1)相对低浓度的IGF-II主要作用于II型IGF受体;2)II型IGF受体与钙门控系统偶联;3)配体与II型IGF受体的结合导致DNA合成的刺激。