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视黄酸对表皮生长因子结合及促有丝分裂活性的影响。

Effects of retinoic acid on the binding and mitogenic activity of epidermal growth factor.

作者信息

Jetten A M

出版信息

J Cell Physiol. 1982 Mar;110(3):235-40. doi: 10.1002/jcp.1041100302.

Abstract

In this study the effects of retinoic acid on the binding and mitogenic activity of epidermal growth factor (EGF) in mouse fibroblast Balb/c 3T6 cells are further examined. Retinoic acid treatment of 3T6 cells results in a sixfold enhancement of 125I-labeled mouse EGF binding when assayed at 37 degrees C. In both retinoic acid-treated and control cells, cell-associated 125I-EGF is rapidly internalized, degraded, and secreted. Retinoic acid treatment does not seem to have a significant effect on the rate of internalization and degradation of EGF. At 0 degrees C, internalization of EGF is strongly inhibited in both retinoic acid-treated and control cells. Under these conditions retinoic acid-treated cells still exhibit a tenfold higher level of EGF binding compared to control cells. When exposed to high concentrations of EGF both retinoic acid-treated and control cells "down-regulate" their EGF receptors. And although the growth rate of retinoic acid-treated cells is about half that of control cells, the rate at which EGF binding capacity is restored after down-regulation is about three times as fast as in control cells. No direct antagonism on EGF binding was observed between the tumor promoter 12-O-tetradecanoyl-phorbol-13-acetate (TPA) and retinoic acid. EGF is a potent mitogen for 3T6 cells in serum-free medium; retinoic acid inhibits the mitogenic activity of EGF even though it increases EGF binding. Retinoic acid also inhibits cell proliferation induced by sarcoma growth factor (SGF) and insulin.

摘要

在本研究中,进一步检测了视黄酸对小鼠成纤维细胞Balb/c 3T6中表皮生长因子(EGF)的结合及促有丝分裂活性的影响。用视黄酸处理3T6细胞后,在37℃测定时,125I标记的小鼠EGF结合增强了6倍。在视黄酸处理的细胞和对照细胞中,与细胞相关的125I-EGF均迅速内化、降解并分泌。视黄酸处理似乎对EGF的内化和降解速率没有显著影响。在0℃时,视黄酸处理的细胞和对照细胞中EGF的内化均受到强烈抑制。在这些条件下,视黄酸处理的细胞与对照细胞相比,EGF结合水平仍高10倍。当暴露于高浓度EGF时,视黄酸处理的细胞和对照细胞均会“下调”其EGF受体。尽管视黄酸处理的细胞生长速率约为对照细胞的一半,但下调后EGF结合能力恢复的速率约为对照细胞的3倍。未观察到肿瘤启动子12-O-十四烷酰佛波醇-13-乙酸酯(TPA)和视黄酸之间对EGF结合有直接拮抗作用。在无血清培养基中,EGF是3T6细胞的一种强效促有丝分裂原;视黄酸抑制EGF的促有丝分裂活性,尽管它增加了EGF结合。视黄酸还抑制肉瘤生长因子(SGF)和胰岛素诱导的细胞增殖。

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