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霍乱毒素和二丁酰环磷酸腺苷抑制未致敏和致敏PC12细胞培养物中神经生长因子诱导的神经丝蛋白表达。

Cholera toxin and dibutyryl cyclic AMP inhibit the expression of neurofilament protein induced by nerve growth factor in cultures of naive and primed PC12 cells.

作者信息

Doherty P, Mann D A, Walsh F S

机构信息

Institute of Neurology, London, England.

出版信息

J Neurochem. 1987 Dec;49(6):1676-87. doi: 10.1111/j.1471-4159.1987.tb02425.x.

Abstract

The effects of nerve growth factor (NGF), dibutyryl cyclic AMP (db cAMP), and cholera toxin on neurofilament protein expression in cultures of PC12 rat pheochromocytoma cells were examined using an enzyme-linked immunoadsorbent assay (ELISA). Morphological differentiation induced by NGF was associated with up to 30-fold increases in the level of neurofilament protein recognised by monoclonal antibody RT97. A more rapid response was apparent from primed as compared to naive PC12 cells. Cholera toxin and db cAMP both induced morphological differentiation of naive PC12 cells, but failed to promote neurite regeneration from primed cells. Neither response was associated with a significant induction of neurofilament protein. Both cholera toxin and db cAMP, but not B-cholera toxin nor antibodies to the toxin receptor, were found to inhibit the neurofilament protein response induced by NGF. Primed cells were more susceptible to this inhibition, and both cholera toxin and db cAMP inhibited neurite regeneration from these cells. These data suggest that increased intracellular cyclic AMP can suppress the expression of neuronal differentiation antigens induced by NGF, and are consistent with a role for neurofilament protein in promoting or facilitating the formation of a stable neuritic network.

摘要

利用酶联免疫吸附测定法(ELISA),研究了神经生长因子(NGF)、二丁酰环磷腺苷(db cAMP)和霍乱毒素对PC12大鼠嗜铬细胞瘤细胞培养物中神经丝蛋白表达的影响。NGF诱导的形态分化与单克隆抗体RT97识别的神经丝蛋白水平高达30倍的增加相关。与未预处理的PC12细胞相比,预处理的细胞有更快速的反应。霍乱毒素和db cAMP均诱导未预处理的PC12细胞发生形态分化,但未能促进预处理细胞的神经突再生。两种反应均未伴随神经丝蛋白的显著诱导。发现霍乱毒素和db cAMP均可抑制NGF诱导的神经丝蛋白反应,但B型霍乱毒素和毒素受体抗体则无此作用。预处理的细胞对这种抑制更敏感,霍乱毒素和db cAMP均抑制这些细胞的神经突再生。这些数据表明,细胞内环磷腺苷增加可抑制NGF诱导的神经元分化抗原的表达,这与神经丝蛋白在促进或便利稳定神经突网络形成中的作用一致。

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