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轴膜成分在含血清和限定培养基中对大鼠坐骨神经施万细胞具有特异性且强效的促有丝分裂作用。

Specific and potent mitogenic effect of axolemmal fraction on Schwann cells from rat sciatic nerves in serum-containing and defined media.

作者信息

Sobue G, Kreider B, Asbury A, Pleasure D

出版信息

Brain Res. 1983 Dec 5;280(2):263-75. doi: 10.1016/0006-8993(83)90056-2.

Abstract

Using cultures of Schwann cells from neonatal rat sciatic nerves, we examined the mitogenic activity of an axolemmal fraction from adult rat CNS. Axolemmal fraction proved a potent mitogen, stimulating [3H]thymidine incorporation into Schwann cell DNA 13.5-fold over control values when axolemmal fraction equivalent to 16 micrograms of protein per culture microwell or more was added. Half maximal stimulation was obtained with addition of axolemmal fraction equivalent to 4 micrograms of protein. The concentration-dependence and magnitude of the mitogenic response of the cultured cells were nearly identical whether they were maintained in vitro for 1 day or for 2 weeks prior to addition of the axolemmal fraction. A study of the time-course of the effect of axolemmal fraction on Schwann cell mitosis showed that maximal [3H]thymidine incorporation took place during the fifth day after addition of axolemmal fraction. Axolemmal fraction also produced stimulation of [3H]thymidine incorporation into Schwann cells, seeded and cultured in a serum-free defined medium. Though the concentration-dependence of the mitogenic effect in the absence of serum was similar to that in a serum-containing medium, maximal stimulation in the defined medium was only 2.8-fold. The mitogenic activity of axolemmal fraction was rapidly and almost totally inactivated by sonication or homogenization, and was partially lost after exposure to heat. The mitogenic activities of plasma membrane fragments from rat skeletal muscle or rat erythrocytes, and of mitochondrial fragments (the major contaminant of the axolemmal fraction) were one-tenth that of axolemmal fraction or less. In contrast to glial growth factor prepared from bovine pituitaries (GGF-BP), which stimulates proliferation of both fibroblasts and Schwann cells, axolemmal fraction induced proliferation of Schwann cells but not of endoneurial fibroblasts; cultures treated with axolemmal fraction demonstrated a 3-fold increase in Schwann cell population in 10 days without detectable increase in number of fibroblasts. Also in contrast to GGF-BP, the mitogenic effect of which is considerably enhanced by simultaneous addition of cholera toxin to the medium, cholera toxin had no effect on the Schwann cell proliferative response to axolemmal fraction.

摘要

我们利用新生大鼠坐骨神经的雪旺细胞培养物,检测了成年大鼠中枢神经系统轴膜组分的促有丝分裂活性。当向每个培养微孔中添加相当于16微克或更多蛋白质的轴膜组分时,轴膜组分被证明是一种有效的促有丝分裂原,可刺激[³H]胸腺嘧啶核苷掺入雪旺细胞DNA,其掺入量比对照值高13.5倍。添加相当于4微克蛋白质的轴膜组分时可获得半数最大刺激。无论在添加轴膜组分之前,培养细胞在体外维持1天还是2周,培养细胞促有丝分裂反应的浓度依赖性和幅度几乎相同。一项关于轴膜组分对雪旺细胞有丝分裂影响的时间进程研究表明,在添加轴膜组分后的第5天,[³H]胸腺嘧啶核苷掺入量达到最大值。轴膜组分还能刺激接种并培养于无血清限定培养基中的雪旺细胞掺入[³H]胸腺嘧啶核苷。尽管在无血清条件下促有丝分裂作用的浓度依赖性与含血清培养基中的相似,但在限定培养基中的最大刺激仅为2.8倍。轴膜组分的促有丝分裂活性经超声处理或匀浆后迅速且几乎完全失活,暴露于热后会部分丧失活性。大鼠骨骼肌或大鼠红细胞的质膜片段以及线粒体片段(轴膜组分的主要污染物)的促有丝分裂活性仅为轴膜组分的十分之一或更低。与从牛垂体制备的胶质生长因子(GGF - BP)不同,GGF - BP可刺激成纤维细胞和雪旺细胞增殖,而轴膜组分仅诱导雪旺细胞增殖,不诱导神经内膜成纤维细胞增殖;用轴膜组分处理的培养物在10天内雪旺细胞数量增加了3倍,而成纤维细胞数量未检测到增加。同样与GGF - BP不同,GGF - BP的促有丝分裂作用在培养基中同时添加霍乱毒素时会显著增强,而霍乱毒素对雪旺细胞对轴膜组分的增殖反应没有影响。

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