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渥曼青霉素可阻断金鱼视网膜磷脂酰肌醇3激酶并抑制神经突生长。

Wortmannin blocks goldfish retinal phosphatidylinositol 3-kinase and neurite outgrowth.

作者信息

Lavie Y, Dybowski J, Agranoff B W

机构信息

Neuroscience Laboratory, University of Michigan, Ann Arbor, Michigan, USA.

出版信息

Neurochem Res. 1997 Apr;22(4):373-8. doi: 10.1023/a:1027391206791.

Abstract

The goldfish retina has been used extensively for the study of nerve regeneration. A role for phosphatidylinositol 3-kinase (PI3K) in neurite outgrowth from goldfish retinal explants has been examined by means of wortmannin (WT), a selective inhibitor of the enzyme. The presence of PI3K in retinal extracts was determined by means of immunoprecipitation as well as by an in vitro assay system for catalytic activity. The relative amount of the p85 subunit of PI3K detected by western blot in the retina following optic nerve crush was unchanged. WT inhibited goldfish brain PI3K activity at concentrations as low as 10(-9) M, approximating that reported for inhibition of mammalian PI3K's. Daily addition of 10(-8) M WT to retinal explants, activated by prior crush of the optic nerve, significantly inhibited neurite outgrowth during a 7 day in vitro culture period, while a single addition of WT to freshly explanted retina had no effect on neurite outgrowth. These results suggest that a PI3K-mediated process may be critical for nerve regrowth.

摘要

金鱼视网膜已被广泛用于神经再生研究。磷脂酰肌醇3激酶(PI3K)在金鱼视网膜外植体神经突生长中的作用已通过渥曼青霉素(WT)进行了研究,渥曼青霉素是该酶的一种选择性抑制剂。通过免疫沉淀以及催化活性的体外检测系统来确定视网膜提取物中PI3K的存在。视神经挤压后,通过蛋白质印迹法检测到的视网膜中PI3K的p85亚基的相对量没有变化。WT在低至10^(-9) M的浓度下就能抑制金鱼脑PI3K活性,这与报道的抑制哺乳动物PI3K的浓度相近。每天向经视神经预先挤压激活的视网膜外植体中添加10^(-8) M的WT,在7天的体外培养期内显著抑制了神经突生长,而向新鲜植入的视网膜中单次添加WT对神经突生长没有影响。这些结果表明,PI3K介导的过程可能对神经再生至关重要。

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