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金鱼视神经再生过程中角蛋白的差异表达。

Differential expression of keratins in goldfish optic nerve during regeneration.

作者信息

Fuchs C, Druger R K, Glasgow E, Schechter N

机构信息

Department of Biochemistry, State University of New York, Stony Brook 11794.

出版信息

J Comp Neurol. 1994 May 8;343(2):332-40. doi: 10.1002/cne.903430211.

Abstract

The goldfish visual pathway, unlike the visual pathway of higher vertebrates, retains continuous growth and development throughout life and is capable of functional regeneration. The structure and expression of proteins that support the physiological attributes of this system are of interest. Glial cells in this pathway express keratins as the predominant intermediate filament proteins rather than the expected glial fibrillary acidic protein. Previously we identified and characterized cDNA clones representing two type I keratins from the goldfish optic nerve, GK48 and GK49. The GK48 protein is the type I keratin partner to the type II keratin ON3, while the GK49 protein is expressed in a different cell type. Here, we extend our studies on the expression of mRNA for the GK48, GK49, and ON3 proteins at the early stages of optic nerve regeneration. RNase protection assays show that at 10 days post-crush, there is no overall change in levels of mRNA for these proteins as compared to uncrushed control nerves and nerves from unoperated fish. In addition, we show by in situ hybridization that the GK49 protein shows no changes in its distribution of mRNA in the optic nerve after crush. In contrast, the levels of GK48 and ON3 mRNA are greatly reduced within the crush zone. However, these two mRNAs are differentially expressed at different time points during regeneration, with GK48 mRNA appearing in the crush zone before ON3. These results indicate that the mRNA for the GK48 and ON3 proteins are differentially regulated during regeneration and that these two proteins are expressed in a different cell type from the GK49 protein.

摘要

与高等脊椎动物的视觉通路不同,金鱼的视觉通路在其一生中都保持着持续的生长和发育,并且具有功能再生能力。支持该系统生理特性的蛋白质的结构和表达备受关注。该通路中的神经胶质细胞表达角蛋白作为主要的中间丝蛋白,而非预期中的神经胶质纤维酸性蛋白。此前我们鉴定并表征了代表金鱼视神经中两种I型角蛋白的cDNA克隆,即GK48和GK49。GK48蛋白是II型角蛋白ON3的I型角蛋白伴侣,而GK49蛋白则在不同的细胞类型中表达。在此,我们扩展了对视神经再生早期阶段GK48、GK49和ON3蛋白mRNA表达的研究。核糖核酸酶保护分析表明,在挤压后10天,与未挤压的对照神经和未手术鱼的神经相比,这些蛋白的mRNA水平没有总体变化。此外,我们通过原位杂交表明,挤压后GK49蛋白mRNA在视神经中的分布没有变化。相比之下,GK48和ON3 mRNA的水平在挤压区内大幅降低。然而,这两种mRNA在再生过程中的不同时间点有差异表达,GK48 mRNA在ON3之前出现在挤压区。这些结果表明,GK48和ON3蛋白的mRNA在再生过程中受到差异调节,并且这两种蛋白与GK49蛋白在不同的细胞类型中表达。

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