Suppr超能文献

野生型和Pro370Leu突变型肌纤蛋白基因真核细胞表达的比较研究

[Comparative study of eukaryotic cell expression of wild-type and Pro370Leu mutation type myocilin gene].

作者信息

Wang Jian-wen, Sun Hui-min, Ji Jian, Li Xiao-rong, Zheng Jian-qiu

机构信息

Ophthalmology Center, Tianjin Medical University, Tianjin 300070, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2006 Mar 14;86(10):700-4.

Abstract

OBJECTIVE

To compare the eukaryotic cell expression of wild-type myocilin (MYOC) (wMYOC) gene and Pro370Leu mutation type MYOC (mMYOC) gene so as to understand the mechanism of primary open angle glaucoma (POAG).

METHODS

HeLa cells were cultured and then transfected with the vector pEGFP-N3-wMYOC, recombinant plasmid with wild type MYOC gene and enhanced green fluorescein gene, or the vector pDsRed2-N1-mMYOC, recombinant plasmid with mutation MYOC gene and red fluorescein gene, respectively, or co-transfected with these 2 plasmids. Corresponding blank vectors pEGFP-N3 and pDsRed2-N1 were used as markers. Fluorescence microscopy was used to observe the localization of red fluorescence and green fluorescence. Laser co-focusing microscopy was used to observe the effect of co-transfection. The green and red fluorescein antibodies were examined by Western blotting.

RESULTS

Green fluorescence was observed in the cytoplasm of the HeLa cells transfected with the blank vector pEGFP-N3, in an even distribution; and red fluorescence was observed in the cytoplasm of the HeLa cells transfected with the blank vector pDsRed2-N1, in an even distribution too. The cells transfected with pEGFP-N3-wMYOC showed evenly-distributed green fluorescence in the cytoplasm, and the cells transfected with pDsRed2-N1-mMYOC showed red fluorescence in the cytoplasm in a state of aggregation. Both red and green fluorescence could be seen in the cells co-transfected with pEGFP-N3-wMYOC and pDsRed2-N1-mMYOC, both in a state of aggregation and co-localization. Laser co-focusing microscopy showed the same results. Protein with the relative molecular weight of 83,000, identical to that of the recombinant protein of wMYOC protein and green fluorescein, could be found in the culture fluid and cell lysate of the pEGFP-N3-wMYOC-transfected cells; however, could be found in the lysate only but not in the culture fluid of the co-transfected cells. Protein with the relative molecular weight of 81,000, identical to that of the recombinant protein of mMYOC protein and red fluorescein, could be found in the cell lysates of the pDsRed2-N1-mMYOC-transfected cells and the pEGFP-N3-wMYOC and pDsRed2-N1-mMYOC co-transfected cells, but not in the culture fluid of both cells.

CONCLUSION

Both the WMYOC and mMYOC genes can be expressed and localized in the cytoplasm. mMYOC protein shoes a tendency of aggregation and disorder in secretion, and affects the expression and secretion of wMYOC, thus influencing the factions of the trabecular meshwork and causing POAG.

摘要

目的

比较野生型肌纤蛋白(MYOC)(wMYOC)基因和Pro370Leu突变型MYOC(mMYOC)基因的真核细胞表达情况,以了解原发性开角型青光眼(POAG)的发病机制。

方法

培养HeLa细胞,然后分别用载体pEGFP-N3-wMYOC(含野生型MYOC基因和增强型绿色荧光蛋白基因的重组质粒)、载体pDsRed2-N1-mMYOC(含突变型MYOC基因和红色荧光蛋白基因的重组质粒)转染细胞,或用这两种质粒共转染细胞。相应的空白载体pEGFP-N3和pDsRed2-N1作为对照。用荧光显微镜观察红色荧光和绿色荧光的定位。用激光共聚焦显微镜观察共转染效果。通过蛋白质免疫印迹法检测绿色和红色荧光抗体。

结果

用空白载体pEGFP-N3转染的HeLa细胞胞质中可见均匀分布的绿色荧光;用空白载体pDsRed2-N1转染的HeLa细胞胞质中也可见均匀分布的红色荧光。用pEGFP-N3-wMYOC转染的细胞胞质中绿色荧光均匀分布,用pDsRed2-N1-mMYOC转染的细胞胞质中红色荧光呈聚集状态。用pEGFP-N3-wMYOC和pDsRed2-N1-mMYOC共转染的细胞中可见红色和绿色荧光,均呈聚集和共定位状态。激光共聚焦显微镜观察结果相同。在pEGFP-N3-wMYOC转染细胞的培养液和细胞裂解物中可检测到相对分子质量为83 000的蛋白,与wMYOC蛋白和绿色荧光蛋白的重组蛋白相同;而在共转染细胞的裂解物中可检测到,但在培养液中未检测到。在pDsRed2-N1-mMYOC转染细胞以及pEGFP-N3-wMYOC和pDsRed2-N1-mMYOC共转染细胞的裂解物中可检测到相对分子质量为81 000的蛋白,与mMYOC蛋白和红色荧光蛋白的重组蛋白相同,但在两种细胞的培养液中均未检测到。

结论

wMYOC和mMYOC基因均可在胞质中表达并定位。mMYOC蛋白在分泌过程中呈现聚集和紊乱的趋势,并影响wMYOC的表达和分泌,进而影响小梁网功能,导致POAG。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验