Suppr超能文献

端锚聚合酶转染对大鼠阴茎海绵体平滑肌细胞的影响。

Effects of sense tankyrase transfection on smooth muscle cells of corpus cavernosum in rat.

作者信息

Wu X-J, Song B, Jin X-Y, Zhang J-H

机构信息

Urinary Surgery Research Center, Southwest Hospital, Third Military Medical University, Chongqing, PR China.

出版信息

Arch Androl. 2006 Mar-Apr;52(2):111-6. doi: 10.1080/01485010500315727.

Abstract

This study was conducted to construct the eukaryotic expression vectors for sense tankyrase and to investigate the effects of tankyrase transfection on smooth muscle cells of corpus cavernosum in the rat. After the eukaryotic expression vectors for sense tankyrase were constructed and identified smooth muscle cells of rat corpus cavernosum were transfected with the recombinant plasmids of sense tankyrase (pcDNA-TNKS). Levels of DNA and RNA were then evaluated. Measurement of telomerase activity was conducted by TRAP-ELISA assay, the length of telomere by Southern blot and the growth curve by MTT assay. We have found that the eukaryotic expression vectors for sense tankyrase were constructed and the recombinant plasmids of sense tankyrase were transfected into smooth muscle cells of rat corpus cavernosum successfully; no significant differences in telomerase activity were observed between TNKS-transfected cells (SMC-TANKS), zero-load- transfected cells (SMC-Zeo), and non-transfected cells (SMC) (P > 0.05). The length of telomere in SMC-TANKS was longer than that in SMC-Zeo or SMC (P < 0.01), and the OD value of TNKS-transfected cell was significantly higher than that of the non-transfected cells (P < 0.01). These results suggested that the eukaryotic expression vectors for sense tankyrase were constructed successfully, which provides the basis for gene therapy. Transfection of recombinant plasmids of sense tankyrase helps change the telomerase length of smooth muscle cells of corpus cavernosum and extend the cell life span.

摘要

本研究旨在构建锚蛋白的真核表达载体,并探讨锚蛋白转染对大鼠阴茎海绵体平滑肌细胞的影响。构建并鉴定锚蛋白的真核表达载体后,用锚蛋白(pcDNA-TNKS)的重组质粒转染大鼠阴茎海绵体平滑肌细胞。然后评估DNA和RNA水平。通过端粒重复序列扩增酶联免疫吸附测定法检测端粒酶活性,通过Southern印迹法检测端粒长度,通过MTT法检测生长曲线。我们发现成功构建了锚蛋白的真核表达载体,并将锚蛋白的重组质粒成功转染到大鼠阴茎海绵体平滑肌细胞中;在转染TNKS的细胞(SMC-TANKS)、空载转染细胞(SMC-Zeo)和未转染细胞(SMC)之间,未观察到端粒酶活性有显著差异(P>0.05)。SMC-TANKS中的端粒长度比SMC-Zeo或SMC中的长(P<0.01),并且转染TNKS的细胞的OD值显著高于未转染细胞(P<0.01)。这些结果表明成功构建了锚蛋白的真核表达载体,为基因治疗提供了依据。转染锚蛋白的重组质粒有助于改变阴茎海绵体平滑肌细胞的端粒酶长度并延长细胞寿命。

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