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Prolonged down regulation of specific gene expression in nucleus pulposus cell mediated by RNA interference in vitro
被引:24
作者:
Kakutani, Kenichiro
Nishida, Kotaro
Uno, Koki
Takada, Toru
Shimomura, Takatoshi
Maeno, Koichiro
Kurosaka, Masahiro
Doita, Minoru
机构:
[1] Kobe Univ, Grad Sch Med, Dept Orthopaed Surg, Chuo Ku, Kobe, Hyogo, Japan
[2] Hyogo Nojigiku Med Ctr Disabled Children, Dept Orthopaed Surg, Kobe, Hyogo, Japan
关键词:
RNA interference (RNAi);
small interfering RNAs (siRNA);
intervertebral disc;
cell proliferation;
D O I:
10.1002/jor.20171
中图分类号:
R826.8 [整形外科学];
R782.2 [口腔颌面部整形外科学];
R726.2 [小儿整形外科学];
R62 [整形外科学(修复外科学)];
学科分类号:
摘要:
To investigate the efficacies and the longevity of RNA interference in nucleus pulposus cells from rat and human, two reporter luciferase plasmids (Firefly and Renilla) were used. These plasmids were cotransfected with siRNA targeting Firefly luciferase to the nucleus pulposus cells extracted from Sprague Dawley rats and scoliosis patients. The inhibitory effects were evaluated by dual luciferase assay for 3 weeks. Proliferation activity of fibroblast-like cells extracted from the subcutaneous tissue of Sprague Dawley rats and the nucleus pulposus cells were measured by proliferation assay (WST-8 assay) every 2 days after plating. The expression of Firefly luciferase was drastically inhibited both in rats (94.7%) and in humans (93.7%). The inhibitory effects were maintained for 2 weeks and had disappeared completely by 3 weeks. The proliferation activity of nucleus pulposus cells was significantly lower than fibroblast-like cells. We have shown, for the first time, siRNA-mediated gene silencing in rat and human disc cells for a relatively sustained period, probably due to the stability of the nucleus pulposus cells in terms of cell proliferation. The demonstration of this study may allow further exploration of the use of siRNA for scientific research and the treatment of disc degenerative diseases. (c) 2006 Orthopaedic Research Society. Published by Wiley Periodicals, Inc.
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页码:1271 / 1278
页数:8
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