High Efficiency Lipid-Based siRNA Transfection of Adipocytes in Suspension

被引:52
|
作者
Kilroy, Gail
Burk, David H.
Floyd, Z. Elizabeth
机构
[1] Ubiquitin Biology Laboratory, Pennington Biomedical Research Center, Baton Rouge, LA
[2] Cell Biology and Bioimaging Core, Pennington Biomedical Research Center, Baton Rouge, LA
来源
PLOS ONE | 2009年 / 4卷 / 09期
关键词
PPAR-GAMMA;
D O I
10.1371/journal.pone.0006940
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Fully differentiated adipocytes are considered to be refractory to introduction of siRNA via lipid-based transfection. However, large scale siRNA-based loss-of-function screening of adipocytes using either electroporation or virally-mediated transfection approaches can be prohibitively complex and expensive. Methodology/Principal Findings: We present a method for introducing small interfering RNA ( siRNA) into differentiated 3T3-L1 adipocytes and primary human adipocytes using an approach based on forming the siRNA/cell complex with the adipocytes in suspension rather than as an adherent monolayer, a variation of "reverse transfection''. Conclusions/Significance: Transfection of adipocytes with siRNA by this method is economical, highly efficient, has a simple workflow, and allows standardization of the ratio of siRNA/cell number, making this approach well-suited for high-throughput screening of fully differentiated adipocytes.
引用
收藏
页数:8
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