Moschos, Sterghios A. and Williams, Andrew E. and Lindsay, Mark A. (2007) Cell-penetrating-peptide-mediated siRNA lung delivery. Biochemical Society. Transactions, 35 (4). pp. 807-810. ISSN 0300-5127
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Official URL: http://www.biochemsoctrans.org/bst/035/bst0350807....
The therapeutic application of siRNA (short interfering RNA) shows promise as an alternative approach to small-molecule inhibitors for the treatment of human disease. However, the major obstacle to its use has been the difficulty in delivering these large anionic molecules in vivo. A potential approach to solving this problem is the chemical conjugation of siRNA to the cationic CPPs (cell-penetrating peptides), Tat-(48–60) (transactivator of transcription) and penetratin, which have been shown previously to mediate protein and peptide delivery in a host of animal models. In this transaction, we review recent studies on the utility of siRNA for the investigation of protein function in the airways/lung. We show that, despite previous studies showing the utility of cationic CPPs in vitro, conjugation of siRNA to Tat-(48–60) and penetratin failed to increase residual siRNA-mediated knockdown of p38 MAPK (mitogen-activated protein kinase) (MAPK14) mRNA in mouse lung in vivo. Significantly, we will also discuss potential non-specific actions and the induction of immunological responses by CPPs and their conjugates and how this might limit their application for siRNA-mediated delivery in vivo.
|Research Community:||University of Westminster > Life Sciences, School of|
|Deposited On:||16 Sep 2011 10:59|
|Last Modified:||16 Sep 2011 10:59|
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