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Lipophilic siRNAs mediate efficient gene silencing in oligodendrocytes with direct CNS delivery
Ist Teil von
Journal of controlled release, 2010-06, Vol.144 (2), p.227-232
Ort / Verlag
Kidlington: Elsevier B.V
Erscheinungsjahr
2010
Quelle
MEDLINE
Beschreibungen/Notizen
Conjugation of small interfering RNA (siRNA) with lipophilic molecules has been demonstrated to enhance cellular uptake in cell culture and to produce efficient endogenous gene silencing in the liver after systemic administration and in neurons after direct local injection. Here, we evaluated the
in vivo delivery of siRNAs conjugated with different linkers to cholesterol by targeting CNPase (2′-3′-cyclic nucleotide 3′-phosphodiesterase) in oligodendrocytes. Cholesterol-conjugated siRNAs administered to the rat corpus callosum by intraparenchymal central nervous system (CNS) infusion show improved silencing ability compared with unconjugated siRNA. Furthermore, conjugation of siRNA to cholesterol with a cleavable disulfide linker appears to be beneficial for improving the potency of silencing of CNPase mRNA in oligodendrocytes
in vivo. Taken together, these findings indicate that cholesterol-conjugated siRNAs are effective for direct CNS delivery to oligodendrocytes, and that the biocleavable disulfide linker appears to be beneficial for improving the potency of silencing of target mRNA
in vivo.
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