| Literature DB >> 20109509 |
Yoon Shin Park1, Yongzhuo Huang, Yoon Jeong Park, Allan E David, Lindsay White, Huining He, Hee Sun Chung, Victor C Yang.
Abstract
Hypoxia is a strong modulator of anpan>giogenesis, accelerating pan> class="Gene">adipose tissue expansion, suggesting that hypoxia inducible factor 1alpha (HIF1alpha) can be a novel target for anti-obesity. We conjugated antisense-HIF1alpha-oligonucleotide (ASO) with low molecular weight protamine (LMWP), a cell-penetrating peptide, to enhance its ability to block hypoxic-angiogenesis, thereby eliciting an anti-obesity effect. Nano-sized ASO-LMWP (AS-L) conjugates enhanced cellular uptake of ASO without yielding a cytotoxic effect and protected the ASO against enzymatic attack and chemical reduction. AS-L showed enhanced intra-cellular localization compared to naked ASO and the complex of ASO with lipofectamine during hypoxic-differentiation. Consequently AS-L induced significant down-regulation of leptin and VEGF gene expressions, thereby reducing fat accumulation in the cell. This proof-of-concept study shows that AS-L produces an inhibitory effect on adipogenesis and angiogenesis during differentiation, indicating LMWP mediated ASO delivery can potentially be a safe and promising treatment for obesity. Copyright 2010 Elsevier B.V. All rights reserved.Entities:
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Year: 2010 PMID: 20109509 PMCID: PMC2862791 DOI: 10.1016/j.jconrel.2010.01.026
Source DB: PubMed Journal: J Control Release ISSN: 0168-3659 Impact factor: 9.776