| Literature DB >> 24806225 |
David P Ferguson1, Lawrence J Dangott2, J Timothy Lightfoot3.
Abstract
Vivo-morpholinos are a promising tool for gene silencing. These oligonucleotide analogs transiently silence genes by blocking either translation or pre-mRNA splicing. Little to no toxicity has been reported for vivo-morpholino treatment. However, in a recent study conducted in our lab, treatment of mice with vivo-morpholinos resulted in high mortality rates. We hypothesized that the deaths were the result of oligonucleotide hybridization, causing an increased cationic charge associated with the dendrimer delivery moiety of the vivo-morpholino. The cationic charge increased blood clot formation in whole blood treated with vivo-morpholinos, suggesting that clotting could have caused cardiac arrest in the deceased mice. Therefore, we investigate the mechanism by which some vivo-morpholinos increase mortality rates and propose techniques to alleviate vivo-morpholino toxicity.Entities:
Keywords: annexin A6; blood clot formation; calsequestrin 1; vivo-morpholino
Mesh:
Substances:
Year: 2014 PMID: 24806225 PMCID: PMC4182913 DOI: 10.2144/000114167
Source DB: PubMed Journal: Biotechniques ISSN: 0736-6205 Impact factor: 1.993