Polydepsipeptide Block-Stabilized Polyplexes for Efficient Transfection of Primary Human Cells.
Weiwei WangToufik NaolouNan MaZijun DengXun XuUlrich MansfeldChristian WischkeManfred GossenAxel T NeffeAndreas LendleinPublished in: Biomacromolecules (2017)
The rational design of a polyplex gene carrier aims to balance maximal effectiveness of nucleic acid transfection into cells with minimal adverse effects. Depsipeptide blocks with an Mn ∼ 5 kDa exhibiting strong physical interactions were conjugated with PEI moieties (2.5 or 10 kDa) to di- and triblock copolymers. Upon nanoparticle formation and complexation with DNA, the resulting polyplexes (sizes typically 60-150 nm) showed remarkable stability compared to PEI-only or lipoplex and facilitated efficient gene delivery. Intracellular trafficking was visualized by observing fluorescence-labeled pDNA and highlighted the effective cytoplasmic uptake of polyplexes and release of DNA to the perinuclear space. Specifically, a triblock copolymer with a middle depsipeptide block and two 10 kDa PEI swallowtail structures mediated the highest levels of transgenic VEGF secretion in mesenchymal stem cells with low cytotoxicity. These nanocarriers form the basis for a delivery platform technology, especially for gene transfer to primary human cells.
Keyphrases
- nucleic acid
- heat shock protein
- mesenchymal stem cells
- single molecule
- circulating tumor
- copy number
- induced apoptosis
- photodynamic therapy
- randomized controlled trial
- genome wide
- cell free
- drug delivery
- cell cycle arrest
- genome wide identification
- drug release
- physical activity
- mental health
- umbilical cord
- endothelial cells
- cancer therapy
- bone marrow
- gene expression
- cell death
- dna methylation
- reactive oxygen species
- resistance training
- cell proliferation
- escherichia coli
- pseudomonas aeruginosa
- transcription factor
- circulating tumor cells
- biofilm formation
- mass spectrometry