Linear-branched poly( β -amino esters)/DNA nano-polyplexes for effective gene transfection and neural stem cell differentiation.
Yuheng CaoHaobo HeKaili CaoYongyang LiuDehua HuangTuanwei LiGuangcun ChenPublished in: Biomedical materials (Bristol, England) (2022)
Controllable regulation of stem cell differentiation is a critical concern in stem cell-based regenerative medicine. In particular, there are still great challenges in controlling the directional differentiation of neural stem cells (NSCs) into neurons. Herein, we developed a novel linear-branched poly( β -amino esters) (S4-TMPTA-BDA-DT, STBD) through a two-step reaction. The synthesized linear-branched polymers possess multiple positively charged amine terminus and degradable intermolecular ester bonds, thus endowing them with excellent properties such as high gene load, efficient gene delivery, and effective gene release and transcription in cells. In the mCherry transfection test, a high transfection efficiency of approximately 70% was achieved in primary NSCs after a single transfection. Moreover, STBD also showed high biocompatibility to NSCs without disturbing their viability and neural differentiation. With the high gene delivery property, STBD is capable of delivering siRNA (shSOX9) expression plasmid into NSCs to significantly interfere with the expression of SOX9, thus enhancing the neuronal differentiation and maturation of NSCs. The STBD/DNA nano-polyplex represents a powerful non-viral approach of gene delivery for manipulating the differentiation of stem cells, showing broad application prospects in NSC-based regenerative therapy for treating neurodegenerative diseases.
Keyphrases
- stem cells
- poor prognosis
- genome wide
- copy number
- transcription factor
- cell therapy
- escherichia coli
- mesenchymal stem cells
- neural stem cells
- single molecule
- genome wide identification
- circulating tumor
- cell free
- sars cov
- spinal cord
- binding protein
- drug delivery
- spinal cord injury
- signaling pathway
- dna methylation
- brain injury
- endoplasmic reticulum stress
- electron transfer