2009
DOI: 10.1016/j.biomaterials.2008.10.020
|View full text |Cite
|
Sign up to set email alerts
|

Non-viral endostatin plasmid transfection of mesenchymal stem cells via collagen scaffolds

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

2
46
0

Year Published

2009
2009
2018
2018

Publication Types

Select...
8

Relationship

1
7

Authors

Journals

citations
Cited by 47 publications
(52 citation statements)
references
References 45 publications
2
46
0
Order By: Relevance
“…The use of scaffolds as delivery systems for therapeutic genes is undergoing considerable investigation. [107][108][109] Gene therapy can be applied to the field of orthopedic regenerative medicine as a method for enhancing the expression of osteogenic and/or chondrogenic tissue inductive factors. 110,111 In this approach, cells seeded on an appropriate scaffold are transfected with plasmid DNA (pDNA; a circular loop of DNA coding) contained within the scaffold, thereby introducing specific DNA sequences into the cells which result in the expression of osteogenic/chondrogenic genes capable of enhancing healing and tissue formation.…”
Section: Collagen Scaffolds For Orthopedic Regenerative Medicinementioning
confidence: 99%
“…The use of scaffolds as delivery systems for therapeutic genes is undergoing considerable investigation. [107][108][109] Gene therapy can be applied to the field of orthopedic regenerative medicine as a method for enhancing the expression of osteogenic and/or chondrogenic tissue inductive factors. 110,111 In this approach, cells seeded on an appropriate scaffold are transfected with plasmid DNA (pDNA; a circular loop of DNA coding) contained within the scaffold, thereby introducing specific DNA sequences into the cells which result in the expression of osteogenic/chondrogenic genes capable of enhancing healing and tissue formation.…”
Section: Collagen Scaffolds For Orthopedic Regenerative Medicinementioning
confidence: 99%
“…The scaffold allows for cells to attach, proliferate and form extracellular matrix (ECM). It should have an open and interconnected pore structure (with a porosity >90 %) that allows nutrients to penetrate into the scaffold in vitro and then vascularisation to occur in vivo [3][4][5][6][7]. It should also degrade at a suitable rate to match the rate of tissue formation.…”
Section: Introductionmentioning
confidence: 99%
“…69 Another approach for controlled gene delivery for tissue engineering purposes is loading biodegradable materials with DNA molecules. [71][72][73] Collagen-based scaffolds have been investigated as carriers for plasmid DNA. 71,73 For example, Capito and Spector have demonstrated that collagen-based scaffolds can serve as nonviral gene delivery vehicles for IGF-1, providing a locally sustained therapeutic level of IGF-1, which enhanced cartilage formation.…”
mentioning
confidence: 99%
“…[71][72][73] Collagen-based scaffolds have been investigated as carriers for plasmid DNA. 71,73 For example, Capito and Spector have demonstrated that collagen-based scaffolds can serve as nonviral gene delivery vehicles for IGF-1, providing a locally sustained therapeutic level of IGF-1, which enhanced cartilage formation. 71 Several gene therapy approaches have been established in preclinical animal models, namely a murine model of collagen-induced arthritis and an immunodeficient mouse model of RA.…”
mentioning
confidence: 99%
See 1 more Smart Citation