| Literature DB >> 26485045 |
Byung Woo Hwang1, Su Jin Kim2, Kyeng Min Park3, Hyemin Kim1, Junseok Yeom1, Jeong-A Yang1, Hyeonseon Jeong1, Hyuntae Jung4, Kimoon Kim5, Young Chul Sung6, Sei Kwang Hahn7.
Abstract
Stem cell therapy has attracted a great deal of attention for treating intractable diseases such as cancer, stroke, liver cirrhosis, and ischemia. Especially, mesenchymal stem cells (MSCs) have been widely investigated for therapeutic applications due to the advantageous characteristics of long life-span, facile isolation, rapid proliferation, prolonged transgene expression, hypo-immunogenicity, and tumor tropism. MSCs can exert their therapeutic effects by releasing stress-induced therapeutic molecules after their rapid migration to damaged tissues. Recently, to improve the therapeutic efficacy, genetically engineered MSCs have been developed for therapeutic transgene expression by viral gene transduction and non-viral gene transfection. In general, the number of therapeutic cells for injection should be more than several millions for effective cell therapy. Adequate carriers for the controlled delivery of MSCs can reduce the required cell numbers and extend the duration of therapeutic effect, which provide great benefits for chronic disease patients. In this review, we describe genetic engineering of MSCs, recent progress of self-assembling supramolecular hydrogels, and their applications to cell therapy for intractable diseases and tissue regeneration.Entities:
Keywords: Cell therapy; Hydrogel; Stem cell; Tissue regeneration; Transgene expression
Mesh:
Substances:
Year: 2015 PMID: 26485045 DOI: 10.1016/j.jconrel.2015.10.034
Source DB: PubMed Journal: J Control Release ISSN: 0168-3659 Impact factor: 9.776