A review of genetic engineering biotechnologies for enhanced chronic wound healing

被引:23
作者
Sessions, John W. [1 ]
Armstrong, David G. [2 ]
Hope, Sandra [3 ]
Jensen, Brian D. [1 ]
机构
[1] Brigham Young Univ, Dept Mech Engn, Provo, UT 84602 USA
[2] Univ Arizona, SALSA, Tucson, AZ USA
[3] Brigham Young Univ, Dept Microbiol & Mol Biol, Provo, UT 84602 USA
基金
美国国家科学基金会;
关键词
chronic wound healing; CRISPR-Cas9; pyrosequencing; transfection nanotechnology; viral transduction; PLASMID DNA; MEDIATED DELIVERY; IMMUNE-RESPONSES; MULTIPLE GENES; DRUG-DELIVERY; KNOCK-IN; THERAPY; SKIN; VECTORS; ELECTROPORATION;
D O I
10.1111/exd.13185
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100227 [皮肤病学];
摘要
Traditional methods for addressing chronic wounds focus on correcting dysfunction by controlling extracellular elements. This review highlights technologies that take a different approach - enhancing chronic wound healing by genetic modification to wound beds. Featured cutaneous transduction/transfection methods include viral modalities (ie adenoviruses, adeno-associated viruses, retroviruses and lentiviruses) and conventional non-viral modalities (ie naked DNA injections, microseeding, liposomal reagents, particle bombardment and electroporation). Also explored are emerging technologies, focusing on the exciting capabilities of wound diagnostics such as pyrosequencing as well as site-specific nuclease editing tools such as CRISPR-Cas9 used to both transiently and permanently genetically modify resident wound bed cells. Additionally, new non-viral transfection methods (ie conjugated nanoparticles, multi-electrode arrays, and microfabricated needles and nanowires) are discussed that can potentially facilitate more efficient and safe transgene delivery to skin but also represent significant advances broadly to tissue regeneration research.
引用
收藏
页码:179 / 185
页数:7
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