Literature DB >> 28448022

Development of an Economical DNA Delivery System by "Acufection" and its Application to Skin Research.

Yu-Jei Lin1, Tsung-Lin Lee1, Chia-Chi Ku2.   

Abstract

Dysregulation of immune response in skin is associated with numerous human skin disorders. Direct transfer of immune-related genes into skin tissue is a fascinating approach to investigate immune modulation of cutaneous inflammation in mouse models of human diseases. Here we present a cost-effective protocol that delivered naked DNA in mouse skin and leads to transgene expression. The method is coined "acufection", denoting acupuncture-mediated DNA transfection. To perform acufection, mouse skin was first infused with DNA in phosphate-buffered saline (PBS) and then pricked lightly with a bundle of acupuncture needles to facilitate the absorption of DNA and transfection into cells. The plasmid DNA is presumably taken up by the keratinocyte and dendritic cells (DCs) in the skin and expressed into protein. Mechanical prick with the needles per se did not cause skin damage or induce keratinocyte activation. The expression of the transfected genes was detected in the skin at both transcriptional and translational levels following acufection for 2 days and maintained up to 7 days. The primary goal for the development of this acufection method was to investigate a previously undefined isoform of IL-15. Using this method, an alternatively spliced IL-15 isoform with partially deleted exon 7 (IL-15ΔE7) was expressed in the skin and subsequently treated with a Toll-like receptor 7 (TLR7) agonist, imiquimod (IMQ), to induce inflammation. Acufection-delivered IL-15ΔE7 in skin suppressed keratinocyte proliferation, epidermal thickness and neutrophil recruitment in IMQ-induced cutaneous inflammation. With increasing interest in identifying the regulatory mechanisms of cutaneous inflammation, the protocol described here provides a cost effective and versatile alternative to the gene gun system or microseeding for DNA delivery in vivo. It may potentially allow discovery of the function of a novel gene in the skin or for investigating new treatment for cutaneous diseases.

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Year:  2017        PMID: 28448022      PMCID: PMC5565090          DOI: 10.3791/55206

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  21 in total

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Journal:  Vaccine       Date:  2005-01-04       Impact factor: 3.641

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Authors:  X Tan; L Lefrançois
Journal:  Genes Immun       Date:  2006-06-22       Impact factor: 2.676

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Review 9.  Particle-mediated DNA vaccine delivery to the skin.

Authors:  Joel R Haynes
Journal:  Expert Opin Biol Ther       Date:  2004-06       Impact factor: 4.388

10.  Human keratinocytes' response to injury upregulates CCL20 and other genes linking innate and adaptive immunity.

Authors:  Milène Kennedy-Crispin; Erika Billick; Hiroshi Mitsui; Nicholas Gulati; Hideki Fujita; Patricia Gilleaudeau; Mary Sullivan-Whalen; Leanne M Johnson-Huang; Mayte Suárez-Fariñas; James G Krueger
Journal:  J Invest Dermatol       Date:  2011-09-01       Impact factor: 8.551

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