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Subject: A method for genetically engineering skin keratinocytes
From: Kofi
Date: 3/16/2008 8:59:34 PM
Toxicol Pathol. 2008;36(1):104-11.
An approach to achieve long-term expression in skin gene therapy.
Therrien JP, Pfutzner W, Vogel JC.
Dermatology Branch, National Cancer Institute, National Institute of
Health, Bethesda, Maryland, USA.
For gene therapy purposes, the skin is an attractive organ to target for
systemic delivery of therapeutic proteins to treat systemic diseases,
skin diseases, or skin cancer. To achieve long-term stable expression of
a therapeutic gene in keratinocytes (KC), we have developed an approach
using a bicistronic retroviral vector expressing the desired therapeutic
gene linked to a selectable marker (multidrug resistant gene, MDR) that
is then introduced into KC and fibroblasts (FB) to create genetically
modified human skin equivalent (HSE). After grafting the HSE onto
immunocompromised mice, topical colchicine treatment is used to select
and enrich for genetically modified keratinocyte stem cells (KSC) that
express MDR and are resistant to colchicine's antimitotic effects. Both
the apparatus for topical colchicine delivery and the colchicine doses
have been optimized for application to human skin. This approach can be
validated by systemic delivery of therapeutic factors such as
erythropoietin and the antihypertensive atrial natriuretic peptide.
PMID: 18337228
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