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Recombinant adeno‐associated virus‐mediated gene delivery of long chain acyl coenzyme A dehydrogenase (LCAD) into LCAD‐deficient mice
Author(s) -
Beattie Stuart G.,
Goetzman Eric,
Tang Qiuishi,
Conlon Thomas,
CampbellThompson Martha,
Matern Dietrich,
Vockley Jerry,
Flotte Terence R.
Publication year - 2008
Publication title -
the journal of gene medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.689
H-Index - 91
eISSN - 1521-2254
pISSN - 1099-498X
DOI - 10.1002/jgm.1242
Subject(s) - steatosis , biology , immunostaining , microbiology and biotechnology , biochemistry , endocrinology , medicine , chemistry , immunology , immunohistochemistry
Background Very long chain acyl coenzyme A (CoA) dehydrogenase (VLCAD) deficiency is a relatively common mitochondrial β‐oxidation disorder. The most severe form of VLCAD deficiency presents with neonatal cardiomyopathy and hepatic failure and is generally fatal within the first year of life. Mice deficient for long chain acyl CoA dehydrogenase (LCAD) closely resemble the clinical syndrome observed in VLCAD‐deficient humans. Recombinant adeno‐associated viral (rAAV) vectors with pseudotype capsids were investigated for their potential towards correcting the phenotype observed in mice heterozygous (+/−) for LCAD (i.e. liver and muscle steatosis). Methods rAAV containing the mouse LCAD cDNA (mLCAD) under the transcriptional control of the CMV/chicken β‐actin hybrid promoter were injected intramuscularly into the tibialis anterior (TA) muscle of LCAD +/− mice or injected into the portal vein to transduce hepatocytes. Results Ten weeks post‐injection of rAAV1‐mLCAD into the TA muscle, significantly increased levels of mLCAD within mitochondria were demonstrated by immunostaining of TA sections, immunoblotting of mitochondrial isolates and by the electron transfer flavoprotein (ETF) fluorescence reduction enzyme activity assay. Magnetic resonance spectroscopy of vector‐injected TA muscle demonstrated a reduction in the lipid content compared to phosphate‐buffered saline‐injected mice, whereas a systemic effect was observed as a reduction in liver macrosteatosis. Eight weeks after portal vein injection of rAAV8‐mLCAD into LCAD +/− mice, increased levels of mLCAD within hepatocyte mitochondria were demonstrated by immunostaining and also by the ETF assay. Scoring of the hepatosteatosis observed in partially deficient LCAD mice indicated a reduction in the lipid content within livers of vector‐treated mice. Conclusions These studies show that rAAV‐mediated delivery of mLCAD was efficient and led to an amelioration of local and systemic pathologies observed in partially deficient LCAD mice. Copyright © 2008 John Wiley & Sons, Ltd.