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Myostatin short interfering hairpin RNA gene transfer increases skeletal muscle mass
Author(s) -
Magee Thomas R.,
Artaza Jorge N.,
Ferrini Monica G.,
Vernet Dolores,
Zuniga Freddi I.,
Cantini Liliana,
ReiszPorszasz Suzanne,
Rajfer Jacob,
GonzalezCadavid Nestor F.
Publication year - 2006
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.946
Subject(s) - myostatin , small hairpin rna , microbiology and biotechnology , small interfering rna , biology , skeletal muscle , gene silencing , transfection , plasmid , blot , muscle hypertrophy , western blot , rna , endocrinology , gene , genetics
Background Myostatin negatively regulates skeletal muscle growth. Myostatin knockout mice exhibit muscle hypertrophy and decreased interstitial fibrosis. We investigated whether a plasmid expressing a short hairpin interfering RNA (shRNA) against myostatin and transduced using electroporation would increase local skeletal muscle mass. Methods Short interfering RNAs (siRNAs) targeting myostatin were co‐transfected with a myostatin‐expressing plasmid into HEK293 cells and identified for myostatin silencing by Western blot. Corresponding shRNAs were cloned into plasmid shRNA expression vectors. Myostatin or a randomer negative control shRNA plasmid was injected and electroporated into the tibialis anterior or its contralateral muscle, respectively, of nine rats that were sacrificed after 2 weeks. Six other rats received a β‐galactosidase reporter plasmid and were sacrificed at 1, 2, and 4 weeks. Uptake of plasmid was examined by β‐galactosidase expression, whereas myostatin expression was determined by real‐time polymerase chain reaction (PCR) and Western blotting. Muscle fiber size was determined by histochemistry. Satellite cell proliferation was determined by PAX7 immunohistochemistry. Myosin heavy chain type II (MHCII) expression was determined by Western blot. Results β‐Galactosidase reporter plasmid was expressed at 1 and 2 weeks but diminished by 4 weeks in tibialis anterior skeletal muscle. Myostatin shRNA reduced myostatin mRNA and protein expression by 27 and 48%, respectively. Tibialis anterior weight, fiber size, and MHCII increased by 10, 34, and 38%, respectively. Satellite cell number was increased by over 2‐fold. Conclusions This is the first demonstration that myostatin shRNA gene transfer is a potential strategy to increase muscle mass. Copyright © 2006 John Wiley & Sons, Ltd.