Long-term enhancement of skeletal muscle mass and strength by single gene administration of myostatin inhibitors

被引:211
作者
Haidet, Amanda M. [1 ,2 ]
Rizo, Liza [1 ]
Handy, Chalonda [1 ,2 ]
Umapathi, Priya [1 ]
Eagle, Amy [1 ]
Shilling, Chris [1 ]
Boue, Daniel [1 ]
Martin, Paul T. [1 ,2 ,3 ]
Sahenk, Zarife [1 ,2 ,3 ]
Mendell, Jerry R. [1 ,3 ]
Kaspar, Brian K. [1 ,2 ,3 ]
机构
[1] Nationwide Childrens Hosp, Res Inst, Columbus, OH 43205 USA
[2] Nationwide Childrens Hosp, Integrated Biomed Sci Program, Columbus, OH 43205 USA
[3] Nationwide Childrens Hosp, Grad Program Neurosci, Columbus, OH 43205 USA
关键词
gene therapy; muscular dystrophy;
D O I
10.1073/pnas.0709144105
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Increasing the size and strength of muscles represents a promising therapeutic strategy for musculoskeletal disorders, and interest has focused on myostatin, a negative regulator of muscle growth. Various myostatin inhibitor approaches have been identified and tested in models of muscle disease with varying efficacies, depending on the age at which myostatin inhibition occurs. Here, we describe a one-time gene administration of myostatin-inhibitor-proteins to enhance muscle mass and strength in normal and dystrophic mouse models for >2 years, even when delivered in aged animals. These results demonstrate a promising therapeutic strategy that warrants consideration. for clinical trials in human muscle diseases.
引用
收藏
页码:4318 / 4322
页数:5
相关论文
共 27 条
[1]   Phenotypic improvement of dystrophic muscles by rAAV/microdystrophin vectors is augmented by Igf1 codelivery [J].
Abmayr, S ;
Gregorevic, P ;
Allen, JM ;
Chamberlain, JS .
MOLECULAR THERAPY, 2005, 12 (03) :441-450
[2]   Muscle-specific expression of insulin-like growth factor I counters muscle decline in mdx mice [J].
Barton, ER ;
Morris, L ;
Musaro, A ;
Rosenthal, N ;
Sweeney, HL .
JOURNAL OF CELL BIOLOGY, 2002, 157 (01) :137-147
[3]   Functional improvement of dystrophic muscle by myostatin blockade [J].
Bogdanovich, S ;
Krag, TOB ;
Barton, ER ;
Morris, LD ;
Whittemore, LA ;
Ahima, RS ;
Khurana, TS .
NATURE, 2002, 420 (6914) :418-421
[4]   The new frontier in muscular dystrophy research: booster genes [J].
Engvall, E ;
Wewer, UM .
FASEB JOURNAL, 2003, 17 (12) :1579-1584
[5]   A deletion in the bovine myostatin gene causes the double-muscled phenotype in cattle [J].
Grobet, L ;
Martin, LJR ;
Poncelet, D ;
Pirottin, D ;
Brouwers, B ;
Riquet, J ;
Schoeberlein, A ;
Dunner, S ;
Menissier, F ;
Massabanda, J ;
Fries, R ;
Hanset, R ;
Georges, M .
NATURE GENETICS, 1997, 17 (01) :71-74
[6]   FLRG (follistatin-related gene), a new target of chromosomal rearrangement in malignant blood disorders [J].
Hayette, S ;
Gadoux, M ;
Martel, S ;
Bertrand, S ;
Tigaud, I ;
Magaud, JP ;
Rimokh, R .
ONCOGENE, 1998, 16 (22) :2949-2954
[7]   Regulation of myostatin in vivo by growth and differentiation factor-associated serum protein-1:: A novel protein with protease inhibitor and follistatin domains [J].
Hill, JJ ;
Qiu, YC ;
Hewick, RM ;
Wolfman, NM .
MOLECULAR ENDOCRINOLOGY, 2003, 17 (06) :1144-1154
[8]   RECOMBINANT EXPRESSION OF HUMAN FOLLISTATIN WITH 315 AND 288 AMINO-ACIDS - CHEMICAL AND BIOLOGICAL COMPARISON WITH NATIVE PORCINE FOLLISTATIN [J].
INOUYE, S ;
GUO, YL ;
DEPAOLO, L ;
SHIMONAKA, M ;
LING, N ;
SHIMASAKI, S .
ENDOCRINOLOGY, 1991, 129 (02) :815-822
[9]   Activin A is a critical component of the inflammatory response, and its binding protein, follistatin, reduces mortality in endotoxemia [J].
Jones, Kristian L. ;
Mansell, Ashley ;
Patella, Shane ;
Scott, Bernadette J. ;
Hedger, Mark P. ;
de Kretser, David M. ;
Phillips, David J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (41) :16239-16244
[10]   Mutations in myostatin (GDF8) in double-muscled Belgian blue and Piedmontese cattle [J].
Kambadur, R ;
Sharma, M ;
Smith, TPL ;
Bass, JJ .
GENOME RESEARCH, 1997, 7 (09) :910-916