The myokine decorin is regulated by contraction and involved in muscle hypertrophy

被引:137
作者
Kanzleiter, Timo [1 ,2 ]
Rath, Michaela [1 ,2 ]
Goergens, Sven W. [2 ,3 ]
Jensen, Jorgen [4 ]
Tangen, Daniel S. [4 ]
Kolnes, Anders J. [5 ]
Kolnes, Kristoffer J. [4 ,5 ]
Lee, Sindre [6 ]
Eckel, Juergen [2 ,3 ]
Schuermann, Annette [1 ,2 ]
Eckardt, Kristin [2 ,3 ,6 ]
机构
[1] German Inst Human Nutr, Dept Expt Diabetol, Potsdam, Germany
[2] German Ctr Diabet Res, Bad Mergentheim, Germany
[3] German Diabet Ctr, Paul Langerhans Grp Integrat Physiol, Dusseldorf, Germany
[4] Norwegian Sch Sport Sci, Dept Phys Performance, Oslo, Norway
[5] Charles Univ Prague, Fac Med 3, Prague, Czech Republic
[6] Univ Oslo, Inst Basic Med Sci, Dept Nutr, N-0317 Oslo, Norway
关键词
Skeletal muscle; Myokines; Exercise; SKELETAL-MUSCLE; GENE-EXPRESSION; MYOSTATIN; DIFFERENTIATION; RESISTANCE; ALIGNMENT;
D O I
10.1016/j.bbrc.2014.06.123
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The health-promoting effects of regular exercise are well known, and myokines may mediate some of these effects. The small leucine-rich proteoglycan decorin has been described as a myokine for some time. However, its regulation and impact on skeletal muscle has not been investigated in detail. In this study, we report decorin to be differentially expressed and released in response to muscle contraction using different approaches. Decorin is released from contracting human myotubes, and circulating decorin levels are increased in response to acute resistance exercise in humans. Moreover, decorin expression in skeletal muscle is increased in humans and mice after chronic training. Because decorin directly binds myostatin, a potent inhibitor of muscle growth, we investigated a potential function of decorin in the regulation of skeletal muscle growth. In vivo overexpression of decorin in murine skeletal muscle promoted expression of the pro-myogenic factor Mighty, which is negatively regulated by myostatin. We also found Myodl and follistatin to be increased in response to decorin overexpression. Moreover, muscle-specific ubiquitin ligases atroginl and MuRF1, which are involved in atrophic pathways, were reduced by decorin overexpression. In summary, our findings suggest that decorin secreted from myotubes in response to exercise is involved in the regulation of muscle hypertrophy and hence could play a role in exercise-related restructuring processes of skeletal muscle. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:1089 / 1094
页数:6
相关论文
共 32 条
[1]   Follistatin complexes Myostatin and antagonises Myostatin-mediated inhibition of myogenesis [J].
Amthor, H ;
Nicholas, G ;
McKinnell, I ;
Kemp, CF ;
Sharma, M ;
Kambadur, R ;
Patel, K .
DEVELOPMENTAL BIOLOGY, 2004, 270 (01) :19-30
[2]  
[Anonymous], SCAND J MED SCI SPOR
[3]  
[Anonymous], BIOCH BIOPHYS ACTA
[4]  
[Anonymous], 2014, HTSEQ PYTHON FRAMEWO
[5]  
BRANDAN E, 1991, EUR J CELL BIOL, V55, P209
[6]   Myokines in insulin resistance and type 2 diabetes [J].
Eckardt, Kristin ;
Gorgens, Sven W. ;
Raschke, Silja ;
Eckel, Juergen .
DIABETOLOGIA, 2014, 57 (06) :1087-1099
[7]   Dynamics of the Skeletal Muscle Secretome during Myoblast Differentiation [J].
Henningsen, Jeanette ;
Rigbolt, Kristoffer T. G. ;
Blagoev, Blagoy ;
Pedersen, Bente Klarlund ;
Kratchmarova, Irina .
MOLECULAR & CELLULAR PROTEOMICS, 2010, 9 (11) :2482-2496
[8]   Overexpression of the orphan receptor Nur77 alters glucose metabolism in rat muscle cells and rat muscle in vivo [J].
Kanzleiter, T. ;
Preston, E. ;
Wilks, D. ;
Ho, B. ;
Benrick, A. ;
Reznick, J. ;
Heilbronn, L. K. ;
Turner, N. ;
Cooney, G. J. .
DIABETOLOGIA, 2010, 53 (06) :1174-1183
[9]   TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions [J].
Kim, Daehwan ;
Pertea, Geo ;
Trapnell, Cole ;
Pimentel, Harold ;
Kelley, Ryan ;
Salzberg, Steven L. .
GENOME BIOLOGY, 2013, 14 (04)
[10]   Decorin enhances the proliferation and differentiation of myogenic cells through suppressing myostatin activity [J].
Kishioka, Yasuhiro ;
Thomas, Mark ;
Wakamatsu, Jun-Ichi ;
Hattori, Akihito ;
Sharma, Mridula ;
Kambadur, Ravi ;
Nishimura, Takanori .
JOURNAL OF CELLULAR PHYSIOLOGY, 2008, 215 (03) :856-867