Dynamics of the Skeletal Muscle Secretome during Myoblast Differentiation

被引:237
作者
Henningsen, Jeanette [1 ,2 ,3 ]
Rigbolt, Kristoffer T. G. [1 ]
Blagoev, Blagoy [1 ]
Pedersen, Bente Klarlund [2 ,3 ]
Kratchmarova, Irina [1 ]
机构
[1] Univ So Denmark, Ctr Expt BioInformat, Dept Biochem & Mol Biol, DK-5230 Odense M, Denmark
[2] Univ Copenhagen, Ctr Inflammat & Metab, Dept Infect Dis, Rigshosp,Fac Hlth Sci, DK-2100 Copenhagen, Denmark
[3] Univ Copenhagen, Copenhagen Muscle Res Ctr, Rigshosp, Fac Hlth Sci, DK-2100 Copenhagen, Denmark
基金
英国医学研究理事会; 新加坡国家研究基金会;
关键词
GROWTH-FACTOR-BETA; NEURAL CHEMOREPELLENT SEMA3A; IGF-BINDING-PROTEINS; TGF-BETA; SATELLITE-CELLS; QUANTITATIVE PROTEOMICS; ENDOCRINE ORGAN; AMINO-ACIDS; IN-VITRO; EXPRESSION;
D O I
10.1074/mcp.M110.002113
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
During recent years, increased efforts have focused on elucidating the secretory function of skeletal muscle. Through secreted molecules, skeletal muscle affects local muscle biology in an auto/paracrine manner as well as having systemic effects on other tissues. Here we used a quantitative proteomics platform to investigate the factors secreted during the differentiation of murine C2C12 skeletal muscle cells. Using triple encoding stable isotope labeling by amino acids in cell culture, we compared the secretomes at three different time points of muscle differentiation and followed the dynamics of protein secretion. We identified and quantitatively analyzed 635 secreted proteins, including 35 growth factors, 40 cytokines, and 36 metallopeptidases. The extensive presence of these proteins that can act as potent signaling mediators to other cells and tissues strongly highlights the important role of the skeletal muscle as a prominent secretory organ. In addition to previously reported molecules, we identified many secreted proteins that have not previously been shown to be released from skeletal muscle cells nor shown to be differentially released during the process of myogenesis. We found 188 of these secreted proteins to be significantly regulated during the process of myogenesis. Comparative analyses of selected secreted proteins revealed little correlation between their mRNA and protein levels, indicating pronounced regulation by posttranscriptional mechanisms. Furthermore, analyses of the intracellular levels of members of the semaphorin family and their corresponding secretion dynamics demonstrated that the release of secreted proteins is tightly regulated by the secretory pathway, the stability of the protein, and/or the processing of secreted proteins. Finally, we provide 299 unique hydroxyproline sites mapping to 48 distinct secreted proteins and have discovered a novel hydroxyproline motif. Molecular & Cellular Proteomics 9:2482-2496, 2010.
引用
收藏
页码:2482 / 2496
页数:15
相关论文
共 79 条
[11]   Novel regulatory mechanisms for the proteoglycans decorin and biglycan during muscle formation and muscular dystrophy [J].
Brandan, Enrique ;
Cabello-Verrugio, Claudio ;
Vial, Cecilia .
MATRIX BIOLOGY, 2008, 27 (08) :700-708
[12]  
Budasz-Rwiderska M, 2005, J Physiol Pharmacol, V56 Suppl 3, P195
[13]   Identification of secreted proteins during skeletal muscle development [J].
Chan, X'avia C. Y. ;
McDermott, John C. ;
Siu, K. W. Michael .
JOURNAL OF PROTEOME RESEARCH, 2007, 6 (02) :698-710
[14]   Cellular and molecular regulation of muscle regeneration [J].
Chargé, SBP ;
Rudnicki, MA .
PHYSIOLOGICAL REVIEWS, 2004, 84 (01) :209-238
[15]   Proteolytic processing converts the repelling signal Sema3E into an inducer of invasive growth and lung metastasis [J].
Christensen, C ;
Ambartsumian, N ;
Gilestro, G ;
Thomsen, B ;
Comoglio, P ;
Tamagnone, L ;
Guldberg, P ;
Lukanidin, E .
CANCER RESEARCH, 2005, 65 (14) :6167-6177
[16]   Angiotensin II type 1 receptor blockade attenuates TGF-β-induced failure of muscle regeneration in multiple myopathic states [J].
Cohn, Ronald D. ;
van Erp, Christel ;
Habashi, Jennifer P. ;
Soleimani, Arshia A. ;
Klein, Erin C. ;
Lisi, Matthew T. ;
Gamradt, Matthew ;
Rhys, Colette M. ap ;
Holm, Tammy M. ;
Loeys, Bart L. ;
Ramirez, Francesco ;
Judge, Daniel P. ;
Ward, Christopher W. ;
Dietz, Harry C. .
NATURE MEDICINE, 2007, 13 (02) :204-210
[17]   A practical guide to the MaxQuant computational platform for SILAC-based quantitative proteomics [J].
Cox, Juergen ;
Matic, Ivan ;
Hilger, Maximiliane ;
Nagaraj, Nagarjuna ;
Selbach, Matthias ;
Olsen, Jesper V. ;
Mann, Matthias .
NATURE PROTOCOLS, 2009, 4 (05) :698-705
[18]   WebLogo: A sequence logo generator [J].
Crooks, GE ;
Hon, G ;
Chandonia, JM ;
Brenner, SE .
GENOME RESEARCH, 2004, 14 (06) :1188-1190
[19]   Inhibition of myogenesis by transforming growth factor β is density-dependent and related to the translocation of transcription factor MEF2 to the cytoplasm [J].
De Angelis, L ;
Borghi, S ;
Melchionna, R ;
Berghella, L ;
Baccarani-Contri, M ;
Parise, F ;
Ferrari, S ;
Cossu, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (21) :12358-12363
[20]   Comprehensive mass-spectrometry-based proteome quantification of haploid versus diploid yeast [J].
de Godoy, Lyris M. F. ;
Olsen, Jesper V. ;
Cox, Juergen ;
Nielsen, Michael L. ;
Hubner, Nina C. ;
Froehlich, Florian ;
Walther, Tobias C. ;
Mann, Matthias .
NATURE, 2008, 455 (7217) :1251-U60