4.7 Article

IL-7 is expressed and secreted by human skeletal muscle cells

Journal

AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
Volume 298, Issue 4, Pages C807-C816

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpcell.00094.2009

Keywords

interleukin-7; interleukin-6; myotubes; myokines

Funding

  1. The Norwegian Cancer Association
  2. Lars Heny Lie's and Dagmar & Reidar Jensens' Legacy for Cancer Research
  3. Legacy in Memory of H. G. & Andrine Berg and their son Hans Gysler Berg
  4. Aktieselskabet Freia Chocolade Fabrik's Medical Foundation
  5. Throne-Holst Foundation for Nutrition Research
  6. Ella & Kristian Nyerrods Foundation for Medical Research at the University of Oslo
  7. Nutrigenomics Organisation, EC-funded Network of Excellence [FOOD-2004-506360]

Ask authors/readers for more resources

Haugen F, Norheim F, Lian H, Wensaas AJ, Dueland S, Berg O, Funderud A, Skalhegg BS, Raastad T, Drevon CA. IL-7 is expressed and secreted by human skeletal muscle cells. Am J Physiol Cell Physiol 298: C807-C816, 2010. First published January 20, 2010; doi:10.1152/ajpcell.00094.2009.-In addition to generating movement, skeletal muscle may have a function as a secretory organ. The aim of the present study was to identify novel proteins with signaling capabilities secreted from skeletal muscle cells. IL-7 was detected in media conditioned by primary cultures of human myotubes differentiated from satellite cells, and concentrations increased with incubation time. By immunoblotting and real-time RT-PCR IL-7 expression was confirmed at both protein and mRNA levels. Furthermore, with immunofluorescence and specific antisera, multinucleated myotubes were found to coexpress IL-7 and myosin heavy chain. During differentiation of human myotubes from satellite cells, IL-7 expression increased at mRNA and protein levels. In contrast, mRNA expression of the IL-7 receptor was 80% lower in myotubes compared with satellite cells. Incubations with recombinant IL-7 under differentiation conditions caused similar to 35% reduction in mRNA for the terminal myogenic markers myosin heavy chain 2 (MYH2) and myogenin (MYOG), suggesting that IL-7 may act on satellite cells to inhibit development of the muscle fiber phenotype. Alternative routes of cell development were investigated, and IL-7 increased migration of satellite cells by 40% after 48 h in a Transwell system, whereas cell proliferation remained unchanged. In vivo, real-time RT-PCR analysis of musculus vastus lateralis (n = 10) and musculus trapezius (n = 7) biopsies taken from male individuals undergoing a strength training program demonstrated that after 11 wk mean IL-7 mRNA increased by threefold (P = 0.01) and fourfold (P = 0.04), respectively. In conclusion, we have demonstrated that IL-7 is a novel myokine regulated both in vitro and in vivo, and it may play a role in the regulation of muscle cell development.

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