Regulation of the Growth of Multinucleated Muscle Cells by an NFATC2-Dependent Pathway

• Published in: The Journal of cell biology 2001-04, Vol.153 (2), p.329-338
• Main Authors: Horsley, Valerie, Friday, Bret B., Matteson, Sarah, Kegley, Kristy Miller, Gephart, Jonathan, Pavlath, Grace K.
• Format: Article
• Language: English
• Subjects: Animals; Blotting, Northern; Cell growth; Cell Nucleus - metabolism; Cells; Cells, Cultured; Cellular biology; DNA-Binding Proteins - genetics; DNA-Binding Proteins - metabolism; Gene expression regulation; Growth rate; Male; Mice; Mice, Knockout; Models, Biological; Muscle cells; Muscle fibers; Muscle Fibers, Skeletal - cytology; Muscle Fibers, Skeletal - metabolism; Muscle, Skeletal - anatomy & histology; Muscle, Skeletal - cytology; Muscle, Skeletal - physiology; Muscles; Myoblasts; Myogenin - metabolism; Myosin Heavy Chains - metabolism; NFAT protein; NFATC Transcription Factors; Nuclear Proteins - genetics; Nuclear Proteins - metabolism; Original; Regeneration - physiology; Retroviridae - genetics; Retroviridae - metabolism; Reverse Transcriptase Polymerase Chain Reaction; Rodents; Skeletal muscle; Skeletal muscle satellite cells; T lymphocytes; Time Factors; Transcription Factors - genetics; Transcription Factors - metabolism
• ISSN: 0021-9525; 1540-8140
• DOI: 10.1083/jcb.153.2.329

The nuclear factor of activated T cells (NFAT) family of transcription factors regulates the development and differentiation of several tissue types. Here, we examine the role of NFATC2 in skeletal muscle by analyzing adult NFATC2-/- mice. These mice exhibit reduced muscle size due to a decrease in myofiber cross-sectional area, suggesting that growth is blunted. Muscle growth was examined during regeneration after injury, wherein NFATC2-null myofibers form normally but display impaired growth. The growth defect is intrinsic to muscle cells, since the lack of NFATC2 in primary muscle cultures results in reduced cell size and myonuclear number in myotubes. Retroviral-mediated expression of NFATC2 in the mutant cells rescues this cellular phenotype. Myonuclear number is similarly decreased in NFATC2-/- mice. Taken together, these results implicate a novel role for NFATC2 in skeletal muscle growth. We demonstrate that during growth of multinucleated muscle cells, myoblasts initially fuse to form myotubes with a limited number of nuclei and that subsequent nuclear addition and increases in myotube size are controlled by a molecular pathway regulated by NFATC2.