Your browser doesn't support javascript.
loading
Zfp697 is an RNA-binding protein that regulates skeletal muscle inflammation and remodeling.
Correia, Jorge C; Jannig, Paulo R; Gosztyla, Maya L; Cervenka, Igor; Ducommun, Serge; Præstholm, Stine M; Dias, José M; Dumont, Kyle D; Liu, Zhengye; Liang, Qishan; Edsgärd, Daniel; Emanuelsson, Olof; Gregorevic, Paul; Westerblad, Håkan; Venckunas, Tomas; Brazaitis, Marius; Kamandulis, Sigitas; Lanner, Johanna T; Teixeira, Ana I; Yeo, Gene W; Ruas, Jorge L.
Afiliação
  • Correia JC; Molecular and Cellular Exercise Physiology, Department of Physiology and Pharmacology, Biomedicum, Karolinska Institutet, Stockholm SE-171 77, Sweden.
  • Jannig PR; Molecular and Cellular Exercise Physiology, Department of Physiology and Pharmacology, Biomedicum, Karolinska Institutet, Stockholm SE-171 77, Sweden.
  • Gosztyla ML; Department of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA 92093.
  • Cervenka I; Sanford Stem Cell Institute Innovation Center and Stem Cell Program, University of California San Diego, La Jolla, CA 92093.
  • Ducommun S; Center for RNA Technologies and Therapeutics, University of California San Diego, La Jolla, CA 92093.
  • Præstholm SM; Molecular and Cellular Exercise Physiology, Department of Physiology and Pharmacology, Biomedicum, Karolinska Institutet, Stockholm SE-171 77, Sweden.
  • Dias JM; Molecular and Cellular Exercise Physiology, Department of Physiology and Pharmacology, Biomedicum, Karolinska Institutet, Stockholm SE-171 77, Sweden.
  • Dumont KD; Molecular and Cellular Exercise Physiology, Department of Physiology and Pharmacology, Biomedicum, Karolinska Institutet, Stockholm SE-171 77, Sweden.
  • Liu Z; Nanomedicine and Spatial Biology, Department of Physiology and Pharmacology, Biomedicum, Karolinska, Stockholm SE-171 77, Sweden.
  • Liang Q; Department of Cell and Molecular Biology, Biomedicum, Karolinska Institutet, Stockholm SE-171 77, Sweden.
  • Edsgärd D; Molecular and Cellular Exercise Physiology, Department of Physiology and Pharmacology, Biomedicum, Karolinska Institutet, Stockholm SE-171 77, Sweden.
  • Emanuelsson O; Molecular Muscle Physiology and Pathophysiology, Department of Physiology and Pharmacology, Biomedicum, Karolinska Institutet, Stockholm SE-171 77, Sweden.
  • Gregorevic P; Department of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA 92093.
  • Westerblad H; Center for RNA Technologies and Therapeutics, University of California San Diego, La Jolla, CA 92093.
  • Venckunas T; Department of Chemistry and Biochemistry, University of California San Diego, La Jolla, CA 92093.
  • Brazaitis M; Science for Life Laboratory, Department of Gene Technology, School of Engineering Sciences in Biotechnology, Chemistry and Health, KTH Royal Institute of Technology, Stockholm SE-100 44, Sweden.
  • Kamandulis S; Science for Life Laboratory, Department of Gene Technology, School of Engineering Sciences in Biotechnology, Chemistry and Health, KTH Royal Institute of Technology, Stockholm SE-100 44, Sweden.
  • Lanner JT; Centre for Muscle Research, Department of Anatomy and Physiology, School of Biomedical Sciences, The University of Melbourne, Parkville, VIC 3010, Australia.
  • Teixeira AI; Muscle Physiology, Department of Physiology and Pharmacology, Biomedicum, Karolinska Institutet, Stockholm SE-171 77, Sweden.
  • Yeo GW; Institute of Sports Science and Innovations, Lithuanian Sports University, Kaunas 44221, Lithuania.
  • Ruas JL; Institute of Sports Science and Innovations, Lithuanian Sports University, Kaunas 44221, Lithuania.
Proc Natl Acad Sci U S A ; 121(34): e2319724121, 2024 Aug 20.
Article em En | MEDLINE | ID: mdl-39141348
ABSTRACT
Skeletal muscle atrophy is a morbidity and mortality risk factor that happens with disuse, chronic disease, and aging. The tissue remodeling that happens during recovery from atrophy or injury involves changes in different cell types such as muscle fibers, and satellite and immune cells. Here, we show that the previously uncharacterized gene and protein Zfp697 is a damage-induced regulator of muscle remodeling. Zfp697/ZNF697 expression is transiently elevated during recovery from muscle atrophy or injury in mice and humans. Sustained Zfp697 expression in mouse muscle leads to a gene expression signature of chemokine secretion, immune cell recruitment, and extracellular matrix remodeling. Notably, although Zfp697 is expressed in several cell types in skeletal muscle, myofiber-specific Zfp697 genetic ablation in mice is sufficient to hinder the inflammatory and regenerative response to muscle injury, compromising functional recovery. We show that Zfp697 is an essential mediator of the interferon gamma response in muscle cells and that it functions primarily as an RNA-interacting protein, with a very high number of miRNA targets. This work identifies Zfp697 as an integrator of cell-cell communication necessary for tissue remodeling and regeneration.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Ligação a RNA / Músculo Esquelético Limite: Animals / Humans Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Ligação a RNA / Músculo Esquelético Limite: Animals / Humans Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2024 Tipo de documento: Article