Zfp697 is an RNA- binding protein that regulates skeletal muscle inflammation and remodeling

被引:2
|
作者
Correia, Jorge C. [1 ]
Jannig, Paulo R. [1 ,2 ,3 ,4 ]
Gosztyla, Maya L.
Cervenka, Igor [1 ]
Ducommun, Serge [1 ]
Praestholm, Stine M. [1 ]
Dias, Jose M. [5 ,6 ]
Dumont, Kyle D. [1 ]
Liu, Zhengye [7 ]
Liang, Qishan [2 ,4 ,8 ]
Edsgaerd, Daniel [9 ]
Emanuelsson, Olof [9 ]
Gregorevic, Paul [10 ]
Westerblad, Hakan [11 ]
Venckunas, Tomas [12 ]
Brazaitis, Marius [12 ]
Kamandulis, Sigitas [12 ]
Lanner, Johanna T. [7 ]
Teixeira, Ana I. [5 ]
Yeo, Gene W. [2 ,3 ,4 ]
Ruas, Jorge L. [1 ,13 ,14 ]
机构
[1] Karolinska Inst, Dept Physiol & Pharmacol, Mol & Cellular Exercise Physiol, Biomedicum, SE-17177 Stockholm, Sweden
[2] Univ Calif San Diego, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Sanford Stem Cell Inst Innovat Ctr, Stem Cell Program, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Ctr RNA Technol & Therapeut, La Jolla, CA 92093 USA
[5] Karolinska Inst, Dept Physiol & Pharmacol, Nanomed & Spatial Biol, Biomedicum, SE-17177 Stockholm, Sweden
[6] Karolinska Inst, Dept Cell & Mol Biol, Biomedicum, SE-17177 Stockholm, Sweden
[7] Karolinska Inst, Dept Physiol & Pharmacol, Mol Muscle Physiol & Pathophysiol, Biomedicum, S-17177 Stockholm, Sweden
[8] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
[9] KTH Royal Inst Technol, Sch Engn Sci Chem Biotechnol & Hlth, Dept Gene Technol, Sci Life Lab, Stockholm, Sweden
[10] Univ Melbourne, Ctr Muscle Res, Sch Biomed Sci, Dept Physiol, Parkville, Vic 3010, Australia
[11] Karolinska Inst, Dept Physiol & Pharmacol, SE-171 77 Stockholm, Sweden
[12] Lithuanian Sports Univ, Inst Sports Sci & Innovat, LT-44221 Kaunas, Lithuania
[13] Univ Michigan, Dept Pharmacol & Stanley, Med Sch, Ann Arbor, MI 48109 USA
[14] Univ Michigan, Judith Frankel Inst Heart & Brain Hlth, Med Sch, Ann Arbor, MI 48109 USA
基金
瑞典研究理事会; 英国医学研究理事会;
关键词
skeletal muscle; Zfp697; muscle atrophy; inflammation; RNA- binding protein; DUCHENNE MUSCULAR-DYSTROPHY; REGENERATION; INJURY; CELLS; PROGRESSION; MECHANISMS; DELETION; GROWTH; CCL2;
D O I
10.1073/pnas.2319724121
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 extra- cellular 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.
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页数:11
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