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Hsp72 preserves muscle function and slows progression of severe muscular dystrophy

Author

Listed:
  • Stefan M. Gehrig

    (Basic and Clinical Myology Laboratory, University of Melbourne)

  • Chris van der Poel

    (Basic and Clinical Myology Laboratory, University of Melbourne
    Present addresses: Department of Human Biosciences, Faculty of Health Sciences, La Trobe University, Bundoora, 3086, Victoria, Australia (C.v.d.P. and J.E.C.); Department of Biochemistry and Biomedical Sciences and Department of Pediatrics, McMaster University, Hamilton, Ontario, L8S 4L8, Canada (J.D.S.).)

  • Timothy A. Sayer

    (Basic and Clinical Myology Laboratory, University of Melbourne)

  • Jonathan D. Schertzer

    (Basic and Clinical Myology Laboratory, University of Melbourne
    Present addresses: Department of Human Biosciences, Faculty of Health Sciences, La Trobe University, Bundoora, 3086, Victoria, Australia (C.v.d.P. and J.E.C.); Department of Biochemistry and Biomedical Sciences and Department of Pediatrics, McMaster University, Hamilton, Ontario, L8S 4L8, Canada (J.D.S.).)

  • Darren C. Henstridge

    (Cellular and Molecular Metabolism Laboratory, Baker-IDI Heart and Diabetes Institute, PO Box 6492, St Kilda Road Central, Victoria, 8008, Australia)

  • Jarrod E. Church

    (Basic and Clinical Myology Laboratory, University of Melbourne
    Present addresses: Department of Human Biosciences, Faculty of Health Sciences, La Trobe University, Bundoora, 3086, Victoria, Australia (C.v.d.P. and J.E.C.); Department of Biochemistry and Biomedical Sciences and Department of Pediatrics, McMaster University, Hamilton, Ontario, L8S 4L8, Canada (J.D.S.).)

  • Severine Lamon

    (Centre for Physical Activity and Nutrition Research, School of Exercise and Nutrition Sciences, Deakin University, Burwood, Victoria, 3125, Australia)

  • Aaron P. Russell

    (Centre for Physical Activity and Nutrition Research, School of Exercise and Nutrition Sciences, Deakin University, Burwood, Victoria, 3125, Australia)

  • Kay E. Davies

    (MRC Functional Genomics Unit, Anatomy and Genetics, University of Oxford, South Parks Road, Oxford OX1 3QX, UK)

  • Mark A. Febbraio

    (Cellular and Molecular Metabolism Laboratory, Baker-IDI Heart and Diabetes Institute, PO Box 6492, St Kilda Road Central, Victoria, 8008, Australia)

  • Gordon S. Lynch

    (Basic and Clinical Myology Laboratory, University of Melbourne)

Abstract

Increasing the expression of intramuscular heat shock protein 72 preserves muscle strength and ameliorates the dystrophic pathology in two mouse models of muscular dystrophy, suggesting a promising way forward for the treatment of muscular dystrophy.

Suggested Citation

  • Stefan M. Gehrig & Chris van der Poel & Timothy A. Sayer & Jonathan D. Schertzer & Darren C. Henstridge & Jarrod E. Church & Severine Lamon & Aaron P. Russell & Kay E. Davies & Mark A. Febbraio & Gord, 2012. "Hsp72 preserves muscle function and slows progression of severe muscular dystrophy," Nature, Nature, vol. 484(7394), pages 394-398, April.
  • Handle: RePEc:nat:nature:v:484:y:2012:i:7394:d:10.1038_nature10980
    DOI: 10.1038/nature10980
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    Cited by:

    1. Ronja Schiemann & Annika Buhr & Eva Cordes & Stefan Walter & Jürgen J. Heinisch & Paola Ferrero & Hendrik Milting & Achim Paululat & Heiko Meyer, 2022. "Neprilysins regulate muscle contraction and heart function via cleavage of SERCA-inhibitory micropeptides," Nature Communications, Nature, vol. 13(1), pages 1-18, December.

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