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DISEASE MECHANISM

FAPs are sensors for skeletal myofibre atrophy

Skeletal muscle denervation leads to myofibre atrophy with fibrosis and fatty infiltration of muscle-resident fibroadipogenic progenitors (FAPs). A study shows that on denervation, FAPs activate pathogenic STAT3–IL-6 signalling. Inhibition of this pathway prevents atrophy and points to potential therapeutic targets.

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Fig. 1: Schematic representation of a signalling role for FAPs in response to denervation.

References

  1. Pannerec, A., Formicola, L., Besson, V., Marazzi, G. & Sassoon, D. A. Development 140, 2879–2891 (2013).

    Article  PubMed  CAS  Google Scholar 

  2. Relaix, F. & Zammit, P. S. Development 139, 2845–2856 (2012).

    Article  PubMed  CAS  Google Scholar 

  3. Heredia, J. E. et al. Cell 153, 376–388 (2013).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  4. Murphy, M. M., Lawson, J. A., Mathew, S. J., Hutcheson, D. A. & Kardon, G. Development 138, 3625–3637 (2011).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  5. Uezumi, A. et al. J. Cell Sci. 124, 3654–3664 (2011).

    Article  PubMed  CAS  Google Scholar 

  6. Joe, A. W. et al. Nat. Cell Biol. 12, 153–163 (2010).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  7. Ibebunjo, C. et al. Mol Cell Biol. 33, 194–212 (2013).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  8. Madaro, L. et al. Nat. Cell Biol. http://doi.org/10.1038/s41556-018-0151-y (2018).

  9. Dupont-Versteegden, E. E., Murphy, R. J., Houle, J. D., Gurley, C. M. & Peterson, C. A. Am. J. Physiol. 277, 589–597 (1999).

    Article  Google Scholar 

  10. McGeachie, J. K. Neuroscience 15, 499–506 (1985).

    Article  PubMed  CAS  Google Scholar 

  11. Schiaffino, S., Dyar, K. A., Ciciliot, S., Blaauw, B. & Sandri, M. FEBS J. 280, 4294–4314 (2013).

    Article  PubMed  CAS  Google Scholar 

  12. Tang, H. et al. Sci Signal 7, ra18 (2014).

    Article  PubMed  CAS  Google Scholar 

  13. Munoz-Canoves, P., Scheele, C., Pedersen, B. K. & Serrano, A. L. FEBS J. 280, 4131–4148 (2013).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  14. Mitchell, K. J. et al. Nat. Cell Biol. 12, 257–266 (2010).

    Article  PubMed  CAS  Google Scholar 

  15. Gurney, M. E. et al. Science 264, 1772–1775 (1994).

    Article  PubMed  CAS  Google Scholar 

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Correspondence to David Sassoon.

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Marazzi, G., Sassoon, D. FAPs are sensors for skeletal myofibre atrophy. Nat Cell Biol 20, 864–865 (2018). https://doi.org/10.1038/s41556-018-0149-5

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