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Cardiac fibrosis

Waging war against cardiac fibrosis by targeting the anthrax toxin receptor

Anthrax toxin receptor 1 (ANTXR1), an integrin-like transmembrane protein, is a docking platform for anthrax toxin and mediates cell–extracellular matrix interactions. New work shows that ANTXR1 stabilizes transforming growth factor-β receptors on cardiac fibroblasts, leading to profibrotic signaling and pathological remodeling of the heart.

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Fig. 1: A model for anthrax toxin receptor-mediated regulation of cardiac fibrosis.

References

  1. Travers, J. G., Tharp, C. A., Rubino, M. & McKinsey, T. A. J. Clin. Invest. 132, e148554 (2022).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Bocella, N. et al. Nat. Cardiovasc. Res. https://doi.org/10.1038/s44161-025-00725-y (2025).

    Article  Google Scholar 

  3. van der Goot, G. & Young, J. A. Mol. Aspects Med. 30, 406–412 (2009).

    Article  PubMed  Google Scholar 

  4. Nanda, A. et al. Cancer Res. 64, 817–820 (2004).

    Article  CAS  PubMed  Google Scholar 

  5. Chaudhary, A. et al. Cancer Cell 21, 212–226 (2012).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Besschetnova, T. Y. et al. Matrix Biol. 42, 56–73 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Hsu, K. S. et al. Nat. Commun. 13, 7078 (2022).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. Yokota, T. et al. Cell 182, 545–562.e523 (2020).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. Hammond, D. E. et al. Mol. Cell Proteom. 21, 100252 (2022).

    Article  CAS  Google Scholar 

  10. Slack, R. J., Macdonald, S. J. F., Roper, J. A., Jenkins, R. G. & Hatley, R. J. D. Nat. Rev. Drug Discov. 21, 60–78 (2022).

    Article  CAS  PubMed  Google Scholar 

  11. Fu, S. et al. PLoS One 5, e11203 (2010).

    Article  PubMed  PubMed Central  Google Scholar 

  12. Santelli, E., Bankston, L. A., Leppla, S. H. & Liddington, R. C. Nature 430, 905–908 (2004).

    Article  CAS  PubMed  Google Scholar 

  13. Vagnozzi, R. J. & McKinsey, T. A. Cell Stem Cell 29, 352–354 (2022).

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

We thank E. Lau (University of Colorado Anschutz Medical Campus) for critical input. T.A.M. was supported by US National Institutes of Health grants R01HL171711 and HL181226 and an American Heart Association Collaborative Sciences Award (24CSA1255857). J.G.C. received support from US National Institutes of Health project grant T32GM158468

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Correspondence to Timothy A. McKinsey.

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T.A.M. is a co-founder of Myracle Therapeutics, is on the scientific advisory boards of Eikonizo Therapeutics and Revier Therapeutics and is a consultant for Augustine Therapeutics.

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Cox, J.G., McKinsey, T.A. Waging war against cardiac fibrosis by targeting the anthrax toxin receptor. Nat Cardiovasc Res 4, 1451–1453 (2025). https://doi.org/10.1038/s44161-025-00741-y

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