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Oxidative stress induces angiogenesis by activating TLR2 with novel endogenous ligands

Abstract

Reciprocity of inflammation, oxidative stress and neovascularization is emerging as an important mechanism underlying numerous processes from tissue healing and remodelling to cancer progression1,2. Whereas the mechanism of hypoxia-driven angiogenesis is well understood3,4, the link between inflammation-induced oxidation and de novo blood vessel growth remains obscure. Here we show that the end products of lipid oxidation, ω-(2-carboxyethyl)pyrrole (CEP) and other related pyrroles5, are generated during inflammation and wound healing and accumulate at high levels in ageing tissues in mice and in highly vascularized tumours in both murine and human melanoma. The molecular patterns of carboxyalkylpyrroles are recognized by Toll-like receptor 2 (TLR2), but not TLR4 or scavenger receptors on endothelial cells, leading to an angiogenic response that is independent of vascular endothelial growth factor. CEP promoted angiogenesis in hindlimb ischaemia and wound healing models through MyD88-dependent TLR2 signalling. Neutralization of endogenous carboxyalkylpyrroles impaired wound healing and tissue revascularization and diminished tumour angiogenesis. Both TLR2 and MyD88 are required for CEP-induced stimulation of Rac1 and endothelial migration. Taken together, these findings establish a new function of TLR2 as a sensor of oxidation-associated molecular patterns, providing a key link connecting inflammation, oxidative stress, innate immunity and angiogenesis.

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Figure 1: CEP, an end product of lipid oxidation, is present in wounds, is elevated in melanoma and accumulates in ageing tissues.
Figure 2: Proangiogenic effects of oxidized adducts are dependent on pyrrole moiety and are mediated by TLR2 but not VEGFR signalling.
Figure 3: CEP-induced angiogenesis in vivo is mediated by TLR2.
Figure 4: Endogenous CEP contributes to wound recovery and melanoma vascularization; TLR2-dependent responses to CEP involve MyD88 and Rac1.

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References

  1. Jackson, J. R., Seed, M. P., Kircher, C. H., Willoughby, D. A. & Winkler, J. D. The codependence of angiogenesis and chronic inflammation. FASEB J. 11, 457–465 (1997)

    Article  CAS  Google Scholar 

  2. Coussens, L. M. & Werb, Z. Inflammation and cancer. Nature 420, 860–867 (2002)

    Article  ADS  CAS  Google Scholar 

  3. Mazzone, M. et al. Heterozygous deficiency of PHD2 restores tumor oxygenation and inhibits metastasis via endothelial normalization. Cell 136, 839–851 (2009)

    Article  CAS  Google Scholar 

  4. Fraisl, P., Mazzone, M., Schmidt, T. & Carmeliet, P. Regulation of angiogenesis by oxygen and metabolism. Dev. Cell 16, 167–179 (2009)

    Article  CAS  Google Scholar 

  5. Crabb, J. W. et al. Drusen proteome analysis: an approach to the etiology of age-related macular degeneration. Proc. Natl Acad. Sci. USA 99, 14682–14687 (2002)

    Article  ADS  CAS  Google Scholar 

  6. Karin, M., Lawrence, T. & Nizet, V. Innate immunity gone awry: linking microbial infections to chronic inflammation and cancer. Cell 124, 823–835 (2006)

    Article  CAS  Google Scholar 

  7. Martin, P. Wound healing—aiming for perfect skin regeneration. Science 276, 75–81 (1997)

    Article  CAS  Google Scholar 

  8. Niethammer, P., Grabher, C., Look, A. T. & Mitchison, T. J. A tissue-scale gradient of hydrogen peroxide mediates rapid wound detection in zebrafish. Nature 459, 996–999 (2009)

    Article  ADS  CAS  Google Scholar 

  9. Segal, A. W. How neutrophils kill microbes. Annu. Rev. Immunol. 23, 197–223 (2005)

    Article  CAS  Google Scholar 

  10. Podrez, E. A. et al. Identification of a novel family of oxidized phospholipids that serve as ligands for the macrophage scavenger receptor CD36. J. Biol. Chem. 277, 38503–38516 (2002)

    Article  CAS  Google Scholar 

  11. Podrez, E. A. et al. Platelet CD36 links hyperlipidemia, oxidant stress and a prothrombotic phenotype. Nature Med. 13, 1086–1095 (2007)

    Article  CAS  Google Scholar 

  12. Gu, X. et al. Carboxyethylpyrrole protein adducts and autoantibodies, biomarkers for age-related macular degeneration. J. Biol. Chem. 278, 42027–42035 (2003)

    Article  CAS  Google Scholar 

  13. Ebrahem, Q. et al. Carboxyethylpyrrole oxidative protein modifications stimulate neovascularization: implications for age-related macular degeneration. Proc. Natl Acad. Sci. USA 103, 13480–13484 (2006)

    Article  ADS  CAS  Google Scholar 

  14. Manley, P. W. et al. Anthranilic acid amides: a novel class of antiangiogenic VEGF receptor kinase inhibitors. J. Med. Chem. 45, 5687–5693 (2002)

    Article  CAS  Google Scholar 

  15. Palm, N. W. & Medzhitov, R. Pattern recognition receptors and control of adaptive immunity. Immunol. Rev. 227, 221–233 (2009)

    Article  CAS  Google Scholar 

  16. Kawai, T. & Akira, S. Pathogen recognition with Toll-like receptors. Curr. Opin. Immunol. 17, 338–344 (2005)

    Article  CAS  Google Scholar 

  17. Shi, H. et al. TLR4 links innate immunity and fatty acid-induced insulin resistance. J. Clin. Invest. 116, 3015–3025 (2006)

    Article  CAS  Google Scholar 

  18. Apetoh, L. et al. Toll-like receptor 4-dependent contribution of the immune system to anticancer chemotherapy and radiotherapy. Nature Med. 13, 1050–1059 (2007)

    Article  CAS  Google Scholar 

  19. Kim, H. S. et al. Toll-like receptor 2 senses beta-cell death and contributes to the initiation of autoimmune diabetes. Immunity 27, 321–333 (2007)

    Article  CAS  Google Scholar 

  20. Vogl, T. et al. Mrp8 and Mrp14 are endogenous activators of Toll-like receptor 4, promoting lethal, endotoxin-induced shock. Nature Med. 13, 1042–1049 (2007)

    Article  CAS  Google Scholar 

  21. Schaefer, L. et al. The matrix component biglycan is proinflammatory and signals through Toll-like receptors 4 and 2 in macrophages. J. Clin. Invest. 115, 2223–2233 (2005)

    Article  CAS  Google Scholar 

  22. Jiang, D. et al. Regulation of lung injury and repair by Toll-like receptors and hyaluronan. Nature Med. 11, 1173–1179 (2005)

    Article  CAS  Google Scholar 

  23. Grote, K. et al. Toll-like receptor 2/6 stimulation promotes angiogenesis via GM-CSF as a potential strategy for immune defense and tissue regeneration. Blood 115, 2543–2552 (2010)

    Article  CAS  Google Scholar 

  24. Zahringer, U., Lindner, B., Inamura, S., Heine, H. & Alexander, C. TLR2—promiscuous or specific? A critical re-evaluation of a receptor expressing apparent broad specificity. Immunobiology 213, 205–224 (2008)

    Article  Google Scholar 

  25. Aliprantis, A. O. et al. Cell activation and apoptosis by bacterial lipoproteins through toll-like receptor-2. Science 285, 736–739 (1999)

    Article  CAS  Google Scholar 

  26. Ozinsky, A. et al. The repertoire for pattern recognition of pathogens by the innate immune system is defined by cooperation between toll-like receptors. Proc. Natl Acad. Sci. USA 97, 13766–13771 (2000)

    Article  ADS  CAS  Google Scholar 

  27. Tan, W. et al. An essential role for Rac1 in endothelial cell function and vascular development. FASEB J. 22, 1829–1838 (2008)

    Article  CAS  Google Scholar 

  28. Arbibe, L. et al. Toll-like receptor 2-mediated NF-κB activation requires a Rac1-dependent pathway. Nature Immunol. 1, 533–540 (2000)

    Article  CAS  Google Scholar 

  29. Mullick, A. E., Tobias, P. S. & Curtiss, L. K. Modulation of atherosclerosis in mice by Toll-like receptor 2. J. Clin. Invest. 115, 3149–3156 (2005)

    Article  CAS  Google Scholar 

  30. Chen, J. et al. Akt1 regulates pathological angiogenesis, vascular maturation and permeability in vivo . Nature Med. 11, 1188–1196 (2005)

    Article  CAS  Google Scholar 

  31. Feng, W. et al. The angiogenic response is dictated by β3 integrin on bone marrow-derived cells. J. Cell Biol. 183, 1145–1157 (2008)

    Article  CAS  Google Scholar 

  32. Mahabeleshwar, G. H., Somanath, P. R. & Byzova, T. V. Methods for isolation of endothelial and smooth muscle cells and in vitro proliferation assays. Methods Mol. Med. 129, 197–208 (2006)

    Google Scholar 

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Acknowledgements

We thank L. Hong for the help with synthesis of CEP and CPP adducts, Y. Cui for expressing and purifying anti-CEP monoclonal antibodies, and J. Crabb for providing anti-CEP monoclonal antibody hybridoma cells. This work was supported by NIH grants HL073311, HL071625, CA126847 to T.V.B., HL077213 to E.A.P. and GM021249 to R.G.S. and an American Heart Association grant (10SDG4300062) to N.L.M.

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Contributions

N.L.M., E.A.P. and T.V.B. designed experiments. In vivo and ex vivo experiments were performed by X.Z.W. with a help from A.A.M. and M.T. In vitro experiments were performed by N.L.M. with help from B.A.K. Melanoma samples and their analysis was done by E.C.B. Synthesis of CAPs was performed by R.G.S. The data were analysed and plotted by X.Z.W. The manuscript was written by N.L.M. and T.V.B.

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Correspondence to Tatiana V. Byzova.

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The authors declare no competing financial interests.

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West, X., Malinin, N., Merkulova, A. et al. Oxidative stress induces angiogenesis by activating TLR2 with novel endogenous ligands. Nature 467, 972–976 (2010). https://doi.org/10.1038/nature09421

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