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Endothelial BMP4 Promotes Leukocyte Rolling and Adhesion and Is Elevated in Patients After Survived Out-of-Hospital Cardiac Arrest

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Abstract

Leukocyte recruitment is a fundamental step in the inflammatory response during ischemia/reperfusion injury (IRI). Rolling and adhesion of leukocytes to activated endothelium promote tissue inflammation after IRI and require presentation of adhesion molecules E-selectin and ICAM-1 on the endothelial surface. Bone morphogenetic protein (BMP) 4 is a prominent member of the BMP family expressed and secreted by endothelial cells. BMP4 derived from endothelial cells has important functions in vascular disease but its influence on the leukocyte adhesion cascade during inflammation is incompletely understood. In the present study, we challenged mice with an inducible endothelial-specific BMP4 deletion (referred to as EC-BMP4−/− mice) and their control littermates (EC-BMP4+/+) with thioglycollate i.p. and assessed extravasation of different leukocyte subsets during peritonitis. Peritoneal lavages were performed and peritoneal cells were counted. Total cell count in lavages of EC-BMP4−/− mice was markedly reduced compared with lavages of EC-BMP4+/+ mice. FACS analyses of thioglycollate-elicited peritoneal cells revealed that diverse leukocyte subsets were reduced in EC-BMP4−/− mice. Intravital microscopy of cremaster venules demonstrated that rolling and adhesion of leukocytes were significantly diminished in EC-BMP4−/− mice in comparison with control mice in response to TNFα. These observations indicate that endothelial BMP4 is essential for rolling, adhesion, and extravasation of leukocytes in vivo. To understand the underlying mechanisms, levels of endothelial adhesion molecules E-selectin and ICAM-1 were quantified in EC-BMP4−/− and EC-BMP4+/+ mice by quantitative PCR and Western blotting. Interestingly, ICAM-1 and E-selectin expressions were reduced in the hearts of EC-BMP4−/− mice. Next we confirmed pro-inflammatory properties of BMP4 in a gain of function experiments and found that administration of recombinant BMP4 in male C57BL/6 mice increased leukocyte rolling and adhesion in cremaster venules in vivo. To assess the regulation of BMP4 in inflammatory disease in humans, we collected plasma samples of patients from day 0 to day 7 after survived out-of-hospital cardiac arrest (OHCA, n = 42). Remarkably, plasma of OHCA patients contained significantly higher BMP4 protein levels compared with patients with coronary artery disease (CAD, n = 12) or healthy volunteers (n = 11). Subgroup analysis revealed that elevated plasma BMP4 levels after ROSC are associated with decreased survival and unfavorable neurological outcome. Collectively, endothelial BMP4 is a potent activator of inflammation in vivo that promotes rolling, adhesion, and extravasation of leukocyte subsets by induction of E-selectin and ICAM-1. Elevation of plasma BMP4 levels in the post-resuscitation period suggests that BMP4 contributes to pathophysiology and poor outcome of post-cardiac arrest syndrome.

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References

  1. Eltzschig, H.K., and T. Eckle. 2011. Ischemia and reperfusion--From mechanism to translation. Nat Med 17 (11): 1391–1401.

    Article  CAS  Google Scholar 

  2. Marchant, D.J., J.H. Boyd, D.C. Lin, D.J. Granville, F.S. Garmaroudi, and B.M. McManus. 2012. Inflammation in myocardial diseases. Circ Res 110 (1): 126–144.

    Article  CAS  Google Scholar 

  3. Hernandez-Resendiz, S., et al. 2018. Responses of endothelial cells towards ischemic conditioning following acute myocardial infarction. Cond Med 1 (5): 247–258.

    PubMed  PubMed Central  Google Scholar 

  4. Ley, K., C. Laudanna, M.I. Cybulsky, and S. Nourshargh. 2007. Getting to the site of inflammation: The leukocyte adhesion cascade updated. Nat Rev Immunol 7 (9): 678–689.

    Article  CAS  Google Scholar 

  5. Dyer, L.A., X. Pi, and C. Patterson. 2014. The role of BMPs in endothelial cell function and dysfunction. Trends Endocrinol Metab 25 (9): 472–480.

    Article  CAS  Google Scholar 

  6. Gomez-Puerto, M.C., P.V. Iyengar, A. García de Vinuesa, P. ten Dijke, and G. Sanchez-Duffhues. 2019. Bone morphogenetic protein receptor signal transduction in human disease. J Pathol 247 (1): 9–20.

    Article  CAS  Google Scholar 

  7. Cai, J., E. Pardali, G. Sánchez-Duffhues, and P. ten Dijke. 2012. BMP signaling in vascular diseases. FEBS Lett 586 (14): 1993–2002.

    Article  CAS  Google Scholar 

  8. Garcia de Vinuesa, A., et al. 2016. BMP signaling in vascular biology and dysfunction. Cytokine Growth Factor Rev 27: 65–79.

    Article  CAS  Google Scholar 

  9. Tian, X.Y., L.H. Yung, W.T. Wong, J. Liu, F.P. Leung, L. Liu, Y. Chen, S.K. Kong, K.M. Kwan, S.M. Ng, P.B.S. Lai, L.M. Yung, X. Yao, and Y. Huang. 2012. Bone morphogenic protein-4 induces endothelial cell apoptosis through oxidative stress-dependent p38MAPK and JNK pathway. J Mol Cell Cardiol 52 (1): 237–244.

    Article  CAS  Google Scholar 

  10. Miriyala, S., M.C. Gongora Nieto, C. Mingone, D. Smith, S. Dikalov, D.G. Harrison, and H. Jo. 2006. Bone morphogenic protein-4 induces hypertension in mice: Role of noggin, vascular NADPH oxidases, and impaired vasorelaxation. Circulation 113 (24): 2818–2825.

    Article  CAS  Google Scholar 

  11. Sorescu, G.P., H. Song, S.L. Tressel, J. Hwang, S. Dikalov, D.A. Smith, N.L. Boyd, M.O. Platt, B. Lassègue, K.K. Griendling, and H. Jo. 2004. Bone morphogenic protein 4 produced in endothelial cells by oscillatory shear stress induces monocyte adhesion by stimulating reactive oxygen species production from a nox1-based NADPH oxidase. Circ Res 95 (8): 773–779.

    Article  CAS  Google Scholar 

  12. Sorescu, G.P., M. Sykes, D. Weiss, M.O. Platt, A. Saha, J. Hwang, N. Boyd, Y.C. Boo, J.D. Vega, W.R. Taylor, and H. Jo. 2003. Bone morphogenic protein 4 produced in endothelial cells by oscillatory shear stress stimulates an inflammatory response. J Biol Chem 278 (33): 31128–31135.

    Article  CAS  Google Scholar 

  13. Helbing, T., L. Arnold, G. Wiltgen, E. Hirschbihl, V. Gabelmann, A. Hornstein, J.S. Esser, P. Diehl, S. Grundmann, H.J. Busch, K. Fink, C. Bode, and M. Moser. 2017. Endothelial BMP4 regulates leukocyte diapedesis and promotes inflammation. Inflammation 40 (6): 1862–1874.

    Article  CAS  Google Scholar 

  14. Helbing, T., G. Wiltgen, A. Hornstein, E.Z. Brauers, L. Arnold, A. Bauer, J.S. Esser, P. Diehl, S. Grundmann, K. Fink, C. Patterson, C. Bode, and M. Moser. 2017. Bone Morphogenetic Protein-Modulator BMPER regulates endothelial barrier function. Inflammation 40 (2): 442–453.

    Article  CAS  Google Scholar 

  15. Zhang, Y., J. Liu, X.Y. Tian, W.T. Wong, Y. Chen, L. Wang, J. Luo, W.S. Cheang, C.W. Lau, K.M. Kwan, N. Wang, X. Yao, and Y. Huang. 2014. Inhibition of bone morphogenic protein 4 restores endothelial function in db/db diabetic mice. Arterioscler Thromb Vasc Biol 34 (1): 152–159.

    Article  CAS  Google Scholar 

  16. Wong, W.T., X.Y. Tian, Y. Chen, F.P. Leung, L. Liu, H.K. Lee, C.F. Ng, A. Xu, X. Yao, P.M. Vanhoutte, G.L. Tipoe, and Y. Huang. 2010. Bone morphogenic protein-4 impairs endothelial function through oxidative stress-dependent cyclooxygenase-2 upregulation: Implications on hypertension. Circ Res 107 (8): 984–991.

    Article  CAS  Google Scholar 

  17. Csiszar, A., N. Labinskyy, H. Jo, P. Ballabh, and Z. Ungvari. 2008. Differential proinflammatory and prooxidant effects of bone morphogenetic protein-4 in coronary and pulmonary arterial endothelial cells. Am J Physiol Heart Circ Physiol 295 (2): H569–H577.

    Article  CAS  Google Scholar 

  18. Winnier, G., M. Blessing, P.A. Labosky, and B.L. Hogan. 1995. Bone morphogenetic protein-4 is required for mesoderm formation and patterning in the mouse. Genes Dev 9 (17): 2105–2116.

    Article  CAS  Google Scholar 

  19. Ghosn, E.E., et al. 2010. Two physically, functionally, and developmentally distinct peritoneal macrophage subsets. Proc Natl Acad Sci U S A 107 (6): 2568–2573.

    Article  CAS  Google Scholar 

  20. Misharin, A.V., R. Saber, and H. Perlman. 2012. Eosinophil contamination of thioglycollate-elicited peritoneal macrophage cultures skews the functional readouts of in vitro assays. J Leukoc Biol 92 (2): 325–331.

    Article  CAS  Google Scholar 

  21. Zelova, H., and J. Hosek. 2013. TNF-alpha signalling and inflammation: Interactions between old acquaintances. Inflamm Res 62 (7): 641–651.

    Article  CAS  Google Scholar 

  22. Fink, K., M. Moebes, C. Vetter, N. Bourgeois, B. Schmid, C. Bode, T. Helbing, and H.J. Busch. 2015. Selenium prevents microparticle-induced endothelial inflammation in patients after cardiopulmonary resuscitation. Crit Care 19: 58.

    Article  Google Scholar 

  23. Bro-Jeppesen, J., P.I. Johansson, C. Hassager, M. Wanscher, S.R. Ostrowski, M. Bjerre, and J. Kjaergaard. 2016. Endothelial activation/injury and associations with severity of post-cardiac arrest syndrome and mortality after out-of-hospital cardiac arrest. Resuscitation 107: 71–79.

    Article  Google Scholar 

  24. Bro-Jeppesen, J., P.I. Johansson, J. Kjaergaard, M. Wanscher, S.R. Ostrowski, M. Bjerre, and C. Hassager. 2017. Level of systemic inflammation and endothelial injury is associated with cardiovascular dysfunction and vasopressor support in post-cardiac arrest patients. Resuscitation 121: 179–186.

    Article  Google Scholar 

  25. Meyer, A.S., et al. 2016. Endothelial Dysfunction in Resuscitated Cardiac Arrest (ENDO-RCA): safety and efficacy of low-dose prostacyclin administration and blood pressure target in addition to standard therapy, as compared to standard therapy alone, in post-cardiac arrest syndrome patients: Study protocol for a randomized controlled trial. Trials 17: 378.

    Article  Google Scholar 

  26. Helbing, T., R. Rothweiler, E. Ketterer, L. Goetz, J. Heinke, S. Grundmann, D. Duerschmied, C. Patterson, C. Bode, and M. Moser. 2011. BMP activity controlled by BMPER regulates the proinflammatory phenotype of endothelium. Blood 118 (18): 5040–5049.

    Article  CAS  Google Scholar 

  27. Chang, K., D. Weiss, J. Suo, J.D. Vega, D. Giddens, W.R. Taylor, and H. Jo. 2007. Bone morphogenic protein antagonists are coexpressed with bone morphogenic protein 4 in endothelial cells exposed to unstable flow in vitro in mouse aortas and in human coronary arteries: Role of bone morphogenic protein antagonists in inflammation and atherosclerosis. Circulation 116 (11): 1258–1266.

    Article  CAS  Google Scholar 

  28. Csiszar, A., M. Ahmad, K.E. Smith, N. Labinskyy, Q. Gao, G. Kaley, J.G. Edwards, M.S. Wolin, and Z. Ungvari. 2006. Bone morphogenetic protein-2 induces proinflammatory endothelial phenotype. Am J Pathol 168 (2): 629–638.

    Article  CAS  Google Scholar 

  29. Grasner, J.T., et al. 2016. EuReCa ONE-27 nations, one Europe, one registry: A prospective one month analysis of out-of-hospital cardiac arrest outcomes in 27 countries in Europe. Resuscitation 105: 188–195.

    Article  Google Scholar 

  30. Grasner, J.T., et al. 2020. Survival after out-of-hospital cardiac arrest in Europe - Results of the EuReCa two study. Resuscitation 148: 218–226.

    Article  Google Scholar 

  31. Chalkias, A., and T. Xanthos. 2012. Pathophysiology and pathogenesis of post-resuscitation myocardial stunning. Heart Fail Rev 17 (1): 117–128.

    Article  Google Scholar 

  32. Adrie, C., M. Adib-Conquy, I. Laurent, M. Monchi, C. Vinsonneau, C. Fitting, F.̧. Fraisse, A.T. Dinh-Xuan, P. Carli, C. Spaulding, J.F.̧. Dhainaut, and J.M. Cavaillon. 2002. Successful cardiopulmonary resuscitation after cardiac arrest as a “sepsis-like” syndrome. Circulation 106 (5): 562–568.

  33. Huang, C.H., M.S. Tsai, K.L. Chien, W.T. Chang, T.D. Wang, S.C. Chen, M.H.M. Ma, H.Y. Hsu, and W.J. Chen. 2016. Predicting the outcomes for out-of-hospital cardiac arrest patients using multiple biomarkers and suspension microarray assays. Sci Rep 6: 27187.

    Article  CAS  Google Scholar 

  34. Peberdy, M.A., L.W. Andersen, A. Abbate, L.R. Thacker, D. Gaieski, B.S. Abella, A.V. Grossestreuer, J.C. Rittenberger, J. Clore, J. Ornato, M.N. Cocchi, C. Callaway, M. Donnino, and National Post Arrest Research Consortium (NPARC) Investigators. 2016. Inflammatory markers following resuscitation from out-of-hospital cardiac arrest-A prospective multicenter observational study. Resuscitation 103: 117–124.

    Article  Google Scholar 

  35. Nolan, J.P., J. Soar, A. Cariou, T. Cronberg, V.R.M. Moulaert, C.D. Deakin, B.W. Bottiger, H. Friberg, K. Sunde, and C. Sandroni. 2015. European Resuscitation Council and European Society of Intensive Care Medicine guidelines for post-resuscitation care 2015: Section 5 of the European Resuscitation Council Guidelines for resuscitation 2015. Resuscitation 95: 202–222.

    Article  Google Scholar 

  36. Huet, O., L. Dupic, F. Batteux, C. Matar, M. Conti, C. Chereau, V. Lemiale, A. Harrois, J.P. Mira, E. Vicaut, A. Cariou, and J. Duranteau. 2011. Postresuscitation syndrome: Potential role of hydroxyl radical-induced endothelial cell damage. Crit Care Med 39 (7): 1712–1720.

    Article  CAS  Google Scholar 

  37. Fink, K., M. Schwarz, L. Feldbrügge, J.N. Sunkomat, T. Schwab, N. Bourgeois, M. Olschewski, C. von zur Mühlen, C. Bode, and H.J. Busch. 2010. Severe endothelial injury and subsequent repair in patients after successful cardiopulmonary resuscitation. Crit Care 14 (3): R104.

    Article  Google Scholar 

  38. Johansson, P.I., et al. 2015. Sympathoadrenal activation and endothelial damage are inter correlated and predict increased mortality in patients resuscitated after out-of-hospital cardiac arrest. A post Hoc sub-study of patients from the TTM-trial. PLoS One 10 (3): e0120914.

    Article  Google Scholar 

  39. Tong, F., B. Dong, R. Chai, K. Tong, Y. Wang, S. Chen, X. Zhou, and D. Liu. 2017. Simvastatin nanoparticles attenuated intestinal ischemia/reperfusion injury by downregulating BMP4/COX-2 pathway in rats. Int J Nanomedicine 12: 2477–2488.

    Article  CAS  Google Scholar 

  40. Yan, Y., F. Tong, and J. Chen. 2019. Endogenous BMP-4/ROS/COX-2 mediated IPC and resveratrol alleviated brain damage. Curr Pharm Des 25 (9): 1030–1039.

    Article  CAS  Google Scholar 

  41. Ogura, Y., N. Ouchi, K. Ohashi, R. Shibata, Y. Kataoka, T. Kambara, T. Kito, S. Maruyama, D. Yuasa, K. Matsuo, T. Enomoto, Y. Uemura, M. Miyabe, M. Ishii, T. Yamamoto, Y. Shimizu, K. Walsh, and T. Murohara. 2012. Therapeutic impact of follistatin-like 1 on myocardial ischemic injury in preclinical models. Circulation 126 (14): 1728–1738.

    Article  Google Scholar 

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Acknowledgments

We are indebted to Jessica Beckert for her outstanding technical assistance.

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Correspondence to Thomas Helbing.

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All animal procedures were approved by the local ethics committee (Regierungspräsidium Freiburg) and were performed according to the respective guidelines. The study was approved by the ethics committee of the University of Freiburg and confirms to the tenets of the declaration of Helsinki.

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Electronic Supplementary Material

Supplement 1

Flow cytometric analysis of mouse thioglycollate-elicited peritoneal cells. Gating strategy used to identify different subsets of peritoneal cells of Figure 1. (AI 1441 kb)

Supplement 2

BMP4 protein expression in total heart tissue extracted from EC-BMP4+/+ and EC-BMP4−/− mice. Cells were lysed and proteins were extracted to perform western blot analysis with an anti-BMP4 and anti-α-tubulin antibody. (AI 527 kb)

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Arnold, L., Weberbauer, M., Herkel, M. et al. Endothelial BMP4 Promotes Leukocyte Rolling and Adhesion and Is Elevated in Patients After Survived Out-of-Hospital Cardiac Arrest. Inflammation 43, 2379–2391 (2020). https://doi.org/10.1007/s10753-020-01307-9

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