Author Correction: Hydrogen Sulfide Recruits Macrophage Migration by Integrin β1-Src-FAK/Pyk2-Rac Pathway in Myocardial Infarction (Scientific Reports, (2016), 6, 1, (22363), 10.1038/srep22363);Hydrogen sulfide recruits macrophage migration by integrin β1-Src-FAK/Pyk2-rac pathway in myocardial infarction

Scientific Reports

Volumn 6, Issue , 2016, Pages

  Miao, Lei ^a   Xin, Xiaoming ^a   Xin, Hong ^a   Shen, Xiaoyan ^a   Zhu, Yi Zhun ^a,b  

^a FUDAN UNIVERSITY   (China)

^b MACAU UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Macao)

Author keywords

[No Author keywords available]

Indexed keywords

BETA1 INTEGRIN; CYSTATHIONINE GAMMA LYASE; FOCAL ADHESION KINASE 2; HYDROGEN SULFIDE; PROTEIN TYROSINE KINASE; PTK2B PROTEIN, MOUSE; RAC1 PROTEIN;

ANIMAL; CARDIAC MUSCLE CELL; CELL HYPOXIA; CELL MOTION; CYTOLOGY; DRUG EFFECTS; ENDOCYTOSIS; GENE SILENCING; HEART INFARCTION; KNOCKOUT MOUSE; MACROPHAGE; METABOLISM; MOUSE; PATHOLOGY; RAW 264.7 CELL LINE; SIGNAL TRANSDUCTION;

ANIMALS; ANTIGENS, CD29; CELL HYPOXIA; CELL MOVEMENT; CYSTATHIONINE GAMMA-LYASE; ENDOCYTOSIS; FOCAL ADHESION KINASE 2; GENE SILENCING; HYDROGEN SULFIDE; MACROPHAGES; MICE; MICE, KNOCKOUT; MYOCARDIAL INFARCTION; MYOCYTES, CARDIAC; RAC1 GTP-BINDING PROTEIN; RAW 264.7 CELLS; SIGNAL TRANSDUCTION; SRC-FAMILY KINASES;

EID: 84959538617     PISSN: None     EISSN: 20452322     Source Type: Journal    
DOI: 10.1038/s41598-022-06168-w     Document Type: Erratum

References (48)

1. Downey, J. M. & Cohen, M. V. Why do we still not have cardioprotective drugs?. Circ. J. 73, 1171-1177 (2009).
2. Lambert, J. M., Lopez, E. F. & Lindsey, M. L. Macrophage roles following myocardial infarction. Int. J. Cardiol. 130, 147-158 (2008).
3. Frantz, S., et al. Monocytes/macrophages prevent healing defects and left ventricular thrombus formation after myocardial infarction. FASEB J. 27, 871-881 (2013).
4. Weinberger, T. & Schulz, C. Myocardial infarction: a critical role of macrophages in cardiac remodeling. Front. Physiol. 6, 107 (2015).
5. Nahrendorf, M., et al. The healing myocardium sequentially mobilizes two monocyte subsets with divergent and complementary functions. J. Exp. Med. 204, 3037-3047 (2007).
6. Schultze, J. L., Schmieder, A. & Goerdt, S. Macrophage activation in human diseases. Semin. Immunol. 27, 249-56 (2015).
7. Sutton, M. G. & Sharpe, N. Left ventricular remodeling after myocardial infarction: pathophysiology and therapy. Circulation 101, 2981-2988 (2000).
8. Nahrendorf, M. & Swirski, F. K. Monocyte and macrophage heterogeneity in the heart. Circ. Res. 112, 1624-1633 (2013).
9. Van Amerongen, M. J., Harmsen, M. C., Van Rooijen, N., Petersen, A. H. & Van Luyn, M. J. Macrophage depletion impairs wound healing and increases left ventricular remodeling after myocardial injury in mice. Am. J. Pathol. 170, 818-829 (2007).
10. Leor, J., et al. Ex vivo activated human macrophages improve healing, remodeling, and function of the infarcted heart. Circulation 114, I94-100 (2006).
11. Qipshidze, N., Metreveli, N., Mishra, P. K., Lominadze, D. & Tyagi, S. C. Hydrogen sulfide mitigates cardiac remodeling during myocardial infarction via improvement of angiogenesis. Int. J. Biol. Sci. 8, 430-441 (2012).
12. Shen, Y., Shen, Z., Luo, S., Guo, W. & Zhu, Y. Z. The Cardioprotective Effects of Hydrogen Sulfide in Heart Diseases: From Molecular Mechanisms to Therapeutic Potential. Oxid. Med. Cell Longev. 2015, 925167 (2015).
13. Pan, L. L., Liu, X. H., Gong, Q. H., Yang, H. B. & Zhu, Y. Z. Role of cystathionine gamma-lyase/hydrogen sulfide pathway in cardiovascular disease: a novel therapeutic strategy?. Antioxid. Redox Signal. 17, 106-118 (2012).
14. Calvert, J. W., Coetzee, W. A. & Lefer, D. J. Novel insights into hydrogen sulfide-mediated cytoprotection. Antioxid. Redox Signal. 12, 1203-1217 (2010).
15. Wang, Y., et al. Role of hydrogen sulfide in the development of atherosclerotic lesions in apolipoprotein E knockout mice. Arterioscler. Thromb. Vasc. Biol. 29, 173-179 (2009).
16. Chuah, S. C., Moore, P. K. & Zhu, Y. Z. S-allylcysteine mediates cardioprotection in an acute myocardial infarction rat model via a hydrogen sulfide-mediated pathway. Am. J. Physiol. Heart Circ. Physiol. 293, H2693-2701 (2007).
17. Zhu, Y. Z., et al. Hydrogen sulfide and its possible roles in myocardial ischemia in experimental rats. J. Appl. Physiol. 102, 261-268 (2007).
18. Huang, C., et al. Cardioprotective effects of a novel hydrogen sulfide agent-controlled release formulation of S-propargyl-cysteine on heart failure rats and molecular mechanisms. PloS one 8, e69205 (2013).
19. Kan, J., et al. S-propargyl-cysteine, a novel water-soluble modulator of endogenous hydrogen sulfide, promotes angiogenesis through activation of signal transducer and activator of transcription 3. Antioxid. Redox Signal. 20, 2303-2316 (2014).
20. Polhemus, D. J., Calvert, J. W., Butler, J. & Lefer, D. J. The cardioprotective actions of hydrogen sulfide in acute myocardial infarction and heart failure. Scientifica (Cairo) 2014, 768607 (2014).
21. Zhang, X., Goncalves, R. & Mosser, D. M. The isolation and characterization of murine macrophages. Curr. Protoc. Immunol. Chapter 14, Unit 14 (2008).
22. Weischenfeldt, J. & Porse, B. Bone Marrow-Derived Macrophages (BMM): Isolation and Applications. CSH Protoc. 2008, pdb prot5080 (2008).
23. Wang, G. W., Schuschke, D. A. & Kang, Y. J. Metallothionein-overexpressing neonatal mouse cardiomyocytes are resistant to H2O2toxicity. Am. J. Physiol. 276, H167-175 (1999).
24. Rakhit, R. D., et al. Nitric oxide-induced cardioprotection in cultured rat ventricular myocytes. Am. J. Physiol. Heart Circ. Physiol. 278, H1211-1217 (2000).
25. Van Buul, J. D., Anthony, E. C., Fernandez-Borja, M., Burridge, K. & Hordijk, P. L. Proline-rich tyrosine kinase 2 (Pyk2) mediates vascular endothelial-cadherin-based cell-cell adhesion by regulating beta-catenin tyrosine phosphorylation. J. Biol. Chem. 280, 21129-21136 (2005).
26. Owen, K. A., et al. Regulation of lamellipodial persistence, adhesion turnover, and motility in macrophages by focal adhesion kinase. J. Cell Biol. 179, 1275-1287 (2007).
27. Rossello, X., Pocock, S. J. & Julian, D. G. Long-Term Use of Cardiovascular Drugs: Challenges for Research and for Patient Care. J. Am. Coll. Cardiol. 66, 1273-1285 (2015).
28. Kain, V. & Halade, G. V. Big eater macrophages dominate inflammation resolution following myocardial infarction. J. Mol. Cell. Cardiol. 87, 225-227 (2015).
29. Nahrendorf, M. & Swirski, F. K. Innate immune cells in ischaemic heart disease: does myocardial infarction beget myocardial infarction?. Eur. Heart J. [Epub ahead of print] (2015).
30. Li, X., et al. Myocardial injury after ischemia-reperfusion in mice deficient in Akt2 is associated with increased cardiac macrophage density. Am. J. Physiol. Heart Circ. Physiol. 301, H1932-1940 (2011).
31. Cha, S. J., et al. CD68 acts as a major gateway for malaria sporozoite liver infection. J. Exp. Med. 212, 1391-1403 (2015).
32. Nagai, T., et al. Decreased myocardial dendritic cells is associated with impaired reparative fibrosis and development of cardiac rupture after myocardial infarction in humans. J. Am. Heart Assoc. 3, e000839 (2014).
33. Frangogiannis, N. G. Regulation of the inflammatory response in cardiac repair. Circ. Res. 110, 159-173 (2012).
34. Mann, D. L. The emerging role of innate immunity in the heart and vascular system: for whom the cell tolls. Circ. Res. 108, 1133-1145 (2011).
35. Liehn, E. A., Postea, O., Curaj, A. & Marx, N. Repair after myocardial infarction, between fantasy and reality: the role of chemokines. J. Am. Coll. Cardiol. 58, 2357-2362 (2011).
36. Frangogiannis, N. G. The mechanistic basis of infarct healing. Antioxid. Redox Signal. 8, 1907-1939 (2006).
37. Caswell, P. T. & Norman, J. C. Integrin trafficking and the control of cell migration. Traffic 7, 14-21 (2006).
38. Lee, H. D., Kim, Y. H. & Kim, D. S. Exosomes derived from human macrophages suppress endothelial cell migration by controlling integrin trafficking. Eur. J. Immunol. 44, 1156-1169 (2014).
39. Tanimizu, N., Kikkawa, Y., Mitaka, T. & Miyajima, A. alpha1- and alpha5-containing laminins regulate the development of bile ducts via beta1 integrin signals. J. Biol. Chem. 287, 28586-28597 (2012).
40. Panicker, A. K., Buhusi, M., Erickson, A. & Maness, P. F. Endocytosis of beta1 integrins is an early event in migration promoted by the cell adhesion molecule L1. Exp. Cell Res. 312, 299-307 (2006).
41. Cera, M. R., et al. JAM-A promotes neutrophil chemotaxis by controlling integrin internalization and recycling. J. Cell Sci. 122, 268-277 (2009).
42. Maa, M. C., et al. Requirement of inducible nitric-oxide synthase in lipopolysaccharide-mediated Src induction and macrophage migration. J. Biol. Chem. 283, 31408-31416 (2008).
43. Thapa, B., Koo, B. H., Kim, Y. H., Kwon, H. J. & Kim, D. S. Plasminogen activator inhibitor-1 regulates infiltration of macrophages into melanoma via phosphorylation of FAK-Tyr(9)(2)(5). Biochem. Biophys. Res. Commun. 450, 1696-1701 (2014).
44. Mitra, S. K., Hanson, D. A. & Schlaepfer, D. D. Focal adhesion kinase: in command and control of cell motility. Nat. Rev. Mol. Cell Biol. 6, 56-68 (2005).
45. Liu, Z., et al. The influence of chitosan hydrogel on stem cell engraftment, survival and homing in the ischemic myocardial microenvironment. Biomaterials 33, 3093-3106 (2012).
46. Kamen, L. A., Schlessinger, J. & Lowell, C. A. Pyk2 is required for neutrophil degranulation and host defense responses to bacterial infection. J. Immunol. 186, 1656-1665 (2011).
47. Rhee, I., Davidson, D., Souza, C. M., Vacher, J. & Veillette, A. Macrophage fusion is controlled by the cytoplasmic protein tyrosine phosphatase PTP-PEST/PTPN12. Mol. Cell. Biol. 33, 2458-2469 (2013).
48. Aflaki, E., et al. Impaired Rho GTPase activation abrogates cell polarization and migration in macrophages with defective lipolysis. Cell. Mol. Life Sci. 68, 3933-3947 (2011).