Stromal cell-derived factor-1 and CXCR4 interaction is critical for development of transplant arteriosclerosis

Circulation

Volumn 110, Issue 18, 2004, Pages 2924-2930

  Sakihama, Hideyasu ^a,b   Masunaga, Taro ^a   Yamashita, Kenichiro ^b   Hashimoto, Taku ^b   Inobe, Manabu ^a   Todo, Satoru ^b   Uede, Toshimitsu ^a  

^a HOKKAIDO UNIVERSITY   (Japan)

^b HOKKAIDO UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

Author keywords

Arteriosclerosis; Rejection; Stem cells; Transplantation

Indexed keywords

CD11B ANTIGEN; CD3 ANTIGEN; CD45 ANTIGEN; CHEMOKINE RECEPTOR CXCR4; MESSENGER RNA; STEM CELL FACTOR RECEPTOR; STROMAL CELL DERIVED FACTOR 1;

ADVENTITIA; ALLOGRAFT; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; AORTA GRAFT; ARTERIOSCLEROSIS; ARTICLE; CELL DIFFERENTIATION; CELL MIGRATION; CONTROLLED STUDY; DIFFERENTIAL DISPLAY; DNA SEQUENCE; GENE EXPRESSION; GRAFT REJECTION; HEMATOPOIETIC STEM CELL; INTIMA; MICROVASCULATURE; MOUSE; NONHUMAN; PRIORITY JOURNAL; REAL TIME POLYMERASE CHAIN REACTION; TRANSPLANT ARTERIOSCLEROSIS; VASCULAR SMOOTH MUSCLE;

ANIMALS; AORTA, THORACIC; AORTIC DISEASES; ARTERIOSCLEROSIS; CELL DIFFERENTIATION; CELL LINEAGE; CHEMOKINES, CXC; GENE EXPRESSION PROFILING; HEMATOPOIETIC STEM CELL MOBILIZATION; HEMATOPOIETIC STEM CELLS; MICE; MICE, INBRED BALB C; MICE, INBRED C3H; MICE, INBRED C57BL; MICE, INBRED ICR; POSTOPERATIVE COMPLICATIONS; RECEPTORS, CXCR4; TRANSPLANTATION, HOMOLOGOUS; TUNICA INTIMA; TUNICA MEDIA; UP-REGULATION;

EID: 8144225160     PISSN: 00097322     EISSN: None     Source Type: Journal    
DOI: 10.1161/01.CIR.0000146890.93172.6C     Document Type: Article

References (27)

1. Libby P, Pober JS. Chronic rejection. Immunity. 2001;14:387-397.
2. Waaga AM, Gasser M, Laskowski I, et al. Mechanisms of chronic rejection. Curr Opin Immunol. 2000;12:517-521.
3. Tilney NL, Guttmann RD. Effects of initial ischemia/reperfusion injury on the transplanted kidney. Transplantation. 1997;64:945-947.
4. Isik FF, McDonald TO, Ferguson M, et al. Transplant arteriosclerosis in a rat aortic model. Am J Pathol 1992;141:1139-1149.
5. Hillebrands J, van den Hurk BM, Klatter FA, et al. Recipient origin of neointimal vascular smooth muscle cells in cardiac allografts with transplant arteriosclerosis. J Heart Lung Transplant. 2000;19:1183-1192.
6. Shimizu K, Sugiyama S, Aikawa M, et al. Host bone-marrow cells are a source of donor intimal smooth-muscle-like cells in murine aortic transplant arteriopathy. Nat Med. 2001;7:738-741.
7. Sata M, Saiura A, Kunisato A, et al. Hematopoietic stem cells differentiate into vascular cells that participate in the pathogenesis of atherosclerosis. Nat Med. 2002;8:403-409.
8. Hu Y, Davison F, Ludewig B, et al. Smooth muscle cells in transplant atherosclerotic lesions are originated from recipients, but not bone marrow progenitor cells. Circulation. 2002;106:1834-1839.
9. Sun H, Valdivia LA, Subbotin V, et al. Improved surgical technique for the establishment of a murine model of aortic transplantation. Microsurgery. 1998;18:368-371.
10. Liang P, Pardee AB. Differential display of eukaryotic messenger RNA by means of the polymerase chain reaction. Science. 1992;257:967-971.
11. Chamley-Campbell J, Campbell GR, Ross R. The smooth muscle cell in culture. Physiol Rev. 1979;59:1-61.
12. Rajeevan MS, Ranamukhaarachchi DG, Vernon SD, et al. Use of real-time quantitative PCR to validate the results of cDNA array and differential display PCR technologies. Methods. 2001;25:443-451.
13. Salcedo R, Wasserman K, Young HA, et al. Vascular endothelial growth factor and basic fibroblast growth factor induce expression of CXCR4 on human endothelial cells: in vivo neovascularization induced by stromal-derived factor-1 alpha. Am J Pathol. 1999;154:1125-1135.
14. Mirshahi F, Pourtau J, Li H, et al. SDF-1 activity on microvascular endothelial cells: consequences on angiogenesis in in vitro and in vivo models. Thromb Res. 2000;99:587-594.
15. Abi-Younes S, Sauty A, Mach F, et al. The stromal cell-derived factor-1 chemokine is a potent platelet agonist highly expressed in atherosclerotic plaques. Circ Res. 2000;86:131-138.
16. Tachibana K, Hirota S, Iizasa H, et al. The chemokine receptor CXCR4 is essential for vascularization of the gastrointestinal tract. Nature. 1998;393:591-594.
17. Nagasawa T, Hirota S, Tachibana K, et al. Defects of B-cell lymphopoiesis and bone-marrow myelopoiesis in mice lacking the CXC chemokine PBSF/SDF-1. Nature. 1996;382:635-638.
18. Nagasawa T, Kikutani H, Kishimoto T. Molecular cloning and structure of a pre-B-cell growth-stimulating factor. Proc Natl Acad Sci U S A. 1994;91:2305-2309.
19. Aiuti A, Webb IJ, Bleul C, et al. The chemokine SDF-1 is a chemoattractant for human CD34+ hematopoietic progenitor cells and provides a new mechanism to explain the mobilization of CD34+ progenitors to peripheral blood. J Exp Med. 1997;185:111-120.
20. Hattori K, Heissig B, Tashiro K, et al. Plasma elevation of stromal cell-derived factor-1 induces mobilization of mature and immature hematopoietic progenitor and stem cells. Blood. 2001;97:3354-3360.
21. Shen H, Cheng T, Olszak I, et al. CXCR-4 desensitization is associated with tissue localization of hemopoietic progenitor cells. J Immunol. 2001;166:5027-5033.
22. Melter M, Exeni A, Reinders ME, et al. Expression of the chemokine receptor CXCR3 and its ligand IP-10 during human cardiac allograft rejection. Circulation. 2001;104:2558-2564.
23. Gao W, Faia KL, Csizmadia V, et al. Beneficial effects of targeting CCR5 in allograft recipients. Transplantation. 2001;72:1199-1205.
24. Bleul CC, Fuhlbrigge RC, Casasnovas JM, et al. A highly efficacious lymphocyte chemoattractant, stromal cell-derived factor 1 (SDF-1). J Exp Med. 1996;184:1101-1109.
25. Gupta SK, Pillarisetti K, Lysko PG. Modulation of CXCR4 expression and SDF-1 alpha functional activity during differentiation of human monocytes and macrophages. J Leukocyte Biol. 1999;66:135-143.
26. Bhattacharya V, McSweeney PA, Shi Q, et al. Enhanced endothelialization and microvessel formation in polyester grafts seeded with CD34(+) bone marrow cells. Blood. 2000;95:581-585.
27. Kollet O, Shivtiel S, Chen YQ, et al. HGF, SDF-1, and MMP-9 are involved in stress-induced human CD34+ stem cell recruitment to the liver. J Clin Invest. 2003;112:160-169.