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BioMed Research International
Volume 2014 (2014), Article ID 945127, 8 pages
Roles of Bone-Marrow-Derived Cells and Inflammatory Cytokines in Neointimal Hyperplasia after Vascular Injury
Department of Medicine, Division of Cardiology, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa-ku,
Tokyo 142-8555, Japan
Received 4 October 2013; Revised 22 November 2013; Accepted 21 December 2013; Published 14 January 2014
Academic Editor: Yoshitaka Iso
Copyright © 2014 Makoto Shoji et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
- R. Ross, “The pathogenesis of atherosclerosis: a perspective for the 1990s,” Nature, vol. 362, no. 6423, pp. 801–809, 1993.
- R. Ross, “Atherosclerosis—an inflammatory disease,” The New England Journal of Medicine, vol. 340, no. 2, pp. 115–126, 1999.
- A. Saiura, M. Sata, Y. Hirata, R. Nagai, and M. Makuuchi, “Circulating smooth muscle progenitor cells contribute to atherosclerosis,” Nature Medicine, vol. 7, no. 5, pp. 382–383, 2001.
- M. Sata, A. Saiura, A. Kunisato et al., “Hematopoietic stem cells differentiate into vascular cells that participate in the pathogenesis of atherosclerosis,” Nature Medicine, vol. 8, no. 4, pp. 403–409, 2002.
- J. E. Rectenwald, L. L. Moldawer, T. S. Huber, J. M. Seeger, and C. K. Ozaki, “Direct evidence for cytokine involvement in neointimal hyperplasia,” Circulation, vol. 102, no. 14, pp. 1697–1702, 2000.
- R. S. Schwartz and T. D. Henry, “Pathophysiology of coronary artery restenosis,” Reviews in Cardiovascular Medicine, vol. 3, no. 5, pp. S4–S9, 2002.
- I. M. Van Der Meer, M. P. M. De Maat, M. L. Bots et al., “Inflammatory mediators and cell adhesion molecules as indicators of severity of atherosclerosis: the rotterdam study,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 22, no. 5, pp. 838–842, 2002.
- M. Shoji, M. Sata, D. Fukuda et al., “Temporal and spatial characterization of cellular constituents during neointimal hyperplasia after vascular injury: potential contribution of bone-marrow-derived progenitors to arterial remodeling,” Cardiovascular Pathology, vol. 13, no. 6, pp. 306–312, 2004.
- M. Dominici, K. Le Blanc, I. Mueller et al., “Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement,” Cytotherapy, vol. 8, no. 4, pp. 315–317, 2006.
- D. G. Phinney and D. J. Prockop, “Concise review: Mesenchymal stem/multipotent stromal cells: the state of transdifferentiation and modes of tissue repair—current views,” Stem Cells, vol. 25, no. 11, pp. 2896–2902, 2007.
- D. T. Scadden, “The stem-cell niche as an entity of action,” Nature, vol. 441, no. 7097, pp. 1075–1079, 2006.
- T. M. Dexter, P. Simmons, R. A. Purnell, E. Spooncer, and R. Schofield, “The regulation of hemopoietic cell development by the stromal cell environment and diffusible regulatory molecules,” Progress in clinical and biological research, vol. 148, pp. 13–33, 1984.
- A. Wilson and A. Trumpp, “Bone-marrow haematopoietic-stem-cell niches,” Nature Reviews Immunology, vol. 6, no. 2, pp. 93–106, 2006.
- H. Kawada, J. Fujita, K. Kinjo et al., “Nonhematopoietic mesenchymal stem cells can be mobilized and differentiate into cardiomyocytes after myocardial infarction,” Blood, vol. 104, no. 12, pp. 3581–3587, 2004.
- D. J. Prockop, “Marrow stromal cells as stem cells for nonhematopoietic tissues,” Science, vol. 276, no. 5309, pp. 71–74, 1997.
- D. J. Prockop, C. A. Gregory, and J. L. Spees, “One strategy for cell and gene therapy: harnessing the power of adult stem cells to repair tissues,” Proceedings of the National Academy of Sciences of the United States of America, vol. 100, no. 1, pp. 11917–11923, 2003.
- C. K. Hashi, Y. Zhu, G.-Y. Yang et al., “Antithrombogenic property of bone marrow mesenchymal stem cells in nanofibrous vascular grafts,” Proceedings of the National Academy of Sciences of the United States of America, vol. 104, no. 29, pp. 11915–11920, 2007.
- X. Wu, L. Huang, Q. Zhou et al., “Mesenchymal stem cells participating in ex vivo endothelium repair and its effect on vascular smooth muscle cells growth,” International Journal of Cardiology, vol. 105, no. 3, pp. 274–282, 2005.
- M. Shoji, A. Oskowitz, C. D. Malone, D. J. Prockop, and R. Pochampally, “Human mesenchymal stromal cells (MSCs) reduce neointimal hyperplasia in a mouse model of flow-restriction by transient suppression of anti-inflammatory cytokines,” Journal of Atherosclerosis and Thrombosis, vol. 18, no. 6, pp. 464–474, 2011.
- J. Kitagawa, T. Hara, H. Tsurumi et al., “Cell cycle-dependent priming action of granulocyte colony-stimulating factor (G-CSF) enhances in vitro apoptosis induction by cytarabine and etoposide in leukemia cell lines,” Journal of Clinical and Experimental Hematopathology, vol. 50, no. 2, pp. 99–105, 2010.
- D. Orlic, J. Kajstura, S. Chimenti et al., “Mobilized bone marrow cells repair the infarcted heart, improving function and survival,” Proceedings of the National Academy of Sciences of the United States of America, vol. 98, no. 18, pp. 10344–10349, 2001.
- S. Minatoguchi, G. Takemura, X.-H. Chen et al., “Acceleration of the healing process and myocardial regeneration may be important as a mechanism of improvement of cardiac function and remodeling by postinfarction granulocyte colony-stimulating factor treatment,” Circulation, vol. 109, no. 21, pp. 2572–2580, 2004.
- Y. Maekawa, T. Anzai, T. Yoshikawa et al., “Effect of granulocyte-macrophage colony-stimulating factor inducer on left ventricular remodeling after acute myocardial infarction,” Journal of the American College of Cardiology, vol. 44, no. 7, pp. 1510–1520, 2004.
- K. C. Wollert, G. P. Meyer, J. Lotz et al., “Intracoronary autologous bone-marrow cell transfer after myocardial infarction: the BOOST randomised controlled clinical trial,” The Lancet, vol. 364, no. 9429, pp. 141–148, 2004.
- K. Suzuki, K. Nagashima, M. Arai et al., “Effect of granulocyte colony-stimulating factor treatment at a low dose but for a long duration in patients with coronary heart disease—a pilot study,” Circulation Journal, vol. 70, no. 4, pp. 430–437, 2006.
- H. Hasegawa, H. Takano, H. Shiraishi et al., “Intracoronary injection of granulocyte colony-stimulating factor ameliorates the progression of left ventricular remodeling after myocardial ischemia/reperfusion in rabbits,” Circulation Journal, vol. 70, no. 7, pp. 942–944, 2006.
- D. Kong, L. G. Melo, M. Gnecchi et al., “Cytokine-induced mobilization of circulating endothelial progenitor cells enhances repair of injured arteries,” Circulation, vol. 110, no. 14, pp. 2039–2046, 2004.
- I. Flamme and W. Risau, “Induction of vasculogenesis and hematopoiesis in vitro,” Development, vol. 116, no. 2, pp. 435–439, 1992.
- A. Kawamoto and T. Asahara, “Role of progenitor endothelial cells in cardiovascular disease and upcoming therapies,” Catheterization and Cardiovascular Interventions, vol. 70, no. 4, pp. 477–484, 2007.
- M. Shoji, Y. Iso, T. Kusuyama et al., “High-dose granulocyte-colony stimulating factor promotes neointimal hyperplasia in the early phase and inhibits neointimal hyperplasia in the late phase after vascular injury,” Circulation Journal, vol. 72, no. 11, pp. 1885–1893, 2008.
- M. Kopf, H. Baumann, G. Freer et al., “Impaired immune and acute-phase responses in interleukin-6-deficient mice,” Nature, vol. 368, no. 6469, pp. 339–342, 1994.
- M. Takaoka, H. Suzuki, S. Shioda et al., “Endovascular injury induces rapid phenotypic changes in perivascular adipose tissue,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 30, no. 8, pp. 1576–1582, 2010.
- T. Oguro, Y. Takahashi, T. Ashino et al., “Involvement of tumor necrosis factor α, rather than interleukin-1α/β or nitric oxides in the heme oxygenase-1 gene expression by lipopolysaccharide in the mouse liver,” FEBS Letters, vol. 516, no. 1–3, pp. 63–66, 2002.
- H. Yang, M. Li, H. Chai et al., “Expression and regulation of neuropilins and VEGF receptors by TNF-α in human endothelial cells,” Journal of Surgical Research, vol. 122, no. 2, pp. 249–255, 2004.
- M. Shibata, H. Sueki, H. Suzuki et al., “Impaired contact hypersensitivity reaction and reduced production of vascular endothelial growth factor in tumor necrosis factor-α gene-deficient mice,” Journal of Dermatology, vol. 32, no. 7, pp. 523–533, 2005.
- A. Ozkok, E. Aktas, A. Yilmaz et al., “Decrease in endothelial progenitor cells associated with inflammation, but not with endothelial dysfunction in chronic hemodialysis patients,” Clinical Nephrology, vol. 79, pp. 21–30, 2013.
- H. Iwata, I. Manabe, K. Fujiu et al., “Bone marrow-derived cells contribute to vascular inflammation but do not differentiate into smooth muscle cell lineages,” Circulation, vol. 122, no. 20, pp. 2048–2057, 2010.
- J. Aoki, P. W. Serruys, H. Van Beusekom et al., “Endothelial progenitor cell capture by stents coated with antibody against CD34: the HEALING-FIM (Healthy Endothelial Accelerated Lining Inhibits Neointimal Growth-First in Man) registry,” Journal of the American College of Cardiology, vol. 45, no. 10, pp. 1574–1579, 2005.
- S. Silber, P. Damman, M. Klomp et al., “Clinical results after coronary stenting with the Genous bio-engineered R stent: 12-month outcomes of the e-HEALING (Healthy Endothelial Accelerated Lining Inhibits Neointimal Growth) worldwide registry,” EuroIntervention, vol. 6, no. 7, pp. 819–825, 2011.
- X. Wu, G. Wang, C. Tang et al., “Mesenchymal stem cell seeding promotes reendothelialization of the endovascular stent,” Journal of Biomedical Materials Research A, vol. 98, no. 3, pp. 442–449, 2011.