Nacházíte se zde: Úvod > Journal of Applied Biomedicine > 9_3 > fang9_3.htm

fang9_3.htm

ISSN 1214-0287 (on-line), ISSN 1214-021X (printed)
J Appl Biomed
Volume 9 (2011) No 3, p 129-141
DOI 10.2478/v10136-011-0001-8

Effects of SDF-1alpha/CXCR4 on vascular smooth muscle cells and bone marrow mesenchymal cells in a rat carotid artery balloon injury model

Wen-Wei Cai, Ning-Yuan Fang, Jing Sheng, Shao-Jun Ma, Zhi-Hui Chen

Address: Ning-Yuan Fang, No. 639, Zhi-Zao-Ju Road, Shanghai 200011, P. R. China
funfeng111@gmail.com

Received 20th December 2010.
Revised 10th February 2011.
Published online 7th April 2011.

Full text article (pdf)
Full text article (html)

SUMMARY
Bone marrow mensenchyme cells(BMSCs) can differentiate into endothelial progenitor cells which then migrate to injured sites for the repair of neointima, and stromal cell-derived factor-1alpha (SDF-1alpha) can mediate the migration of CXCR4 expressing stem/progenitor cells to injured sites for repair. Protein and mRNA expression of SDF-1alpha and CXCR4 were determined by RT-PCR, Western blot and ELISA. Immediately after common carotid artery balloon injury, the mRNA expression of SDF-1alpha in vascular smooth muscle cells(VSMCs) first increased and then decreased 7 days later. VSMCs transfected with SDF-1alpha siRNA did not express SDF-1alpha mRNA, but after transfection with SDF-1alpha siRNA, the SDF-1alpha content in injured VSMCs gradually returned to the baseline level. Normal BMSCs rarely expressed CXCR4 mRNA, but the CXCR4 mRNA expression on BMSCs increased significantly 4 days after common carotid artery injury and was maintained. The migration of BMSCs after artery injury was enhanced when compared with normal BMSCs, but SDF-1alpha siRNA transfection of VSMCs and AMD3100 treatment remarkably decreased the chemotaxis of BMSCs to VSMCs and SDF-1alpha, respectively. We conclude that the SDF-1alpha/CXCR4 axis plays an important role in the migration of BMSCs after balloon injury and can ultimately cause abnormal proliferation of the intima.

KEY WORDS
bone marrow mensenchyme cells; vascular smooth muscle cells; stromal cell-derived factor-1alpha

REFERENCES
Amara A, Lorthioir O, Valenzuela A, Magerus A, Thelen M, Montes M, Virelizier JL, Delepierre M, Baleux F, Lortat-Jacob H, Arenzana-Seisdedos F. Stromal cell-derived factor-1 associates with heparin sulfates through the first beta-strand of the chemokine. J Biol Chem. 274: 23916-23925, 1999.
[CrossRef]

Anderson DM, Lyman SD, Baird A, Wignall JM, Eisenman J, Rauch C, March CJ, Boswell HS, Gimpel SD, Cosman D. Molecular cloning of mast cell growth factor, a hematopoietin that is active in both membrane bound and soluble forms. Cell. 63: 235-243, 1990.
[CrossRef]

Asahara T, Murohara T, Sullivan A, Silver M, van der Zee R, Li T, Witzenbichler B, Schatteman G, Isner JM. Isolation of putative progenitor endothelial cells for angiogenesis. Science. 275: 964-966, 1997.
[CrossRef]

Asahara T, Takahashi T, Masuda H, Kalka C, Chen D, Iwaguro H, Inai Y, Silver M, Isner JM. VEGF contributes to postnatal neovascularization by mobilizing bone marrow-derived endothelial progenitor cells. EMBO J. 18: 3964-3972, 1999.
[CrossRef]

Barry FP, Murphy JM. Mesenchymal stem cells: clinical applications and biological characterization. Int J Biochem Cell Biol. 36: 568-584, 2004.
[CrossRef]

Bochaton-Piallat ML, Ropraz P, Gabbiani F, Gabbiani G. Phenotypic heterogeneity of rat arterial smooth muscle cell clones. Implications for the development of experimental intimal thickening. Arterioscler Thromb Vasc Biol. 16: 815-820, 1996.
[CrossRef]

Dowell JD, Rubart M, Pasumarthi KB, Soonpaa MH, Field LJ. Myocyte and myogenic stem cell transplantation in the heart. Cardiovasc Res. 58: 336-350, 2003.
[CrossRef]

Feng Y, Broder CC, Kennedy PE. HIV-1 entry co-factor: functional cDNA cloning of a seven-transmemberane, G protein-coupled receptor. Science. 272: 872, 1996.
[CrossRef]

Fibbe WE, Pruijt JF, von Kooyk Y. The role of metalloproteinases and adhesion molecules in interleukine-8-induced stem-cell mobilization. Semin Hematol. 37: 19-24, 2000.
[CrossRef]

Folkman J, Shing Y. Angiogenesis. J Biol Chem. 267: 10931-10934, 1992.

Gao C, Li Y. SDF-1 plays a key role in the repairing and remodeling process on rat allo-orthotopic abdominal aorta grafts. Transplant Proc. 39: 268-272, 2007.
[CrossRef]

Gleichmann M, Gillen C, Czardybon M, Bosse F, Greiner-Petter R, Auer J, Muller HW. Cloning and characterization of SDF-1gamma, a novel SDF-1 chemokine transcript with developmentally regulated expression in the nervous system. Eur J Neurosci. 12: 1857-1866, 2000.
[CrossRef]

Hattori K, Heissig B, Tashiro K, Honjo T, Tateno M, Shieh JH, Hackett NR, Quitoriano MS, Crystal RG, Rafii S, Moore MA. Plasma elevation of stromal cell-derived factor-1 induces mobilization of mature and immature hematopoietic progenitor and stem cells. Blood. 97: 3354-3360, 2000.
[CrossRef]

Hattori K, Dias S, Heissig B, Hackett NR, Lyden D, Tateno M, Hicklin DJ, Zhu Z, Witte L, Crystal RG, Moore MA, Rafii S. Vascular endothelial growth factor and angiopoitin-1 stimulate postnatal hematopoiesis by recruitment of vasculogenic and hematopoietic stem cells. J Exp Med. 193: 1005-1014, 2001.
[CrossRef]

Kucia M, Dawn B, Hunt G, Guo Y, Wysoczynski M, Majka M, Ratajczak J, Rezzoug F, Ildstad ST, Bolli R, Ratajczak MZ. Cells expressing early cardiac markers reside in the bone marrow and are mobilized into the peripheral blood after myocardial infarction. Circ Res. 95: 1191-1199, 2004a.
[CrossRef]

Kucia M, Jankowski K, Reca R, Wysoczynski M, Bandura L, Allendorf DJ, Zhang J, Ratajczak J, Ratajczak MZ. CXCR4-SDF-1 signaling, locomotion, chemotaxis and adhesion. J Mol Histol. 35: 233-245, 2004b.
[CrossRef]

Lapidot T, Petit I. Current understanding of stem cell mobilization: the roles of chemokines, proteolytic enzymes, adhesion molecules, cytokines, and stromal cells. Exp Hematol. 30: 973, 2002.
[CrossRef]

Laterveer L, Lindley IJ, Hamilton MS, Willemze R, Fibbe WE. Interleukin-8 induces rapid mobilization of hematopoietic stem cells with radioprotective capacity and long-term myelolymphoid repopulating ability. Blood. 85: 2269-2275, 1995.

Law RE, Meehan WP, Xi XP, Graf K, Wuthrich DA, Coats W, Faxon D, Hsueh WA. Troglitazone inhibits vascular smooth muscle cell growth and intimal hyperplasia. J Clin Invest. 98: 1897-1905, 1996.
[CrossRef]

Loetscher M, Geiser T, O’Reilly T, Zwahlen R, Baggiolini M, Moser B. Cloning of a human seven-transmembrane domain receptor, LESTR, that is highly expressed in leukocytes. J Biol Chem. 269: 232, 1994.

Mathur A, Martin JF. Stem cells and repair of the heart. Lancet. 364: 183-192, 2004.
[CrossRef]

Metcalf D, Nicola NA. Proliferative effects of purified granulocyte colony-stimulating factor, G-CSF on normal mouse hemopoietic cells. J Cell Physiol. 16: 198-206, 1983.
[CrossRef]

Minguell JJ, Erices A, Conget P. Mesechymal stem cells. Exp Biol Med. 226, 6: 507-552, 2001.

Misao Y, Takemura G, Arai M, Ohno T, Onogi H, Takahashi T, Minatoguchi S, Fujiwara T, Fujiwara H. Importance of recruitment of bone marrow-derived CXCR4+ cells in post-infarct cardiac repair mediated by G-CSF. Cardiovasc Res. 71: 455-465, 2006.
[CrossRef]

Moore MA, Hattori K, Heissig B, Shieh JH, Dias S, Crystal RG, Rafii S. Mobilization of endothelial and hematopoietic stem and progenitor cells by adenovector-mediated elevation of serum levels of SDF-1, VEGF, and angiopoietin-1. Ann NY Acad Sci. 938: 36-45, 2001.
[CrossRef]

Orlic D, Hill JM, Arai AE. Stem cells for myocardial regeneration. Circ Res. 91: 1092-1102, 2002.
[CrossRef]

Papayannopoulou T. Mechanisms of stem-/progenitor-cell mobilization: The anti-VLA-4 paradigm. Semin Hematol. 37 (Suppl. 2): 11-18, 2000.
[CrossRef]

Paul S, Steven N. Understanding coronary artery disease: Tomographic imaging with intravascular ultrasound. Heart. 88: 91-96, 2002.
[CrossRef]

Petit I, Szyper-Kravitz M, Nagler A. G-CSF induces stem cell mobilization by decreasing bone marrow SDF-1and up-regulating CXCR4. Nat Immunol. 3: 687-694, 2002.
[CrossRef]

Pittenger MF, Mackay AM, Beck SC, Jaiswal RK, Douglas R, Mosca JD, Moorman MA, Simonetti DW, Craig S, Marshak DR. Multilineage potential of adult human mesenchymal stem cells. Science. 284, 5411: 143-147, 1999.
[CrossRef]

Ratajczak MZ, Kucia M, Reca R, Majka M, Janowska-Wieczorek A, Ratajczak J. Stem cell plasticity revisited: CXCR4-positive cells expressing mRNA for early muscle. liver and neural cells ‘hide out’ in the bone marrow. Leukemia. 18: 29-40, 2004.
[CrossRef]

Ross R. The smooth muscle cell II. Growth of smooth cells in culture and formation of elastic fibers. J Cell Biol. 50: 172-176, 1971.
[CrossRef]

Schwartz SM. Biology of the neointima. Exp Nephrol. 2: 63-67, 1994.

Shi Q, Rafii S, Wu MH, Wijelath ES, Yu C, Ishida A, Fujita Y, Kothari S, Mohle R, Sauvage LR, Moore MA, Storb RF, Hammond WP. Evidence for circulating bone marrow-derived endothelial cells. Blood. 92: 362-367, 1998.

Simons M, Ware JA. Therapeutic angiogenesis in cardiovascular disease. Nat Rev Drug Discov. 2: 863-871, 2003.
[CrossRef]

Suda T, Suda J, Kajigaya S, Nagata S, Asano S, Saito M, Miura Y. Effects of recombinant murine granulocyte colony-stimulating factor on granulocyte-macrophage and blast colony formation. Exp Hematol. 15: 958-965, 1987.

Takahashi T, Kalka C, Masuda H, Chen D, Silver M, Kearney M, Magner M, Isner JM, Asahara T. Ischemia- and cytokine-induced mobilization of bone marrow-derived endothelial progenitor cells for neovascularization. Nat Med. 5: 434-438, 1999.
[CrossRef]

Tulis DA, Durante W, Peyton KJ, Evans AJ, Schafer AI. Heme oxygenase-1 attenuates vascular remodeling following balloon injury in rat carotid arteries. Atherosclerosis. 155: 113-122, 2001.
[CrossRef]

Ulich TR, del Castillo J, Yi ES, Yin S, McNiece I, Yung YP, Zsebo KM. Hematologic effects of stem cell factor in vivo and in vitro in rodents. Blood. 78: 645-650, 1991.

Yamaguchi J, Kusano KF, Masuo O, Kawamoto A, Silver M, Murasawa S, Bosch-Marce M, Masuda H, Losordo DW, Isner JM, Asahara T. Stromal cell-derived factor-1 effects on ex vivo expanded endothelial progenitor cell recruitment for ischemic neovascularization. Circulation. 107: 1322-1328, 2003.
[CrossRef]

Zhang Y, Wang C, Yang Q. Establishing an organic model of SMC proliferation with cultured aorta of rats and exploring the underlying mechanism (in Chinese). Sheng Wu Yi Xue Gong Cheng Xue Za Zhi. 25: 1405-1410, 2008.
CITED

0


BACK