Arteriogenesis as a new therapeutic intervention strategy in chronic artery disorders. Cellular mechanism and experimental models;Arteriogenesis: Egy új terápiás intervenciós stratégia krónikus artériabetegségekben. Sejtes mechanizmus és kísérletes modellek

Orvosi Hetilap

Volumn 148, Issue 14, 2007, Pages 633-642

  Erdo, Franciska ^a,c   Ivo, R Buschmann ^b  

^a Gyogyszereszeti Intezet   (Hungary)

^b CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^c NONE   (Hungary)

Author keywords

Animal models; Arteriogenesis; Cerebrovascular disease; Coronary heart disease; Endothelial cells; Growth factors; Monocytes; Peripheral artery disease

Indexed keywords

ANTIGEN; BASIC FIBROBLAST GROWTH FACTOR; CD151 ANTIGEN; CHEMOKINE; COMPLEMENTARY DNA; GRANULOCYTE MACROPHAGE COLONY STIMULATING FACTOR; GROWTH FACTOR; HEAT SHOCK PROTEIN 90; INTERLEUKIN 8; LYMPHOTACTIN; MONOCYTE CHEMOTACTIC PROTEIN 1; NERVE GROWTH FACTOR; NEUTROPHIL ACTIVATING PROTEIN 2; PLATELET DERIVED ENDOTHELIAL CELL GROWTH FACTOR; PROTEIN DERIVATIVE; TRANSFORMING GROWTH FACTOR BETA1; UNCLASSIFIED DRUG; VASCULOTROPIN; ANGIOGENIC FACTOR; SIGNAL PEPTIDE;

ANGIOGENESIS; ARTERY DISEASE; ARTERY OCCLUSION; BRAIN BLOOD VESSEL; BRAIN INFARCTION; CEREBROVASCULAR ACCIDENT; CEREBROVASCULAR DISEASE; CHRONIC DISEASE; COLLATERAL CIRCULATION; COMBINATION CHEMOTHERAPY; DRUG DELIVERY SYSTEM; DRUG DOSE REGIMEN; ENDOTHELIUM CELL; EX VIVO STUDY; FOLLOW UP; HEART BLOOD VESSEL; HEART FUNCTION; HEART MUSCLE ISCHEMIA; HUMAN; IN VIVO STUDY; ISCHEMIC HEART DISEASE; MONOCYTE; MONOTHERAPY; NONHUMAN; PERIPHERAL OCCLUSIVE ARTERY DISEASE; REVIEW; SMOOTH MUSCLE FIBER; TIME; TISSUE BLOOD FLOW; ANIMAL; BRAIN CIRCULATION; CORONARY ARTERY ATHEROSCLEROSIS; CORONARY ARTERY BLOOD FLOW; CYTOLOGY; DRUG EFFECT; PATHOPHYSIOLOGY; PERIPHERAL VASCULAR DISEASE; VASCULAR SMOOTH MUSCLE;

ANGIOGENESIS INDUCING AGENTS; ANIMALS; ARTERIAL OCCLUSIVE DISEASES; CEREBROVASCULAR CIRCULATION; CEREBROVASCULAR DISORDERS; CHEMOKINES; CHRONIC DISEASE; COLLATERAL CIRCULATION; CORONARY ARTERIOSCLEROSIS; CORONARY CIRCULATION; ENDOTHELIAL CELLS; HUMANS; INTERCELLULAR SIGNALING PEPTIDES AND PROTEINS; MONOCYTES; MUSCLE, SMOOTH, VASCULAR; NEOVASCULARIZATION, PHYSIOLOGIC; PERIPHERAL VASCULAR DISEASES;

EID: 34347216355     PISSN: 00306002     EISSN: 17886120     Source Type: Journal    
DOI: 10.1556/OH.2007.27916     Document Type: Review

References (50)

1. Buschmann, I., Schaper, W: Arteriogenesis Versus Angiogenesis: Two Mechanisms of Vessel Growth. News Physiol. Sci., 1999, 14, 121-125.
2. Schaper, W. és Buschmann, I.: Artetiogenesis, the good and bad of it. Cardiovasc. Res., 1999, 43, 835-837.
3. Frye, R. L., Gura, G. M., Chesebro, J. H. és mtsa: Complete occlusion of the left main coronary artery and the importance of coronary collateral circulation. Mayo Clin. Proc., 1977, 52, 742-745.
4. Ward, D. E., Valantine, H. és Hui, W.: Occluded left main stem coronary artery. Report of five patients and review of published reports. Br. Heart Journal, 1983, 49, 276-279.
5. Heil, M., Schaper, W.: Influence of mechanical, cellular, and molecular factors on collateral artery growth (arteriogenesis). Circ. Res., 2004, 95, 449-458.
6. Asabara, T., Murohara, T., Sullivan, A. és mtsai: Isolation of putative progenitor endothelial cells for angiogenesis. Science, 1997, 275, 964-967.
7. Orlic, D., Kajstura, J., Chimenti, S., Limana, F. és mtsai: Mobilized bone marrow cells repair the infarcted heart, improving function and survival. Proc. Natl. Acad. Sci. USA, 2001, 98, 10344-10349.
8. Shi, Q., Rafii, S., Wu, M. H. és mtsai: Evidence for circulating bone marrow-derived endothelial cells. Blood, 1998, 92, 362-367.
9. Kalka, C., Masuda, H., Takahashi, T. és mtsai: Transplantation of ex vivo expanded endothelial progenitor cells for therapeutic neovascularization. Proc. Natl. Acad. Sci. USA, 2000, 97, 3422-3427.
10. Orlic, D., Kajstura, J., Chimenti, S. és mtsai: Transplanted adult bone marrow cells repair myocardial infarcts in mice. Ann. NY Acad. Sci., 2001, 938, 221-229.
11. Wolf, C., Cai, W. J., Vosschulte, R. és mtsai: Vascular remodeling and altered protein expression during growth of coronary collateral arteries. J. Mol. Cell. Cardiol., 1998, 30, 2291-2305.
12. Schaper, W., Piek, J. J., Munoz-Chapuli, R. és mtsai: In Angiogenesis and Cardivascular Disease. Szerk.: Ware, J. A. és Simons, M. Oxford University Press, New York, 159-198.
13. Matsunaga, T., Warltier, D. C., Weihrauch, D. W. és mtsai: Ischemia-induced coronary collateral growth is dependent on vascular endothelial growth factor and nitric oxide. Circulation, 2000, 102, 3098-3103.
14. Weihrauch, D., Tessmer, J., Warltier, D. C. és mtsa: Repetitive coronary artery occlusions induce release of growth factors into the myocardial interstitium. Am. J. Physiol., 1998, 275, (3 Pt 2) H969-976.
15. Lamping, K. G., Zheng, W., Xing, D. és mtsai: Bradycardia stimulates vascular growth during gradual coronary occlusion. Arterioscler. Thromb. Vasc. Biol., 2005, 25, 2122-2127.
16. White, F. C., Bloor, C. M., McKirnan, M. D. és mtsa: Exercise training in swine promotes growth of arteriolar bed and capillary angiogenesis in heart. J. Appl. Physiol., 1998, 85, 1160-1168.
17. White, F. C., Carroll, S. M., Magnet, A. és mtsa: Coronary collateral development in swine after coronary artery occlusion. Circ. Res., 1992, 71, 1490-1500.
18. Toyota, E., Warltier, D. C., Brock, T. és mtsai: Vascular endothelial growth factor is required for coronary collateral growth in the rat. Circulation, 2005, 112, 2108-2113.
19. Boodhwani, M., Nakai, Y., Mieno, S. és mtsai: Hypercholesterolemia impairs the myocardial angiogenic response in a swine model of chronic ischemia: role of endostatin and oxidative stress. Ann. Thorac. Surg., 2006, 81, 634-642.
20. Kamihata, H., Matsubara, H., Nishiue, T. és mtsai: Implantation of bone marrow mononuclear cells into ischemic myocardium enhances collateral perfusion and regional function via sides upply of angioblasts, angiogenic ligands, and cytokines. Circulation, 2001, 104, 1046-1052.
21. Waksman, R. és Baffour, R.: Bone marrow and bone marrow derived mononuclear stem cells therapy for the chronically ischemic myocardium. Cardiovasc. Radiation Medicine, 2003, 4, 164-168.
22. Scholz, D., Ito, W., Flweming, I. és mtsai: Ultrastructure and molecular histology of rabbit hind-limb collateral artery growth (arteriogenesis). Virchows Arch., 2000, 436, 257-270.
23. Hershey, J. C., Baskin, E. P., Glass, J. D. és mtsai: Revascularization in the rabbit hindlimb: dissociation between capillary sprouting and arteriogenesis. Cardiovasc. Res., 2001, 49, 618-625.
24. Grundmann, S., Hoefer, I., Ulusans, S. és mtsai: Anti-tumor necrosis factor-{alpha} therapies attenuate adaptive arteriogenesis in the rabbit. Am. J. Physiol. Heart Circ. Physiol., 2005, 289, H1497-H1505.
25. Hoefer, I. E., van Royen, N., Rectenwald, J. E. és mtsai: Arteriogenesis proceeds via ICAM-1/Mac-1-mediated mechanisms. Circ. Res., 2004, 94, 1179-1185.
26. Hoefer, I. E., Grundmann, S., van Royen, N. és mtsai: Leukocyte subpopulations and arteriogenesis: specific role of monocytes, lymphocytes and granulocytes. Atherosclerosis, 2005, 181, 285-293.
27. van Royen, N., Hoefer, I., Buschmann, I. és mtsai: Exogenous application of transforming growth factor beta 1 stimulates arteriogenesis in the peripheral circulation. FASEB, 2002, 16, 432-434.
28. Buschmann, I. R., Hoefer, I. E., van Royen, N. és mtsai: GMCSF: a strong arteriogenic factor acting by amplification of monocyte function. Atherosclerosis, 2001, 159, 343-356.
29. Herold, J., Pipp, F., Fernandez, B. és mtsai: Transplantation of monocytes: a novel strategy for in vivo augmentation of collateral vessel growth. Human Gene Therapy, 2004, 15, 1-12.
30. Hoefer, I. E., Grundmann, S., Schirmer, S. és mtsai: Aspirin, but not clopidogrel, reduces collateral conductance in a rabbit model of femoral artery occlusion. J. Am. Coll. Cardiol. 2005, 46, 994-1001.
31. Tirziu, D., Moodie, K. L., Zhuang, Z. W. és mtsai: Delayed arteriogenesis in hypercholesterolemic mice. Circulation, 2005, 112, 2501-2509.
32. Hossmann, K. A.: Collateral circulation of the brain. In Collateral Cirulation. Szerk.: Schaper, W. és Schaper, J. Kluwer Academic Publisher, Amsterdam, 1993, 291-315.
33. Wei, L., Erinjeri, J. P., Rovainen, C. M. és mtsa: Collateral growth and angiogenesis around cortical stroke. Stroke, 2001, 32, 2179-2184.
34. Erdo F., Trapp, T., Mies, G. és mtsa: Immunohistochemical analysis of protein expression after middle cerebral artery occlusion in mice. Acta Neuropathol., 2004, 107, 127-136.
35. Hata, R., Maeda, K., Hermann, D. és mtsai: Dynamics of regional brain metabolism and gene expression after middle cerebral artery occlusion in mice. J. Cereb. Blood Flow Metab., 2000, 20, 306-315.
36. Mies, G., Ishimaru, S., Xie, Y. és mtsai: Ischemic thresholds of cerebral protein synthesis and energy state following middle cerebral artery occlusion in rat. J. Cereb. Blood Flow Metab., 1991, 11, 753-761.
37. Busch, H. J., Buschmann, I. R., Mies, G. és mtsai: Arteriogenesis in hypoperfused rat brain. J. Cereb. Blood Flow. Metab., 2003, 23, 621-628.
38. Buschmann, I. R., Busch, H. J., Mies, G. és mtsa: Therapeutic induction of arteriogenesis in hypoperfused rat brain via granulocyte-macrophage colony-stimulating factor. Circulation, 2003, 108, 610-615.
39. Schneeloch, E., Mies, G., Busch, H. J. és mtsai: Granulocyte-macrophage colony-stimulating factor-induced arteriogenesis reduces energy failure in hemodynamic stroke. Proc. Natl. Acad. Sci. USA, 2004, 101, 12730-12735
40. Choy, M., Ganesan, V., Thomas, D. L. és mtsai: The chronic vascular and haemodynamic response after permanent bilateral common carotid occlusion in newborn and adult rats. J. Cereb. Blood Flow Metab., 2006, 26, 1066-1075.
41. Muhs, A., Lenter, M. C., Seidler, R. W. és mtsai: Nonviral monocyte chemoattractant protein-1 gene transfer improves arteriogenesis after femoral artery occlusion. Gene Ther., 2004, 11, 1685-1693.
42. Srivastava, S., Terjung, R. L. és Yang, H. T.: Basic fibroblast growth factor increases collateral blood flow in spontaneously hypertensive rats. Am. J. Physiol. Heart Circ. Physiol., 2003, 285, H1190-1197.
43. Lebberz, C., von Degenfeld, G., Karl, A. és mtsai: Therapeutic anigiogenesis/arteriogenesis in the chronic ischemic rabbit hindlimb: effect of venous basic fibroblast growth factor retroinfusion. Endothelium, 2003, 10, 257-265.
44. Deng, X. L., Wu, X. B., Jiang, J. és mtsai: Recombinant adeno-associated viral vector 2-mediated gene transfer of VEGF165 improved porcine chronic myocardial ischemia. Zonghua Xin Xue Guan Bing Za Zhi, 2005, 33, 732-737.
45. Jiang, H., Zhang, T. és Sun, X.: Vascular endothelial growth factor gene delivery by magnetic DNA nanospheres ameliorates limb ischemia in rabbits. J. Surg. Res., 2005, 126, 48-54.
46. Zhang, Z. G., Zhang, L, Jiang, Q. és mtsai: VEGF enhances angiogenesis and promotes blood brain barrier leakage in the ischemic brain. J. Clin. Invest., 2000, 106, 829-838.
47. Lan, R. F., Liu, Z. X., Liu, X. C. és mtsai: CD151 promotes neovascularization and improves blood perfusion in a rat hind-limb ischemia model. J. Endovasc. Ther., 2005, 12, 469-478.
48. Pfosser, A., Thalgott, M., Buttner, K. és mtsai: Liposomal Hsp90 cDNA induces neovascularization via nitric oxide in chronic ischemia. Cardiovasc. Res., 2005, 65, 728-736.
49. Li, W., Tanaka, K., Ihaya, A. és mtsai: Gene therapy for chronic myocardial ischemia using platelet-derived endothelial cell growth factor in dogs. Am. J. Physiol. Heart Circ. Physiol., 2005, 288, H408-415.
50. Salis, M. B., Graiani, G., Desortes E. és mtsai: Nerve growth factor supplementation reverses the impairment, induced by Type 1 diabetes, of hindlimb postischemic recovery in mice. Diabetogia, 2004, 47, 1055-1063.