The role of fibrin E on the modulation of endothelial progenitors adhesion, differentiation and angiogenic growth factor production and the promotion of wound healing

Biomaterials

Volumn 32, Issue 29, 2011, Pages 7096-7105

  Caiado, Francisco ^a,b   Carvalho, Tânia ^a,b   Silva, Fernanda ^a,b   Castro, Catarina ^c   Clode, Nuno ^c   Dye, Julian F ^d   Dias, Sérgio ^a,b,e  

^a INSTITUTO PORTUGUÊS DE ONCOLOGIA DE LISBOA FRANCISCO GENTIL   (Portugal)

^b INSTITUTO GULBENKIAN DE CIÊNCIA   (Portugal)

^c HOSPITAL DE SANTA MARIA   (Portugal)

^d Raft Research Institute   (United Kingdom)

^e UNIVERSITY OF LISBON   (Portugal)

Author keywords

Angiogenesis; Endothelial progenitors; Fibrin E; Wound healing

Indexed keywords

ANGIOGENESIS; ANGIOGENIC GROWTH FACTORS; CLINICAL PROBLEMS; COLLAGEN-BASED SCAFFOLDS; CONDITIONED MEDIAS; CRITICAL STEPS; CUTANEOUS WOUNDS; DIFFERENT SUBSTRATES; ENDOTHELIAL DIFFERENTIATION; ENDOTHELIAL PROGENITOR; ENDOTHELIAL PROGENITOR CELLS; ENDOTHELIAL PROGENITORS; EXTRACELLULAR MATRICES; FIBRIN E; GENE EXPRESSION ANALYSIS; IN-VITRO; IN-VIVO; INTEGRINS; MOUSE MODELS; NEUTRALIZING ANTIBODIES; PARACRINE; TUBE FORMATION; VASCULARIZATION; WOUND CLOSURE; WOUND HEALING; WOUND HEALING EFFECTS; WOUND HEALING PROCESS;

ADHESION; BIOMATERIALS; COLLAGEN; GENE EXPRESSION; MAMMALS; SCAFFOLDS (BIOLOGY);

ENDOTHELIAL CELLS;

ALGINIC ACID; BIOMATERIAL; COLLAGEN; FIBRIN; FIBRIN DEGRADATION PRODUCT; FIBRIN FRAGMENT E; FIBRONECTIN; GROWTH FACTOR; INTEGRIN; INTERLEUKIN 8; MACROPHAGE INFLAMMATORY PROTEIN 1ALPHA; NEUTRALIZING ANTIBODY; STROMAL CELL DERIVED FACTOR 1; TISSUE SCAFFOLD; TRANSFORMING GROWTH FACTOR BETA1; UNCLASSIFIED DRUG; VASCULOTROPIN A; VERY LATE ACTIVATION ANTIGEN 5;

ANGIOGENESIS; ANIMAL EXPERIMENT; ARTICLE; CELL ADHESION; CELL DIFFERENTIATION; CELL GROWTH; CELL PROLIFERATION; CONTROLLED STUDY; CULTURE MEDIUM; ENDOTHELIAL PROGENITOR CELL; EXTRACELLULAR MATRIX; FEMALE; GENE EXPRESSION; HUMAN; HUMAN CELL; HUMAN TISSUE; IN VITRO STUDY; IN VIVO STUDY; MOUSE; NONHUMAN; PARACRINE SIGNALING; PRIORITY JOURNAL; PROTEIN FUNCTION; REGULATORY MECHANISM; UMBILICAL CORD BLOOD; VASCULARIZATION; WOUND CLOSURE; WOUND HEALING;

ANIMALS; BIOLOGICAL MARKERS; CELL ADHESION; CELL DIFFERENTIATION; CELL PROLIFERATION; CELLS, CULTURED; ENDOTHELIAL CELLS; EXTRACELLULAR MATRIX; FEMALE; FIBRIN; HUMANS; MICE; MICE, INBRED BALB C; MICE, SCID; NEOVASCULARIZATION, PHYSIOLOGIC; PROTEIN ISOFORMS; STEM CELLS; VASCULAR ENDOTHELIAL GROWTH FACTOR A; WOUND HEALING;

EID: 79960839631     PISSN: 01429612     EISSN: 18785905     Source Type: Journal    
DOI: 10.1016/j.biomaterials.2011.06.022     Document Type: Article

References (42)

1. Mustoe T. Understanding chronic wounds: a unifying hypothesis on their pathogenesis and implications for therapy. Am J Surg 2004, 187(5):65-70.
2. Clark R.A.F., Ghosh K., Tonnesen M.G. Tissue engineering for cutaneous wounds. J Invest Dermatol 2007, 127(5):1018-1029.
3. Martin P. Wound healing - aiming for perfect skin regeneration. Science 1997, 276(5309):75-81.
4. Epstein F.H., Singer A.J., Clark R.A.F. Cutaneous wound healing. N Engl J Med 1999, 341(10):738-746.
5. Tonnesen M.G., Clark R.A. Angiogenesis in wound healing. J Investig Dermatol Symp Proc 2000, 5(1):40-46.
6. Asahara T., Murohara T., Sullivan A., Silver M., van der Zee R., Li T., et al. Isolation of putative progenitor endothelial cells for angiogenesis. Science 1997, 275(5302):964-966.
7. Asahara T., Masuda H., Takahashi T., Kalka C., Pastore C., Silver M., et al. Bone marrow origin of endothelial progenitor cells responsible for postnatal vasculogenesis in physiological and pathological neovascularization. Circ Res 1999, 85(3):221-228.
8. Caiado F., Real C., Carvalho T., Dias S. Notch pathway modulation on bone marrow-derived vascular precursor cells regulates their angiogenic and wound healing potential. PLoS One 2008, 3(11):e3752.
9. Zhao-Jun Liu O.C.V. Hyperoxia, endothelial progenitor cell mobilization, and diabetic wound healing. Antioxid Redox Signal 2008, 10(11):1869-1882.
10. Suh W., Kim K.L., Kim J.-M., Shin I.-S., Lee Y.-S., Lee J.-Y., et al. Transplantation of endothelial progenitor cells accelerates dermal wound healing with increased recruitment of monocytes/macrophages and neovascularization. Stem Cells 2005, 23(10):1571-1578.
11. Kim Ji Yeon, S.-H.S., Kim Koung Li, Maeng Yong-Sun, Im Ji-Eun, Yie Se Won, Ahn Young Keun, et al. Human cord blood-derived endothelial progenitor cells and their conditioned media exhibit therapeutic equivalence for diabetic wound healing. Cell Transplant 2010, 19(12):1635-1644.
12. Gallagher K.A., L.Z., Xiao M., Chen H., Goldstein L.J., Buerk D.G., Nedeau A., et al. Diabetic impairments in NO-mediated endothelial progenitor cell mobilization and homing are reversed by hyperoxia and SDF-1 alpha. J Clin Invest 2007, 117(5):1249-1259.
13. Barcelos L.S., Duplaa C., Krankel N., Graiani G., Invernici G., Katare R., et al. Human CD133+ progenitor cells promote the healing of diabetic ischemic ulcers by paracrine stimulation of angiogenesis and activation of Wnt signaling. Circ Res 2009, 104(9):1095-1102.
14. Kelton P. Skin grafts and skin substitutes. Select Read Plast Surg 1999, 9(1):1-24.
15. Auger F.A., Lacroix D., Germain L. Skin substitutes and wound healing. Skin Pharmacol Physiol 2009, 22(2):94-102.
16. Orgill D.P. Excision and skin grafting of thermal burns. N Engl J Med 2009, 360(9):893-901.
17. Potter M.J., Linge C., Cussons P., Dye J.F., Sanders R. An investigation to optimize angiogenesis within potential dermal replacements. Plast Reconstr Surg 2006, 117(6):1876-1885.
18. Thompson W.D., Kazmi M.A., Stout A.J. Fibrinolysis and angiogenesis in wound healing. J Pathol 1991, 165(4):311-318.
19. Jennewein C., Paulus P., Ellinghaus P., Eble J.A., Zacharowski K. Novel aspects of fibrin(ogen) fragments in the course of inflammation. Mol Med 2011, 5-6(17):568-573.
20. Allie D.E., Lirtzman M.D., Wyatt C.H., Keller V.A., Khan M.H., Khan M.A., et al. Critical limb ischemia: a global epidemic. A critical analysis of current treatment unmasks the clinical and economic costs of CLI. EuroIntervention 2005, 1(1):75-84.
21. Andrew J.M.B., Loretta V., Gunnel R.-T., Jan A. The global burden of diabetic foot disease. Lancet 2005, 366(9498):1719-1724.
22. Nele Brusselaers S.M., Dirk Vogelaers, Eric Hoste, Stijn Blot Severe burn injury in europe: a systematic review of the incidence, etiology, morbidity, and mortality. Crit Care 2010, 14(5).
23. Bitsch M., Engel A.M., Christiansen M., Larsen S.O., Iversen L., Holstein P.E., et al. Epidemiology of chronic wound patients and relation to serum levels of mannan-binding lectin. Acta Derm Venereol 2009, 89(6):607-611.
24. Mould A.P., Askari J.A., Aota S.-i., Yamada K.M., Irie A., Takada Y., et al. Defining the topology of integrin alpha5beta1-fibronectin interactions using inhibitory anti-alpha5 and anti-beta1 monoclonal antibodies. J Biol Chem 1997, 272(28):17283-17292.
25. Smith J.W., Cheresh D.A. Integrin (alpha v beta 3)-ligand interaction. Identification of a heterodimeric RGD binding site on the vitronectin receptor. J Biol Chem 1990, 265(4):2168-2172.
26. Kodama M., Naito M., Nomura H., Iguchi A., Thompson W.D., Stirk C.M., et al. Role of D and E domains in the migration of vascular smooth muscle cells into fibrin gels. Life Sci 2002, 71(10):1139-1148.
27. Bootle-Wilbraham C.A., Tazzyman S., Thompson W.D., Stirk C.M., Lewis C.E. Fibrin fragment E stimulates the proliferation, migration and differentiation of human microvascular endothelial cells in vitro. Angiogenesis 2001, 4(4):269-275.
28. Wijelath E.S., Rahman S., Murray J., Patel Y., Savidge G., Sobel M. Fibronectin promotes VEGF-induced CD34+ cell differentiation into endothelial cells. J Vasc Surg 2004, 39(3):655-660.
29. Lee M.J., Lee K.I., Shin J.M., Chae J.I., Chung H.M. Enhancement of wound healing by secretory factors of endothelial precursor cells derived from human embryonic stem cells. Cytotherapy 2011, 13(2):165-178.
30. Senger D.R., Claffey K.P., Papadopoulos-Sergiou A., Peruzzi C.A., Detmar M. Stimulation of endothelial cell migration by vascular permeability factor/vascular endothelial growth factor through cooperative mechanisms involving the alphavbeta3 integrin, osteopontin, and thrombin. Am J Pathol 1996, 149(1):293-305.
31. Watanabe Yoshifumi, S.W.L., Detmar Michael, Ajioka Itsuki, Dvorak Harold F. Vascular permeability factor/vascular endothelial growth factor (VPF/VEGF) delays and induces escape from senescence in human dermal microvascular endothelial cells. Oncogene 1997, 14(17):2025-2032.
32. Galiano R.D., Michaels V.J., Dobryansky M., Levine J.P., Gurtner G.C. Quantitative and reproducible murine model of excisional wound healing. Wound Repair Regen 2004, 164(6):1935-1947.
33. Riedel K., Riedel F., Goessler U.R., Germann G., Sauerbier M. TGF-beta antisense therapy increases angiogenic potential in human keratinocytes in vitro. Arch Med Res 2007, 38(1):45-51.
34. Bandyopadhyay B., Guan S., Li Y., Chen M., Woodley D.T., Li W. A " traffic control" role for TGFbeta3: orchestrating dermal and epidermal cell motility during wound healing. J Cell Biol 2006, 172(7):1093-1105.
35. Barrientos S., Stojadinovic O., Golinko M.S., Brem H., Tomic-Canic M. Perspective article: growth factors and cytokines in wound healing. Wound Repair Regen 2008, 16(5):585-601.
36. Grunewald M., Avraham I., Dor Y., Bachar-Lustig E., Itin A., Yung S., et al. VEGF-induced adult neovascularization: recruitment, retention, and role of accessory cells. Cell 2006, 124(1):175-189.
37. Salcedo R., Young H.A., Grimm M.C., Howard O.M., Anver M.R., Kleinman H.K., 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-1alpha. Am J Pathol 1999, 154(4):1125-1135.
38. Florin L., Maas-Szabowski N., Werner S., Szabowski A., Angel P. Increased keratinocyte proliferation by JUN-dependent expression of PTN and SDF-1 in fibroblasts. J Cell Sci 2005, 118(9):1981-1989.
39. Rennekampff H.O., Hansbrough J.F., Kiessig V., Doré C., Sticherling M., Schroder J.-M. Bioactive interleukin-8 is expressed in wounds and enhances wound healing. J Surg Res 2000, 93(1):41-54.
40. Tuschil A., Haslberger A., Lindley I. Interleukin-8 stimulates calcium transients and promotes epidermal cell proliferation. J Invest Dermatol 1992, 99(3):294-298.
41. Li A., Varney M.L., Valasek J., Godfrey M., Dave B.J., Singh R.K. Autocrine role of interleukin-8 in induction of endothelial cell proliferation, survival, migration and MMP-2 production and angiogenesis. Angiogenesis 2005, 8(1):63-71.
42. Low Q.E., Duffner L.A., Quinn D.G., Cook D.N., Rollins B.J., Kovacs E.J., et al. Wound healing in MIP-1alpha(-/-) and MCP-1(-/-) mice. Am J Pathol 2001, 159(2):457-463.