Role of Tie1 in Shear Stress and Atherosclerosis

Trends in Cardiovascular Medicine

Volumn 21, Issue 4, 2011, Pages 118-123

  Woo, Kel Vin ^a   Baldwin, H Scott ^a  

^a VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANGIOPOIETIN 1; ANGIOPOIETIN 2; ANGIOPOIETIN RECEPTOR; CD31 ANTIGEN; ENDOTHELIAL NITRIC OXIDE SYNTHASE; G PROTEIN COUPLED RECEPTOR; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; INTEGRIN; INTERCELLULAR ADHESION MOLECULE 1; ION CHANNEL; MITOGEN ACTIVATED PROTEIN KINASE; MITOGEN ACTIVATED PROTEIN KINASE 1; MITOGEN ACTIVATED PROTEIN KINASE 3; MONOCYTE CHEMOTACTIC PROTEIN 1; PHOSPHATIDYLINOSITOL 3 KINASE; TIE 1 RECEPTOR; TUMOR NECROSIS FACTOR ALPHA; VASCULAR CELL ADHESION MOLECULE 1; VASCULOTROPIN RECEPTOR 2;

ANGIOGENESIS; ATHEROGENESIS; ATHEROSCLEROSIS; BLOOD FLOW; CYTOSKELETON; ENDOTHELIUM; HUMAN; IMMUNOHISTOCHEMISTRY; LAMINAR FLOW; MECHANOTRANSDUCTION; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; REVIEW; SHEAR STRESS; THROMBOGENESIS;

ANIMALS; ATHEROSCLEROSIS; FORECASTING; HUMANS; INFLAMMATION; MECHANOTRANSDUCTION, CELLULAR; MICE; NEOVASCULARIZATION, PATHOLOGIC; RECEPTOR, TIE-1; STRESS, MECHANICAL;

EID: 84861902913     PISSN: 10501738     EISSN: 18732615     Source Type: Journal    
DOI: 10.1016/j.tcm.2012.03.009     Document Type: Review

References (52)

1. Asakura T., Karino T. Flow patterns and spatial distribution of atherosclerotic lesions in human coronary arteries. Circ Res 1990, 66:1045-1066.
2. Caro C.G., Fitz-Gerald J.M., Schroter R.C. Atheroma and arterial wall shear: Observation, correlation and proposal of a shear dependent mass transfer mechanism for atherogenesis. Proc R Soc Lond B Biol Sci 1971, 177:109-159.
3. Chan B., Sukhatme V.P. Suppression of Tie-1 in endothelial cells in vitro induces a change in the genome-wide expression profile reflecting an inflammatory function. FEBS Lett 2009, 583:1023-1028.
4. Chan B., Yuan H.T., Ananth Karumanchi S. Receptor tyrosine kinase Tie-1 overexpression in endothelial cells upregulates adhesion molecules. Biochem Biophys Res Commun 2008, 371:475-479.
5. Cheng C., van Haperen R., de Waard M., et al. Shear stress affects the intracellular distribution of eNOS: Direct demonstration by a novel in vivo technique. Blood 2005, 106:3691-3698.
6. Chen-Konak L., Guetta-Shubin Y., Yahav H., et al. Transcriptional and post-translation regulation of the Tie1 receptor by fluid shear stress changes in vascular endothelial cells. FASEB J 2003, 17:2121-2123.
7. D'Amico G., Korhonen E.A., Waltari M., et al. Loss of endothelial Tie1 receptor impairs lymphatic vessel development: Brief report. Arterioscler Thromb Vasc Biol 2010, 30:207-209.
8. Davies P.F., Polacek D.C., Handen J.S., et al. A spatial approach to transcriptional profiling: Mechanotransduction and the focal origin of atherosclerosis. Trends Biotechnol 1999, 17:347-351.
9. Dimmeler S., Haendeler J., Rippmann V., et al. Shear stress inhibits apoptosis of human endothelial cells. FEBS Lett 1996, 399:71-74.
10. Eriksson E.E. Intravital microscopy on atherosclerosis in apolipoprotein E-deficient mice establishes microvessels as major entry pathways for leukocytes to advanced lesions. Circulation 2011, 124:2129-2138.
11. Freund J.B., Goetz J.G., Hill K.L. Fluid flows and forces in development: Functions, features and biophysical principles. Development 2012, 139:1229-1245.
12. Gimbrone M.A., Anderson K.R., Topper J.N., et al. Special communication: The critical role of mechanical forces in blood vessel development, physiology and pathology. J Vasc Surg 1999, 29:1104-1151.
13. Gimbrone M.A., Topper J.N., Nagel T., et al. Endothelial dysfunction, hemodynamic forces, and atherogenesis. Ann N Y Acad Sci 2000, 902:230-239. Discussion:239-240.
14. Goel R., Schrank B.R., Arora S., et al. Site-specific effects of PECAM-1 on atherosclerosis in LDL receptor-deficient mice. Arterioscler Thromb Vasc Biol 2008, 28:1996-2002.
15. Harry B.L., Sanders J.M., Feaver R.E., et al. Endothelial cell PECAM-1 promotes atherosclerotic lesions in areas of disturbed flow in ApoE-deficient mice. Arterioscler Thromb Vasc Biol 2008, 28:2003-2008.
16. Hauer A.D., Habets K.L., van Wanrooij E.J., et al. Vaccination against TIE2 reduces atherosclerosis. Atherosclerosis 2009, 204:365-371.
17. Kaipainen A., Vlaykova T., Hatva E., et al. Enhanced expression of the tie receptor tyrosine kinase messenger RNA in the vascular endothelium of metastatic melanomas. Cancer Res 1994, 54:6571-6577.
18. Kim K.L., Shin I.S., Kim J.M., et al. Interaction between Tie receptors modulates angiogenic activity of angiopoietin2 in endothelial progenitor cells. Cardiovasc Res 2006, 72:394-402.
19. Koskinas K.C., Chatzizisis Y.S., Baker A.B., et al. The role of low endothelial shear stress in the conversion of atherosclerotic lesions from stable to unstable plaque. Curr Opin Cardiol 2009, 24:580-590.
20. Lee H.J., Koh G.Y. Shear stress activates Tie2 receptor tyrosine kinase in human endothelial cells. Biochem Biophys Res Commun 2003, 304:399-404.
21. Levesque M.J., Nerem R.M., Sprague E.A. Vascular endothelial cell proliferation in culture and the influence of flow. Biomaterials 1990, 11:702-707.
22. Li Y.S., Haga J.H., Chien S. Molecular basis of the effects of shear stress on vascular endothelial cells. J Biomech 2005, 38:1949-1971.
23. Lin W.C., Li A.F., Chi C.W., et al. Tie-1 protein tyrosine kinase: A novel independent prognostic marker for gastric cancer. Clin Cancer Res 1999, 5:1745-1751.
24. Malinauskas R.A., Herrmann R.A., Truskey G.A. The distribution of intimal white blood cells in the normal rabbit aorta. Atherosclerosis 1995, 115:147-163.
25. Marron M.B., Hughes D.P., Edge M.D., et al. Evidence for heterotypic interaction between the receptor tyrosine kinases TIE-1 and TIE-2. J Biol Chem 2000, 275:39741-39746.
26. Marron M.B., Hughes D.P., McCarthy M.J., et al. Tie-1 receptor tyrosine kinase endodomain interaction with SHP2: Potential signalling mechanisms and roles in angiogenesis. Adv Exp Med Biol 2000, 476:35-46.
27. Marron M.B., Singh H., Tahir T.A., et al. Regulated proteolytic processing of Tie1 modulates ligand responsiveness of the receptor-tyrosine kinase Tie2. J Biol Chem 2007, 282:30509-30517.
28. Moncada S. Adventures in vascular biology: A tale of two mediators. Philos Trans R Soc Lond B Biol Sci 2006, 361:735-759.
29. Moreno P.R., Purushothaman K.R., Fuster V., et al. Plaque neovascularization is increased in ruptured atherosclerotic lesions of human aorta: Implications for plaque vulnerability. Circulation 2004, 110:2032-2038.
30. Moulton K.S., Vakili K., Zurakowski D., et al. Inhibition of plaque neovascularization reduces macrophage accumulation and progression of advanced atherosclerosis. Proc Natl Acad Sci U S A 2003, 100:4736-4741.
31. Papapetropoulos A., Fulton D., Mahboubi K., et al. Angiopoietin-1 inhibits endothelial cell apoptosis via the Akt/survivin pathway. J Biol Chem 2000, 275:9102-9105.
32. Partanen J., Armstrong E., Mäkelä T.P., et al. A novel endothelial cell surface receptor tyrosine kinase with extracellular epidermal growth factor homology domains. Mol Cell Biol 1992, 12:1698-1707.
33. Partanen J., Puri M.C., Schwartz L., et al. Cell autonomous functions of the receptor tyrosine kinase TIE in a late phase of angiogenic capillary growth and endothelial cell survival during murine development. Development 1996, 122:3013-3021.
34. Patan S. TIE1 and TIE2 receptor tyrosine kinases inversely regulate embryonic angiogenesis by the mechanism of intussusceptive microvascular growth. Microvasc Res 1998, 56:1-21.
35. Peacock J.A. An in vitro study of the onset of turbulence in the sinus of Valsalva. Circ Res 1990, 67:448-460.
36. Porat R.M., Grunewald M., Globerman A., et al. Specific induction of tie1 promoter by disturbed flow in atherosclerosis-prone vascular niches and flow-obstructing pathologies. Circ Res 2004, 94:394-401.
37. Puri M.C., Bernstein A. Requirement for the TIE family of receptor tyrosine kinases in adult but not fetal hematopoiesis. Proc Natl Acad Sci U S A 2003, 100:12753-12758.
38. Puri M.C., Rossant J., Alitalo K., et al. The receptor tyrosine kinase TIE is required for integrity and survival of vascular endothelial cells. EMBO J 1995, 14:5884-5891.
39. Qu X., Tompkins K., Batts L.E., et al. Abnormal embryonic lymphatic vessel development in Tie1 hypomorphic mice. Development 2010, 137:1285-1295.
40. Saharinen P., Kerkelä K., Ekman N., et al. Multiple angiopoietin recombinant proteins activate the Tie1 receptor tyrosine kinase and promote its interaction with Tie2. J Cell Biol 2005, 169:239-243.
41. Sato T.N., Tozawa Y., Deutsch U., et al. Distinct roles of the receptor tyrosine kinases Tie-1 and Tie-2 in blood vessel formation. Nature 1995, 376:70-74.
42. Seegar T.C., Eller B., Tzvetkova-Robev D., et al. Tie1-Tie2 interactions mediate functional differences between angiopoietin ligands. Mol Cell 2010, 37:643-655.
43. Shahrara S., Volin M.V., Connors M.A., et al. Differential expression of the angiogenic Tie receptor family in arthritic and normal synovial tissue. Arthritis Res 2002, 4:201-208.
44. Singh H., Hansen T.M., Patel N. The molecular balance between receptor tyrosine kinases Tie1 and Tie2 is dynamically controlled by VEGF and TNFα and regulates angiopoietin signalling. PLoS ONE 2012, 7:e29319.
45. Suo J., Ferrara D.E., Sorescu D., et al. Hemodynamic shear stresses in mouse aortas: Implications for atherogenesis. Arterioscler Thromb Vasc Biol 2007, 27:346-351.
46. Taichman D.B., Schachtner S.K., Li Y., et al. A unique pattern of Tie1 expression in the developing murine lung. Exp Lung Res 2003, 29:113-122.
47. Tsiamis A.C., Morris P.N., Marron M.B. Vascular endothelial growth factor modulates the Tie-2:Tie-1 receptor complex. Microvasc Res 2002, 63:149-158.
48. Van Epps J.S., Chew D.W., Vorp D.A. Effects of cyclic flexure on endothelial permeability and apoptosis in arterial segments perfused ex vivo. J Biomech Eng 2009, 131:101005.
49. Woo K.V., Qu X., Babaev V.R., et al. Tie1 attenuation reduces murine atherosclerosis in a dose-dependent and shear stress-specific manner. J Clin Invest 2011, 121:1624-1635.
50. Yabkowitz R., Meyer S., Black T., et al. Inflammatory cytokines and vascular endothelial growth factor stimulate the release of soluble tie receptor from human endothelial cells via metalloprotease activation. Blood 1999, 93:1969-1979.
51. Yuan H.T., Venkatesha S., Chan B., et al. Activation of the orphan endothelial receptor Tie1 modifies Tie2-mediated intracellular signaling and cell survival. FASEB J 2007, 21:3171-3183.
52. Zheng W., Christensen L.P., Tomanek R.J. Stretch induces upregulation of key tyrosine kinase receptors in microvascular endothelial cells. Am J Physiol Heart Circ Physiol 2004, 287:H2739-H2745.