Skip to main content
Erschienen in:
Buchtitelbild

2013 | OriginalPaper | Buchkapitel

Mechanical and Chemical Regulation of Arterial and Venous Specification

verfasst von : Thomas N. Sato

Erschienen in: Mechanical and Chemical Signaling in Angiogenesis

Verlag: Springer Berlin Heidelberg

Aktivieren Sie unsere intelligente Suche, um passende Fachinhalte oder Patente zu finden.

search-config
loading …

Abstract

The fact that blood circulates through vessels was realized by William Harvey in the early seventeenth century. The blood flows away from the heart via arteries delivering oxygen and nutrients to peripheral organs and return to the heart via veins. Until late the 1990s, the distinction between artery and vein was recognized solely based on anatomical and function differences, basis, and it had been believed that arterial and venous specific characteristics are controlled by the respective hemodynamic forces that they are exposed to. However, in the past 15 years or so, it has become clear that they are also distinguished by the molecules that they express. Furthermore, their phenotypes are also regulated by genetic, hence, molecular (chemical), programs. In this chapter, I will summarize historical perspectives of the recognition of arteries and veins, and will review recent advance in our understating of mechanisms underlying arterial and venous specification mediated by mechanical and chemical signals. I conclude this chapter by proposing three models, morphogenetic, habituation, and integrative models, explaining how these two classes of signals become integrated to specify arteries and veins.

Sie haben noch keine Lizenz? Dann Informieren Sie sich jetzt über unsere Produkte:

Springer Professional "Wirtschaft+Technik"

Online-Abonnement

Mit Springer Professional "Wirtschaft+Technik" erhalten Sie Zugriff auf:

  • über 102.000 Bücher
  • über 537 Zeitschriften

aus folgenden Fachgebieten:

  • Automobil + Motoren
  • Bauwesen + Immobilien
  • Business IT + Informatik
  • Elektrotechnik + Elektronik
  • Energie + Nachhaltigkeit
  • Finance + Banking
  • Management + Führung
  • Marketing + Vertrieb
  • Maschinenbau + Werkstoffe
  • Versicherung + Risiko

Jetzt Wissensvorsprung sichern!

Springer Professional "Technik"

Online-Abonnement

Mit Springer Professional "Technik" erhalten Sie Zugriff auf:

  • über 67.000 Bücher
  • über 390 Zeitschriften

aus folgenden Fachgebieten:

  • Automobil + Motoren
  • Bauwesen + Immobilien
  • Business IT + Informatik
  • Elektrotechnik + Elektronik
  • Energie + Nachhaltigkeit
  • Maschinenbau + Werkstoffe




 

Jetzt Wissensvorsprung sichern!

Literatur
1.
Zurück zum Zitat Harvey, W.: Exercitatio anatomica de motu cordis et sanguinis in animalibus (1628) Harvey, W.: Exercitatio anatomica de motu cordis et sanguinis in animalibus (1628)
2.
Zurück zum Zitat Garcia-Cardena, G., Gimbrone, M.A., Jr.: Biomechanical modulation of endothelial phenotype: implications for health and disease. Handb. Exp. Pharmacol. 176(Pt 2) 79–95 (2006)CrossRef Garcia-Cardena, G., Gimbrone, M.A., Jr.: Biomechanical modulation of endothelial phenotype: implications for health and disease. Handb. Exp. Pharmacol. 176(Pt 2) 79–95 (2006)CrossRef
3.
Zurück zum Zitat Gimbrone Jr, M.A.: Endothelial dysfunction, hemodynamic forces, and atherosclerosis. Thromb. Haemost. 82, 722–726 (1999) Gimbrone Jr, M.A.: Endothelial dysfunction, hemodynamic forces, and atherosclerosis. Thromb. Haemost. 82, 722–726 (1999)
4.
Zurück zum Zitat Gimbrone Jr, M.A.: Vascular endothelium, hemodynamic forces, and atherogenesis. Am. J. Pathol. 155, 1–5 (1999)CrossRef Gimbrone Jr, M.A.: Vascular endothelium, hemodynamic forces, and atherogenesis. Am. J. Pathol. 155, 1–5 (1999)CrossRef
5.
Zurück zum Zitat Gimbrone Jr, M.A., Nagel, T., Topper, J.N.: Biomechanical activation: an emerging paradigm in endothelial adhesion biology. J. Clin. Invest. 100, S61–S65 (1997) Gimbrone Jr, M.A., Nagel, T., Topper, J.N.: Biomechanical activation: an emerging paradigm in endothelial adhesion biology. J. Clin. Invest. 100, S61–S65 (1997)
6.
Zurück zum Zitat Gimbrone, M.A., Jr., Resnick, N., Nagel, T., Khachigian, L.M., Collins, T., and Topper, J.N.: Hemodynamics, endothelial gene expression, and atherogenesis. Ann. N Y. Acad. Sci. 811, 1–10; discussion 10–11 (1997) Gimbrone, M.A., Jr., Resnick, N., Nagel, T., Khachigian, L.M., Collins, T., and Topper, J.N.: Hemodynamics, endothelial gene expression, and atherogenesis. Ann. N Y. Acad. Sci. 811, 1–10; discussion 10–11 (1997)
7.
Zurück zum Zitat Resnick, N., Gimbrone Jr, M.A.: Hemodynamic forces are complex regulators of endothelial gene expression. FASEB. J. 9, 874–882 (1995) Resnick, N., Gimbrone Jr, M.A.: Hemodynamic forces are complex regulators of endothelial gene expression. FASEB. J. 9, 874–882 (1995)
8.
Zurück zum Zitat Topper, J.N., Gimbrone Jr, M.A.: Blood flow and vascular gene expression: fluid shear stress as a modulator of endothelial phenotype. Mol. Med. Today 5, 40–46 (1999)CrossRef Topper, J.N., Gimbrone Jr, M.A.: Blood flow and vascular gene expression: fluid shear stress as a modulator of endothelial phenotype. Mol. Med. Today 5, 40–46 (1999)CrossRef
9.
Zurück zum Zitat Papaioannou, T.G., Stefanadis, C.: Vascular wall shear stress: basic principles and methods. Hellenic. J. Cardiol. 46, 9–15 (2005) Papaioannou, T.G., Stefanadis, C.: Vascular wall shear stress: basic principles and methods. Hellenic. J. Cardiol. 46, 9–15 (2005)
10.
Zurück zum Zitat Jones, E.A., Yuan, L., Breant, C., Watts, R.J., Eichmann, A.: Separating genetic and hemodynamic defects in neuropilin 1 knockout embryos. Development 135, 2479–2488 (2008)CrossRef Jones, E.A., Yuan, L., Breant, C., Watts, R.J., Eichmann, A.: Separating genetic and hemodynamic defects in neuropilin 1 knockout embryos. Development 135, 2479–2488 (2008)CrossRef
11.
Zurück zum Zitat Chong, D.C., Koo, Y., Xu, K., Fu, S., Cleaver, O.: Stepwise arteriovenous fate acquisition during mammalian vasculogenesis. Dev. Dyn. 240, 2153–2165 (2011)CrossRef Chong, D.C., Koo, Y., Xu, K., Fu, S., Cleaver, O.: Stepwise arteriovenous fate acquisition during mammalian vasculogenesis. Dev. Dyn. 240, 2153–2165 (2011)CrossRef
12.
Zurück zum Zitat le Noble, F., Moyon, D., Pardanaud, L., Yuan, L., Djonov, V., Matthijsen, R., Breant, C., Fleury, V., Eichmann, A.: Flow regulates arterial-venous differentiation in the chick embryo yolk sac. Development 131, 361–375 (2004)CrossRef le Noble, F., Moyon, D., Pardanaud, L., Yuan, L., Djonov, V., Matthijsen, R., Breant, C., Fleury, V., Eichmann, A.: Flow regulates arterial-venous differentiation in the chick embryo yolk sac. Development 131, 361–375 (2004)CrossRef
13.
Zurück zum Zitat Cornhill, J.F., Roach, M.R.: A quantitative study of the localization of atherosclerotic lesions in the rabbit aorta. Atherosclerosis 23, 489–501 (1976)CrossRef Cornhill, J.F., Roach, M.R.: A quantitative study of the localization of atherosclerotic lesions in the rabbit aorta. Atherosclerosis 23, 489–501 (1976)CrossRef
14.
Zurück zum Zitat Wong, L.C., Langille, B.L.: Developmental remodeling of the internal elastic lamina of rabbit arteries: effect of blood flow. Circ. Res. 78, 799–805 (1996)CrossRef Wong, L.C., Langille, B.L.: Developmental remodeling of the internal elastic lamina of rabbit arteries: effect of blood flow. Circ. Res. 78, 799–805 (1996)CrossRef
15.
Zurück zum Zitat Wang, H.U., Chen, Z.F., Anderson, D.J.: Molecular distinction and angiogenic interaction between embryonic arteries and veins revealed by ephrin-B2 and its receptor Eph-B4. Cell 93, 741–753 (1998)CrossRef Wang, H.U., Chen, Z.F., Anderson, D.J.: Molecular distinction and angiogenic interaction between embryonic arteries and veins revealed by ephrin-B2 and its receptor Eph-B4. Cell 93, 741–753 (1998)CrossRef
16.
Zurück zum Zitat Zhong, T.P., Childs, S., Leu, J.P., Fishman, M.C.: Gridlock signalling pathway fashions the first embryonic artery. Nature 414, 216–220 (2001)CrossRef Zhong, T.P., Childs, S., Leu, J.P., Fishman, M.C.: Gridlock signalling pathway fashions the first embryonic artery. Nature 414, 216–220 (2001)CrossRef
17.
Zurück zum Zitat Zhong, T.P., Rosenberg, M., Mohideen, M.A., Weinstein, B., Fishman, M.C.: Gridlock, an HLH gene required for assembly of the aorta in zebrafish. Science 287, 1820–1824 (2000)CrossRef Zhong, T.P., Rosenberg, M., Mohideen, M.A., Weinstein, B., Fishman, M.C.: Gridlock, an HLH gene required for assembly of the aorta in zebrafish. Science 287, 1820–1824 (2000)CrossRef
18.
Zurück zum Zitat Weinstein, B.M., Stemple, D.L., Driever, W., Fishman, M.C.: Gridlock, a localized heritable vascular patterning defect in the zebrafish. Nat. Med. 1, 1143–1147 (1995)CrossRef Weinstein, B.M., Stemple, D.L., Driever, W., Fishman, M.C.: Gridlock, a localized heritable vascular patterning defect in the zebrafish. Nat. Med. 1, 1143–1147 (1995)CrossRef
19.
Zurück zum Zitat Lawson, N.D., Scheer, N., Pham, V.N., Kim, C.H., Chitnis, A.B., Campos-Ortega, J.A., Weinstein, B.M.: Notch signaling is required for arterial-venous differentiation during embryonic vascular development. Development 128, 3675–3683 (2001) Lawson, N.D., Scheer, N., Pham, V.N., Kim, C.H., Chitnis, A.B., Campos-Ortega, J.A., Weinstein, B.M.: Notch signaling is required for arterial-venous differentiation during embryonic vascular development. Development 128, 3675–3683 (2001)
20.
Zurück zum Zitat Villa, N., Walker, L., Lindsell, C.E., Gasson, J., Iruela-Arispe, M.L., Weinmaster, G.: Vascular expression of Notch pathway receptors and ligands is restricted to arterial vessels. Mech. Dev. 108, 161–164 (2001)CrossRef Villa, N., Walker, L., Lindsell, C.E., Gasson, J., Iruela-Arispe, M.L., Weinmaster, G.: Vascular expression of Notch pathway receptors and ligands is restricted to arterial vessels. Mech. Dev. 108, 161–164 (2001)CrossRef
21.
Zurück zum Zitat Jones, E.A., Clement-Jones, M., Wilson, D.I.: JAGGED1 expression in human embryos: correlation with the Alagille syndrome phenotype. J. Med. Genet. 37, 658–662 (2000)CrossRef Jones, E.A., Clement-Jones, M., Wilson, D.I.: JAGGED1 expression in human embryos: correlation with the Alagille syndrome phenotype. J. Med. Genet. 37, 658–662 (2000)CrossRef
22.
Zurück zum Zitat Loomes, K.M., Underkoffler, L.A., Morabito, J., Gottlieb, S., Piccoli, D.A., Spinner, N.B., Baldwin, H.S., Oakey, R.J.: The expression of Jagged1 in the developing mammalian heart correlates with cardiovascular disease in Alagille syndrome. Hum. Mol. Genet. 8, 2443–2449 (1999)CrossRef Loomes, K.M., Underkoffler, L.A., Morabito, J., Gottlieb, S., Piccoli, D.A., Spinner, N.B., Baldwin, H.S., Oakey, R.J.: The expression of Jagged1 in the developing mammalian heart correlates with cardiovascular disease in Alagille syndrome. Hum. Mol. Genet. 8, 2443–2449 (1999)CrossRef
23.
Zurück zum Zitat Krebs, L.T., Xue, Y., Norton, C.R., Shutter, J.R., Maguire, M., Sundberg, J.P., Gallahan, D., Closson, V., Kitajewski, J., Callahan, R., et al.: Notch signaling is essential for vascular morphogenesis in mice. Genes Dev. 14, 1343–1352 (2000) Krebs, L.T., Xue, Y., Norton, C.R., Shutter, J.R., Maguire, M., Sundberg, J.P., Gallahan, D., Closson, V., Kitajewski, J., Callahan, R., et al.: Notch signaling is essential for vascular morphogenesis in mice. Genes Dev. 14, 1343–1352 (2000)
24.
Zurück zum Zitat Lindner, V., Booth, C., Prudovsky, I., Small, D., Maciag, T., Liaw, L.: Members of the Jagged/Notch gene families are expressed in injured arteries and regulate cell phenotype via alterations in cell matrix and cell-cell interaction. Am. J. Pathol. 159, 875–883 (2001)CrossRef Lindner, V., Booth, C., Prudovsky, I., Small, D., Maciag, T., Liaw, L.: Members of the Jagged/Notch gene families are expressed in injured arteries and regulate cell phenotype via alterations in cell matrix and cell-cell interaction. Am. J. Pathol. 159, 875–883 (2001)CrossRef
25.
Zurück zum Zitat Reaume, A.G., Conlon, R.A., Zirngibl, R., Yamaguchi, T.P., Rossant, J.: Expression analysis of a Notch homologue in the mouse embryo. Dev. Biol. 154, 377–387 (1992)CrossRef Reaume, A.G., Conlon, R.A., Zirngibl, R., Yamaguchi, T.P., Rossant, J.: Expression analysis of a Notch homologue in the mouse embryo. Dev. Biol. 154, 377–387 (1992)CrossRef
26.
Zurück zum Zitat Del Amo, F.F., Smith, D.E., Swiatek, P.J., Gendron-Maguire, M., Greenspan, R.J., McMahon, A.P., Gridley, T.: Expression pattern of Motch, a mouse homolog of Drosophila Notch, suggests an important role in early postimplantation mouse development. Development 115, 737–744 (1992) Del Amo, F.F., Smith, D.E., Swiatek, P.J., Gendron-Maguire, M., Greenspan, R.J., McMahon, A.P., Gridley, T.: Expression pattern of Motch, a mouse homolog of Drosophila Notch, suggests an important role in early postimplantation mouse development. Development 115, 737–744 (1992)
27.
Zurück zum Zitat Uyttendaele, H., Closson, V., Wu, G., Roux, F., Weinmaster, G., Kitajewski, J.: Notch4 and Jagged-1 induce microvessel differentiation of rat brain endothelial cells. Microvasc. Res. 60, 91–103 (2000)CrossRef Uyttendaele, H., Closson, V., Wu, G., Roux, F., Weinmaster, G., Kitajewski, J.: Notch4 and Jagged-1 induce microvessel differentiation of rat brain endothelial cells. Microvasc. Res. 60, 91–103 (2000)CrossRef
28.
Zurück zum Zitat Shirayoshi, Y., Yuasa, Y., Suzuki, T., Sugaya, K., Kawase, E., Ikemura, T., Nakatsuji, N.: Proto-oncogene of int-3, a mouse Notch homologue, is expressed in endothelial cells during early embryogenesis. Genes Cells 2, 213–224 (1997)CrossRef Shirayoshi, Y., Yuasa, Y., Suzuki, T., Sugaya, K., Kawase, E., Ikemura, T., Nakatsuji, N.: Proto-oncogene of int-3, a mouse Notch homologue, is expressed in endothelial cells during early embryogenesis. Genes Cells 2, 213–224 (1997)CrossRef
29.
Zurück zum Zitat Shutter, J.R., Scully, S., Fan, W., Richards, W.G., Kitajewski, J., Deblandre, G.A., Kintner, C.R., Stark, K.L.: Dll4, a novel Notch ligand expressed in arterial endothelium. Genes Dev. 14, 1313–1318 (2000) Shutter, J.R., Scully, S., Fan, W., Richards, W.G., Kitajewski, J., Deblandre, G.A., Kintner, C.R., Stark, K.L.: Dll4, a novel Notch ligand expressed in arterial endothelium. Genes Dev. 14, 1313–1318 (2000)
30.
Zurück zum Zitat Duarte, A., Hirashima, M., Benedito, R., Trindade, A., Diniz, P., Bekman, E., Costa, L., Henrique, D., Rossant, J.: Dosage-sensitive requirement for mouse Dll4 in artery development. Genes Dev. 18, 2474–2478 (2004)CrossRef Duarte, A., Hirashima, M., Benedito, R., Trindade, A., Diniz, P., Bekman, E., Costa, L., Henrique, D., Rossant, J.: Dosage-sensitive requirement for mouse Dll4 in artery development. Genes Dev. 18, 2474–2478 (2004)CrossRef
31.
Zurück zum Zitat Fischer, A., Schumacher, N., Maier, M., Sendtner, M., Gessler, M.: The Notch target genes Hey1 and Hey2 are required for embryonic vascular development. Genes Dev. 18, 901–911 (2004)CrossRef Fischer, A., Schumacher, N., Maier, M., Sendtner, M., Gessler, M.: The Notch target genes Hey1 and Hey2 are required for embryonic vascular development. Genes Dev. 18, 901–911 (2004)CrossRef
32.
Zurück zum Zitat Kokubo, H., Miyagawa-Tomita, S., Tomimatsu, H., Nakashima, Y., Nakazawa, M., Saga, Y., Johnson, R.L.: Targeted disruption of hesr2 results in atrioventricular valve anomalies that lead to heart dysfunction. Circ. Res. 95, 540–547 (2004)CrossRef Kokubo, H., Miyagawa-Tomita, S., Tomimatsu, H., Nakashima, Y., Nakazawa, M., Saga, Y., Johnson, R.L.: Targeted disruption of hesr2 results in atrioventricular valve anomalies that lead to heart dysfunction. Circ. Res. 95, 540–547 (2004)CrossRef
33.
Zurück zum Zitat Krebs, L.T., Shutter, J.R., Tanigaki, K., Honjo, T., Stark, K.L., Gridley, T.: Haploinsufficient lethality and formation of arteriovenous malformations in Notch pathway mutants. Genes Dev. 18, 2469–2473 (2004)CrossRef Krebs, L.T., Shutter, J.R., Tanigaki, K., Honjo, T., Stark, K.L., Gridley, T.: Haploinsufficient lethality and formation of arteriovenous malformations in Notch pathway mutants. Genes Dev. 18, 2469–2473 (2004)CrossRef
34.
Zurück zum Zitat Visconti, R.P., Richardson, C.D., Sato, T.N.: Orchestration of angiogenesis and arteriovenous contribution by angiopoietins and vascular endothelial growth factor (VEGF). Proc. Natl. Acad. Sci. U S A. 99, 8219–8224 (2002)CrossRef Visconti, R.P., Richardson, C.D., Sato, T.N.: Orchestration of angiogenesis and arteriovenous contribution by angiopoietins and vascular endothelial growth factor (VEGF). Proc. Natl. Acad. Sci. U S A. 99, 8219–8224 (2002)CrossRef
35.
Zurück zum Zitat Mukouyama, Y.S., Shin, D., Britsch, S., Taniguchi, M., Anderson, D.J.: Sensory nerves determine the pattern of arterial differentiation and blood vessel branching in the skin. Cell 109, 693–705 (2002)CrossRef Mukouyama, Y.S., Shin, D., Britsch, S., Taniguchi, M., Anderson, D.J.: Sensory nerves determine the pattern of arterial differentiation and blood vessel branching in the skin. Cell 109, 693–705 (2002)CrossRef
36.
Zurück zum Zitat Mukouyama, Y.S., Gerber, H.P., Ferrara, N., Gu, C., Anderson, D.J.: Peripheral nerve-derived VEGF promotes arterial differentiation via neuropilin 1-mediated positive feedback. Development 132, 941–952 (2005)CrossRef Mukouyama, Y.S., Gerber, H.P., Ferrara, N., Gu, C., Anderson, D.J.: Peripheral nerve-derived VEGF promotes arterial differentiation via neuropilin 1-mediated positive feedback. Development 132, 941–952 (2005)CrossRef
37.
Zurück zum Zitat Lawson, N.D., Vogel, A.M., Weinstein, B.M.: Sonic hedgehog and vascular endothelial growth factor act upstream of the Notch pathway during arterial endothelial differentiation. Dev. Cell 3, 127–136 (2002)CrossRef Lawson, N.D., Vogel, A.M., Weinstein, B.M.: Sonic hedgehog and vascular endothelial growth factor act upstream of the Notch pathway during arterial endothelial differentiation. Dev. Cell 3, 127–136 (2002)CrossRef
38.
Zurück zum Zitat Peterson, R.T., Shaw, S.Y., Peterson, T.A., Milan, D.J., Zhong, T.P., Schreiber, S.L., MacRae, C.A., Fishman, M.C.: Chemical suppression of a genetic mutation in a zebrafish model of aortic coarctation. Nat. Biotechnol. 22, 595–599 (2004)CrossRef Peterson, R.T., Shaw, S.Y., Peterson, T.A., Milan, D.J., Zhong, T.P., Schreiber, S.L., MacRae, C.A., Fishman, M.C.: Chemical suppression of a genetic mutation in a zebrafish model of aortic coarctation. Nat. Biotechnol. 22, 595–599 (2004)CrossRef
39.
Zurück zum Zitat Hong, C.C., Peterson, Q.P., Hong, J.Y., Peterson, R.T.: Artery/vein specification is governed by opposing phosphatidylinositol-3 kinase and MAP kinase/ERK signaling. Curr. Biol. 16, 1366–1372 (2006)CrossRef Hong, C.C., Peterson, Q.P., Hong, J.Y., Peterson, R.T.: Artery/vein specification is governed by opposing phosphatidylinositol-3 kinase and MAP kinase/ERK signaling. Curr. Biol. 16, 1366–1372 (2006)CrossRef
40.
Zurück zum Zitat Lawson, N.D., Mugford, J.W., Diamond, B.A., Weinstein, B.M.: phospholipase C gamma-1 is required downstream of vascular endothelial growth factor during arterial development. Genes Dev. 17, 1346–1351 (2003)CrossRef Lawson, N.D., Mugford, J.W., Diamond, B.A., Weinstein, B.M.: phospholipase C gamma-1 is required downstream of vascular endothelial growth factor during arterial development. Genes Dev. 17, 1346–1351 (2003)CrossRef
41.
Zurück zum Zitat Takahashi, T., Shibuya, M.: The 230 kDa mature form of KDR/Flk-1 (VEGF receptor-2) activates the PLC-gamma pathway and partially induces mitotic signals in NIH3T3 fibroblasts. Oncogene 14, 2079–2089 (1997)CrossRef Takahashi, T., Shibuya, M.: The 230 kDa mature form of KDR/Flk-1 (VEGF receptor-2) activates the PLC-gamma pathway and partially induces mitotic signals in NIH3T3 fibroblasts. Oncogene 14, 2079–2089 (1997)CrossRef
42.
Zurück zum Zitat Liu, Z.J., Shirakawa, T., Li, Y., Soma, A., Oka, M., Dotto, G.P., Fairman, R.M., Velazquez, O.C., Herlyn, M.: Regulation of Notch1 and Dll4 by vascular endothelial growth factor in arterial endothelial cells: implications for modulating arteriogenesis and angiogenesis. Mol. Cell. Biol. 23, 14–25 (2003)CrossRef Liu, Z.J., Shirakawa, T., Li, Y., Soma, A., Oka, M., Dotto, G.P., Fairman, R.M., Velazquez, O.C., Herlyn, M.: Regulation of Notch1 and Dll4 by vascular endothelial growth factor in arterial endothelial cells: implications for modulating arteriogenesis and angiogenesis. Mol. Cell. Biol. 23, 14–25 (2003)CrossRef
43.
Zurück zum Zitat Liu, Z.J., Xiao, M., Balint, K., Soma, A., Pinnix, C.C., Capobianco, A.J., Velazquez, O.C., Herlyn, M.: Inhibition of endothelial cell proliferation by Notch1 signaling is mediated by repressing MAPK and PI3K/Akt pathways and requires MAML1. FASEB. J. 20, 1009–1011 (2006)CrossRef Liu, Z.J., Xiao, M., Balint, K., Soma, A., Pinnix, C.C., Capobianco, A.J., Velazquez, O.C., Herlyn, M.: Inhibition of endothelial cell proliferation by Notch1 signaling is mediated by repressing MAPK and PI3K/Akt pathways and requires MAML1. FASEB. J. 20, 1009–1011 (2006)CrossRef
44.
Zurück zum Zitat Seo, S., Fujita, H., Nakano, A., Kang, M., Duarte, A., Kume, T.: The forkhead transcription factors, Foxc1 and Foxc2, are required for arterial specification and lymphatic sprouting during vascular development. Dev. Biol. 294, 458–470 (2006)CrossRef Seo, S., Fujita, H., Nakano, A., Kang, M., Duarte, A., Kume, T.: The forkhead transcription factors, Foxc1 and Foxc2, are required for arterial specification and lymphatic sprouting during vascular development. Dev. Biol. 294, 458–470 (2006)CrossRef
45.
Zurück zum Zitat Kume, T., Jiang, H., Topczewska, J.M., Hogan, B.L.: The murine winged helix transcription factors, Foxc1 and Foxc2, are both required for cardiovascular development and somitogenesis. Genes Dev. 15, 2470–2482 (2001)CrossRef Kume, T., Jiang, H., Topczewska, J.M., Hogan, B.L.: The murine winged helix transcription factors, Foxc1 and Foxc2, are both required for cardiovascular development and somitogenesis. Genes Dev. 15, 2470–2482 (2001)CrossRef
46.
Zurück zum Zitat Thurston, G., Yancopoulos, G.D.: Gridlock in the blood. Nature 414, 163–164 (2001)CrossRef Thurston, G., Yancopoulos, G.D.: Gridlock in the blood. Nature 414, 163–164 (2001)CrossRef
47.
Zurück zum Zitat You, L.R., Lin, F.J., Lee, C.T., DeMayo, F.J., Tsai, M.J., Tsai, S.Y.: Suppression of Notch signalling by the COUP-TFII transcription factor regulates vein identity. Nature 435, 98–104 (2005)CrossRef You, L.R., Lin, F.J., Lee, C.T., DeMayo, F.J., Tsai, M.J., Tsai, S.Y.: Suppression of Notch signalling by the COUP-TFII transcription factor regulates vein identity. Nature 435, 98–104 (2005)CrossRef
48.
Zurück zum Zitat Krishnan, V., Elberg, G., Tsai, M.J., Tsai, S.Y.: Identification of a novel sonic hedgehog response element in the chicken ovalbumin upstream promoter-transcription factor II promoter. Mol. Endocrinol. 11, 1458–1466 (1997) Krishnan, V., Elberg, G., Tsai, M.J., Tsai, S.Y.: Identification of a novel sonic hedgehog response element in the chicken ovalbumin upstream promoter-transcription factor II promoter. Mol. Endocrinol. 11, 1458–1466 (1997)
49.
Zurück zum Zitat Devic, E., Rizzoti, K., Bodin, S., Knibiehler, B., Audigier, Y.: Amino acid sequence and embryonic expression of msr/apj, the mouse homolog of Xenopus X-msr and human APJ. Mech. Dev. 84, 199–203 (1999)CrossRef Devic, E., Rizzoti, K., Bodin, S., Knibiehler, B., Audigier, Y.: Amino acid sequence and embryonic expression of msr/apj, the mouse homolog of Xenopus X-msr and human APJ. Mech. Dev. 84, 199–203 (1999)CrossRef
50.
Zurück zum Zitat Saint-Geniez, M., Argence, C.B., Knibiehler, B., Audigier, Y.: The msr/apj gene encoding the apelin receptor is an early and specific marker of the venous phenotype in the retinal vasculature. Gene Expr. Patterns 3, 467–472 (2003)CrossRef Saint-Geniez, M., Argence, C.B., Knibiehler, B., Audigier, Y.: The msr/apj gene encoding the apelin receptor is an early and specific marker of the venous phenotype in the retinal vasculature. Gene Expr. Patterns 3, 467–472 (2003)CrossRef
51.
Zurück zum Zitat Cox, C.M., D’Agostino, S.L., Miller, M.K., Heimark, R.L., Krieg, P.A.: Apelin, the ligand for the endothelial G-protein-coupled receptor, APJ, is a potent angiogenic factor required for normal vascular development of the frog embryo. Dev. Biol. 296, 177–189 (2006)CrossRef Cox, C.M., D’Agostino, S.L., Miller, M.K., Heimark, R.L., Krieg, P.A.: Apelin, the ligand for the endothelial G-protein-coupled receptor, APJ, is a potent angiogenic factor required for normal vascular development of the frog embryo. Dev. Biol. 296, 177–189 (2006)CrossRef
52.
Zurück zum Zitat Ishida, J., Hashimoto, T., Hashimoto, Y., Nishiwaki, S., Iguchi, T., Harada, S., Sugaya, T., Matsuzaki, H., Yamamoto, R., Shiota, N., et al.: Regulatory roles for APJ, a seven-transmembrane receptor related to angiotensin-type 1 receptor in blood pressure in vivo. J. Biol. Chem. 279, 26274–26279 (2004)CrossRef Ishida, J., Hashimoto, T., Hashimoto, Y., Nishiwaki, S., Iguchi, T., Harada, S., Sugaya, T., Matsuzaki, H., Yamamoto, R., Shiota, N., et al.: Regulatory roles for APJ, a seven-transmembrane receptor related to angiotensin-type 1 receptor in blood pressure in vivo. J. Biol. Chem. 279, 26274–26279 (2004)CrossRef
53.
Zurück zum Zitat Cermenati, S., Moleri, S., Cimbro, S., Corti, P., Del Giacco, L., Amodeo, R., Dejana, E., Koopman, P., Cotelli, F., Beltrame, M.: Sox18 and Sox7 play redundant roles in vascular development. Blood 111, 2657–2666 (2008)CrossRef Cermenati, S., Moleri, S., Cimbro, S., Corti, P., Del Giacco, L., Amodeo, R., Dejana, E., Koopman, P., Cotelli, F., Beltrame, M.: Sox18 and Sox7 play redundant roles in vascular development. Blood 111, 2657–2666 (2008)CrossRef
54.
Zurück zum Zitat Herpers, R., van de Kamp, E., Duckers, H.J., Schulte-Merker, S.: Redundant roles for sox7 and sox18 in arteriovenous specification in zebrafish. Circ. Res. 102, 12–15 (2008)CrossRef Herpers, R., van de Kamp, E., Duckers, H.J., Schulte-Merker, S.: Redundant roles for sox7 and sox18 in arteriovenous specification in zebrafish. Circ. Res. 102, 12–15 (2008)CrossRef
55.
Zurück zum Zitat Pendeville, H., Winandy, M., Manfroid, I., Nivelles, O., Motte, P., Pasque, V., Peers, B., Struman, I., Martial, J.A., Voz, M.L.: Zebrafish Sox7 and Sox18 function together to control arterial-venous identity. Dev. Biol. 317, 405–416 (2008)CrossRef Pendeville, H., Winandy, M., Manfroid, I., Nivelles, O., Motte, P., Pasque, V., Peers, B., Struman, I., Martial, J.A., Voz, M.L.: Zebrafish Sox7 and Sox18 function together to control arterial-venous identity. Dev. Biol. 317, 405–416 (2008)CrossRef
56.
Zurück zum Zitat Chun, C.Z., Kaur, S., Samant, G.V., Wang, L., Pramanik, K., Garnaas, M.K., Li, K., Field, L., Mukhopadhyay, D., Ramchandran, R.: Snrk-1 is involved in multiple steps of angioblast development and acts via notch signaling pathway in artery-vein specification in vertebrates. Blood 113, 1192–1199 (2009)CrossRef Chun, C.Z., Kaur, S., Samant, G.V., Wang, L., Pramanik, K., Garnaas, M.K., Li, K., Field, L., Mukhopadhyay, D., Ramchandran, R.: Snrk-1 is involved in multiple steps of angioblast development and acts via notch signaling pathway in artery-vein specification in vertebrates. Blood 113, 1192–1199 (2009)CrossRef
57.
Zurück zum Zitat Nicoli, S., Tobia, C., Gualandi, L., De Sena, G., Presta, M.: Calcitonin receptor-like receptor guides arterial differentiation in zebrafish. Blood 111, 4965–4972 (2008)CrossRef Nicoli, S., Tobia, C., Gualandi, L., De Sena, G., Presta, M.: Calcitonin receptor-like receptor guides arterial differentiation in zebrafish. Blood 111, 4965–4972 (2008)CrossRef
58.
Zurück zum Zitat Loughna, S., Sato, T.N.: A combinatorial role of angiopoietin-1 and orphan receptor TIE1 pathways in establishing vascular polarity during angiogenesis. Mol. Cell 7, 233–239 (2001)CrossRef Loughna, S., Sato, T.N.: A combinatorial role of angiopoietin-1 and orphan receptor TIE1 pathways in establishing vascular polarity during angiogenesis. Mol. Cell 7, 233–239 (2001)CrossRef
59.
Zurück zum Zitat Sato, T.N., Loughna, S., Davis, E.C., Visconti, R.P., Richardson, C.D.: Selective functions of angiopoietins and vascular endothelial growth factor on blood vessels: the concept of “vascular domain”. Cold Spring Harb. Symp. Quant. Biol. 67, 171–180 (2002)CrossRef Sato, T.N., Loughna, S., Davis, E.C., Visconti, R.P., Richardson, C.D.: Selective functions of angiopoietins and vascular endothelial growth factor on blood vessels: the concept of “vascular domain”. Cold Spring Harb. Symp. Quant. Biol. 67, 171–180 (2002)CrossRef
60.
Zurück zum Zitat Yancopoulos, G.D., Klagsbrun, M., Folkman, J.: Vasculogenesis, angiogenesis, and growth factors: ephrins enter the fray at the border. Cell 93, 661–664 (1998)CrossRef Yancopoulos, G.D., Klagsbrun, M., Folkman, J.: Vasculogenesis, angiogenesis, and growth factors: ephrins enter the fray at the border. Cell 93, 661–664 (1998)CrossRef
Metadaten
Titel
Mechanical and Chemical Regulation of Arterial and Venous Specification
verfasst von
Thomas N. Sato
Copyright-Jahr
2013
Verlag
Springer Berlin Heidelberg
DOI
https://doi.org/10.1007/978-3-642-30856-7_1

Neuer Inhalt