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Published in: Angiogenesis 2/2009

Open Access 01-06-2009 | Review Paper

Molecular differentiation and specialization of vascular beds

Authors: Susana F. Rocha, Ralf H. Adams

Published in: Angiogenesis | Issue 2/2009

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Abstract

Transport in the large and complex bodies of vertebrate organisms is mediated by extensive and highly branched tubular networks that are formed by endothelial cells. Blood vessels are responsible for systemic circulation, while the lymphatic vasculature drains extravasated plasma, proteins, particles, and cells from the interstitium. Endothelial cells of blood vessels and lymphatic vessels can be distinguished by the expression of certain molecular markers, which accompany or even contribute to functional and morphological differences. Even within the blood vessel network, some molecules and pathways selectively mark the endothelium of arteries, veins and capillaries and are thought to contribute to the differentiation of these vessels. Moreover, microvessels can acquire organ-specific specialization in response to local tissue-derived signals. This review summarizes molecular markers and pathways that are specifically expressed in the endothelium of certain vascular beds and vessel types. Special attention will be given to known functional roles in the morphogenesis of these vessels.
Literature
3.
go back to reference Adams RH et al (1999) Roles of ephrinB ligands and EphB receptors in cardiovascular development: demarcation of arterial/venous domains, vascular morphogenesis, and sprouting angiogenesis. Genes Dev 13:295–306. doi:10.1101/gad.13.3.295 PubMedCrossRef Adams RH et al (1999) Roles of ephrinB ligands and EphB receptors in cardiovascular development: demarcation of arterial/venous domains, vascular morphogenesis, and sprouting angiogenesis. Genes Dev 13:295–306. doi:10.​1101/​gad.​13.​3.​295 PubMedCrossRef
4.
go back to reference Bastide B et al (1993) Gap junction protein connexin40 is preferentially expressed in vascular endothelium and conductive bundles of rat myocardium and is increased under hypertensive conditions. Circ Res 73:1138–1149PubMed Bastide B et al (1993) Gap junction protein connexin40 is preferentially expressed in vascular endothelium and conductive bundles of rat myocardium and is increased under hypertensive conditions. Circ Res 73:1138–1149PubMed
6.
go back to reference Bruzzone R et al (1993) Connexin40, a component of gap junctions in vascular endothelium, is restricted in its ability to interact with other connexins. Mol Biol Cell 4:7–20PubMed Bruzzone R et al (1993) Connexin40, a component of gap junctions in vascular endothelium, is restricted in its ability to interact with other connexins. Mol Biol Cell 4:7–20PubMed
7.
go back to reference Shutter JR et al (2000) Dll4, a novel Notch ligand expressed in arterial endothelium. Genes Dev 14:1313–1318PubMed Shutter JR et al (2000) Dll4, a novel Notch ligand expressed in arterial endothelium. Genes Dev 14:1313–1318PubMed
12.
go back to reference Martyn U, Schulte-Merker S (2004) Zebrafish neuropilins are differentially expressed and interact with vascular endothelial growth factor during embryonic vascular development. Dev Dyn 231:33–42. doi:10.1002/dvdy.20048 PubMedCrossRef Martyn U, Schulte-Merker S (2004) Zebrafish neuropilins are differentially expressed and interact with vascular endothelial growth factor during embryonic vascular development. Dev Dyn 231:33–42. doi:10.​1002/​dvdy.​20048 PubMedCrossRef
13.
go back to reference Moyon D et al (2001) Plasticity of endothelial cells during arterial–venous differentiation in the avian embryo. Development 128:3359–3370PubMed Moyon D et al (2001) Plasticity of endothelial cells during arterial–venous differentiation in the avian embryo. Development 128:3359–3370PubMed
14.
go back to reference Yuan L et al (2002) Abnormal lymphatic vessel development in neuropilin 2 mutant mice. Development 129:4797–4806PubMed Yuan L et al (2002) Abnormal lymphatic vessel development in neuropilin 2 mutant mice. Development 129:4797–4806PubMed
17.
go back to reference Lawson ND et al (2001) Notch signaling is required for arterial–venous differentiation during embryonic vascular development. Development 128:3675–3683PubMed Lawson ND et al (2001) Notch signaling is required for arterial–venous differentiation during embryonic vascular development. Development 128:3675–3683PubMed
23.
go back to reference Benjamin LE et al (1998) A plasticity window for blood vessel remodelling is defined by pericyte coverage of the preformed endothelial network and is regulated by PDGF-B and VEGF. Development 125:1591–1598PubMed Benjamin LE et al (1998) A plasticity window for blood vessel remodelling is defined by pericyte coverage of the preformed endothelial network and is regulated by PDGF-B and VEGF. Development 125:1591–1598PubMed
30.
go back to reference Kurpinski K et al (2006) Regulation of vascular smooth muscle cells and mesenchymal stem cells by mechanical strain. Mol Cell Biomech 3:21–34PubMed Kurpinski K et al (2006) Regulation of vascular smooth muscle cells and mesenchymal stem cells by mechanical strain. Mol Cell Biomech 3:21–34PubMed
42.
go back to reference Dickson MC et al (1995) Defective haematopoiesis and vasculogenesis in transforming growth factor-beta 1 knock out mice. Development 121:1845–1854PubMed Dickson MC et al (1995) Defective haematopoiesis and vasculogenesis in transforming growth factor-beta 1 knock out mice. Development 121:1845–1854PubMed
53.
go back to reference Jia H et al (2004) Vascular endothelial growth factor (VEGF)-D and VEGF-A differentially regulate KDR-mediated signaling and biological function in vascular endothelial cells. J Biol Chem 279:36148–36157. doi:10.1074/jbc.M401538200 PubMedCrossRef Jia H et al (2004) Vascular endothelial growth factor (VEGF)-D and VEGF-A differentially regulate KDR-mediated signaling and biological function in vascular endothelial cells. J Biol Chem 279:36148–36157. doi:10.​1074/​jbc.​M401538200 PubMedCrossRef
56.
58.
go back to reference Kawasaki T et al (1999) A requirement for neuropilin-1 in embryonic vessel formation. Development 126:4895–4902PubMed Kawasaki T et al (1999) A requirement for neuropilin-1 in embryonic vessel formation. Development 126:4895–4902PubMed
68.
go back to reference Krebs LT et al (2000) Notch signaling is essential for vascular morphogenesis in mice. Genes Dev 14:1343–1352PubMed Krebs LT et al (2000) Notch signaling is essential for vascular morphogenesis in mice. Genes Dev 14:1343–1352PubMed
70.
83.
go back to reference Roberts WG, Palade GE (1995) Increased microvascular permeability and endothelial fenestration induced by vascular endothelial growth factor. J Cell Sci 108(Pt 6):2369–2379PubMed Roberts WG, Palade GE (1995) Increased microvascular permeability and endothelial fenestration induced by vascular endothelial growth factor. J Cell Sci 108(Pt 6):2369–2379PubMed
89.
go back to reference Inai T et al (2004) Inhibition of vascular endothelial growth factor (VEGF) signaling in cancer causes loss of endothelial fenestrations, regression of tumor vessels, and appearance of basement membrane ghosts. Am J Pathol 165:35–52PubMed Inai T et al (2004) Inhibition of vascular endothelial growth factor (VEGF) signaling in cancer causes loss of endothelial fenestrations, regression of tumor vessels, and appearance of basement membrane ghosts. Am J Pathol 165:35–52PubMed
91.
go back to reference Wallow IH, Geldner PS (1980) Endothelial fenestrae in proliferative diabetic retinopathy. Invest Ophthalmol Vis Sci 19:1176–1183PubMed Wallow IH, Geldner PS (1980) Endothelial fenestrae in proliferative diabetic retinopathy. Invest Ophthalmol Vis Sci 19:1176–1183PubMed
92.
93.
go back to reference Roberts WG et al (1998) Host microvasculature influence on tumor vascular morphology and endothelial gene expression. Am J Pathol 153:1239–1248PubMed Roberts WG et al (1998) Host microvasculature influence on tumor vascular morphology and endothelial gene expression. Am J Pathol 153:1239–1248PubMed
102.
go back to reference Breiteneder-Geleff S et al (1999) Angiosarcomas express mixed endothelial phenotypes of blood and lymphatic capillaries: podoplanin as a specific marker for lymphatic endothelium. Am J Pathol 154:385–394PubMed Breiteneder-Geleff S et al (1999) Angiosarcomas express mixed endothelial phenotypes of blood and lymphatic capillaries: podoplanin as a specific marker for lymphatic endothelium. Am J Pathol 154:385–394PubMed
106.
go back to reference Irrthum A et al (2003) Mutations in the transcription factor gene SOX18 underlie recessive and dominant forms of hypotrichosis-lymphedema-telangiectasia. Am J Hum Genet 72:1470–1478. doi:10.1086/375614 PubMedCrossRef Irrthum A et al (2003) Mutations in the transcription factor gene SOX18 underlie recessive and dominant forms of hypotrichosis-lymphedema-telangiectasia. Am J Hum Genet 72:1470–1478. doi:10.​1086/​375614 PubMedCrossRef
Metadata
Title
Molecular differentiation and specialization of vascular beds
Authors
Susana F. Rocha
Ralf H. Adams
Publication date
01-06-2009
Publisher
Springer Netherlands
Published in
Angiogenesis / Issue 2/2009
Print ISSN: 0969-6970
Electronic ISSN: 1573-7209
DOI
https://doi.org/10.1007/s10456-009-9132-x

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