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Genes regulating lymphangiogenesis control venous valve formation and maintenance in mice
Eleni Bazigou, … , Nigel A. Brown, Taija Makinen
Eleni Bazigou, … , Nigel A. Brown, Taija Makinen
Published July 18, 2011
Citation Information: J Clin Invest. 2011;121(8):2984-2992. https://doi.org/10.1172/JCI58050.
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Research Article Vascular biology

Genes regulating lymphangiogenesis control venous valve formation and maintenance in mice

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Abstract

Chronic venous disease and venous hypertension are common consequences of valve insufficiency, yet the molecular mechanisms regulating the formation and maintenance of venous valves have not been studied. Here, we provide what we believe to be the first description of venous valve morphogenesis and identify signaling pathways required for the process. The initial stages of valve development were found to involve induction of ephrin-B2, a key marker of arterial identity, by venous endothelial cells. Intriguingly, developing and mature venous valves also expressed a repertoire of proteins, including prospero-related homeobox 1 (Prox1), Vegfr3, and integrin-α9, previously characterized as specific and critical regulators of lymphangiogenesis. Using global and venous valve–selective knockout mice, we further demonstrate the requirement of ephrin-B2 and integrin-α9 signaling for the development and maintenance of venous valves. Our findings therefore identified molecular regulators of venous valve development and maintenance and highlighted the involvement of common morphogenetic processes and signaling pathways in controlling valve formation in veins and lymphatic vessels. Unexpectedly, we found that venous valve endothelial cells closely resemble lymphatic (valve) endothelia at the molecular level, suggesting plasticity in the ability of a terminally differentiated endothelial cell to take on a different phenotypic identity.

Authors

Eleni Bazigou, Oliver T.A. Lyons, Alberto Smith, Graham E. Venn, Celia Cope, Nigel A. Brown, Taija Makinen

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Figure 3

Unique molecular identity of venous valve endothelial cells.

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Unique molecular identity of venous valve endothelial cells.
(A–L) Immun...
(A–L) Immunofluorescence staining of murine venous valves using antibodies against integrin-α9 (A, B, D, E, and G), Prox1 (D, F, J, and K), and Fn-EIIIA (G and H) at the indicated stages. Visualization of ephrin-B2 and Vegfr3 expression was achieved using reporter mice expressing nuclear GFP (Efnb2GFP; A, C, J, and K) or β-gal (Vegfr3lacZ; I and L), respectively. (K) Higher-magnification view of the boxed region in J. Note high expression of Prox1 in ephrin-B2–negative cells on the free edges of valve leaflets (asterisk). (I and L) Vegfr3lacZ reporter activity was present in developing (I) but not in adult (L; asterisk) valves. Arrows denote an adjacent lymphatic vessel; dotted lines outline the iliac vein. (M and N) Immunostaining of adult human venous valve using antibodies against PROX1. (N) Higher-magnification view of the boxed region in M. Arrow denotes a Prox1-positive (dark blue) endothelial cell on the free edge of the valve leaflet; arrowhead denotes a cell on the wall of the vein. Scale bars: 50 μm (A–J and L); 20 μm (K and N); 100 μm (M).

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ISSN: 0021-9738 (print), 1558-8238 (online)

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