Lyons, O;
Saha, P;
Seet, C;
Kuchta, A;
Arnold, A;
Grover, S;
Rashbrook, V;
Sabine, A;
Vizcay-Barrena, G;
Patel, A;
et al.
Lyons, O; Saha, P; Seet, C; Kuchta, A; Arnold, A; Grover, S; Rashbrook, V; Sabine, A; Vizcay-Barrena, G; Patel, A; Ludwinski, F; Padayachee, S; Kume, T; Kwak, BR; Brice, G; Mansour, S; Ostergaard, P; Mortimer, P; Jeffery, S; Brown, N; Makinen, T; Petrova, TV; Modarai, B; Smith, A
(2017)
Human venous valve disease caused by mutations in FOXC2 and GJC2.
Journal of Experimental Medicine, 214 (8).
pp. 2437-2452.
ISSN 1540-9538
https://doi.org/10.1084/jem.20160875
SGUL Authors: Ostergaard, Pia
|
PDF
Published Version
Available under License Creative Commons Attribution Non-commercial Share Alike. Download (3MB) | Preview |
|
|
PDF
Accepted Version
Available under License Creative Commons Attribution Non-commercial Share Alike. Download (887kB) | Preview |
Abstract
Venous valves (VVs) prevent venous hypertension and ulceration. We report that FOXC2 and GJC2 mutations are associated with reduced VV number and length. In mice, early VV formation is marked by elongation and reorientation (“organization”) of Prox1hi endothelial cells by postnatal day 0. The expression of the transcription factors Foxc2 and Nfatc1 and the gap junction proteins Gjc2, Gja1, and Gja4 were temporospatially regulated during this process. Foxc2 and Nfatc1 were coexpressed at P0, and combined Foxc2 deletion with calcineurin-Nfat inhibition disrupted early Prox1hi endothelial organization, suggesting cooperative Foxc2–Nfatc1 patterning of these events. Genetic deletion of Gjc2, Gja4, or Gja1 also disrupted early VV Prox1hi endothelial organization at postnatal day 0, and this likely underlies the VV defects seen in patients with GJC2 mutations. Knockout of Gja4 or Gjc2 resulted in reduced proliferation of Prox1hi valve-forming cells. At later stages of blood flow, Foxc2 and calcineurin-Nfat signaling are each required for growth of the valve leaflets, whereas Foxc2 is not required for VV maintenance.
Item Type: | Article | ||||||||
---|---|---|---|---|---|---|---|---|---|
Additional Information: | © Lyons et al., 2017. Originally published in the Journal of Experimental Medicine. https://doi.org/10.1084/jem.20160875 | ||||||||
Keywords: | Immunology, 11 Medical And Health Sciences | ||||||||
SGUL Research Institute / Research Centre: | Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) > Cell Sciences (INCCCS) |
||||||||
Journal or Publication Title: | Journal of Experimental Medicine | ||||||||
ISSN: | 1540-9538 | ||||||||
Dates: |
|
||||||||
Publisher License: | Creative Commons: Attribution-Noncommercial-Share Alike 4.0 | ||||||||
Projects: |
|
||||||||
URI: | https://openaccess.sgul.ac.uk/id/eprint/108990 | ||||||||
Publisher's version: | https://doi.org/10.1084/jem.20160875 |
Statistics
Actions (login required)
![]() |
Edit Item |