Background: Endothelial cell junctions control blood vessel permeability. Altered permeability can be associated with vascular fragility that leads to vessel weakness and haemorrhage formation. In vivo studies on the function of genes involved in the maintenance of vascular integrity are essential to better understand the molecular basis of diseases linked to permeability defects. Ve-ptp (Vascular Endothelial-Protein Tyrosine Phosphatase) is a transmembrane protein present at endothelial adherens junctions (AJs). Methodology/Principal Findings: We investigated the role of Ve-ptp in AJ maturation/stability and in the modulation of endothelial permeability using zebrafish (Danio rerio). Whole-mount in situ hybridizations revealed zve-ptp expression exclusively in the developing vascular system. Generation of altered zve-ptp transcripts, induced separately by two different splicing morpholinos, resulted in permeability defects closely linked to vascular wall fragility. The ultrastructural analysis revealed a statistically significant reduction of junction complexes and the presence of immature AJs in zve-ptp morphants but not in control embryos. Conclusions/Significance: Here we show the first in vivo evidence of a potentially critical role played by Ve-ptp in AJ maturation, an important event for permeability modulation and for the development of a functional vascular system.

Ve-ptp modulates vascular integrity by promoting adherens junction maturation / S. Carra, E. Foglia, S. Cermenati, E. Bresciani, C. Giampietro, C. Lora Lamia Donin, E. Dejana, M. Beltrame, F. Cotelli. - In: PLOS ONE. - ISSN 1932-6203. - 7:12(2012), pp. e51245.1-e51245.12. [10.1371/journal.pone.0051245]

Ve-ptp modulates vascular integrity by promoting adherens junction maturation

S. Carra;E. Foglia;S. Cermenati;C. Giampietro;C. Lora Lamia Donin;E. Dejana;M. Beltrame;F. Cotelli
2012

Abstract

Background: Endothelial cell junctions control blood vessel permeability. Altered permeability can be associated with vascular fragility that leads to vessel weakness and haemorrhage formation. In vivo studies on the function of genes involved in the maintenance of vascular integrity are essential to better understand the molecular basis of diseases linked to permeability defects. Ve-ptp (Vascular Endothelial-Protein Tyrosine Phosphatase) is a transmembrane protein present at endothelial adherens junctions (AJs). Methodology/Principal Findings: We investigated the role of Ve-ptp in AJ maturation/stability and in the modulation of endothelial permeability using zebrafish (Danio rerio). Whole-mount in situ hybridizations revealed zve-ptp expression exclusively in the developing vascular system. Generation of altered zve-ptp transcripts, induced separately by two different splicing morpholinos, resulted in permeability defects closely linked to vascular wall fragility. The ultrastructural analysis revealed a statistically significant reduction of junction complexes and the presence of immature AJs in zve-ptp morphants but not in control embryos. Conclusions/Significance: Here we show the first in vivo evidence of a potentially critical role played by Ve-ptp in AJ maturation, an important event for permeability modulation and for the development of a functional vascular system.
endothelial cell junction; vascular permeability; endothelium; ve-ptp; protein-tyrosine-phosphatase; blood-vessel development; cell-cell adhesion; molecular-organization; paracellular pathway; endothelial-cells; in-vivo; phosphorylation; zebrafish; cadherin
Settore MED/04 - Patologia Generale
Settore BIO/06 - Anatomia Comparata e Citologia
Settore BIO/18 - Genetica
Settore BIO/11 - Biologia Molecolare
2012
Article (author)
File in questo prodotto:
File Dimensione Formato  
journal.pone.0051245.pdf

accesso aperto

Tipologia: Publisher's version/PDF
Dimensione 879.9 kB
Formato Adobe PDF
879.9 kB Adobe PDF Visualizza/Apri
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/233034
Citazioni
  • ???jsp.display-item.citation.pmc??? 9
  • Scopus 16
  • ???jsp.display-item.citation.isi??? 13
social impact