Emilin1 Links TGF-β Maturation to Blood Pressure Homeostasis

TGF-β proteins are main regulators of blood vessel development and maintenance. Here, we report an unprecedented link between TGF-β signaling and arterial hypertension based on the analysis of mice mutant for Emilin1, a cysteine-rich secreted glycoprotein expressed in the vascular tree. Emilin1 knoc...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cell 2006-03, Vol.124 (5), p.929-942
Hauptverfasser: Zacchigna, Luca, Vecchione, Carmine, Notte, Antonella, Cordenonsi, Michelangelo, Dupont, Sirio, Maretto, Silvia, Cifelli, Giuseppe, Ferrari, Alessandra, Maffei, Angelo, Fabbro, Carla, Braghetta, Paola, Marino, Gennaro, Selvetella, Giulio, Aretini, Alessandra, Colonnese, Claudio, Bettarini, Umberto, Russo, Giovanni, Soligo, Sandra, Adorno, Maddalena, Bonaldo, Paolo, Volpin, Dino, Piccolo, Stefano, Lembo, Giuseppe, Bressan, Giorgio M.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:TGF-β proteins are main regulators of blood vessel development and maintenance. Here, we report an unprecedented link between TGF-β signaling and arterial hypertension based on the analysis of mice mutant for Emilin1, a cysteine-rich secreted glycoprotein expressed in the vascular tree. Emilin1 knockout animals display increased blood pressure, increased peripheral vascular resistance, and reduced vessel size. Mechanistically, we found that Emilin1 inhibits TGF-β signaling by binding specifically to the proTGF-β precursor and preventing its maturation by furin convertases in the extracellular space. In support of these findings, genetic inactivation of Emilin1 causes increased TGF-β signaling in the vascular wall. Strikingly, high blood pressure observed in Emilin1 mutants is rescued to normal levels upon inactivation of a single TGF-β1 allele. This study highlights the importance of modulation of TGF-β availability in the pathogenesis of hypertension.
ISSN:0092-8674
1097-4172
DOI:10.1016/j.cell.2005.12.035