Endothelial Msx1 transduces hemodynamic changes into an arteriogenic remodeling response

Autor: Michel Koole, Jan Schrooten, Aernout Luttun, Xabier L. Aranguren, Frederik Maes, Nick van Gastel, Ine Vandersmissen, Sander Craps, Lieve Umans, Giulia Coppiello, Geert Carmeliet, Olivier Gheysens, Maarten Depypere, Elizabeth A. V. Jones, Roland Devlieger, An Zwijsen
Jazyk: angličtina
Rok vydání: 2015
Předmět:
MSX1 Transcription Factor/genetics
Endothelium
Knockout
Endothelium
Vascular/cytology

Intercellular Adhesion Molecule-1
Vascular Cell Adhesion Molecule-1
Smad Proteins
Hemodynamics/physiology
Vascular Remodeling
Biology
Vascular Cell Adhesion Molecule-1/genetics
Bone morphogenetic protein
Article
Muscle
Smooth
Vascular

Bone Morphogenetic Proteins/genetics
Proinflammatory cytokine
Mice
medicine
Animals
Smad Proteins/genetics
Mechanotransduction
Research Articles
Intercellular Adhesion Molecule-1/genetics
MSX1 Transcription Factor
Mice
Knockout

Vascular Remodeling/physiology
Signal Transduction/physiology
Cell adhesion molecule
Hemodynamics
Cell Biology
Vascular/cytology
Cell biology
stomatognathic diseases
medicine.anatomical_structure
PSI_MIC
Muscle
Smooth
Vascular/cytology

Bone Morphogenetic Proteins
Knockout mouse
Immunology
Muscle
Endothelium
Vascular

Smooth
Signal transduction
Signal Transduction
Zdroj: The Journal of Cell Biology
Journal of Cell Biology, 210(7), 1239-56. Rockefeller University Press
ISSN: 0021-9525
Popis: During peripheral arterial disease, MSX1 acts downstream of BMP–SMAD signaling to transduce the arterial shear stimulus into an arteriogenic remodeling response. MSX1 activates collateral endothelium into a proinflammatory state through ICAM1/VCAM1 up-regulation, resulting in increased leukocyte infiltration and collateral remodeling.
Collateral remodeling is critical for blood flow restoration in peripheral arterial disease and is triggered by increasing fluid shear stress in preexisting collateral arteries. So far, no arterial-specific mediators of this mechanotransduction response have been identified. We show that muscle segment homeobox 1 (MSX1) acts exclusively in collateral arterial endothelium to transduce the extrinsic shear stimulus into an arteriogenic remodeling response. MSX1 was specifically up-regulated in remodeling collateral arteries. MSX1 induction in collateral endothelial cells (ECs) was shear stress driven and downstream of canonical bone morphogenetic protein–SMAD signaling. Flow recovery and collateral remodeling were significantly blunted in EC-specific Msx1/2 knockout mice. Mechanistically, MSX1 linked the arterial shear stimulus to arteriogenic remodeling by activating the endothelial but not medial layer to a proinflammatory state because EC but not smooth muscle cellMsx1/2 knockout mice had reduced leukocyte recruitment to remodeling collateral arteries. This reduced leukocyte infiltration in EC Msx1/2 knockout mice originated from decreased levels of intercellular adhesion molecule 1 (ICAM1)/vascular cell adhesion molecule 1 (VCAM1), whose expression was also in vitro driven by promoter binding of MSX1.
Databáze: OpenAIRE