Immunofluorescence of Cell-Cell and Cell-Extracellular Matrix Adhesive Defects in In Vitro Endothelial CCM Model: Juxtacrine Role of Mutant Extracellular Matrix on Wild-Type Endothelial Cells.
Adherens Junctions
/ metabolism
Animals
Biomarkers
Cell Adhesion
Cell Communication
Cytoskeleton
/ metabolism
Endothelial Cells
/ metabolism
Endothelium, Vascular
/ metabolism
Extracellular Matrix
/ metabolism
Fluorescent Antibody Technique
Focal Adhesions
/ metabolism
Hemangioma, Cavernous, Central Nervous System
/ etiology
Human Umbilical Vein Endothelial Cells
Humans
Intercellular Junctions
/ metabolism
Mechanotransduction, Cellular
Models, Biological
Actomyosin cytoskeleton
Adherens junctions
CCM
Contractility
Extracellular matrix
Focal adhesion
Integrins
Mechanotransduction
VE-cadherin
Journal
Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969
Informations de publication
Date de publication:
2020
2020
Historique:
entrez:
12
6
2020
pubmed:
12
6
2020
medline:
13
3
2021
Statut:
ppublish
Résumé
Endothelial cells lining cerebral cavernous malformations (CCM) present strong adhesive and mechanical defects. Increased cell contractility is a driver to the onset and the expansion of the CCM lesions. 2D in vitro endothelial models have been developed from either endothelial cells isolated from ccm1-3 knock-out mice or CCM1-3-silenced primary endothelial cells. These in vitro models faithfully recapitulate the adhesive and contractile defects of the CCM-deficient endothelial cells such as increased cell-extracellular matrix (ECM) adhesion through β1 integrin-anchored actin stress fibers, abnormal remodeling of the ECM, and destabilized VE-cadherin-dependent cell-cell junctions. Using such 2D in vitro CCM models, we have shown that the ECM remodeled by CCM-depleted endothelial cells can propagate CCM-like adhesive defects to wild-type endothelial cells, a process potentially pertinent to CCM lesion expansion. Here, we detail methods for studying the morphology of focal adhesions, actomyosin cytoskeleton, and VE-cadherin-dependent Adherens junctions by immunofluorescence and morphometric analyses. Moreover, we detail the protocols to produce and purify remodeled ECM and to test its effect on endothelial cell adhesion.
Identifiants
pubmed: 32524568
doi: 10.1007/978-1-0716-0640-7_29
doi:
Substances chimiques
Biomarkers
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM