Regulation of the endothelial barrier function: a filum granum of cellular forces, Rho-GTPase signaling and microenvironment
Abstract
Although the endothelium is an extremely thin single-cell layer, it performs exceedingly well in preventing blood fluids from leaking into the surrounding tissues. However, specific pathological conditions can affect this cell layer, compromising the integrity of the barrier. Vascular leakage is a hallmark of many cardiovascular diseases and despite its medical importance, no specialized therapies are available to prevent it or reduce it. Small guanosine triphosphatases (GTPases) of the Rho family are known to be key regulators of various aspects of cell behavior and studies have shown that they can exert both positive and negative effects on endothelial barrier integrity. Moreover, extracellular matrix stiffness has now been implicated in the regulation of Rho-GTPase signaling, which has a direct impact on the integrity of endothelial junctions. However, knowledge about both the precise mechanism of this regulation and the individual contribution of the specific regulatory proteins remains fragmentary. In this review, we discuss recent findings concerning the balanced activities of Rho-GTPases and, in particular, aspects of the regulation of the endothelial barrier. We highlight the role of Rho-GTPases in the intimate relationships between biomechanical forces, microenvironmental influences and endothelial intercellular junctions, which are all interwoven in a beautiful filigree-like fashion.
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Small GTPases of the Rho family and MLCK stimulate remodeling of the cortical actin cytoskeleton into contractile actin stress fibers, generating cellular tension after inflammatory stimulation.
“Small GTPases of the Rho family and myosin light chain (MLC) kinase (MLCK) also stimulate remodeling of the cortical actin cytoskeleton of stable endothelial monolayers into contractile actin stress fibers, generating cellular tension after inflammatory stimulation (4).”
From Targeting β1-integrin inhibits vascular leakage in endotoxemia (2018) · cites this paper as [4]
These inflammatory agents activate signals that converge on common downstream pathways, including dismantling of VE-cadherin from EC-EC junctions.
“These inflammatory agents activate signals that converge on common downstream pathways, including dismantling of vascular endothelial (VE)-cadherin (Cadherin 5, CDH5) from EC–EC junctions (4, 5).”
From Targeting β1-integrin inhibits vascular leakage in endotoxemia (2018) · cites this paper as [4]
Proinflammatory cytokines, microbial components such as LPS, thrombin, and VEGF induce endothelial permeability by binding to their cognate receptors on ECs.
“Proinflammatory cytokines, microbial components such as lipopolysaccharide (LPS), thrombin, and vascular endothelial growth factor (VEGF) induce endothelial permeability by binding to their cognate receptors on ECs.”
From Targeting β1-integrin inhibits vascular leakage in endotoxemia (2018) · cites this paper as [4]
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References 237 · Cited by 36
- Authors
- Amado-Azevedo, J., Valent, E. T., & Van Nieuw Amerongen, G. P.
- Affiliations
- Amsterdam Cardiovascular Sciences (NL)
- ORCID
- Valent, Erik T.
- Venue
- Cell and Tissue Research
- Published
- 2014-03
- Volume
- 355
- Issue
- 3
- Pages
- 557-576
- ISSN
- 0302-766X (ISSN-L)
- 1432-0878
- OpenAlex
- W2012278629
- Cited by
- 36
- References
- 237
- Citations by year
- 2026: 1 · 2023: 1 · 2022: 4 · 2021: 2 · 2020: 3 · 2019: 2 · 2018: 6 · 2017: 5 · 2016: 6 · 2015: 4 · 2014: 2
- FWCI
- 0.57
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Cell and Tissue Research (publishedVersion)
- PubMed (publishedVersion)
- Pure Amsterdam UMC (publishedVersion)
- Amsterdam UMC (VU Amsterdam) - Institutional Repository (publishedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
- Life Sciences › Neuroscience › Neurology › Barrier Structure and Function Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Keywords
- endothelial barrier function, Rho GTPases, vascular leakage, extracellular matrix stiffness, endothelial cell mechanics, endothelial junctions, microenvironment, biomechanical forces, cardiovascular disease
- MeSH terms
- Animals, Capillary Permeability, Endothelium, Vascular, Humans, Signal Transduction, rho GTP-Binding Proteins, Endothelial Cells
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