Cited by 1,047Liver physiology and pathologyLiver Disease and TransplantationOrgan Transplantation Techniques and Outcomes

Liver sinusoidal endothelial cells: Physiology and role in liver diseases

Poisson, Johanne, Lemoinne, Sara, Boulanger, Chantal, Durand, François, Moreau, Richard, Valla, Dominique, Rautou, Pierre-Emmanuel·2017·Journal of Hepatology

Abstract

Liver sinusoidal endothelial cells (LSECs) are highly specialized endothelial cells representing the interface between blood cells on the one side and hepatocytes and hepatic stellate cells on the other side. LSECs represent a permeable barrier. Indeed, the association of 'fenestrae', absence of diaphragm and lack of basement membrane make them the most permeable endothelial cells of the mammalian body. They also have the highest endocytosis capacity of human cells. In physiological conditions, LSECs regulate hepatic vascular tone contributing to the maintenance of a low portal pressure despite the major changes in hepatic blood flow occurring during digestion. LSECs maintain hepatic stellate cell quiescence, thus inhibiting intrahepatic vasoconstriction and fibrosis development. In pathological conditions, LSECs play a key role in the initiation and progression of chronic liver diseases. Indeed, they become capillarized and lose their protective properties, and they promote angiogenesis and vasoconstriction. LSECs are implicated in liver regeneration following acute liver injury or partial hepatectomy since they renew from LSECs and/or LSEC progenitors, they sense changes in shear stress resulting from surgery, and they interact with platelets and inflammatory cells. LSECs also play a role in hepatocellular carcinoma development and progression, in ageing, and in liver lesions related to inflammation and infection. This review also presents a detailed analysis of the technic…

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Registry

Crossref · 10.1016/j.jhep.2016.07.009

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4 of 4 references verified0 citation errors · 0 not checkable

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  • Excessive shear stress can lead to damage of liver sinusoidal endothelial cells and haemorrhagic necrosis.

    “However, studies have also demonstrated that excessive shear stress can lead to damage of liver sinusoidal endothelial cells (LSECs) and haemorrhagic necrosis[42].”
  • Excessive increases in portal pressure beyond approximately 20 mmHg, such as after 90% hepatectomy, are associated with liver sinusoidal endothelial damage, hemorrhagic necrosis, and post-hepatectomy liver failure.

    “excessive increases beyond approximately 20 mmHg, such as after 90% hepatectomy, are associated with liver sinusoidal endothelial damage, hemorrhagic necrosis, and post-hepatectomy liver failure (PHLF).”
  • Sinusoidal dysfunction, including defenestration and HSC activation, precedes scar formation and liver fibrosis.

    “Sinusoidal dysfunction, including defenestration and HSC activation, precedes scar formation and liver fibrosis”

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Authors
Poisson, J., Lemoinne, S., Boulanger, C., Durand, F., Moreau, R., Valla, D., & Rautou, P.-E.
Affiliations
Inserm (FR)
Corresponding author
Rautou, Pierre-Emmanuel
Venue
Journal of Hepatology
Publisher
Elsevier BV
Published
2017-01
Volume
66
Issue
1
Pages
212-227
ISSN
0168-8278 (ISSN-L)
OpenAlex
W2470906679
Cited by
1,047
References
4
Citations by year
2026: 116 · 2025: 133 · 2024: 143 · 2023: 116 · 2022: 119 · 2021: 142 · 2020: 122 · 2019: 64 · 2018: 70 · 2017: 19 · 2015: 1 · 2014: 1
FWCI
6.36
Type
journal article
Language
en
Open access
closed
Locations
  • Journal of Hepatology (publishedVersion)
  • PubMed (publishedVersion)
  • HAL (submittedVersion)
Funders
  • Agence Nationale pour la Recherche (ANR-14-CE12-0011, ANR-14-CE35-0022)
  • Association Francaise pour l’Etude du foie (AFEF 2014)
  • poste d’accueil INSERM
Topics
  • Health Sciences › Medicine › Hepatology › Liver physiology and pathology
  • Health Sciences › Medicine › Hepatology › Liver Disease and Transplantation
  • Health Sciences › Medicine › Surgery › Organ Transplantation Techniques and Outcomes
Keywords
liver sinusoidal endothelial cells, fenestrated endothelium, endothelial permeability, portal pressure, liver fibrosis, chronic liver disease, liver regeneration, shear stress, platelet interaction, hepatocellular carcinoma, aging, liver inflammation, transgenic mouse model
MeSH terms
Humans, Liver Diseases, Hepatocytes

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