Cargando…

Prominent Receptors of Liver Sinusoidal Endothelial Cells in Liver Homeostasis and Disease

Liver sinusoidal endothelial cells (LSECs) are the most abundant non-parenchymal cells lining the sinusoidal capillaries of the hepatic system. LSECs are characterized with numerous fenestrae and lack basement membrane as well as a diaphragm. These unique morphological characteristics of LSECs makes...

Descripción completa

Detalles Bibliográficos
Autores principales: Pandey, Ekta, Nour, Aiah S., Harris, Edward N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7396565/
https://www.ncbi.nlm.nih.gov/pubmed/32848838
http://dx.doi.org/10.3389/fphys.2020.00873
_version_ 1783565611356389376
author Pandey, Ekta
Nour, Aiah S.
Harris, Edward N.
author_facet Pandey, Ekta
Nour, Aiah S.
Harris, Edward N.
author_sort Pandey, Ekta
collection PubMed
description Liver sinusoidal endothelial cells (LSECs) are the most abundant non-parenchymal cells lining the sinusoidal capillaries of the hepatic system. LSECs are characterized with numerous fenestrae and lack basement membrane as well as a diaphragm. These unique morphological characteristics of LSECs makes them the most permeable endothelial cells of the mammalian vasculature and aid in regulating flow of macromolecules and small lipid-based structures between sinusoidal blood and parenchymal cells. LSECs have a very high endocytic capacity aided by scavenger receptors (SR), such as SR-A, SR-B (SR-B1 and CD-36), SR-E (Lox-1 and mannose receptors), and SR-H (Stabilins). Other high-affinity receptors for mediating endocytosis include the FcγRIIb, which assist in the antibody-mediated removal of immune complexes. Complemented with intense lysosomal activity, LSECs play a vital role in the uptake and degradation of many blood borne waste macromolecules and small (<280 nm) colloids. Currently, seven Toll-like receptors have been investigated in LSECs, which are involved in the recognition and clearance of pathogen-associated molecular pattern (PAMPs) as well as damage associated molecular pattern (DAMP). Along with other SRs, LSECs play an essential role in maintaining lipid homeostasis with the low-density lipoprotein receptor-related protein-1 (LRP-1), in juxtaposition with hepatocytes. LSECs co-express two surface lectins called L-Specific Intercellular adhesion molecule-3 Grabbing Non-integrin Receptor (L-SIGN) and liver sinusoidal endothelial cell lectin (LSECtin). LSECs also express several adhesion molecules which are involved in the recruitment of leukocytes at the site of inflammation. Here, we review these cell surface receptors as well as other components expressed by LSECs and their functions in the maintenance of liver homeostasis. We further discuss receptor expression and activity and dysregulation associated with the initiation and progression of many liver diseases, such as hepatocellular carcinoma, liver fibrosis, and cirrhosis, alcoholic and non-alcoholic fatty liver diseases and pseudocapillarization with aging.
format Online
Article
Text
id pubmed-7396565
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-73965652020-08-25 Prominent Receptors of Liver Sinusoidal Endothelial Cells in Liver Homeostasis and Disease Pandey, Ekta Nour, Aiah S. Harris, Edward N. Front Physiol Physiology Liver sinusoidal endothelial cells (LSECs) are the most abundant non-parenchymal cells lining the sinusoidal capillaries of the hepatic system. LSECs are characterized with numerous fenestrae and lack basement membrane as well as a diaphragm. These unique morphological characteristics of LSECs makes them the most permeable endothelial cells of the mammalian vasculature and aid in regulating flow of macromolecules and small lipid-based structures between sinusoidal blood and parenchymal cells. LSECs have a very high endocytic capacity aided by scavenger receptors (SR), such as SR-A, SR-B (SR-B1 and CD-36), SR-E (Lox-1 and mannose receptors), and SR-H (Stabilins). Other high-affinity receptors for mediating endocytosis include the FcγRIIb, which assist in the antibody-mediated removal of immune complexes. Complemented with intense lysosomal activity, LSECs play a vital role in the uptake and degradation of many blood borne waste macromolecules and small (<280 nm) colloids. Currently, seven Toll-like receptors have been investigated in LSECs, which are involved in the recognition and clearance of pathogen-associated molecular pattern (PAMPs) as well as damage associated molecular pattern (DAMP). Along with other SRs, LSECs play an essential role in maintaining lipid homeostasis with the low-density lipoprotein receptor-related protein-1 (LRP-1), in juxtaposition with hepatocytes. LSECs co-express two surface lectins called L-Specific Intercellular adhesion molecule-3 Grabbing Non-integrin Receptor (L-SIGN) and liver sinusoidal endothelial cell lectin (LSECtin). LSECs also express several adhesion molecules which are involved in the recruitment of leukocytes at the site of inflammation. Here, we review these cell surface receptors as well as other components expressed by LSECs and their functions in the maintenance of liver homeostasis. We further discuss receptor expression and activity and dysregulation associated with the initiation and progression of many liver diseases, such as hepatocellular carcinoma, liver fibrosis, and cirrhosis, alcoholic and non-alcoholic fatty liver diseases and pseudocapillarization with aging. Frontiers Media S.A. 2020-07-21 /pmc/articles/PMC7396565/ /pubmed/32848838 http://dx.doi.org/10.3389/fphys.2020.00873 Text en Copyright © 2020 Pandey, Nour and Harris. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Pandey, Ekta
Nour, Aiah S.
Harris, Edward N.
Prominent Receptors of Liver Sinusoidal Endothelial Cells in Liver Homeostasis and Disease
title Prominent Receptors of Liver Sinusoidal Endothelial Cells in Liver Homeostasis and Disease
title_full Prominent Receptors of Liver Sinusoidal Endothelial Cells in Liver Homeostasis and Disease
title_fullStr Prominent Receptors of Liver Sinusoidal Endothelial Cells in Liver Homeostasis and Disease
title_full_unstemmed Prominent Receptors of Liver Sinusoidal Endothelial Cells in Liver Homeostasis and Disease
title_short Prominent Receptors of Liver Sinusoidal Endothelial Cells in Liver Homeostasis and Disease
title_sort prominent receptors of liver sinusoidal endothelial cells in liver homeostasis and disease
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7396565/
https://www.ncbi.nlm.nih.gov/pubmed/32848838
http://dx.doi.org/10.3389/fphys.2020.00873
work_keys_str_mv AT pandeyekta prominentreceptorsofliversinusoidalendothelialcellsinliverhomeostasisanddisease
AT nouraiahs prominentreceptorsofliversinusoidalendothelialcellsinliverhomeostasisanddisease
AT harrisedwardn prominentreceptorsofliversinusoidalendothelialcellsinliverhomeostasisanddisease