The Space of Disse: The Liver Hub in Health and Disease

Since it was first described by the German anatomist and histologist, Joseph Hugo Vincenz Disse, the structure and functions of the space of Disse, a thin perisinusoidal area between the endothelial cells and hepatocytes filled with blood plasma, have acquired great importance in liver disease. The...

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Detalles Bibliográficos
Autores: Sanz García, Carlos, Fernández Iglesias, Anabel, Gracia Sancho, Jordi, Arráez Aybar, Luis Alfonso, Nevzorova, Yulia, Cubero Palero, Francisco Javier
Tipo de recurso: artículo
Fecha de publicación:2021
País:España
Institución:Universidad Complutense de Madrid (UCM)
Repositorio:Docta Complutense
Idioma:inglés
OAI Identifier:oai:docta.ucm.es:20.500.14352/7354
Acceso en línea:https://hdl.handle.net/20.500.14352/7354
Access Level:acceso abierto
Palabra clave:616.3
612.017
Chronic liver disease
Hepatic stellate cells (HSCs)
Liver sinusoidal endothelial cells (LSECs)
Fibrosis
Kupffer cells (KCs)
Extracellular matrix (ECM)
Medicina
Gastroenterología y hepatología
Inmunología
32 Ciencias Médicas
3205.03 Gastroenterología
2412 Inmunología
Descripción
Sumario:Since it was first described by the German anatomist and histologist, Joseph Hugo Vincenz Disse, the structure and functions of the space of Disse, a thin perisinusoidal area between the endothelial cells and hepatocytes filled with blood plasma, have acquired great importance in liver disease. The space of Disse is home for the hepatic stellate cells (HSCs), the major fibrogenic players in the liver. Quiescent HSCs (qHSCs) store vitamin A, and upon activation they lose their retinol reservoir and become activated. Activated HSCs (aHSCs) are responsible for secretion of extracellular matrix (ECM) into the space of Disse. This early event in hepatic injury is accompanied by loss of the pores—known as fenestrations—of the endothelial cells, triggering loss of balance between the blood flow and the hepatocyte, and underlies the link between fibrosis and organ dysfunction. If the imbalance persists, the expansion of the fibrotic scar followed by the vascularized septae leads to cirrhosis and/or end-stage hepatocellular carcinoma (HCC). Thus, researchers have been focused on finding therapeutic targets that reduce fibrosis. The space of Disse provides the perfect microenvironment for the stem cells niche in the liver and the interchange of nutrients between cells. In the present review article, we focused on the space of Disse, its components and its leading role in liver disease development.